Intervening in Psychosis - A Team Approach

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“Grounded in research but illustrated with clinical experience and the
voice of the consumer, this book brings to life the treatment of first-episode psycho-
sis. The book takes a broad and detailed approach, from policy and public health
to individual and family engagement and treatment. The theme of the book is re-
covery, and the focus on improving outcomes permeates the various chapters. This
book makes a significant contribution to the field of early intervention.”
Intervening Early in PSYCHOSIS

Donald Addington, Professor, Department of Psychiatry, University of Calgary;
Member, Mathison Centre for Mental Health Research and Education
“This book, which is based on a wealth of clinical and research experience, is
A TEAM APPROACH
an invaluable resource for clinicians and agencies who are all working toward early
intervention in psychosis with transitional-age youth. The authors offer a compre-
hensive understanding of all aspects of early intervention, including both young
people who may be at serious risk of developing psychosis and those who are expe-
riencing a first episode. This highly user-friendly text offers case descriptions, step-
by-step instructions for assessments and interventions, and excellent guidelines for
a team-based approach to early intervention for psychosis.”
Jean Addington, Ph.D., Professor of Psychiatry, Cumming School of Medicine,
University of Calgary
With expert guidance on developing specialty care services for young peo-
ple experiencing first-episode psychosis, Intervening Early in Psychosis: A Team
Intervening
Approach offers a multimodal approach that aims for recovery and remission. The
first book of its kind to focus on the U.S. health care environment, it provides a
detailed examination of a range of evidence-based treatments, from the psycho-
Early in
PSYCHOSIS
logical and psychosocial to peer, family, lifestyle, and technological interventions,
all punctuated by clinical case examples.
Special emphasis is placed on the interplay between these individual interventions,
as well as the collaboration between multidisciplinary partners, including licensed
therapists, medical providers, peers, and vocational specialists. An individual and
family perspective on the experience of living with psychosis complements this
interdisciplinary care model, underscoring the importance of engaging clients and
A Team Approach
their support network within a philosophy of shared decision making.
With additional chapters that discuss advocacy issues and policy considerations
when establishing coordinated specialty care services, Intervening Early in Psycho-
sis is the most comprehensive resource available for those interested in expanding
their knowledge of the early identification and treatment of adolescents and young
adults with psychotic disorders. Hardy
Ballon
Noordsy
ISBN 978-1- 61537-175- 4 Adelsheim Edited by
9 0 0 00
Kate V. Hardy, Clin.Psych.D.
Jacob S. Ballon, M.D., M.P.H.
9 7 8 1 6 1 5 3 71 7 5 4 WWW.APPI.ORG Douglas L. Noordsy, M.D.
Cover design: Rick A. Prather
Cover image: © iStock.com Steven Adelsheim, M.D.
Intervening Early in
PSYCHOSIS
A TEAM APPROACH
Intervening Early in
PSYCHOSIS
A TEAM APPROACH
Edited by
Douglas L. Noordsy, M.D.
Steven Adelsheim, M.D.
Note: The authors have worked to ensure that all information in this book is ac-
curate at the time of publication and consistent with general psychiatric and
medical standards, and that information concerning drug dosages, schedules,
and routes of administration is accurate at the time of publication and consis-
tent with standards set by the U.S. Food and Drug Administration and the gen-
eral medical community. As medical research and practice continue to advance,
however, therapeutic standards may change. Moreover, specific situations may
require a specific therapeutic response not included in this book. For these rea-
sons and because human and mechanical errors sometimes occur, we recom-
mend that readers follow the advice of physicians directly involved in their care
or the care of a member of their family.
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Library of Congress Cataloging-in-Publication Data
Names: Hardy, Kate V., editor. | Ballon, Jacob S., editor. | Noordsy, Douglas L.,
1959– editor. | Adelsheim, Steven, editor. | American Psychiatric Association, is-
suing body.
Title: Intervening early in psychosis : a team approach / edited by Kate V. Har-
dy, Jacob S. Ballon, Douglas L. Noordsy, and Steven Adelsheim.
Description: First edition. | Washington, D.C. : American Psychiatric Associa-
tion Publishing, [2019] | Includes bibliographical references and index.
Identifiers: LCCN 2019006911 (print) | LCCN 2019007351 (ebook) | ISBN
9781615372584 (ebook) | ISBN 9781615371754 (pbk. : alk. paper)
Subjects: | MESH: Psychotic Disorders—prevention & control | Early Medical
Intervention | Patient Care Team
Classification: LCC RC512 (ebook) | LCC RC512 (print) | NLM WM 200 | DDC
616.89—dc23
LC record available at https://lccn.loc.gov/2019006911
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Contents
Contributors . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . ix
Foreword . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . xvii
Acknowledgments . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . xix
1 Introduction: EARLY INTERVENTION IN PSYCHOSIS—

BEACHHEAD FOR TRANSFORMATIONAL REFORM IN
MENTAL HEALTH CARE . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1
Patrick D. McGorry, A.O., M.D., Ph.D., FRCP, FRANZCP,
FAA, FAHMS, FASSA
2 Growth of Early Intervention in Psychosis in the

United States . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11
Kate V. Hardy, Clin.Psych.D., Jacob S. Ballon, M.D., M.P.H.,
Douglas L. Noordsy, M.D., and Steven Adelsheim, M.D.
3 Early Detection of Schizophrenia: A POPULATION

HEALTH APPROACH . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .23
Maria Ferrara, M.D., Walter Mathis, M.D.,
John D. Cahill, M.D., Ph.D., Jessica Pollard, Ph.D., and
Vinod H. Srihari, M.D.
4 Early Intervention and Policy . . . . . . . . . . . . . . . . . . . . . . . 45

Abram Rosenblatt, Ph.D., and
Howard H. Goldman, M.D., Ph.D.
5 First-Person Accounts of Psychosis and

Advocacy Work. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 59
Carlos Larrauri, M.S.N., APRN, PMHNP-BC, FNP-BC, and
Chantel Garrett, B.S.
6 Engaging Families and Individuals in Care . . . . . . . . . . .79
Sarah Lynch, LCSW, Rebecca Jaynes, LCPC, and
Nyamuon Nguany Machar
7 Assessment of People in the Early Stages of

Psychosis . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .95
Barbara C. Walsh, Ph.D.
8 Assessment and Targeted Intervention in

Individuals at Clinical High Risk for Psychosis . . . . . . .107
Skylar Kelsven, M.S., and Kristin Cadenhead, M.D.
9 Medical Workup for First-Episode Psychosis . . . . . . . . .133

Agnieszka Kalinowski, M.D., Ph.D., and
10 Assessing and Treating Trauma in Team-Based

Early Psychosis Care. . . . . . . . . . . . . . . . . . . . . . . . . . . . . .151
Rachel L. Loewy, Ph.D., Tara Niendam, Ph.D., and
Paula Wadell, M.D.
11 Intervening Early: A TEAM-BASED APPROACH . . . . . . . . . . . . 171

Iruma Bello, Ph.D., Debra R. Hrouda, Ph.D., and
Lisa Dixon, M.D., M.P.H.
12 Psychopharmacology for People in Early Psychosis . . .187

Jian-Ping Zhang, M.D., Ph.D., and Douglas L. Noordsy, M.D.
13 Psychotherapeutic Interventions for

Early Psychosis . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 211
Kate V. Hardy, Clin.Psy.D., Yulia Landa, Psy.D., M.S.,
Piper Meyer-Kalos, Ph.D., and Kim T. Mueser, Ph.D.
14 Substance Use and Early Psychosis . . . . . . . . . . . . . . . . .241

Jeffrey D. Reed, D.O., and Mary F. Brunette, M.D.
15 Role of Aerobic Exercise in the Treatment of

Early Psychosis . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .265
Luz H. Ospina, Ph.D., Jacob S. Ballon, M.D., M.P.H., and
David Kimhy, Ph.D.
16 Supported Employment and Education for
People in Early Psychosis . . . . . . . . . . . . . . . . . . . . . . . . . 281
Deborah R. Becker, M.Ed., CRC, and
Robert E. Drake, M.D., Ph.D.
17 Implementing Peer Support in Early Psychosis

Programs . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 295
Megan Sage, M.S.W., LCSW, Tamara Sale, M.A.,
Nybelle Caruso, B.S., PSS, Michael Haines, QMHA, PSS,
Ryan Melton, Ph.D., and Ally Linfoot, PSS
18 Family Intervention and Support in Early Psychosis . . 309

Shirley M. Glynn, Ph.D.
19 Suicide Risk, Assessment, and Intervention in

Early Psychosis . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 335
Jill Harkavy-Friedman, Ph.D.
20 Using Technology to Advance Early Psychosis

Intervention . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 349
Benjamin Buck, Ph.D., and Dror Ben-Zeev, Ph.D.
21 Inpatient Care for Early Psychosis:

A RECOVERY-ORIENTED PERSPECTIVE . . . . . . . . . . . . . . . . . . . . . . .365
Zheala Qayyum, M.D., Kristen Sayles, M.S., R.N.,
Hyun Jung Kim, M.D., and Gerrit Van Schalkwyk, M.B., Ch.B.
22 Care for Adolescents on the First-Episode Psychosis

Continuum. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 383
Rhoshel K. Lenroot, M.D., and Tresha A. Gibbs, M.D.
23 Special Populations: College and

University Students . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 403
Kate V. Hardy, Clin.Psych.D., Jacob S. Ballon, M.D., M.P.H.
Mehak Chopra, D.O., and Douglas L. Noordsy, M.D.
Index . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 417
Contributors

Clinical Professor, Department of Psychiatry and Behavioral Sciences,
Stanford University School of Medicine, Stanford, California

Clinical Associate Professor, Department of Psychiatry and Behavioral
Sciences, Stanford University, Stanford, California
Deborah R. Becker, M.Ed., CRC

Senior Research Associate, Westat, Lebanon, New Hampshire
Iruma Bello, Ph.D.

Assistant Professor of Psychology, Department of Psychiatry, New York
State Psychiatric Institute and Columbia University Medical Center,
New York, New York
Dror Ben-Zeev, Ph.D.

Professor, Department of Psychiatry and Behavioral Sciences, Univer-
sity of Washington, Seattle, Washington
Mary F. Brunette, M.D.

Associate Professor of Psychiatry, Geisel School of Medicine, Dart-
mouth College, Hanover, New Hampshire; Medical Director, Bureau of
Behavioral Health, New Hampshire Department of Health and Human
Services, Concord, New Hampshire
Benjamin Buck, Ph.D.

Advanced Fellow, Health Services Research and Development, VA
Puget Sound: Seattle; Senior Fellow, Department of Health Services,
School of Public Health, University of Washington, Seattle, Washington
Kristin Cadenhead, M.D.

Professor of Psychiatry, Department of Psychiatry, University of Cali-
fornia–San Diego, La Jolla, California
ix
x Intervening Early in Psychosis
John D. Cahill, M.D., Ph.D.

Assistant Professor, Department of Psychiatry, Yale University; Medical
Director, Program for Specialized Treatment Early in Psychosis (STEP),
New Haven, Connecticut
Nybelle Caruso, B.S., PSS

Co-chair, EASA Young Adult Leadership Council, Portland, Oregon
Mehak Chopra, D.O.

Student Health and Counseling Services, University of California, San
Francisco, San Francisco, California

Edna L. Edison Professor of Psychiatry, New York State Psychiatric In-
stitute, Columbia University Vagelos College of Physicians and Sur-
geons and New York Presbyterian, New York, New York

Vice President, Westat, Lebanon, New Hampshire
Maria Ferrara, M.D.

Postdoctoral Associate, Department of Psychiatry, Yale University; Re-
search coordinator, Program for Specialized Treatment Early in Psycho-
sis (STEP), New Haven, Connecticut

Founding Director, Strong 365, Rutherford, California
Tresha A. Gibbs, M.D.

Department of Psychiatry, Columbia University College of Physicians
and Surgeons, New York, New York

Research Psychologist, Semel Institute of Neuroscience and Human Be-
havior, UCLA; Clinical Research Psychologist, VA Greater Los Angeles
Healthcare System at West Los Angeles, Los Angeles, California

Professor of Psychiatry, University of Maryland School of Medicine,
Baltimore, Maryland
Michael Haines, QMHA, PSS

Lead Peer Support Specialist, PeaceHealth, Eugene, Oregon
Contributors xi

Clinical Associate Professor, Department of Psychiatry and Behavioral
Sciences, Stanford University, Stanford, California

Vice President of Research, American Foundation for Suicide Preven-
tion, New York, New York
Debra R. Hrouda, Ph.D.

Director of Practice Implementation and Evaluation, Northeast Ohio
Medical University, Rootstown, Ohio
Rebecca Jaynes, LCPC

Clinical Counselor, PIER Program, Maine Medical Center, Portland,
Maine
Agnieszka Kalinowski, M.D., Ph.D.

Clinical Instructor, Department of Psychiatry and Behavioral Sciences,
Stanford University, Stanford, California
Skylar Kelsven, M.S.

Doctoral student, San Diego State University/University of California–
San Diego Joint Doctoral Program in Clinical Psychology, San Diego,
California
Hyun Jung Kim, M.D.

Psychiatrist in Charge, Psychotic Disorders Division, McLean Hospital,
Belmont, Massachusetts; Instructor in Psychiatry, Harvard Medical
School, Cambridge, Massachusetts
David Kimhy, Ph.D.

Associate Professor and Program Leader in New Interventions in
Schizophrenia; Director, Experimental Psychopathology Lab; Depart-
ment of Psychiatry, Icahn School of Medicine at Mount Sinai, New York,
New York; Mental Illness Research, Education and Clinical Center
(MIRECC), James J. Peters VA Medical Center, Bronx, New York
Yulia Landa, Psy.D., M.S.

Assistant Professor and Director, CBT for Psychosis Research and Clin-
ical Program, Department of Psychiatry, Icahn School of Medicine at
Mount Sinai, New York, New York; Director, Advanced Psychology Fel-
lowship Program, Mental Illness Research, Education and Clinical Cen-
ter, VISN 2 South, James J. Peters VA Medical Center, Bronx, New York
xii Intervening Early in Psychosis
Carlos Larrauri, M.S.N., APRN, PMHNP-BC, FNP-BC

Lecturer, School of Nursing and Health Studies, University of Miami,
Miami, Florida
Rhoshel K. Lenroot, M.D.

Department of Psychiatry and Behavioral Sciences, University of New
Mexico, Albuquerque, New Mexico
Ally Linfoot, PSS

Peer Services Coordinator, Clackamas Behavioral Health Services, Ore-
gon City, Oregon
Rachel L. Loewy, Ph.D.

Associate Professor of Psychiatry, University of California, San Fran-
cisco, San Francisco, California
Sarah Lynch, LCSW

Director, PIER Program, Maine Medical Center, Portland, Maine

Peer Support Regional Coordinator, Youth Move Maine, Portland,
Maine
Walter Mathis, M.D.

Assistant Professor, Yale School of Medicine, New Haven, Connecticut
Patrick D. McGorry, A.O., M.D., Ph.D., FRCP, FRANZCP, FAA,

FAHMS, FASSA
Executive Director, Orygen, National Centre of Excellence in Youth
Mental Health; Professor of Youth Mental Health, Centre for Youth
Mental Health, University of Melbourne, Parkville, Victoria, Australia
Ryan Melton, Ph.D.

Clinical Training Director, OHSU-PSU School of Public Health, Port-
land Oregon
Piper Meyer-Kalos, Ph.D.

Executive Director, Minnesota Center for Chemical and Mental Health,
University of Minnesota School of Social Work, St. Paul, Minnesota
Kim T. Mueser, Ph.D.

Professor, Departments of Occupational Therapy, Psychological and
Brain Sciences, and Psychiatry, Boston University, Boston, Massachusetts
Contributors xiii
Tara Niendam, Ph.D.

Associate Professor of Psychiatry, University of California, Davis, Da-
vis, California; Executive Director, UC Davis Early Psychosis Programs
(EDAPT and SacEDAPT Clinics), Sacramento, California

Clinical Professor of Psychiatry and Behavioral Sciences, Stanford Uni-
versity School of Medicine, Stanford, California; Professor of Psychia-
try, Geisel School of Medicine at Dartmouth, Hanover, New Hampshire;
Chief of Mental Health and Behavioral Science Services, Veterans Ad-
ministration Medical Center, White River Junction, Vermont
Luz H. Ospina, Ph.D.

Project Director, Experimental Psychopathology Laboratory, Icahn
School of Medicine at Mount Sinai, New York, New York
Jessica Pollard, Ph.D.

Assistant Professor, Department of Psychiatry, Yale University; Clinical
Director, Program for Specialized Treatment Early in Psychosis (STEP),
Zheala Qayyum, M.D.

Assistant Clinical Professor, Department of Psychiatry, Yale University,
Jeffrey D. Reed, D.O.

Instructor in Psychiatry, Geisel School of Medicine, Dartmouth College,
Hanover, New Hampshire; Staff Psychiatrist, West Central Behavioral
Health, Affiliate of Geisel School of Medicine, Lebanon, New Hamp-
shire
Abram Rosenblatt, Ph.D.

Associate Director, Westat, Rockville, Maryland
Megan Sage, M.S.W., LCSW

Senior Research Associate, OHSU-PSU School of Public Health, Port-
land, Oregon
Tamara Sale, M.A.

Director, EASA Center for Excellence, OHSU-PSU School of Public
Health, Portland, Oregon
xiv Intervening Early in Psychosis
Kristen Sayles, M.S., R.N.

Nurse Manager, Adolescent Unit, Butler Hospital, Providence, Rhode
Island

Associate Professor, Department of Psychiatry, Yale University; Direc-
tor, Program for Specialized Treatment Early in Psychosis (STEP), New
Haven, Connecticut
Gerrit Van Schalkwyk, M.B., Ch.B.

Assistant Professor (Clinician Educator) of Psychiatry and Human Be-
havior, Warren Alpert School of Medicine, Brown University; Unit
Chief, Adolescent Unit, Butler Hospital, Providence, Rhode Island
Paula Wadell, M.D.

Associate Professor of Psychiatry, University of California, Davis, Da-
vis, California; Medical Director, UC Davis Early Psychosis Programs
(EDAPT and SacEDAPT Clinics), Sacramento, California

Clinical Coordinator, PRIME Clinic, Yale University School of Medi-
cine, New Haven, Connecticut
Jian-Ping Zhang, M.D., Ph.D.

Assistant Professor, Early Treatment Program, Department of Psychia-
try, Zucker Hillside Hospital, Northwell Health; [Please provide title],
Department of Psychiatry, Donald and Barbara Zucker School of Medi-
cine at Hofstra/Northwell, Glen Oaks, New York
Disclosure of Interests
The following contributors to this book have indicated a financial inter-
est in or other affiliation with a commercial supporter, a manufacturer
of a commercial product, a provider of a commercial service, a nongov-
ernmental organization, and/or a government agency, as listed below:
Dror Ben-Zeev, Ph.D. Intervention content licensing agreement: Pear

Therapeutics.
Carlos Larrauri, M.S.N., APRN, PMHNP-BC, FNP-BC Consultant:
Alkermes. Proposal review committee: Alkermes Inspiration Grants.
Rachel L. Loewy, Ph.D. Faculty: Lundbeck International Neurosci-
ence Foundation.
Contributors xv
The following contributors have indicated that they have no financial

interests or other affiliations that represent or could appear to represent
a competing interest with the contributions to this book:
Deborah R. Becker, M.Ed., CRC; Iruma Bello, Ph.D.; Benjamin Buck, Ph.D.;
John D. Cahill, M.D., Ph.D.; Lisa Dixon, M.D., M.P.H.; Robert E. Drake,
M.D, Ph.D.; Maria Ferrara, M.D.; Chantel Garrett, B.S.; Tresha A. Gibbs,
M.D.; Howard H. Goldman, M.D., Ph.D.; Jill Harkavy-Friedman, Ph.D.;
Debra R. Hrouda, Ph.D.; Rebecca Jaynes, LCPC; Agnieszka Kalinowski,
M.D., Ph.D.; Skylar Kelsven, M.S.; Hyun Jung Kim, M.D.; David Kimhy,
Ph.D.; Rhoshel K. Lenroot, M.D.; Ally Linfoot, PSS; Sarah Lynch, LCSW;
Nyamuon Nguany Machar; Walther Mathis, M.D.; Ryan Melton, Ph.D.;
Tara Niendam, Ph.D.; Luz H. Ospina, Ph.D.; Jessica Pollard, Ph.D.; Zheala
Qayyum, M.D.; Jeffrey D. Reed, D.O.; Abram Rosenblatt, Ph.D.; Megan
Sage, M.S.W., LCSW; Kristen Sayles, M.S., R.N.; Vinod H. Srihari, M.D.;
Gerrit Van Schalkwyk, M.B., Ch.B.; Paula Wadell, M.D.; Jian-Ping Zhang,
M.D., Ph.D.
Foreword
THE past three decades have witnessed an exponential growth of early

intervention services for people with psychosis around the globe. Early
intervention has moved from research-driven clinical studies to having
a significant impact on mental health service reform, with large-scale
clinical implementation in many countries. This growth has not been
without its challenges. The concept of early intervention to improve
long-term outcomes in physical health has been common practice in
medicine for many years, but early intervention in mental health has
faced fierce resistance. This resistance strengthened the resolve of many
early intervention clinicians and researchers to join forces across disci-
plines and to reach out to young people with psychosis and their families
and caregivers to build a strong evidence base for early intervention. This
approach has been very fruitful and has been the platform for policy
changes and service reform. The debate has shifted away from disput-
ing the concept of early intervention in psychosis, and pessimism re-
garding long-term outcome of young people who experience psychosis
has been replaced by guarded optimism.
As early intervention is becoming more established, we still face a
number of important challenges. In the United States, recent funding
has been dedicated to the expansion of early psychosis care across the
country, but in many other countries, service provision and implemen-
tation is still patchy and poorly funded. More research is needed to bet-
ter understand the mechanisms that trigger the onset of psychosis as
well as the contextual and individual factors that help build resilience
and enhance recovery. It is time to further increase the participatory na-
ture of our work and implement peer support in services. There is a
need for personalized treatments that consider the personal history,
strengths, and weaknesses of young people with psychosis and their
families and that enable these youth to benefit from evidence-based
treatments. In order to increase access to services, we need to investi-
gate the effectiveness of new technologies in delivering interventions.
These topics, and the early intervention ethos of interdisciplinary col-
xvii
xviii Intervening Early in Psychosis
laboration, are reflected in the content of this volume. This book will
prove useful to anyone who is a policy maker, who is active clinically in
early intervention, who studies or researches psychosis, who teaches
about mental health, or who has experienced psychosis or cares for
someone who has experienced psychosis.
Lucia Valmaggia, Ph.D., M.Sc., B.Sc.

President, IEPA–Early Intervention in Mental Health and Reader in Clinical
Psychology and Digital Mental Health, Institute of Psychiatry, Psychology
and Neuroscience, King’s College London, London, UK
Acknowledgments
THIS book is dedicated to the many clients and families who have
taught us about the transformative power of living well with, and recov-
ery from, psychosis. We are also indebted to the many chapter authors for
their gracious contributions. This book could not have happened without
the intellectual stimulation within our clinic group and the support of
many fine colleagues, including Nichole Olson, Agnes Kalinowski, Katie
Eisen, and Justin Cheng of the INSPIRE clinic team. We owe the greatest
debt of gratitude to Laura Roberts, both for her vision and leadership in
forming the INSPIRE clinic and for her encouragement to create this
much-needed book. Laura has long insisted that academic departments
have a responsibility to be fully engaged with, and to demonstrate lead-
ership in, addressing the pressing problems of our time, including devel-
oping and demonstrating optimal care models for people most in need,
such as those at risk for and facing early psychosis.
We each have specific people in our lives to thank for their professional
and personal support in guiding us toward the creation of this book:
I have been very fortunate to have benefited greatly from expert guid-
ance, mentoring, and collaboration with numerous exceptional individ-
uals in the field and extend my heartfelt thanks to Moggie McGowan,
Anthony Morrison, Paul French, Ali Brabban, David Kingdon, Douglas
Turkington, Rory Byrne, Richard Bentall, Rachel Loewy, Tamara Sale,
Robert Heinssen, Kim Mueser, and David Shern. It has been a privilege
to work with my coeditors, both on this book and in our clinic. Each of
them brings a deep commitment and passion for working with individ-
uals experiencing psychosis. I am humbled to learn from the many pro-
viders with whom I have had the privilege to work in community
settings, who inspired the focus of this book, and who embody the
ethos of a team approach in early psychosis intervention. In addition, I
want to thank Bethan Reading, who taught me early on the importance
of resilience, unwavering compassion, and always emphasizing the po-
tential for recovery. On a personal note, I want to thank my parents, Rita
xix
xx Intervening Early in Psychosis
and David Hardy, for their unerring support across two continents, my
husband, Jon, for his endless patience and encouragement, and my son,
Theo, for all the joy he brings.
K.V.H.
I wish to thank my first mentors in psychiatry, Steve Marder and Donna

Ames, who provided me, as an undergraduate student in their research
clinic, inspiration in thinking that care for people meant more than fix-
ing symptoms. Their work in understanding the importance of treating
the whole person pushed important ground for the field and laid a key
foundation for the direction of my career. I am grateful for the mentor-
ing and for the encouragement to take risks in my career that I had
during my training at Stanford from Alan Schatzberg and Jennifer Ho-
blyn. I am also grateful for the mentorship of Jeffrey Lieberman, Scott
Stroup, and Fred Jarskog, who further helped me define my voice
within the academic community. I am very lucky to have the support
and encouragement of my wife, Alana, in pursuing my goals and push-
ing me to see the world from multiple perspectives. Last, I dedicate my
work in this area to my mom, Debbie, a dedicated psychiatric nurse, for
providing my earliest inspiration and showing me through her passion
the joy it is to work with people who have experienced psychosis.
J.S.B.
I am grateful to Bob Drake, Fred Osher, Kim Mueser, Tom Fox, Lindy Fox
Smith, Chris O’Keefe ,and many others for showing me the value of multi-
disciplinary, team-based, recovery-oriented care at a formative stage in my
career. Their approach to engagement, mutual respect, and shared decision
making have guided care for people with psychosis throughout my career.
I am also grateful to Alan Green for entrusting me with a study of medica-
tion treatment for people in early psychosis and to Laura Roberts for creat-
ing the opportunity for me to join the INSPIRE clinic team. Finally, and most
importantly, I am grateful to my dear wife, Mary, my beautiful children,
Charlotte and Jack, and my loving family for inspiring me to strive for ex-
cellence and patiently tolerating the many hours dedicated to this volume.
D.L.N.
My professional thanks go to wonderful colleagues who provide critical

education, guidance, patience, and support in educating me about the
world of clinical high risk and early psychosis, allowing me to become in-
volved in this critical effort. Thank you to Jane Lowe, Bill McFarlane,
Donna Downing, Sarah Lynch, Gary Blau, Bob Heinssen, Susan Azrin,
David Shern, John Kane, Delbert Robinson, Margaret Migliorati, Melina
Salvador, David Graeber, Lisa Dixon, Tamara Sale, Ryan Melton, Cam-
eron Carter, Rachel Loewy, Tara Niendam, Kate Hardy, Pat McGorry,
and Laura Roberts. On a personal note, I want to thank my parents,
Acknowledgments xxi
Marcia and Richard Adelsheim, for their lifelong support and my wife,
Tara Ford, who is my daily role model and guide as I strive to hold com-
passion in all of my interactions. Thank you all!
S.A.
Resources:
https://med.stanford.edu/psychiatry/patient_care/inspire.html
https://med.stanford.edu/peppnet.html
CHAPTER
1
Introduction
EARLY INTERVENTION IN PSYCHOSIS—
BEACHHEAD FOR TRANSFORMATIONAL
REFORM IN MENTAL HEALTH CARE
Patrick D. McGorry, A.O., M.D., Ph.D., FRCP, FRANZCP,
FAA, FAHMS, FASSA
The Challenge
Even in high-income countries, only a small minority of people with
mental illness obtain access to evidence-based care in a timely way and
in cultures of care that are welcoming and effective. The human and
economic consequences of this global neglect are enormous (Bloom et
al., 2011), especially because mental disorders begin largely in young
people on the threshold of productive life, and the damage extends
across decades of adult life (Insel and Fenton 2005). Therefore, the op-
portunity to save lives, restore and safeguard futures, and strengthen
the global economy is correspondingly huge (The Economist 2014). The
evidence-based reform of early intervention in psychosis, pioneered
around the world for the last two to three decades, represents a blue-
print and launch pad for dissolving the barriers that have constrained
effective mental health care for so long, paves the way for early inter-
vention across the full spectrum of disorders affecting young people,
and fundamentally strengthens societies across the globe.
1
2 Intervening Early in Psychosis
Optimism in mental health care has always been in short supply.

Mental disorders have been hidden from public gaze, permeated by
fear, discrimination, and maltreatment. Even today most people fail to
realize how common and treatable these illnesses actually are. This is
due to a toxic mix of flawed concepts, prejudice, learned helplessness
within professional groups, and funding neglect. Nowhere is this better
illustrated than in the phenomenon of dementia praecox, later schizo-
phrenia, which was deliberately associated conceptually by Emil Krae-
pelin and his contemporaries with an essentially hopeless future. This
was a serious conceptual and strategic mistake, one that has still to be
corrected, and the corrosive pessimism it reinforced was to sabotage the
care of people with psychosis for over a century. There have been chal-
lenges to this orthodoxy, but it is particularly tenacious, sustained as it
has been by deep and pervasive neglect of those with mental illness,
which in turn has reinforced the “clinician’s illusion” that the prognosis
is much worse than it truly is (Cohen and Cohen 1984).
The facts soon began to get in the way of the Kraepelinian paradigm,
with recovery proving more possible than had been allowed (Bleuler et
al. 1976). However, even the advent of effective antipsychotic drugs, de-
veloped in the 1950s, and the rise of community psychiatry failed to dis-
pel this pessimism. It was not until the 1980s that focus turned to the
early stages of psychotic illness and the notion of early diagnosis would
become a realistic proposition. Initially, this was driven by a research
agenda, which correctly proposed that studying individuals with first-
episode psychosis free of the many confounding variables that were
present in chronic and multi-episode samples would shed more light on
etiological questions. At the outset it was unforeseen that this research
agenda, which led to the establishment of streamed, or discrete, early
psychosis programs in the 1980s and 1990s, would also reveal the clini-
cal imperatives of both viewing psychosis from a harm reduction per-
spective and providing an opportunity for reductions in premature
death and disability and more complete functional recovery.
This was certainly our own experience in Melbourne, Australia,
where in 1984 we established a 10-bed clinical research unit for patients
with first-episode psychosis (Copolov et al. 1989; McGorry 1985). Their
clinical needs were starkly different from those of older multi-episode
patients. These young individuals were typically propelled into the
hospital after a prolonged period of untreated psychosis as a result of a
suicidal or behavioral crisis, usually with police involvement. They
were terrified by their Dickensian surroundings and the confrontation
in the admission ward with an acutely disturbed cohort of much older
chronically mentally ill individuals. Deep pessimism regarding their fu-
ture was communicated to them on every level, directly by psychiatrists
and nursing staff true to the Kraepelinian traditions of the time and sub-
tly reinforced by the compelling, yet illusory, evidence of the chronicity
Introduction 3
of the illness that surrounded them in the form of their older co-patients
(Cohen and Cohen 1984). These acute units were dangerous and fright-
ening places (sadly, even in the general hospital settings of today, they
all too often still are). Not only were their fellow patients disorganized,
frightened, and often aggressive; this was the era of rapid neuroleptiza-
tion, and young, drug-naïve people with first-episode psychosis were
at risk of receiving vastly more medication than they needed to achieve
remission. Their families were equally shattered by these experiences.
The task was simple. First, we had to reduce or prevent the harm
that patients were exposed to by separating them from the longer-term
patients and the toxic messages and treatments that were draining hope
and optimism for the future and then find the minimally effective dose
of antipsychotics that would result in remission with no, or minimal,
side effects. Second, we had to develop and evaluate psychosocial inter-
ventions for both these young people and their families that were truly
relevant for their stage of illness and psychosocial development and
that would promote recovery (McGorry 1992). Third, we had to build
cultures of care that were capable of guaranteeing safe, humane, and ef-
fective care and scale them up to replace the existing system.
An Idea Whose Time Has Come

Growing research interest in first-episode psychosis that had begun at
Northwick Park in London (Crow et al. 1986) and Hillside Hospital in
New York (Kane et al. 1982; Lieberman et al. 1992) and the seminal pa-
per by Richard Wyatt assembling the evidence demonstrating the de-
structive impact of treatment delay (Wyatt 1991) created the context for
the exponential growth not only in early psychosis research but in new
treatments and models of care that were to follow. With the benefit of
hindsight, it is often said of an idea that has spread that “its time had
come.” However, many such ideas fail to flourish and spread. Powerful
ideas must also be actively spread or translated into reality, a process
that requires many additional ingredients other than mere vision, cre-
ativity, or even research evidence. Key among these is the demonstra-
tion that the idea can work in a real-world setting and that it can
subsequently be scaled up in many other locations. Thanks to a phalanx
of inspirational leaders and early adopters around the world, this adap-
tation and scaling-up process gained momentum during the late 1990s
and early 2000s. This reform was powered by a new global community,
the International Early Psychosis Association (IEPA), which has held 11
conferences from 1996 to 2018 to drive research, clinical care, and ser-
vice reform. Another catalyst has been the journal Early Intervention in
Psychiatry, founded in 2007 as the official journal of the IEPA, which has
successfully helped to grow capacity and evidence transdiagnostically

in the early intervention field.
The scientific literature in early psychosis has expanded exponen-
tially over the past 20 years, and many textbooks have appeared as well.
The neurobiology of onset became much better understood, and the ev-
idence base for optimal treatment and culture of care is much stronger.
More than 60 nations are represented at IEPA conferences, and hun-
dreds of early psychosis services, first-episode centers, and clinical
high-risk centers have been developed in many countries. These have
typically been local initiatives, and they vary in terms of fidelity to a
core or optimal model (Table 1–1). However, some nations have scaled
up services more systematically, some even with widespread or full na-
tional coverage. The latter include England, Canada, Denmark, Hong
Kong, Singapore, and Australia.
Although U.S. researchers have played a leading role in first-epi-
sode research (Kirch et al. 1992; Lieberman et al. 1992), especially neu-
robiological research, because of the limitations of the U.S. health care
system, service reform has been piecemeal until recently. Oregon has
been the pioneer in service reform, with a statewide commitment to
early psychosis care for several years based on the Early Assessment
and Support Alliance model (Tamara Sale and colleagues, www.easa-
community.org). The Recovery After an Initial Schizophrenia Episode
(RAISE) Project (Kane et al. 2016) has been a game changer that is cata-
lyzing a nationwide wave of service reform. The National Institute of
Mental Health under the directorship of Dr. Tom Insel and the inspired
and strategic yet unassuming leadership of Dr. Robert Heinssen in as-
sembling and nurturing national early psychosis research collabora-
tions and using the data to leverage new federal funding have been
absolutely crucial in ensuring that early intervention has now been
placed at the apex of U.S. mental health reform.
Resistance to Reform: Genuine

Skeptics or Merchants of Doubt?
Despite this wave of evidence-based reform, progress has been slower
than ideal. When one surveys the landscape of premature death, pre-
ventable suffering, and multiple risks and the blighted lives and the re-
coveries against the odds despite the often harmful, poor quality, and at
best patchy care on offer in most traditional settings for psychotic ill-
ness and contrasts this with the effectiveness and cost-effectiveness of
expert care for early psychosis when it is provided and sustained, one
might wonder why early care has not been scaled up even more rapidly
and why a small cadre of critics, especially in the United Kingdom and
Introduction 5
TABLE 1–1. Core components of a specialized early psychosis

service
Core components can be loosely grouped according to their function within
the service, with certain components operating across the whole model and
others more closely aligned to one of the three key functions of early
detection, acute care, and recovery. This allows for a flexible yet
comprehensive service that is able to respond quickly and appropriately to
the individual needs of the young person and his or her family.
Early detection
1. Community education to improve awareness of young people’s mental
health issues among the general public and those who work closely with
young people
2. Easy access to the service through one clear entry point with a “no wrong
door” policy and guaranteed referral for those who do not meet entry criteria
3. Home-based assessment and care available via a mobile multidisciplinary
team able to provide triage, assessment, crisis intervention, and home-based
acute treatment 24 hours a day, 7 days a week
Acute care
4. Acute phase care delivered in the community by the mobile team or, when
necessary, in a dedicated youth-friendly inpatient unit
5. Access to subacute care for additional support after an acute episode
Continuing care
6. Case management with an individual case manager who provides an
individually tailored treatment approach as well as support with practical
issues
7. Medical interventions, primarily low-dose pharmacotherapy
8. Psychological interventions, including psychoeducation, individual
psychotherapy, and cognitive-behavioral therapy
9. A functional recovery program with an emphasis on returning to full social,
educational, and vocational functioning
10. Group programs to enhance psychosocial and functional recovery; focus
should be on topics of interest to young people, ranging from health-
related issues such as stress management, coping with anxiety, and
reducing drug use to study, school, and work issues, as well as social and
leisure activities such as music, art, and outdoor adventure
11. Family programs and family peer support for the families and friends of
young people with early psychosis
12. Youth participation and peer support for maintaining youth friendliness
and accountability to young people in these services
TABLE 1–1. Core components of a specialized early psychosis

service (continued)
13. Mobile outreach for those young people with complex issues who have
difficulty engaging with services
14. Partnerships with other organizations that can enhance the support for
young people with mental health issues
15. Workforce development to create highly skilled and clinically expert
mental health professionals specializing in youth mental health
16. Ultra-high-risk young people should be treated within a specialized
service, with the aim of minimizing symptoms and distress and
maintaining a normal functional trajectory to prevent further deterioration
in functioning and thus to prevent a first episode of psychosis
Source. Adapted from Hughes et al. 2014.
Australia, has fiercely resisted its advance. Although the safety of

screening and proactive early treatment in cancer and elsewhere has
been debated in a logical fashion, the debates concerning early inter-
vention in psychosis have taken on a more strident and, at times, emo-
tional, even personal, tone (e.g., Frances 2011).
Skepticism and debate are, of course, crucial scientific processes to
guide and safeguard effective reform. However, extreme or excessive
skepticism, especially in relation to a reform with strong face validity
and strong, if incomplete, evidence, should prompt an analysis of mo-
tives because vested interests and ideological groups have been known
to misuse science to undermine valid change and reform (Oreskes and
Conway 2010). The timing of this skepticism appears to coincide with a
shift of momentum from pure research studies to substantial new in-
vestment in early psychosis services. To an extent, this resistance is un-
derstandable in the context of the neglect of the mental health care of
even people with severe and persistent illnesses. Clinicians working in
these underfunded and low-morale cultures of care, barely beyond the
shadows of the asylum, genuinely feel that more must be done to re-
lieve the suffering of their patients and their families, especially when
this neglect is leading to homelessness and the widespread incarcera-
tion of the mentally ill in prisons. These clinicians fear that early inter-
vention will divert scarce, finite, and precious resources from these
neglected patients to notionally less deserving patients, often citing the
experience of the 1960s, when this did, in fact, occur in the United
States.
However, the fundamental fallacy that these well-intentioned, yet
essentially simplistic, emotion-based critiques promote is that this is a
zero-sum game, that substantial growth in funding for mental health
Introduction 7
care is not an achievable goal and that only one focus should be pur-
sued—a classic false dichotomy. Yet, compellingly, the evidence that
early intervention actually saves money in all kinds of ways means that
it is almost certainly part of the solution in relation to better funding for
longer-term care (McCrone et al. 2010; Mihalopoulos et al. 2009). The
notion that individuals with prolonged and severe mental illness
should receive sole priority until their care is truly optimal is part of the
mantra of many critics, yet it is not a principle that has been accepted in
cancer and cardiovascular medicine. In these illnesses, we do not see
the trivialization of the needs of patients in earlier stages or with less se-
vere or persistent forms of illness as the “worried well” or the fanning
of fears of labeling and overtreatment. In cancer, we do not see pallia-
tive care being pitted against early diagnosis. It is important that these
conversations, debates, dilemmas, and choices are faced honestly and
openly in the light of the facts and the evidence and that they are not
buried, distorted, or hijacked by ideologues, vested interests, irrespon-
sible journalists, or even misguided humanitarians. Complex scientific
and sociological forces must be understood within the cycle of innova-
tion and reform.
Next Wave of Reform: Beyond Psychosis

The clinical epidemiology of the onset of mental disorders is more or
less the mirror image of that seen in physical illness, with 75% of mental
and substance use disorders emerging for the first time by age 25. Some
of these disorders, notably neurodevelopmental disorders and some be-
havioral and anxiety disorders, commence in childhood before age 12;
however, the dominant and potentially persistent and disabling mental
and substance use disorders of adult life are a phenomenon of adoles-
cence and emerging adulthood. Until recently, there has been no sense
of urgency to intervene to alter their course and outcome. This obvi-
ously has to change.
A conceptual underpinning of this change is the wider application
of early intervention beyond psychosis to all emerging disorders, par-
ticularly, but not only, in young people. This conceptual framework will
be difficult to progress given the silos present in psychiatric research
and the organization of specialist clinical care. However, buttressed by
more flexible research and diagnostic approaches such as the Research
Domain Criteria (Insel et al. 2010) and clinical staging (McGorry 2007a),
a transdiagnostic focus for early intervention (McGorry and Nelson
2016) sits alongside a new wave of service reforms in youth mental
health in an increasing number of countries (McGorry et al. 2013, 2014).
These reforms aim to create a comprehensive, fully integrated youth
mental health service stream for young people that offers seamless
mental health care from puberty to mature adulthood up to around age

25 years, with soft transitions at either boundary with child and older
adult mental health care. Such a vertically integrated system embraces
the reality of dynamic biopsychosocial development and recognizes the
complexity of the challenges faced by young people as they become in-
dependent adults, as well the burden of disease imposed on this age
group by mental ill health. It responds by blurring the distinctions and
borders between the tiers of primary and specialist care in recognition
of the complexity of the presentation of much of the mental ill health ap-
parent in young people, allowing a flexible and appropriate response
for each individual (McGorry et al. 2013, 2014). A corresponding in-
crease in flexibility and sophistication is required on the diagnostic side
of the endeavor (McGorry and Nelson 2016; Nelson et al. 2017).
The foundations for reform in mental health must be built on the prin-
ciples of demonstrable need, capacity to benefit, and evidence-informed
care, including indicative evidence of value for better health outcomes
and value for money, which, given the timing of morbidity, is likely to
trump almost any other domain of health and social care (McGorry
2007b; McGorry et al. 2011). Youth mental health is emerging as a new
professional field, and more evidence will be created as the field
evolves. However, we can be optimistic here, not least because of the
success of the early psychosis paradigm, which not only has provided
proof of concept for early intervention but has largely driven the cur-
rent transformation of psychiatry toward a more preventive and per-
sonalized focus, analogous to the approach now widespread in physical
medicine. Early intervention, the essential element of preemptive psy-
chiatry, is now being explored across the full diagnostic spectrum, and
this exciting new field promises human, economic, and public health
benefits on a much larger scale than could have been envisioned even a
decade ago.
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CHAPTER
2
Growth of Early Intervention

in Psychosis in the United
States
A Brief History of Early Intervention

in Psychosis
Throughout medicine, it is generally considered the best practice to initi-
ate treatment as early in the course of an illness as possible. The Framing-
ham risk criteria help predict the likelihood of heart disease, and
numerous screening tools, such as colonoscopy or mammography, try
to identify the earliest signs of otherwise occult cancers. In psychiatry,
however, early identification often proves difficult because there are no
definitive tests to identify the precise onset, or definitive at-risk state, to
guide decisions about when to initiate treatment. Concerns over poten-
tially stigmatizing diagnoses further necessitate diagnostic precision at
the onset of symptoms.
Psychiatric diagnosis has certainly evolved over the decades. The
publication of the first Diagnostic and Statistical Manual of Mental Disor-
ders (DSM) in 1952 (American Psychiatric Association 1952) came be-
fore the commercial release of chlorpromazine, the first antipsychotic
medication, and it was written with a psychoanalytic mindset reflective
11
of the time in which it was developed. The third edition of DSM first
brought the concept of diagnostic criteria to the mainstream in 1980
(American Psychiatric Association 1980). It was with DSM-III that a
person could be diagnosed as having schizophrenia if he or she experi-
enced a subset of the listed symptoms, including hallucinations, delu-
sions, and decrease in functioning. The shift to a diagnostic framework
based on observable symptoms marked a change in how and when
treatment was expected to initiate. In concert with the cultural changes,
the onset of the medication era also changed the available modes of
treatment from primarily psychoanalytic to include psychopharmacol-
ogy and other biologically based treatments and heralded the medical
model that became the dominant paradigm for that era.
Notably, it was in the DSM-III that the concept of a prodrome to
schizophrenia was put forth as a formal component of diagnosis. How-
ever, this was not the first time that the concept of a prodrome, or high-
risk state, was first posited. Early work, including that by Chapman
(1966), showed a premorbid increase in symptom severity without
treatment. Notably, it was in this time that it was initially reported that
a longer duration of untreated psychosis (DUP) related to a worsened
prognosis overall.
This recognition about DUP, along with revisions to the diagnostic
classifications of schizophrenia overall, led to a need to better character-
ize the nature of the earliest stages of psychotic illness. Additionally, a
greater emphasis on prevention led to a greater recognition of the puta-
tively prodromal, or clinical high-risk state, and the value of defining
interventions for this population of people with early symptoms of
schizophrenia. McGorry et al. (2006) developed a clinical staging
model, described in the section “Staging Model,” that serves as an effec-
tive framework for marking the stages of development in psychotic ill-
ness. Delineating this model effectively set the stage for a line of
research focused on the earlier phases of illness.
Transitioning From Chronic Care

to Early Intervention
Research on the pathophysiology, diagnosis, and treatment of psycho-
sis has predominantly focused on advanced phases of disease. Promi-
nent psychiatrists who defined schizophrenia spectrum disorders, such
as Emil Kraepelin, Eugen Bleuler, and Kurt Schneider, identified mani-
festations of florid psychosis, including first-rank psychotic symptoms,
catatonia, and cognitive decline. Treatment during the compassionate
care era of the nineteenth and twentieth centuries centered on long-
term hospital-based care communities for people with psychoses. With
the advent of medications and changes in attitudes toward civil rights,
Growth of Early Intervention in Psychosis in the United States 13
there was a shift toward deinstitutionalization beginning in the 1960s.

Over the past 50 years, the effects of moving people out of long-term
hospitals have changed the focus of care for people with severe mental
illness to community-based treatment programs.
Although this change in focus has not come without challenges, peo-
ple with psychosis primarily live immersed in their communities, and
therefore the goal of care had to shift to one that supports individuals with
advanced disease to adapt to life outside a hospital. Unfortunately, the ef-
fects of long-term institutionalization had contributed to beliefs about
schizophrenia as an inevitably disabling disease. Pervasive among pro-
viders were attitudes about the chronicity of schizophrenia and a belief in
the need for paternalistic protection and involuntary treatment. Psychoso-
cial rehabilitation interventions were developed to counter the effects of
institutionalization and negative symptoms on social functioning but
were typically viewed as only partially ameliorative. The pioneering work
of Harding et al. (1987) identified that many people with schizophrenia
go on to achieve remission of psychosis. This work set the stage for
changes in the perceived potential prognosis for people with psychotic
disorders by identifying variability of outcomes and the bias inherent in
selective attention to people seen in institutional treatment settings. This
experience is similar to the recognition that if a clinician saw only patients
with stage 4 skin cancer, by analogy, that clinician’s perception of the prog-
nosis of skin cancer on all people’s lives would be distorted.
Another line of work began to identify the impact of DUP at the outset
of psychosis on long-term outcomes. Documentation of higher rates of re-
sponse to antipsychotic medication treatment and remission among peo-
ple in their first episode of psychosis compared with those with multiple
episodes also heightened interest in focusing on early stages of illness
(Robinson et al. 1999). These observations led to the development of
specialized clinical programs focused on intervening early in psychosis
in both Australia and across Europe. These programs provided both in-
valuable clinical experience and an essential evidence base from which
further developments in the field have grown (Amminger et al. 2011,
Melle et al. 2008). Collectively, this work generated recognition that
early psychosis was an evolving process and that there might be an op-
portunity to intervene early in the progression of symptoms and delay
or even potentially prevent the movement toward more serious psychi-
atric illness. The early intervention movement had arrived.
Principles of Intervening Early

in Psychosis
The introduction of early intervention in psychosis represented a para-
digm shift in the field of mental health care. In particular, this shift en-
couraged providers, researchers, consumers, families, and society at

large to reconsider how emerging serious mental health problems are
assessed, treated, and conceptualized and shifted the focus from under-
standing psychosis as a chronic and debilitating illness to embracing
the potential for early intervention and recovery. As such, a number of
key principles unite the early intervention in psychosis movement in-
ternationally. These principles provide a foundation on which, argu-
ably, all early psychosis services are developed and offer guidance
regarding multiple aspects of service provision, including workforce
development and training, the breadth of interventions offered, and
overall ethos of the service.
In 2005 the World Health Organization issued the seminal consen-
sus statement on early intervention (Bertolote and McGorry 2005).
Within this consensus document, five key principles were highlighted,
and the core values and vision for early intervention were described.
The five key principles are 1) raising community awareness, 2) improv-
ing access and engagement, 3) promoting recovery, 4) encouraging fam-
ily engagement and support, and 5) providing workforce training. The
principles are outlined below in the following subsections and are elab-
orated on in later chapters of this book.
Raising Community Awareness

A key tenet of early intervention is community education to support the
early identification of individuals who may be experiencing early signs
of psychosis. There are multiple community education initiatives that
draw on innovative means of reaching the target audience (e.g., via so-
cial media, advertisements in movie theaters, information outreach
talks to key stakeholders) and provide information on early psychosis
at an appropriate level. Taking the approach of going into the commu-
nity and educating stakeholders (e.g., young people, educators, family
members, primary care doctors) contrasts with the traditional approach
of many mental health centers that rely on established referral path-
ways for consumers to access treatment. However, this traditional ap-
proach has been associated with delays in accessing care, resulting in an
extended DUP, shown to result in poorer long-term outcomes (Kane et
al. 2016). Another important element of raising community awareness
is the opportunity to provide up-to-date, accurate information about
psychosis symptoms, address misconceptions about mental health, and
address head-on the stigma that is often associated with acknowledging
mental illness in our homes and families.
Improving Access and Engagement

The very essence of early intervention is ensuring that individuals ac-
cess treatments shown to be effective for early psychosis in a timely
manner. As such, ensuring that services are accessible, responsive, and
prioritize engaging the young person is essential to this approach. In the
United States the median of duration of untreated psychosis is 74 weeks
(Addington et al. 2015). This time frame far exceeds the internationally
recommended standard of 12 weeks. Although the reasons for an ex-
tended duration of psychosis are multifaceted, this principle of easy
and early access encourages early psychosis teams to respond rapidly
to referrals (including developing models for triaging referrals and sup-
porting waitlist management) and ensuring that services are offered in
youth-friendly settings to aid overall engagement.
Promoting Recovery
The third principle emphasizes that the focus should be on recovery,
healing, functioning, and shared decision making rather than disability
and illness management. This core principle permeates all aspects of an
early psychosis service, including medication management, individual
and family psychosocial interventions, peer support, and support for
education and employment. It is essential that all members of the early
intervention team have a full understanding of this principle and that
they adhere to this recovery frame in their interactions with the client,
the family, and other stakeholders. Recovery is a concept typically de-
fined by the client on the basis of the goals and values that they identify
and helps to drive treatment in order to support the individual in reach-
ing those goals.
Encouraging Family Engagement and Support

Given the age at onset of early psychosis, many symptomatic individu-
als are often still closely connected to or living with their family or other
support systems. As such, family members should have access to infor-
mation regarding psychosis and how best to support their loved one.
The developmental needs of this young population also need to be con-
sidered in service development. In contrast to traditional adult mental
health services, families are generally actively engaged in the treatment
process. Early psychosis programs may need to consider how best to
support family members, navigate family dynamics, and ensure that in-
formation provided on psychosis is culturally salient.
Providing Workforce Training

One element of early psychosis treatment has been a dedication to pro-
viding evidence-based treatments. This principle requires commitment
to training providers in these specialized approaches and ensuring ongo-
ing, sustainable consultation to help practitioners access cutting-edge
treatments and stay abreast of the field. As such, early psychosis services
should consider training at multiple levels, including preimplementation
planning, training implementation, ongoing consultation, and repeating
training efforts to respond to staff turnover.
Developmental Framework
The first episode of psychosis typically occurs in late adolescence or
early adulthood. This time frame spans a key developmental period
from 16 to 24 years, with individuals of this age range often referred to
as transitional-age youth (TAY). This developmental stage can chal-
lenge mental health services that are traditionally divided into services
for children (up to age 18) and adults (ages 18 and older). Because indi-
viduals with early psychosis generally span two different systems of
mental health care, it is critical to consider how best to support naviga-
tion of these two often disparate systems.
The needs of the TAY population vary greatly from those of children
or adults. Consideration should be given to the developmental needs of
each of these populations, and services should be adapted accordingly.
This reality requires workforce training in developmental approaches,
recognition of the different medication and physical health needs of in-
dividuals younger than 18 years, consideration of medicolegal issues of
consent and confidentiality, adaptation of evidence-based individual
and family therapy approaches, and the importance of supporting con-
tinued educational attainment through specialized services designed
specifically for secondary school and higher education. In addition, the
environment of the clinical space needs to reflect this developmental
stage, and services should be encouraged to develop youth-friendly en-
vironments. Providers must also recognize these young people as a dy-
namic and changing age group who are evolving in terms of their
personality, sexuality and gender orientation, sense of autonomy and
independence, and social supports. In particular, the role of the family
may change over the course of providing care for an individual receiv-
ing services for early psychosis. Chapter 22, “Care for Adolescents on
the First-Episode Psychosis Continuum,” provides more information
on developmental approaches for this population.
Staging Model
McGorry and colleagues developed a clinical staging model that serves as
an effective framework for marking the stages of psychotic illness devel-
opment (Fusar-Poli et al. 2017; McGorry et al. 2006). This model, which
is based on the model of staging other developing and/or chronic ill-
nesses such as cancer or osteoporosis, sets benchmarks for delineating
the steps through which an individual might progress in moving from
very early symptoms to a full psychotic disorder. The stages range from
stage 0, which occurs without symptoms but with elevated risk for psy-
chosis, to stage 1, with the first identification of concerning symptoms,
through stage 2, which is the first episode of psychosis, stage 3, with re-
lapses of the first episode, and ultimately, stage 4, which is a fully estab-
lished, more chronic disorder. Not everyone progresses through each
stage, but the stages are designed to help better understand the nature
of the current state for the individual and to guide stage-specific treat-
ment to help provide appropriate levels of intervention.
Clinical staging can be useful in guiding treatment selection and de-
termining potential impacts of an intervention. Preventive, neuropro-
tective interventions are indicated in stages 0–1, whereas specific
therapeutic interventions are indicated in stages 2–4 (Fusar-Poli et al.
2017). As in cancer, therapeutic interventions have the highest opportu-
nity for efficacy in earlier stages of disease, and relapse raises the need for
more complex care. These relationships serve to advance understanding
that one of the most important ways that our field can improve the effi-
cacy of interventions for psychosis is to apply them in an early, timely,
and consistent manner, before tertiary disease develops. There may be as
much potential gain from efforts to improve the timing of application of
existing treatments as there is in trying to develop new, more efficacious
treatments. This reality has implications for both the design and availabil-
ity of clinical services and for public health efforts to ensure broad public
awareness of psychosis.
Historical Context of United States

Early Intervention Support
and Funding
Although intervening early in the course of psychosis has been broadly
adopted in Australia and several European countries over the past two
decades, the United States was a relative latecomer to the systematic
implementation of early psychosis service models. Challenges related
to funding services, access through insurance, and a lack of a coordi-
nated infrastructure to support widespread implementation all acted as

initial barriers to the growth of this approach in the United States and
hampered policy development that would have otherwise supported
implementation.
Initial early psychosis programs in the United States were devel-
oped at either a community level (e.g., Early Assessment and Support
Alliance [EASA], Portland Identification and Early Referral [PIER]),
through community-academic partnerships (e.g., Prevention and Re-
covery in Early Psychosis [PREP; Hardy et al. 2011]), or in an academic
setting (e.g., Specialized Treatment Early in Psychosis [STEP; Srihari et
al. 2014]) and drew on early psychosis models prevalent in Australia
and the United Kingdom. These models often integrated evidence-
based practices for psychosis with local adaptations reflecting cultural
and geographical needs. In addition to this grassroots development, the
National Institute of Mental Health (NIMH) sponsored both the North
American Prodromal Longitudinal Study (NAPLS) and Recovery After
an Initial Schizophrenia Episode (RAISE) studies. NAPLS is now in its
third iteration, focusing on people with elevated risk for psychosis.
Critical results include refinement of the components of the at-risk
state, leading to the recent development of a risk calculator for deter-
mining the risk of conversion to psychosis from the clinical high-risk
state (Carrión et al. 2016).
In addition, the RAISE studies are the largest clinical trials to focus
on people in their first episode of psychosis (Dixon et al. 2015; Kane et
al. 2016). Research into the optimal treatment for the first episode of
schizophrenia in general has been difficult to undertake in large num-
bers for many reasons. Despite difficulty in initiating treatment for
many people, once an individual is identified as having an early psy-
chotic illness, treatment is often initiated before potential enrollment in
pretreatment research can be arranged. Further, the effects of medica-
tion in the first episode are rapid, and the timing of initial treatments, or
delay of recognition for initiating treatment, can have a profound im-
pact on the later course of illness. Furthermore, recruitment and reten-
tion of research subjects in this stage of illness are challenging, and
alignment between clinicians and clients and families on the need for
treatment is often difficult to achieve.
One important outcome of RAISE was the development and valida-
tion of the coordinated specialty care (CSC) model for comprehensive
treatment of people experiencing an initial episode of psychosis and the
importance of interdisciplinary teams to partner with both clients and
family members on service implementation. This CSC approach was
implemented within community mental health centers across the
United States to allow for evaluation of this approach in a real-world
setting and trained staff in these centers to deliver the interventions.
In addition, the Robert Wood Johnson Foundation funded the Early

Detection, Intervention, and Prevention of Psychosis Program
(EDIPPP) clinical high-risk study at six U.S. sites (McFarlane et al. 2015).
Whereas the RAISE studies focused on early interventions for persons
with psychotic illness, others, such as NALPS and EDIPPP, focused on
broad outreach and case finding to bring those at clinical high risk for
psychosis in for early intervention, with the hope of delaying or possi-
bly preventing the movement to a first psychotic episode.
The success of RAISE and other early psychosis services in the
United States contributed to the federal decision to allocate an additional
5% to each state’s Mental Health Services Block Grant for early psycho-
sis recognition and treatment, which was doubled to 10% in 2016. These
funds are dedicated to the development and provision of programs for
young people experiencing early psychosis. This expansion has resulted
in the exponential growth of early psychosis programs across the United
States, with approximately 200 programs across 40 states in EASA at this
time (EASA Center for Excellence 2016). In 2018 the Substance Abuse
and Mental Health Services Administration released the first funding
for programs supporting persons at clinical high risk for psychosis,
thereby expanding the potential continuum of federal funding support
for early psychosis programs nationally.
Coordinated Specialty Care

in the United States
The NIMH sponsored the RAISE studies to establish that effective early
intervention services for psychosis could be broadly implemented in
the United States (Dixon et al. 2015, 2018; Kane et al. 2016). The CSC
model was developed on the basis of evidence-based care strategies
previously implemented with people with chronic psychosis, as well as
successful global early intervention models. CSC was designed to pro-
vide comprehensive treatment for people experiencing an initial epi-
sode of psychosis, including case management, psychotherapy,
pharmacotherapy, family intervention, and supported education and
employment. Care is delivered by interdisciplinary teams that provide
services to both clients and their family members. Although most early
intervention studies are not designed to test the individual components
of CSC or similar models, multidisciplinary, team-based care has been
shown to be effective in reducing symptom severity and improving
functional outcomes for people in first-episode psychosis. Multimodal
care models are used in effective early intervention programs across the
globe and are now considered the standard of care.
Throughout the chapters of this book, you will find details on spe-
cific interventions and modalities of care. It is important to be mindful
that these interventions are intended for use within a team-based care
program and may not be as effective in isolation. Intervening early in
psychosis works best in a team approach with coordination between
multiple disciplines and stakeholders and strong partnerships with cli-
ents and their support network. We encourage you to consider how you
can incorporate an early and comprehensive range of interventions, de-
livered in a multidisciplinary setting, in partnership with individuals
with early psychosis and their families.
KEY CONCEPTS
• Traditionally, mental health services took a watch-and-wait
approach to psychosis, with a focus on managing chronic
psychotic symptoms.
• International efforts to intervene early in the course of
psychosis have provided guiding principles for the devel-
opment of early intervention services in the United States.
• In the United States, these international guiding principles
were integrated into models of early psychosis care called
coordinated specialty care (CSC).
• There has been a growth in the availability of CSC services
across the United States over the past decade.
• A developmentally based approach to working with indi-
viduals with early psychosis and their family is critical for
treatment success.
Discussion Questions
1. Where is your closest CSC service?
2. How is an individual experiencing a first episode of psycho-

sis, and his or her family, currently provided with evidence-
based interventions for early psychosis in your area?
3. What resources are locally available to support the growth of

CSC in your area?
Suggested Readings
Articles and Reports

Dixon LB, Goldman HH, Srihari VH, et al: Transforming the treatment
of schizophrenia in the United States: the RAISE initiative. Annu
Rev Clin Psychol 14(1):237–258, 2018
Heinssen RK, Goldstein AB, Azrin ST: Evidence-Based Treatments for
First Episode Psychosis: Components of Coordinated Specialty Care.
Bethesda, MD, National Institute of Mental Health, April 14, 2014.
Available at: www.nimh.nih.gov/health/topics/schizophrenia/
raise/nimh-white-paper-csc-for-fep_147096.pdf. Accessed Septem-
ber 27, 2018.
Sale T, Fetzer P, Humensky J, et al: The Integration of Early Psychosis
Services in a System of Care Framework: Opportunities, Issues, and
Recommendations. Stanford, CA, Stanford Medicine, April 2018.
Available at: http://med.stanford.edu/content/dam/sm/peppnet/
documents/Integration-of-Early-Psychosis-Services-in-SoC-
Framework-Final.pdf. Accessed January 18, 2019.
Website
Prodrome and Early Psychosis Program Network (PEPPNET): https://
med.stanford.edu/peppnet.html
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2014 25471062
CHAPTER
3
Early Detection of
Schizophrenia
A POPULATION HEALTH APPROACH
Maria Ferrara, M.D.
Walter Mathis, M.D.
John D. Cahill, M.D., Ph.D.
Jessica Pollard, Ph.D.
Case Example
Langston is a 21-year-old African American male who has lived with his
mother since being asked to take a leave of absence from a 4-year col-
lege. While a freshman 3 years ago, he was taken to the college counsel-
ing center by his roommate because he was displaying disorganized
thinking and experiencing auditory hallucinations. After assessment by
a primary care physician and psychiatrist, Langston was diagnosed
with a primary psychotic disorder. His mother recalls that, aside from
mild “clumsiness” as a child, he had met usual developmental mile-
stones on time. She remembered noticing, a year or so prior to the psy-
chotic episode, that Langston appeared less interested in socializing
with friends and that he would sometimes become preoccupied with
the notion that his peers at school were talking about him. She is wor-
ried about whether her son will be able to return to college as he wishes.
She blames herself for not acting sooner on his behalf to get help and has
a lot of questions about Langston’s current medications and how to
manage his frequent requests to stop treatment.
23
The schizophrenia spectrum disorders (henceforth schizophrenia) are a

family of illnesses with diverse etiologies that can exert their impact over
an extended period of neurodevelopment (from pregnancy through early
adulthood) and cause varied clinical presentations and courses. Despite
this heterogeneity, much is known about the course and treatment of
schizophrenia. Over the past 20 years, the early intervention services
(EIS) paradigm has brought two conceptually overlapping approaches to
improve the lives of those afflicted and their family members: early de-
tection seeks to reduce delays to care, and first-episode services (FES), the
provision of packages of empirically based interventions by specialty
teams, has emerged as a best practice. FES can improve a variety of out-
comes in the first few years after psychosis onset. Called coordinated
specialty care (CSC) in the United States, these teams are equipped to
provide a range of relevant services to clients like Langston (e.g., med-
ication treatment, psychotherapy, vocational assistance) and his mother
and other caregivers (e.g., education, support) (Srihari et al. 2012). The
delivery of CSC care is detailed in the rest of this book; in this chapter
we focus on early detection and specifically on how FES services can
conceptualize and implement approaches to shortening delays to care.
The onset of frank psychotic symptoms, usually in late adolescence
or early adulthood, can be a distressing and confusing experience. The
proactive involvement of humane and competent health care profes-
sionals can significantly reduce unnecessary suffering for affected cli-
ents and families. This is reason enough to advocate changing the status
quo of unacceptably long delays to best practice FES. There is also
strong evidence linking prolonged delays in providing care, with
poorer long-term outcomes. This association has been consistent across
many health care systems and many methods of measuring the time be-
tween onset of full-blown psychosis and initiation of appropriate treat-
ment, operationalized as the duration of untreated psychosis (DUP;
(Perkins et al. 2005). Furthermore, tests of early detection strategies to
reduce DUP have demonstrated reductions in suicidality and symptom
severity at presentation to care and improvements in outcomes that are
measurable up to 10 years later (Hegelstad et al. 2012). Shorter DUP is
associated with reduced social isolation, unemployment, and home-
lessness. Hastening access to care may also reduce the community bur-
den of suicides and homicides among early psychosis populations
(Srihari et al. 2014).
Efforts toward reducing DUP should be contextualized in the rich
and longstanding literature pointing to the severe human costs of de-
layed and inadequate care. Prospective studies of schizophrenia spec-
trum disorders suggest that most of the clinical and psychosocial
deterioration occurs within the first 2–5 years after psychosis onset
(Birchwood et al. 1998). This is also a high-risk period for suicide, highest
in the first year after first hospitalization for psychotic disorder. In the
Early Detection of Schizophrenia 25
first 12 months after a psychosis diagnosis, mortality rates were 24 times

higher than those of an age-matched cohort in the U.S. general popula-
tion (Simon et al. 2018b).
This early, turbulent period is usually followed not by progressive
decline but rather a plateau in symptoms and impairment, even under
usual systems of care. Reassuringly, 75% or more of individuals in treat-
ment for first-episode psychosis (FEP) experience symptomatic remis-
sion within the first year (Lieberman et al. 1993; Tohen et al. 2000), but
this is often followed by treatment discontinuation and relapse, and less
than one-third achieve minimal age appropriate employment or educa-
tional functioning in the first few years after frank psychosis has
emerged (Menezes et al. 2006). EIS holds the promise of significantly
improving on these outcomes of usual care.
Duration of Untreated Psychosis or

Duration of Untreated Illness?
Case Example (continued)

When asked about when he first noticed a change, Langston was able to
recall a period 2 years before his first hospitalization when he felt more
sensitive to sounds. Occasionally, other people’s voices sounded louder
than usual, and, at other times, he heard his name being called but turned
around and realized it might have been his imagination. These experi-
ences were infrequent and resolved after a few months, but after this he
started hearing whispers. He began to feel “on edge,” especially around
other people. His mother recalled that during this period he appeared
more distracted and was less interested in spending time with his friends
after class. Langston also reported that his teachers used “more and more
words” he could not follow, and his grades began to drop.
Psychotic symptoms that are severe enough to warrant clinical care

are usually preceded by months to even years of prodromal abnormal-
ities in thought (e.g., mild or attenuated positive symptoms), feeling, or
behavior (e.g., social withdrawal). There are also measurable declines in
cognitive performance and social and school functioning. However,
these changes are often apparent only in retrospect as precursors to
schizophrenia. The first episode of frank psychosis remains the most re-
liable way of identifying the presence of a disorder that will likely re-
quire chronic treatment. The first episode of psychosis is thus best
understood not as the true beginning but rather as the end of the begin-
ning of a complex biopsychosocial process wherein vulnerabilities (e.g.,
genetic, in utero exposures) interact with a wide range of environmen-
tal factors to drive progression toward diagnosable illness. Reliable
identification of individuals during the pre-FEP phase is an area of ac-

tive research, and promising possibilities have been tested to prevent or
delay progression to full blown psychosis (Millan et al. 2016). Neverthe-
less, the state of the art for early detection, at the time of this writing,
remains focused on targeting FEP (to reduce DUP).
The actions of individuals in a wide variety of roles both within and
outside health care agencies (e.g., police, educators, youth and family or-
ganizations, clergy) can make a substantial impact on DUP. First-episode
services or CSC services need to engage with these stakeholders to imple-
ment early detection. In the next section, we provide a conceptual model
for such efforts.
Population Health for Early

Intervention

Langston is of African American descent and the youngest of three sib-
lings raised by their mother, a high school principal. His father had been
incarcerated for a drug-related offense and lost contact with the family
during Langston’s childhood. His older brother, also a schoolteacher,
lives nearby with his wife and 3-year-old daughter and helps pay for
Langston’s living expenses. Langston’s sister, the middle sibling, is a
physician and has been a strong source of support and a role model for
Langston, who attended the same college that she did.
Population health is the goal of “achieving measurable improvements

in the health of a defined population” (Kindig et al. 2008, pp. 2081–2083).
This perspective turns a critical eye to the definition and measurement
of health outcomes (dependent variables) as well as the determinants of
health, construed broadly (independent variables). Importantly, there is
an embedded concern with social justice; assessing differences in out-
comes within the target population—health disparities—is integral to
population health. This model can be visualized in a table with mortality
and morbidity paired with disparities measured across race and ethnic-
ity, socioeconomic status, geographic location, and sex (Kindig et al.
2008). In our adaptation of Kindig et al.’s (2008) conceptualization, Fig-
ure 3–1 lists examples of determinants for early psychosis to illustrate
factors that EIS should consider. In addition, quality of life in Kindig’s
original formulation is enlarged to include a variety of measures of
morbidity that are relevant to schizophrenia.
The weighting or relative importance given to various population
health outcomes should be determined by the social valuation of local
stakeholders. This means that the list of outcomes chosen for the mor-
DETERMINANTS POPULATION HEALTH OUTCOMES
Medical care: Mortality disparities

Duration of untreated psychosis
Enrollment in specialty care Race/ethnicity
Population mean
Individual behavior: Socioeconomic status
mortality Lethal means
Substance use disorders
Geographic location
Socialization
Sex
Early Detection of Schizophrenia
Social environment:
Migrant or ethnic minority
Early life adversity Health-related
Population mean morbidity disparities
Physical environment:
morbidity Race/ethnicity
Urban environment
Environmental pollution (measured by, e.g.,
hospitalization, Socioeconomic status
vocational
Genetics: Geographic location
SPECIFIC functioning, quality
Parent with psychotic disorder of life)
Rapid metabolizer INTERVENTIONS Sex
FIGURE 3–1. Population health and early intervention services for schizophrenia.
27
Source. Adapted from Kindig et al. 2008.

bidity cell can vary across regions. In contrast, the weighting of the rel-
ative impact of the determinants should be derived empirically (i.e., not
by social valuation). The Evans-Stoddart model (Evans et al. 1994) pro-
poses five broad categories of determinants: medical care, individual
behavior, social environment, physical environment, and genetics. Fac-
tors within these categories can interact with each other in complex
ways, limiting inferences about the independent impact of individual
determinants. Additionally, these determinants can have differential
impacts on different subgroups, contributing to health disparities. For
example, minority racial status and residence in a high-crime neighbor-
hood can lead to aversive pathways to care (e.g., via the criminal justice
system) that, if not assertively addressed, can contribute to poor engage-
ment with FES and poorer outcomes. As these interactions are better un-
derstood, they can be leveraged as targets for specific interventions.
Interventions to improve outcomes can be aimed at moderating the
effects of determinants on outcomes (e.g., care models that intentionally
intersect with criminal justice agencies [Wasser et al. 2017]), or modify-
ing the determinants directly (e.g., reducing delays to care). Such ap-
proaches may require collaboration with diverse community
stakeholders because many determinants are not within the direct con-
trol of clinics and will need to address a wide mix of population needs
that may also have distinct regional profiles. The population health
model thus provides a bridge between the poles of the traditional pub-
lic health focus on more distal determinants of health in mostly non-ill
populations (e.g., fortification of salt with iodine, promotion of seat belt
use) and the clinical focus on more proximal factors in samples already
enrolled in care. For FES staff, the population health framework pro-
vides a way to “step out” of the clinic and engage local stakeholders in
impacting determinants that operate earlier in the pathway to care, as
well as to influence responsiveness to treatment. Geopolitical areas
rather than simple geographic zones have been recommended in using
the population health framework because funding decisions and regu-
lations are inherently political in nature (Dawn and Teutsch 2012).
How can this framework be made operational by clinics that are
seeking to reduce delays to care in their localities? In the next section,
we offer a vocabulary for population health–informed early detection
and examples and lessons from the application of this approach by an
EIS in southern Connecticut, the program for Specialized Treatment
Early in Psychosis (STEP).
Pathways, Networks, and Systems:

A Vocabulary for Population Health–
Based Early Detection

When Langston’s mother first heard about his difficulties in college, she
was mostly concerned that his academic performance not suffer and
worried aloud to him that his reduced enthusiasm and social with-
drawal in the last year of high school might have persisted into college.
She saw this largely as a problem he could address with more effort. She
encouraged Langston to seek out more tutoring. When he raised con-
cerns—which he was unable to clearly articulate—about his safety on
campus, she suggested that these worries were likely unfounded and
advised him to speak to his resident advisor. Instead, Langston repeat-
edly called the campus police, who were unable to find any evidence to
substantiate his concerns and grew increasingly wary of his phone calls.
Over the course of the semester, Langston began going to classes in an
increasingly disheveled state, wearing sunglasses even while indoors,
and was seen talking to himself in the dormitory corridors. When his sis-
ter talked to him on the phone, she grew concerned about his mental state
and requested that his roommate accompany him to the college counsel-
ing center. This was Langston’s first experience of mental health care and
resulted in the recommendation that he withdraw from college to attend
to his health. Although there was an appointment scheduled in 1 month’s
time with the primary care physician, Langston’s mother was able to ar-
range for him to be evaluated earlier by a psychiatrist, who diagnosed
him with a schizophrenia spectrum disorder and prescribed antipsy-
chotic medication.
After Langston returned home, he asked to stop seeing the psychia-
trist. He noted feeling safe at home and said that the medication made
him feel “emotionally flat.” He did not think his psychiatrist under-
stood his concerns; “he just wants me to take the medications.” Eventu-
ally, Langston prevailed in his wishes to stop seeing the psychiatrist and
to discontinue antipsychotic medication. After he discontinued treat-
ment, he appeared indifferent about most of his prior interests, includ-
ing playing the guitar (a long-standing passion), and seemed content to
stay in his room. His brother sometimes found him staring at the wall
and grew frustrated after trying repeatedly to get him to spend more
time with his family or go out with friends from high school.
Six months later, when Langston again started paying less attention
to his personal hygiene, as he had before his first psychotic episode, his
mother grew more concerned. Langston became increasingly irritable
and voiced suspicions that the neighbors were watching him and send-
ing him messages through their shared wall. One evening, his mother
had to call the police after he pushed her to the floor. The police officer
found Langston to be markedly disheveled, loudly alleging that “[the

neighbors are] messing with my business” and that his mother “does
not believe me.” The officer had to threaten him with arrest to have him
agree to an evaluation at the local emergency department.
Langston arrived at the hospital upset and refusing to cooperate
with the psychiatric evaluation. He was placed in soft leather restraints
and given involuntary intramuscular tranquilizing medications after he
threw his food tray at a staff member and attempted to run out of the
emergency room. After a brief hospitalization of 6 days, during which
he agreed to take antipsychotic medications and follow up with after-
care, Langston was discharged with a referral to a local clinic. However,
he did not arrive for this visit, explaining to his mother that he now felt
better and saw no need for care.
One week later, Langston was sent back to the emergency depart-
ment from a local community college where, per the police report, he
was found “wandering on campus” in a severely disorganized state. Af-
ter two more involuntary hospitalizations, he was referred to a local
FES, the STEP clinic. This was 18 months after the onset of the psychotic
symptoms that had led to his leaving college.
Langston’s journey (a composite of many individual narratives) is

marked by inordinate delay, lost opportunities for referral and engage-
ment with FES, and aversive interactions with criminal justice and in-
voluntary medical care. However, this journey to FES can also be
viewed as involving many community members with important roles
in this young person’s life who can be empowered to assist his passage
to optimal care and eventual return to a full role in these communities.
In the next subsection, we seek to provide a set of useful concepts and
approaches toward this goal.
Pathways and Networks: Essential Concepts

for Early Detection
A diverse group of actors are often involved in a young person’s jour-
ney, or pathway, to FES. Psychotic illnesses can cause behavioral disrup-
tions in many settings, but perhaps unlike other public medical events
(e.g., cardiac arrest, seizures), these behaviors can be met with combina-
tions of fear of violence, aversion, or shaming responses from unedu-
cated observers. This means that a network of care needs to extend
beyond traditional clinical settings to include all who might be ex-
pected to facilitate pathways to and through FES.
Langston’s pathway to care can be divided into two periods that con-
stitute the DUP: the demand side (illness identification and attempts to ac-
cess health care) and supply side (diagnosis of psychosis, initiation of
treatment, and referral to FES) (Srihari et al. 2014). The demand side of
DUP includes all the actors, events, and opportunities that emerge in the
window of time that begins with the onset of frank psychosis and ends
with contact with a health care provider or facility with the ability to initiate
treatment and referral to best practice care. The supply side begins with
such contact and ends with entry into best practice care or FES. Delays in
both the demand and supply sides are implicated in prolonged DUP.
A heuristic model of Langston’s pathways to FES, as used by the
STEP program, is provided in Figure 3–2. The dashed line depicts the
demand side of delay, which in this client’s case intersected with at least
five distinct groups (family, friends, college staff, police, and mental
health services) before engagement with STEP. In Langston’s case, there
was a delay between the onset of symptoms and signs and the recogni-
tion of a need for professional care (at college counseling). Rather than
entry into FES, this resulted in visits to an available psychiatrist covered
by Langston’s mother’s health insurance plan. Although this ended the
demand side of the journey, it certainly did not mark the end of DUP.
Rather, this was the beginning of the supply side of delay. The needs of
individuals with FEP and their families for education and iterative, ex-
tended attempts at engagement into care proved beyond the capacity of
the private psychiatrist. However, when the psychiatrist was unable to
provide needed care, effective referral to local FES was not made. After
disengagement with this provider, Langston unfortunately reentered
the medical system in a manner that required the intervention of the po-
lice. This aversive, involuntary process likely led to an understandable
reluctance on Langston’s part to engage with psychiatric services after
discharge from the hospital. Thus, even when best practice care is lo-
cally available, supply-side delays can be considerable and can be me-
diated by a dynamic mix of factors, including a lack awareness of the
client of the need for care, the potentially alienating experience of invol-
untary care, and the various ways in which providers may be unaware
of, or unable to make, appropriate referrals to FES.
How can this inform an early detection strategy? An FES that takes
a population health approach to early detection will need to decide on
a target region and then consider how to intervene on these variables to
shorten DUP. One way to begin is to consider who the relevant actors
may be in the local network. Figure 3–3 depicts eight stakeholder
groups identified in the planning phases of STEP’s early detection strat-
egy, which is focused on a geopolitical catchment of 10 towns, with ap-
proximately 400,000 residents. The list was prepared by consulting the
literature as well as clinicians and administrators with tenure in the re-
gion of interest. These categories can help organize a strategy and can
be expanded or narrowed as data are gathered on actual local path-
ways. These data can be gathered passively from electronic health re-
cords of integrated health care networks and/or claims databases
(Simon et al. 2018a) or, ideally, national registries (Srihari 2018) that can
inform the FES on the distribution of contacts that clients with FEP have
Community agencies Acute clinical settings

• Police/jail diversion • Emergency rooms
• Church/mosque • Outpatient triage
• Inpatient units
Non-acute clinical settings

• Community mental health
centers
• College counseling centers STEP
• School-based clinics
• Primary care (Internist,
pediatrician)
Patient
Components of DUP and/or
caregiver
Demand
Supply
FIGURE 3–2. Heuristic model for DUP in STEP’s catchment.

Abbreviations. DUP= duration of untreated psychosis; STEP= Specialized Treatment Early in
Psychosis.
Source. Adapted from Srihari et al. 2014.
made, within and outside the health care sector. Additionally, the FES
can use structured questionnaires to query entrants about all their prior
help-seeking attempts, which allows the FES to gather information
about contacts outside formal systems of care. However, these data will
suffer from a sampling bias by being able to include only clients who
have been able to enroll at the service. Such questionnaires (Judge et al.
2005) can nevertheless provide the FES with useful information about
local referral partners and targets for professional outreach.
Information gathered about local pathways will raise the need for a
response. For example, long delays on the demand side may suggest
that individuals with FEP and their families are waiting too long to seek
care. This may reflect a low degree of awareness in the community of
the common signs and symptoms of psychosis. Information campaigns,
such as those tested by the Norwegian Early Treatment and Interven-
tion in Psychosis (TIPS) investigators using print, broadcast, and online
media, were partly directed at this possibility (Johannessen et al. 2001).
Such delays, however, could also be due to the relative inaccessibility or
unattractiveness of available care. A few of the interventions that can
Distributed networks of care
PRIMARY CARE EDUCATION
BETHANY
NORTH
HAVEN CIVIC/RELIGIOUS
MENTAL HEALTH SERVICES HAMDEN
NEW HAVEN
EAST
ORANGE HAVEN BRANFORD
JUDICIAL WEST
HAVEN
GOVERNMENT
MILFORD
SOCIAL WELFARE CONSUMER/YOUTH

ORGANIZATIONS
FIGURE 3–3. Understanding local networks to transform pathways to

early intervention services.
have an impact include quick, flexible responses to requests for help; the
ability to conduct assessments in familiar (e.g., homes, college campuses)
or acute care (e.g., emergency departments, inpatient units) settings; and
the lowering of structural barriers to care access (e.g., insurance coverage,
age restrictions, transportation costs).
To shorten the supply side of DUP, interfacing with members of the
local referral network (i.e., individuals and agencies that are or can be in-
fluential on local pathways to care for FEP) emerges as a key task. Con-
ducting educational workshops with provision of continuing education
credits that are ideally followed up by recurring visits to places of work
can be used as a platform to build relationships wherein the FEP is more
likely to be detected early in the pathway (e.g., by the college counseling
staff who are worried but yet uncertain about a psychosis diagnosis).
There is also a need for quick and welcoming responses to calls for con-
sultation from these colleagues. Many of these calls may not concern eli-
gible clients, but responding to them promptly will establish networks
that enable rapid identification of other individuals experiencing FEP. Lo-
cal groups that have not generated referrals (e.g., primary care clinics)
may require proactive outreach efforts from the FES.
Finally, delays on the supply side can happen at the “front door” of
the FES. The time between receipt of an appropriate referral and entry
into FES care can be prolonged by a collusion of many factors, including
the common ambivalence of the client to entering treatment, the work-

flow of busy clinicians who may struggle to prioritize new assessments
over established clients, and myriad other factors that are often idiosyn-
cratic to each case. The use of a dedicated early detection team tasked with
the mission of reducing DUP can help assure good customer service to all
calls for assistance and arrange rapid assessments for eligibility. In order
to facilitate rapid enrollment into care, program leadership is vital to en-
sure careful handoff to the clinicians on the FES team. Regular audits of
times between referral and enrollment, within a performance improve-
ment ethos and under oversight by program leadership, can help the
team discover sources of delay that might require more systematic atten-
tion, while also ensuring organizational learning about how to respond
in a more personalized manner to modifiable and client-specific sources
of delay. It is vital to avoid the enactment of implicit waitlists for FES.
The list of tasks needed to enable early detection can be culled from
approaches used by systematic efforts to reduce DUP but can also be
developed over time by an FES that is gathering knowledge of local
pathways. Early detection can be a resource-intensive project, and there
is a related paradox that will confront an FES that seeks to shorten DUP:
although most clinicians can easily recall cases where any of a variety
of efforts demonstrably reduced delays and improved the experience of
entry for particular clients, it can be difficult to demonstrate this at a
population level. Reviews of prior research point to the challenges of ef-
fecting measurable reductions in regional DUP (Oliver et al. 2018), with
a plethora of factors likely implicated in these delays. The fact that all of
these factors cannot be feasibly addressed by an FES or even multiple
agencies within the health care sector is a sobering reality.
Some features of U.S. health care, including fragmented payment and
delivery and the lack of established gatekeepers to specialty care, make
early detection more challenging. The multifactorial and dynamic nature
of these interactive factors necessitates the use of many strategies at once.
Furthermore, the distribution of factors across geopolitical regions will
vary, along with their relative responsiveness to intervention: what works
in one region may not work in another. Campaigns that have succeeded in-
cluded multiyear strategies targeting multiple sources of delay in demand
and supply. The seminal Norwegian TIPS study used an intensive media
campaign along with early detection teams that could rapidly assess refer-
rals in the community. STEP’s ongoing early detection effort (the MindMap
campaign; Srihari et al. 2014) has acted on this insight to implement a so-
cioecological approach that targets a very wide range of putative levers for
DUP reduction that are generalizable as categories across diverse U.S.
health care ecologies but engages actors who are specifically salient within
the targeted geopolitical region.
Given these challenges, FES providers may reasonably worry about
the diversion of limited resources from the treatment of already admit-
ted patients toward early detection efforts. However, the reduction of

DUP can reduce unnecessary suffering in a community, may reduce sui-
cide and violence during a critical period of elevated risk, and has been
shown to have durable effects on long-term outcomes (Hegelstad et al.
2012). Allocating resources between these two components (early detec-
tion and FES) of EIS presents a difficult trade-off. One way to navigate
this tension is to conceptualize the role of the clinical service as an integra-
tor of a local network of actors wherein the work of improving population
outcomes becomes a shared task. This is taken up in the next section.
Building Systems for Early Intervention

Services
We prefer to use system to refer to a set of activities with a common set
of objectives to contrast with the common usage of the term to connote
the fixed features of some aggregation of health care agencies or actors.
Our putative population health systems include the dynamic caregiv-
ing activities of a wide and variable group of actors (in Langston’s case,
his peers in college, campus security, his family, and college instructors)
who may or may not be coordinating efforts or even be aware of them-
selves as assisting help seeking, are mostly outside the formal health
care sector, and may have limited prior experience with accessing FES.
Along with health care agencies, such de facto regional networks deter-
mine the quality and speed of clients’ pathways to and through the
health care system and the resources available for recovery (Figure 3–4).
The hosting and self-aware integration of such a regional network
should become a priority for FES staff who wish to provide a regional
system of EIS.
When services are organized into a functioning system of care (Srihari
et al. 2016), the following occurs:
1. There is a common overall aim.

2. Objectives are drawn from a list of outcomes that, per the population
health framework, have been prioritized on the basis of the social
valuation of local stakeholders.
3. These objectives are tied to “achievable” standards of what is feasible
locally and continually aspire to what has been accomplished in best
practice international EIS. The objectives are explicit and linked to
outcome measures that are client centered but also include measures
of relevance to other agents who are important for optimal path-
ways to care and can be leveraged to become active stakeholders in
this system.
36
Mental health Judicial

services • Police Policy
• Hospitals • Jail diversion • Government
• Outpatient • CITs • Civic Primary care
clinics organizations • Adult
• Pediatric
Education Pathways to care

• College Network
counselors
• High school Family/consumer/advocacy
staff Client/ groups, e.g., local chapter of
• NAMI
family
• MHA
Youth and STEP clinic

community
organizations
• Sports
• Religious
• Other System: A set of activities with
a common set of objectives
Population health system of care Network: A set of organizations
• Early detection and best practice treatment and individuals that deliver
• Explicit, measurable, and high standards the system of care
• Accountable to regional stakeholders
Pathway: the routes that clients
• Resource efficient
follow through the network
FIGURE 3–4. Early intervention services as integrators of regional systems of care for psychosis.
Intervening Early in Psychosis
Abbreviations. CITs=crisis intervention teams; MHA=Mental Health America; NAMI=National Alliance on Mental Illness.
One working example of such a system specification from the STEP

program is depicted in Table 3–1.
The generation of a list of objectives (which is dynamic) involves it-
erative and systematic querying of local stakeholders, conversion of
their values to rigorous and feasible measurement protocols, and estab-
lishing a culture of practice within the clinical service that respects such
measurement and welcomes changes in care processes to respond to
gaps between achievable and aspirational standards. The description of
how to do this is beyond the scope of this chapter, but we seek here to
highlight the need for local ownership of the system and the role of the
clinic in hosting the generation of a system specification that can hold
the EIS accountable to local stakeholders but also engage them in col-
laborative efforts to improve outcomes of shared interest.
Regular auditing (e.g., in an annual report or actively maintained
dashboard) of progress toward espoused standards can drive refine-
ments of care within an iterative process. This requires flexibility, cre-
ativity, responsiveness, and collaboration from all stakeholders—there
are no recipes or key ingredients that will deliver improvement across
all valued outcomes. In this way, the mission of early detection is em-
bedded as one objective within the overall goal of improving outcomes
for early psychosis populations, and each objective can be prioritized
on the basis of measured performance of a particular EIS. Baseline as-
sessments of pathways to care for FES enrollees might suggest oppor-
tunities for improvement with traditional plan-do-study-act cycles. For
example, to address poor rates of follow-up from inpatient referrals,
providers of the STEP program have used brief visits to meet patients
on referring inpatient units to effectively decrease no-shows for first ap-
pointments.
The development and use of reliable measurement procedures for
these or other outcomes is an important consideration but beyond the
scope of this chapter. Some combination of passive harvesting from
electronic health records (when possible), with dedicated and trained
staff to administer a limited number of measures (e.g., the Positive and
Negative Syndrome Scale [PANSS]), would meet the needs of most EIS
that wish to demonstrate impact to their stakeholders. As we have ar-
gued elsewhere (Pollard et al. 2016; Srihari et al. 2016), keeping this end
in mind should be part of the implementation of new services rather
than an afterthought. Although there are no consensually accepted
measures for DUP, early detection efforts can begin by choosing one of
several available conceptualizations (Polari et al. 2011) and investing re-
sources over time to improve reliability.
TABLE 3–1. System specification for STEP’s population health–

based early intervention services in southern
Connecticut
Objectivea Measure Standard
Access
Rapidity DUP 1<3 monthsb Achievable (30%);

aspirational (75%)
DUP 2<12 monthsc Achievable (50%);
aspirational (75%)
Equity Proportion of females Achievable (20%);
aspirational (30%)
Ratio of ethnic groups Aspirational: matches
census percentages
Ratio of towns of residence Aspirational: matches
percentage of towns
Proportion ages <18 Achievable (5%);
aspirational (10%)
Coverage Number annually offered Achievable (15%);
STEP care/expected aspirational (80%)
annual incidence in the
zone
Pathways to care Proportion of individuals Achievable (<60%);
admitted to STEP after aspirational (<30%)
psychiatric
hospitalization
Engagement
Overall engagement In contact with FES at 12 Achievable (70%);
months postadmission aspirational (90%)
Exposure to family Family participation in at Achievable (75%);
education and support least one qualifying event aspirational (90%)
in first month
Exposure to specialized, Engagement in qualifying Achievable (75%);
empirically based event in first month aspirational (90%)
psychotherapy
Outcomes
Hospitalization Psychiatric admission in Achievable (<25%);
months 1–6 and 7–12 aspirational (<10%)
Suicide prevention Patients making attempt in Achievable (<10%);
first year of admission aspirational (<1%)
TABLE 3–1. System specification for STEP’s population health–

based early intervention services in southern
Connecticut (continued)
Objectivea Measure Standard
Outcomes (continued)
Remission PANSS positive subscore Achievable (70%);
<3 at 6 months aspirational (85%)
PANSS positive subscore Achievable (80%);
<3 at 1 year aspirational (90%)
Recovery GF: Role scale level 8 or Achievable (70%);
better aspirational (85%)
GF: Social scale level 8 or Achievable (70%);
better aspirational (85%)
Vocational engagement Not in labor market (NEET Achievable (<10%);
full or part time; not a aspirational (<5%)
full-time caregiver)
Cardiovascular risk
Smoking New smokers at 6 months Achievable (<20%);
aspirational (<10%)
Smoking rate at 6 months Achievable (<60%);
aspirational (<30%)
Overweight or obese BMI <25 at 12 months Achievable (30%);
aspirational (75%)
Normal BMIs retained at 12 Achievable (60%);
months aspirational (75%)
Disposition Successfully transitioned to Achievable (70%);
mainstream health care aspirational (80%)
services at or before 2
years
aThe overall aim of population health system for early intervention is to “transform out-
comes of all individuals within the first 3 years of psychosis onset within a catchment
zone of 10 surrounding towns” (extracted from the program for Specialized Treatment
Early in Psychosis [STEP] in New Haven, Connecticut).
bDUP 1: time between psychosis onset and first antipsychotic medication trial.
cDUP 2: time between psychosis onset and enrollment in STEP.
Abbreviations. BMI=body mass index (calculated as weight in kilograms divided by

height in meters squared); DUP=duration of untreated psychosis; FES=first-episode ser-
vices; NEET=not in education, employment, or training; GF=Global Functioning: Role
and Social Scale; PANSS=Positive and Negative Syndrome Scale; STEP=Specialized
Treatment Early in Psychosis.
Source. Adapted from Srihari et al. 2016.
Early Detection and the Future

of Early Intervention Services

Soon after entering the STEP clinic, Langston expressed a strong wish to
return to college and added that he experienced his visits to the clinic
and his interaction with psychiatric care in general as an interruption in
his education and planned trajectory to train to become a nurse.
Langston’s clinician connected him to the vocational counselor on the
CSC team, who first helped him navigate his way out of liability for
most of his tuition for his last semester. She also helped him prepare an
application to a local community college.
Two months after enrollment, Langston accepted a low dose of an
antipsychotic medication and reported that it helped him sleep and was
not causing him to feel emotionally dulled. He continued to voice con-
cerns about his neighbors but learned to not bring up his concerns di-
rectly with them but rather to discuss them with his clinician.
Six months after entering the STEP clinic, Langston was able to return
part time to a local community college with a plan to eventually transfer to
a nearby state university, where he planned to work toward a bachelor’s
degree in nursing. He has allowed regular contact with his family, espe-
cially his sister, and his mother and brother have visited individually with
clinic staff and attended workshops with other family members.
The first few years after the onset of frank psychosis can be turbu-
lent ones for those affected and for their caregivers, along with the
many other community members who are also typically involved. In
usual care systems, this period is marked by elevated risks for suicide,
aggression, and cycles of treatment discontinuation and symptomatic
relapse that can exact a disproportionate toll on long-term functioning
by derailing educational and vocational trajectories at a developmen-
tally vulnerable period of young adulthood. Conversely, the provision
of EIS can address many modifiable prognostic factors at once and can
achieve gratifying results for all stakeholders. This is an optimistic time
for early psychosis care in the United States: leadership from the Na-
tional Institute of Mental Health and the Substance Abuse and Mental
Health Services Administration has catalyzed the establishment of mul-
tiple new CSC services across the country (Dixon et al. 2018). These
could serve as a platform for adding early detection to further maxi-
mize population health impact.
As knowledge of the pre-psychotic phases of schizophrenia evolves,
the population health systems we advocate for in this chapter could
also serve to implement earlier intervention to potentially delay or even
prevent FEP. In the interim, these EIS can participate in necessary re-
search to better delineate the trajectory of prodromal states and to test

preventive approaches.
KEY CONCEPTS
• The period between psychosis onset and entry into care is
associated with significant suffering, disability, risk for vio-
lence, suicide, and the emergence of comorbidities (e.g.,
substance abuse).
• Evidence from worldwide early detection studies to shorten
the duration of untreated psychosis (DUP) and efforts by
first-episode services (FES) or, in the United States, coordi-
nated specialty care (CSC) suggest that many of these
sources of suffering, disability, and premature mortality are
modifiable, and the early period after emergence of psycho-
sis is a particularly important window of opportunity.
• Early detection efforts focused on shortening DUP offer a
way to further improve on outcomes of established FES or
CSC teams.
• Population health approaches to early detection can help
transform community-based FES or CSC into comprehen-
sive EIS programs.
• FES or CSC teams can have a powerful influence on local sys-
tems of care while attempting to reduce DUP and improve
pathways to care.
1. Which geopolitical region do you wish to target for early de-

tection efforts?
2. Who are the key stakeholders in this region, and what are
their expectations of your EIS? How can you make common
cause with them on your goals?
3. Which population outcome benchmarks are you hoping to

meet with your EIS? How will you include your local net-
work as full stakeholders in these outcomes?
4. What barriers to early detection do you expect within your

FES or health care agency?
5. How do you envision integrating emerging knowledge about

detection of prodromal states into your service?
Suggested Readings
Birchwood M, Todd P, Jackson C: Early intervention in psychosis: the
critical period hypothesis. Br J Psychiatry Suppl 172(33):53–59,
1998. An excellent summary of observational data supporting the
critical period hypothesis that continues to provide a useful orga-
nizing principle for early intervention services.
Kane JM, Robinson DG, Schooler NR, et al: Comprehensive versus usu-
al community care for first-episode psychosis: 2-year outcomes
from the NIMH RAISE early treatment program. Am J Psychiatry
173(4):362–372, 2016. Multisite cluster randomized trial of a first-
episode service that established the feasible application of this
model of care across multiple nonacademic clinical settings in the
United States.
Srihari VH, Cahill JD: Early intervention for schizophrenia: building
systems of care for knowledge translation, in Youth Mental Health:
Vulnerability and Opportunities for Prevention and Early Interven-
tion. Strüngmann Forum Rep Vol 28. Edited by Uhlhaas PJ, Wood
SW. Cambridge, MA, MIT Press, 2019. An elaboration of the popu-
lation health–based model for national implementation that in-
vokes the concept of learning health care systems.
Srihari VH, Shah J, Keshavan MS: Is early intervention for psychosis
feasible and effective? Psychiatr Clin North Am 35(3):613–631,
2012. Picking up from Birchwood’s summary of observational data,
this paper reviews subsequent experimental data from randomized
trials of first-episode services from around the world prior to the
U.S. STEP and RAISE trials.
Srihari VH, Tek C, Pollard J, et al: Reducing the duration of untreated
psychosis and its impact in the U.S.: the STEP-ED study. BMC Psy-
chiatry 14(1):335, 2014. Details of the rationale and design of the
first U.S. attempt to adapt and replicate the TIPS study.
Srihari VH, Tek C, Kucukgoncu S, et al: First-episode services for psy-
chotic disorders in the U.S. public sector: a pragmatic randomized
controlled trial. Psychiatr Serv 66(7):705–712, 2015. First random-
ized controlled study of a first-episode service in the United States,
which showed effectiveness of specialty team–based care within a
public-academic collaboration.
Srihari VH, Jani A, Gray M: Early intervention for psychotic disorders:

building population health systems. JAMA Psychiatry 73(2):101–
102, 2016.The STEP program’s vision for population-based early in-
tervention services.
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CHAPTER
4
Early Intervention and Policy

Abram Rosenblatt, Ph.D.
SIGNIFICANT advances in the early treatment of psychosis occur in

the nexus of numerous challenges for contemporary mental health policy
formulation in the United States. Adolescents and young adults typically
develop psychosis in the transitional age range of 15–25 years, when ser-
vices must bridge child- and adult-focused delivery systems. Effective
constellations of services for early psychosis require a broad range of
therapeutic treatments, psychosocial interventions, and educational or
vocational services. By definition, early treatment often requires provid-
ing preventive-based services before young people fully meet specific di-
agnostic and disability criteria. Evidence-based service delivery models
for early psychosis are most effectively applied to those persons for
whom the interventions were originally developed. To maximize their ef-
fectiveness, these services require fidelity and quality monitoring as well
as sufficient training and ongoing supports. All the policy-relevant as-
pects of financing and delivering services for the early treatment of psy-
chosis transpire against the backdrop of a continually shifting health
policy landscape, especially with the Affordable Care Act (ACA) facing
ongoing legislative and administrative modifications.
In this chapter, we focus on policy considerations pertinent to the
early treatment of psychosis within the broader context of contempo-
rary challenges for health and mental health policy. Financing effective
early treatment services remains at the core of policy formulation, with
the overall goal of providing affordable and accessible health insurance
45
coverage (Goldman 2017). Although financing is a necessary condition

for humane policy formation, it is far from sufficient in assuring access
to services (Saloner et al. 2017) or in enhancing the effectiveness and ef-
ficiency of service delivery (Dixon et al. 2018). Additional challenges for
policy development include fragmentation in categorically based ser-
vice delivery systems, translating and implementing evidence-based
services in community settings, monitoring fidelity and quality, estab-
lishing a sufficient workforce, and addressing discriminatory attitudes
and practices.
Financing Early Psychosis Treatment

In the United States, individuals with schizophrenia have high rates of
morbidity and mortality. People with psychotic disorders, including
schizophrenia, die an average of 11 years earlier than the general popu-
lation, and up to 10% die by suicide (Druss et al. 2011). Individuals have
a three times higher rate of mortality in the 3 years following an initial
diagnosis of psychosis when compared with a general outpatient pop-
ulation (Simon et al. 2018). By any measure, schizophrenia constitutes a
serious public health problem. The emergent understanding of schizo-
phrenia as a modifiable illness, with the initial onset of symptoms rep-
resenting an optimal time for intervention, underlies current early
intervention treatment approaches that carry the promise of clinical and
functional recovery for persons with schizophrenia (Dixon et al. 2015).
Current evidence establishes that early intervention in psychosis, spe-
cifically coordinated specialty care (CSC), can improve symptoms and
functioning when compared with usual care (Dixon et al. 2018).
CSC is a team-based intervention developed for persons with first-
episode psychosis that fosters recovery and strives to prevent disability,
focusing particularly on the first episode of psychosis. It combines var-
ious well-established evidence-based treatments, including assertive
case management, individual or group psychotherapy, supported em-
ployment and education services, family education and support, and,
as necessary, low doses of antipsychotic medications. These services are
also closely coordinated with primary health care (Azrin et al. 2015). In
addition to its multidisciplinary team-based approach, CSC relies on a
suite of recovery-oriented person-centered treatment approaches com-
bined in a shared decision-making framework. This approach is de-
signed to engage young people in treatment and keep them
participating while respecting their preferences and treatment goals.
When appropriate, CSC engages the individual’s close friends, family
members, or peer supports as active participants (Dixon et al. 2018).
Early Intervention and Policy 47
A series of studies (e.g., Dixon et al. 2018) demonstrates the feasibil-

ity, acceptability, and effectiveness of CSC in U.S. community mental
health settings. Yet the adoption of the model is far from universal,
largely because of a lack of adequate financing (Lieberman et al. 2013).
Financing first-episode psychosis (FEP) services is complex and diffi-
cult, requiring funding an array of services that are not typically cov-
ered by public or private health insurance (Shern et al. 2017). Medicaid
can fund psychotherapy, case management, family support and educa-
tion, medication, and, in some states, supported employment and edu-
cation or peer support. However, Medicaid does not cover community
outreach and the full cost of supported employment and education ser-
vices, among other program costs. Commercial health insurance pro-
grams are more restrictive, allowing for billing of psychotherapy, case
management, and medication while leaving other services unreim-
bursed. Consequently, states rely on additional local funding sources
for CSC program implementation, including highly variable state gen-
eral funds. Some states, such as Oregon and New York, are using Sec-
tion 1115 waiver demonstrations to address early psychosis. These
demonstrations originate from Section 1115 of the Social Security Act,
which allows the U.S. Department of Health and Human Services to ap-
prove experimental, pilot, or demonstration projects that further the ob-
jectives of Medicaid and the Children’s Health Insurance Program
(CHIP). Waiver demonstrations allow for the flexibility to design and
improve programs; demonstrate and evaluate policy approaches; and
use innovative service delivery systems to improve care, increase effi-
ciency, and reduce costs.
Adding to the complexity is the age at onset for psychosis, which of-
ten falls during late adolescence or early adulthood. Funding for ser-
vices to children and adolescents who are 21 years of age and younger
includes options that have no comparable adult funding mechanisms.
Medicaid-eligible children with a mental health diagnosis that meets
medical necessity criteria are federally entitled to receive mental health
services through the Early and Periodic Screening, Diagnostic, and
Treatment (EPSDT) program. This program includes young people in
the dependency and juvenile justice systems. EPSDT is relatively com-
prehensive, funding a wide variety of services, including some of those
that are necessary for CSC.
Although usually underfunded and difficult to access, special edu-
cation enabled through the Individuals with Disabilities Education Act
(IDEA) also provides a federal entitlement to mental health services to
assist children in achieving educational benefits. IDEA eligibility ends
at age 21. In addition, civil rights law (Section 504) prohibits discrimi-
nation on the basis of disabling conditions such as psychosis by schools
benefiting from federal financial assistance. Unfortunately, the criteria
for identification, eligibility, appropriate education, and due process
procedures vary between IDEA and Section 504, complicating transi-

tions in educational services. Similarly, as youth younger than age 21
who are in the early stages of psychosis transition to the adult mental
health system, they may lose coverage for a range of services consistent
with CSC. Additionally, when youth become adults, those youth who
are not Medicaid eligible must typically meet a means test and stringent
mental illness criteria to access public services.
The ACA improved funding opportunities for CSC services through
both expanded private insurance and increased Medicaid coverage.
Prior to the passage of the ACA, youth were removed from parental
health insurance unless they were full-time students, lost insurance if
they left the workplace, and were potentially excluded from insurance
because their mental illness was considered a preexisting condition
(Goldman et al. 2013). Under the ACA, many individuals younger than
age 26 remain on parental insurance even if they are not full-time stu-
dents. The removal of preexisting condition limitations allows individ-
uals to purchase insurance on the health exchanges even though their
FEP would previously have been considered a preexisting condition.
More individuals now qualify for Medicaid in Medicaid expansion
states, even if they are not yet disabled and receiving Supplemental Se-
curity Income. Preventive services and essential health benefits are ex-
panded. A state can also modify its Medicaid plan to include CSC under
the 1915i provisions of the ACA (Goldman et al. 2013). Yet with all of
these positive changes, states still need to supplement CSC services and
provide resources for staff training as well as outreach and engagement
(Goldman and Karakus 2014).
Also potentially relevant to funding CSC services, the ACA in-
cluded provisions for the establishment of health homes. Health homes
are intended to improve the treatment of chronic conditions, including
for individuals with schizophrenia and other mental health disorders,
by providing flexibility in both the array and intensity of services pro-
vided. States have considerable flexibility, but the provisions for these
health homes do not allow for funding the provision of direct, individ-
ual treatment services. Potential supports such as information technol-
ogy, training, and oversight can be funded. States are currently
experimenting with implementing CSC services within health homes
(Shern et al. 2017).
The Substance Abuse and Mental Health Services Administration
(SAMHSA) provides essential support for FEP services, including the
implementation of CSC. Community Mental Health Block Grants allow
states to implement models across a continuum, including those that
are required for CSC. SAMHSA’s Mental Health Services Block Grants
(MHBGs) are noncompetitive and provide funding for community-
based mental health services for adults with serious mental illness or
children with serious emotional disturbance. A 5% allocation set aside
for CSC programs began in 2015 and was doubled to 10% in 2016, provid-
ing $50 million that states can use to develop CSC programs. Currently,
36 states are implementing one or more CSC programs. The 21st Century
Cures Act reinforces the allocation, requiring states to use at least 10% of
their block grant funds on CSC for individuals with early psychosis.
SAMHSA, in collaboration with the National Institute of Mental Health
(NIMH) and Office of the Assistant Secretary for Planning and Evalua-
tion, contracted with a research corporation (Westat) to lead an evalua-
tion of this Mental Health Block Grant 10% SetAside. This national
evaluation will provide information on the implementation and out-
comes of FEP sites funded through the MHBG (Rosenblatt 2018).
In 2017, SAMHSA also awarded funding to eight states to partici-
pate in a 2-year demonstration project to expand access to behavioral
health services in community-based settings (Shern et al. 2017). Partici-
pating states receiving the funding will develop certified community
behavioral health clinics (CCBHCs), which will receive enhanced Med-
icaid reimbursement rates to better align with the costs of providing
community-based care. The services provided through the CCBHCs are
suitable for providing CSC and include crisis services; screening, as-
sessment, and diagnosis (including risk assessment); client-centered
treatment and planning; outpatient behavioral health services; outpa-
tient primary care screening and monitoring; targeted case manage-
ment; psychiatric rehabilitation services; peer support and family
support services; and intensive community care for veterans and mem-
bers of the armed forces. CCBHCs prioritize 24-hour crisis services, ev-
idence-based practices, care coordination, and the integration of
physical and behavioral health care.
In 2018, SAMHSA broadened funding opportunities to include
awards for services delivered to youth who are at clinical high risk for
psychosis (the Community Programs for Outreach and Intervention
With Youth and Young Adults at Clinical High Risk for Psychosis Grant
Program, CFDA 93.243). The purpose of this program is to identify
youth and young adults up to age 25 who are at clinical high risk for
psychosis and provide evidence-based interventions to prevent the on-
set of psychosis or lessen the severity of psychotic disorder. NIMH is ex-
pected to announce funding availability for researchers studying and
evaluating the effectiveness of these programs and interventions, and
SAMHSA is encouraging partnerships between funded sites and re-
searchers to conduct such studies.
Financing Patchwork
As is evident from the discussion to this point, there is little that is com-
prehensive or coordinated about the financing of early intervention ser-
vices for psychosis, including CSC. The capacity to use Medicaid
effectively depends in part on states, which have latitude in implement-

ing the program, including whether to participate in the expansion per-
mitted by the ACA. Adolescents and young adults often find their
coverage under Medicaid shifting dramatically simply by virtue of ag-
ing out of the EPSDT program. Private health insurance does not cover
the full range of services required to implement CSC. SAMHSA funding,
including the MHBG and, to a lesser degree, CCBHCs, serves to drive re-
form and leverage Medicaid and private insurance while providing
funds for development and implementation. Nonetheless, SAMHSA
funds are appropriation based and are insufficient to fully fund CSC ser-
vices nationally. For the foreseeable future, funding CSC programs will
require using a patchwork of state and federal funds to fill in the funding
gaps in Medicaid and private health insurance.
Access and Quality of Care

Providing access to services, which is inextricably linked to funding,
comes with a unique set of policy-related concerns. Goldman (2017)
strikes a cautionary note regarding the limitations of improved insur-
ance coverage. For example, using data from the National Survey on
Drug Use and Health (NSDUH), Saloner et al. (2017) found that health
insurance coverage increased subsequent to the implementation of the
ACA, yet utilization of services for treating substance use disorder did
not improve, and there was limited, if any, increase in other behavioral
health services use. This finding is consistent with prior studies of im-
provements in health insurance coverage such as parity, in which utili-
zation of behavioral health services does not increase with improved
coverage. This dilemma is not due to lack of need; the NSDUH study
and others demonstrate that need continues to exceed use. As Goldman
(2017) and Dixon (2017) explain, providing coverage for services does
not fully address the problem of access to services. Stigma; lack of
trained providers and appropriate referral mechanisms; and fragmen-
tation between schools, social service organizations, law enforcement
and justice systems, and child and adult services systems all conspire to
establish barriers to timely care, even when coverage is available.
Providing sufficient quality of care literally begins with timely refer-
ral and access to services. The Recovery After an Initial Schizophrenia
Episode Early Treatment Program (RAISE-ETP) study (Kane et al. 2015)
demonstrated that individuals with a shorter duration of untreated
psychosis (less than 74 weeks) had better outcomes than those with a
longer duration of untreated psychosis. Clinical quality reporting pro-
grams are required though the CHIP Re-authorization Act of 2009
(CHIPRA), the Health Information Technology for Economic and Clin-
ical Health Act of 2009 (HITECH), and the ACA. The Centers for Medi-
care and Medicaid Services adopted a core set of children’s and adult
health care quality measures for Medicaid and CHIP participants, in-
cluding measures focused on behavioral health. This brief set of mea-
sures includes follow-up after hospitalization for mental illness for both
children and adults. Other measures relate to suicide risk; attention-
deficit/hyperactivity disorder; depression medication; and cessation
and treatment for tobacco, alcohol, and other drugs. In addition, pursu-
ant to the ACA, SAMHSA developed the National Behavioral Health
Quality Framework and the National Quality Forum. SAMHSA grant-
ees report a range of child and adult behavioral health–related out-
comes through the national outcomes measures resulting from the
Government Performance and Results Modernization Act. Finally,
many states use a range of performance monitoring and quality mea-
sures, with limited consistency between states and sometimes even
within states.
These performance measures are not specific to CSC and the early
treatment of psychosis, although they do result in indicators that could
conceivably be compared across different types of mental health pro-
grams. Fidelity to CSC as a model is a different matter, falling some-
where between more global quality indicators of behavioral health care
and specific fidelity measures used in effectiveness studies. The First-
Episode Psychosis Services Fidelity Scale (FEPS-FS) (Addington et al.
2016), for example, is brief and feasible and has demonstrable reliability
and validity. This scale is designed to be used to assess adherence to ev-
idence-based practices for FEP services across a range of service deliv-
ery settings. Taking a somewhat different approach to pragmatically
assessing fidelity, Essock et al. (2015) used measures commonly avail-
able in existing data sets linked to billing practices, combined with in-
terviews with clients, to assess fidelity of key components. This
approach illustrates that fidelity to CSC models can be assessed using
existing data sets and minimally intrusive performance monitoring
methods. Methods and measures exist to maintain fidelity to CSC in
public and private service delivery agencies. Federal, state, and local
policy can all encourage or even mandate their use.
Training, Workforce, and Service

Delivery Systems
Numerous broader challenges related to training, the workforce, and
the existing structure of service delivery systems can, in part, be ad-
dressed through ongoing and future policy making at federal, state, and
local levels. With regard to child and adolescent behavioral health ser-
vices, over the past three decades, federal and state policy has focused
extensively on improving the organization, coordination, and delivery

of children’s mental health services. The systems of care approach that
emerged from these efforts involves collaboration across agencies with
youth and families to provide an array of effective, community-based,
culturally and linguistically appropriate services and supports for chil-
dren, youth, and young adults with or at risk for behavioral health chal-
lenges and their families (Stroul and Blau 2008). Behavioral health
services to adults with severe mental illness also historically address the
problem of systems integration and coordination, including, but not
limited to, more recent work on integrating behavioral health and pri-
mary care.
The considerable progress made toward understanding methods for
better coordinating and integrating care for adults with severe mental
illness and children and youth with severe emotional disturbance is rele-
vant to the effective and efficient delivery of early intervention services
for psychosis, including CSC. Of special note, however, is the problem of
the transition between the child and adult service systems. Children and
adolescents may experience severe emotional disturbances that seriously
hinder functional capacities across age ranges. Adolescents and young
adults experiencing FEP, however, are typically in the 15- to 25-year age
range considered transitional age. This stage of life encompasses life
changes that are especially difficult for those youth living with a serious
mental health condition, resulting in struggles to complete high school,
enroll in and complete college, and establish adult work lives. Transi-
tional-age youth with serious mental health conditions also receive ser-
vices in multiple public child and adult systems, including mental
health, justice systems, foster care, and vocational rehabilitation. Each
of these service systems is organized by inconsistent age groups. Child
welfare services may be provided up to age 18 or 21, whereas adult
mental health services usually begin at age 18 and special education ser-
vices may continue up to age 21 (Davis et al. 2018). Varying eligibility
criteria, funding streams, accountability structures, staff training, and
service cultures add to system fragmentation.
This gap between the adult- and child-focused service systems has
numerous implications for early psychosis treatment and CSC. The
most obvious is the problem discussed earlier in the section “Financing
Early Psychosis Treatment” of the lack of continuity between financing
systems that create confusion and gaps in coverage and service delivery
during a crucial developmental stage, particularly for persons experi-
encing FEP. Little is actually understood about programs that collabo-
rate across this age divide, especially with regard to transitional-age
youth with severe mental health conditions (Davis et al. 2018). As Dixon
(2017) noted, however, there are other less direct but equally important
concerns. Clinicians, for example, are typically trained to work with
children and adolescents or to work with adults. Treatments for chil-
dren and adolescents are often different from those for adults, and es-
pecially at the younger age ranges are typically not focused specifically
on severe mental illness. Family members are commonly integral parts
of service delivery for children and adolescents and may be less directly
involved in adult services. Legal responsibility changes dramatically
when a young person becomes an adult, and service organizations are
usually specialized to work within individual age groups. Conse-
quently, working with transitional-age youth requires unique skill sets
that are generally not taught in the professional training of social work-
ers, psychologists, psychiatrists, and other providers.
Also important, particularly with regard to legislative and other pol-
icy-related activities, are the gaps between the advocacy communities for
children and adolescents and those for adults. Historically adult-focused
organizations such as the National Alliance for the Mentally Ill are dif-
ferent from child-focused organizations such as the Federation of Fam-
ilies for Children’s Mental Health and Youth MOVE National. In part,
this is because the advocacy needs for children and adolescents with se-
vere emotional disturbance vary from those of adults with severe men-
tal illness. Lived experience can have diverse meanings, and many
youth receiving services within the public child and adolescent behav-
ioral health service system who are experiencing potentially serious
and significantly disabling emotional disturbances do not develop or
have a history of specific severe mental illnesses such as schizophrenia
and bipolar disorder. Transitional-age youth and their families, particu-
larly those experiencing FEP, may navigate varying advocacy and self-
help organizations and structures. Such divides and potential confu-
sion can dilute the strength of advocacy efforts and hamper activating
the policy voice of young people experiencing early psychosis.
Implementation of Coordinated
Special Care: California
Federal legislation and national initiatives provide an essential back-
drop and an array of financial and policy guidance that significantly in-
fluence the provision of services to individuals experiencing FEP.
Services are, nonetheless, provided primarily at the local level, and
states retain considerable flexibility in the implementation of service
delivery and the application of federal guidelines and funding require-
ments. State and local policies provide essential contours and detail re-
garding the overall landscape for CSC programs. The variability across
all U.S. states and territories precludes an adequate summary in this
chapter. Nonetheless, California, as the nation’s most populous and di-
verse state, provides an illustrative example of the complexities inher-
ent at the state level along with an example of how state initiatives can
profoundly influence service delivery to individuals experiencing FEP.
Behavioral health services in California are administered largely
through the 58 individual county health and behavioral health systems.
Although there are some exceptions, eligibility for services is tied to
counties, and service recipients can lose or gain eligibility for specific
services by moving—in some cases just a few miles or less—across
county lines. Because of California’s sheer size (39.5 million residents in
2017), federal initiatives such as Mental Health Block Grant 10% Set-
Aside funding often result in relatively small allocations at the county
level, requiring counties to significantly supplement MHBG funds to
establish local FEP programs. The challenges to funding CSC programs
outlined throughout this chapter apply to California counties in vary-
ing ways, depending on county composition and size.
In 2004, advocates and legislators in California, recognizing the lim-
itations of existing funding streams for individuals with serious mental
illness, including those experiencing FEP, succeeded in using the initia-
tive process in the state to pass Proposition 63, the Mental Health Ser-
vices Act (MHSA), which placed a 1% state tax on incomes over 1 million
dollars to transform and expand the reach of the state’s mental health
services. The MHSA mandates that counties spend between 75% and
80% of the funds allocated for community services and supports for
people in immediate mental health crisis and between 15% and 20% on
prevention and early intervention. Counties can also allocate up to 10%
of the funding for innovative practices. In 2017, Assembly Bill 1315 es-
tablished an advisory committee to the Proposition 63 Mental Health
Services Oversight and Accountability Commission, which was de-
signed to encourage the expansion of detection and intervention ser-
vices for early psychosis and mood disorder.
The MHSA, although variable in implementation and overall suc-
cess, nonetheless resulted in a plethora of experimentation and innova-
tion at the county level in the provision of mental health services. This
included the establishment and ongoing funding of FEP programs,
mostly using the prevention and early intervention or innovative prac-
tice components of the MHSA. Some MHSA-funded programs
emerged as state and national models (e.g., the Sacramento Early Diag-
nosis and Preventative Treatment [Sac-EDAPT] clinic). Many of these
programs combined available patchwork funding, including Medicaid,
EPSDT, and MHBG resources, with substantially more flexible and gen-
erous MHSA resources to establish and sustain their CSC programs.
The flexibility in county implementation of the MHSA promoted
variability and innovation. However, limited guidance on how MHSA
dollars are allocated and used also allowed for variation from estab-
lished fidelity, training, and quality improvement practices. Conse-
quently, behavioral health services, including CSC and other FEP
programs, may not be consistently implemented or available across

counties. Other aspects of CSC implementation beyond funding, such
as training, availability of providers, stigma, and broader systemic is-
sues in the adult- and child-focused behavioral health systems, can re-
main barriers in implementing effective CSC programs even with the
availability of relatively flexible MHSA funds. A central lesson from the
implementation of MHSA in California to date mirrors those discussed
earlier: adequate and flexible funding, although essential and poten-
tially promoting innovation, is nonetheless not sufficient for assuring
efficient, equitable, and effective service delivery, including CSC, for in-
dividuals with FEP.
KEY CONCEPTS
Evidence strongly suggests that providing effective early psychosis
services, including coordinated specialty care (CSC), constitutes an
important component to addressing the significant public health
problem posed by schizophrenia. There are numerous key policy
concerns that emerge in considering how to promote the wide-scale
implementation of these services, including the following:
• Financing CSC programs is currently complex and difficult.
Public financing, mostly provided through Medicaid, does
not cover all the necessary components of CSC. Private
insurance covers even fewer components. Consequently,
states currently rely on a combination of state general funds
and federal grants and waivers to cover CSC services. States
vary with regard to both how widely Medicaid is imple-
mented under the ACA and how extensively they use local
funds or apply for waivers and grants. Legislative changes or
administrative modifications to the ACA could serve to roll
back gains made by the legislation, including expanded
Medicaid services; extended commercial insurance options
for youth younger than age 26 who are covered by parental
plans; and the protection afforded individuals with preexist-
ing conditions, including schizophrenia.
• The transition of adolescents with psychosis from child-
serving behavioral health and related systems to adult ser-
vice systems creates particular policy challenges for this
population. Funding options exist for children and adoles-
cents that do not have comparable adult mechanisms. The
gap between adult- and child-serving systems also creates
problems for continuity of care, for consistency in the

skills of providers and organizations, and for advocacy on
behalf of youth and young adults with psychosis.
• Access to services and quality of care both have unique
policy concerns that extend beyond financing. Increased
coverage does not directly translate to increased access.
Stigma, inadequate referral mechanisms, workforce issues,
and service system fragmentation all may create barriers to
accessing services. Services also may be provided without
sufficient fidelity and to populations beyond those experi-
encing first or early episodes of psychosis for which they
were not originally intended, reducing their potential
effectiveness.
• Creating and maintaining a well-trained workforce who
can address the special needs of transitional-age youth
experiencing psychosis requires bridging adult and child
modalities; drawing from different therapeutic and train-
ing traditions; and modifying curricula, practicum, and
continuing education requirements. Creating teams dedi-
cated to treating early psychosis may prove difficult in
areas with small populations and/or low population den-
sity and in more remote locations.
• Mobilizing for policy change is essential and remains
potentially difficult for adolescents and young adults expe-
riencing psychosis. Child- and adult-focused advocacy
organizations vary in perspective and approach. The
involvement of young adults, adolescents, and families can
be hampered by stigma and competing interests for scarce
resources. Provider groups similarly vary, potentially creat-
ing additional confusion among policy makers and admin-
istrators.
1. How can policy for early treatment of psychosis create more

seamless funding options across the child- and adult-focused
services systems while addressing the existing gaps in fund-
ing for CSC services so that the existing patchwork financing
quilt is more coherent?
2. What policies best address the need to improve access, fidel-

ity, and quality of care and at what level should they be im-
plemented? For example, are federal or state guidelines more
likely to impact local service delivery?
3. What can professional organizations, institutions of higher

education, and accrediting bodies do to improve the work-
force of providers skilled in the treatment of early psychosis?
4. How can advocates across the child- and adult-serving sys-

tems unite to bring a coherent youth and family voice to the
policy debate?
5. What is the optimal role of temporary, allocated, or leveraged

funding such as waivers and block grants in creating sustain-
able and effective service delivery systems for young people
experiencing a first or early episode of psychosis?
Suggested Readings
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the first-episode Psychosis Services Fidelity Scale. Psychiatr Serv
67(9):1023–1025, 2016
Dixon LB, Goldman H, Srihari VH, et al: Transforming the treatment of
schizophrenia in the United States: the RAISE initiative. Annu Rev
Clin Psychol 14:237–258, 2018
Essock SM, Nossel IR, McNamara K, et al: Practical monitoring of treat-
ment fidelity: examples from a team-based intervention for people
with early psychosis. Psychiatr Serv 66(7):674–676, 2015
Goldman HH, Karakus M, Frey W, et al: Economic grand rounds: fi-
nancing first-episode psychosis services in the United States. Psy-
chiatr Serv 64(6):506–508, 2013
Shern D, Neylon K, Kazandjian MA, et al: Use of Medicaid to Finance Co-
ordinated Specialty Care Services for First Episode Psychosis. Alex-
andria, VA, National Association of State Mental Health Program
Directors, 2017. Available at: www.nasmhpd.org/sites/default/
files/Medicaid_brief_1.pdf. Accessed September 27, 2018.
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episode Psychosis Services Fidelity Scale. Psychiatr Serv 67(9):1023–1025,
2016 27032665
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553, 2015
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delity: examples from a team-based intervention for people with early psy-
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health system when the ACA is fully implemented. J Behav Health Serv
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first-episode psychosis: background, rationale, and study design. J Clin
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www.nasmhpd.org/sites/default/files/Medicaid_brief_1.pdf. Accessed
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Brookes, 2008
CHAPTER
5
First-Person Accounts of
Psychosis and Advocacy
Work
Carlos Larrauri, M.S.N., APRN, PMHNP-BC, FNP-BC
AN often overlooked aspect of the recovery process is the shift in both

an individual’s perspective about his or her own identity and that of
family and close friends. Changing the way we perceive experiences of
psychosis and learning that we are not alone in them is nearly as critical
as clinical intervention because it is often stigma—both self-imposed
stigma and societal misconceptions—that serves as the first barriers to
early intervention. Stigma promotes isolation, lack of information, and
shame. The ignorance and apathy that stigma breeds also constrain
funding for much-needed innovation in preventing and treating psy-
chosis. In our own personal journeys, we have found that the impact of
stigma is perhaps the biggest barrier to full functional recovery.
One of the most powerful tools we possess for chipping away at the
harmful effects of stigma is the sharing of personal narratives that sup-
port new, empowering notions about what it looks like to experience
mental illness (Rüsch et al. 2005). Connection—whether virtual or per-
sonal—with those who have fought for recovery has inspired each of us
along our own recovery paths. This chapter is meant to illuminate
many of the challenges that we faced and insights gained along this
path to help bring a more nuanced understanding of the power that
peers, strong support networks, and community support wield in the
recovery process.
59
The Role of Community and Family

Support in My Recovery
Carlos Larrauri
My Family and Childhood Years

I am the first-born son of Cuban immigrants and a child of the Ameri-
can Dream. My mother’s family came to the United States having
crossed the Rio Grande River when she was 6 years old. She crossed the
river in a rubber raft at the mercy of the people her family were paying
to smuggle them in. My father’s family immigrated from Cuba to Ven-
ezuela. He studied medicine in Spain and returned to Venezuela to
practice; however, facing economic and political uncertainty, he de-
cided to come to the United States. He started his career over in his late
thirties as a landscaper and used car salesman. My parents and their
families faced tremendous challenges as immigrants, but they never-
theless achieved the coveted American Dream that we often spoke of in
aspiring and revered tones.
My mother worked 35 years as a graphic journalist for the Miami
Herald. My father continued to simultaneously work and study, becom-
ing first a registered nurse and then a physician assistant. My parents
inculcated the expectation among my two brothers and myself that any-
thing was achievable and that much of the rest of the world did not
have the privilege of such economic or political security. Hundreds of
thousands of people leave their homes and family, risk their lives and
health, all for the opportunities we were born into. My parents worked
hard and made necessary sacrifices so that we could be raised within
the security and comfort of a middle-class life.
As a child I was happy and sociable. I enjoyed school work, and my
mother nicknamed me the mini-mayor for my outgoing personality. My
parents enrolled me in Little League Baseball and paid for piano and
guitar lessons, but I was mostly interested in playing Super Mario and
Donkey Kong. We spent summers at the beach watching Shark Week
and playing dominoes. I remember my grandmother in the kitchen fry-
ing croquetas and my grandfather drinking whiskey and smoking his
pipe. We spent winter vacations on road trips to the Great Smoky
Mountains, the closest place from Miami where we could see snow, and
there were several family vacations to European castles and monu-
ments.
By all measures I had an extremely privileged childhood. The only
darker memories of my childhood were the occasional instances of cor-
poral punishment for a poor grade or fighting among my brothers. In
First-Person Accounts of Psychosis and Advocacy Work 61
retrospect, it was within the context of what is normal for my parents’

culture and generation, but I do recall them as frightening experiences.
Otherwise, I am grateful for a fortunate and delightful childhood.
Adolescence and Prodromal Period

It was by the end of my eighth-grade summer that a shift began to occur
in my behavior and mood. I was introduced to weed by my older
cousin, and shortly thereafter, the focus of most of my efforts in high
school was on figuring out how to get high. I would meet a fellow stu-
dent on my walk to school, poke holes in a soda can and smoke weed,
and then we would start our day at school. On some days I would take
our half-hour lunch break to smoke cigarettes or a joint on my walk
home after school.
Toward the later years of high school, I experimented with harder
drugs. I would take ecstasy and dance all night at rave parties or trip on
mushrooms and LSD with friends at musical festivals or house parties.
There were a handful of times I tried cocaine and prescription medica-
tions such as Xanax and Valium. I identified with party subcultures
such as the rave and electronic music scene or hippie and psychedelic
music, but it was always weed that was the most frequent and consis-
tent drug I used to cope or connect with people. There were long peri-
ods of time when I was smoking weed every day or several times a day
and getting high with friends or alone.
Nevertheless, I was a good student throughout high school. I was in
mostly AP and Honors courses, and I graduated summa cum laude, par-
tially attending a dual enrollment program, where I earned college cred-
its at the local community college. The best opportunity I had available
after finishing high school was to attend an Early Admission Placement
program at the Ohio State University College of Medicine. At 18 years
old, I was offered a seat in medical school, and as long as I could maintain
a reasonable 3.2 GPA, I could avoid taking the dreaded MCAT. It was a
great opportunity that also included great expectations and pressures as
the first-born son in an immigrant family.
Crisis During the College Years

In hindsight, I may have gone through an untreated episode of depres-
sion during my freshman year at Ohio State. In my first couple of semes-
ters, I skipped classes, slept in for 10–12 hours, and gained 20–30 pounds,
and my GPA dropped to a 1.80. I remember for the first time feeling like
a minority person now that I was no longer among mostly Hispanic
people like at home in Miami. Furthermore, I had not yet developed the
study skills or coping skills to succeed in a more competitive environ-
ment, so I struggled without knowing whom to talk with or reach out
to. I befriended a few other minority people in the program, and we

quickly became stoner buddies who spent most of our time in the dorm
room, sheltered away from the unforgiving Midwest winter, getting
high and playing video games.
By the end of my second semester, I called my mom and told her I
wanted to come back home. She remembers that when she saw me for
the first time since going away for college, she was struck by how I had
let my beard grow unkempt. I came back home, started working, and
studied for a couple semesters at the local community college. With a re-
newed sense of momentum, I left home to complete a bachelor’s de-
gree, this time at New College of Florida. I was moving forward with
completing my studies, but I continued to struggle academically and
was placed on academic probation.
I can recall what was initially trouble with concentration and per-
forming school work. I would sit at my computer desk to write my se-
nior year thesis, but I would either space out or find it impossible to
focus. I also had increasing difficulty sleeping and would stay up until
the early hours in the morning, talking or rhyming to myself as if in a
spoken word contest. I began my studies at New College of Florida as
a literature major, with the reasoning that I could write well, so I should
develop this skill, but by my senior year I was taking mostly religious
coursework and becoming increasingly preoccupied with reading reli-
gious texts.
At the time, I felt something was off, so I went to see the school psy-
chologist. We had several visits and talked about the pressure of writing
a senior-year thesis, but we failed to intervene or identify the growing
severity of the situation. I continued to develop a profound sense that I
was having a religious experience. I started hearing whispers assuring
me I was a prophet and an angel being initiated into a greater realm of
spiritual existence. The voices grew louder and began saying, “You are
so good...you are so beautiful....” What started as whispers grew into
a noisy cacophony of conversations and chaos. I started to believe that
the religious text I was reading was speaking directly to me and telling
me that I would live to a hundred years or that I would be rewarded
with great financial prosperity. There were nights when I would lie
down to smoke a cigarette and watch with wonder and awe as the
smoke from my cigarettes and clouds in the night sky coalesced to form
crucifixes, doves, and other religious imagery. I was experiencing what
felt like the heavens directly opening up, and it was driving me toward
incessant tears, laughter, and joy.
Psychosis is an enigmatic experience that can be challenging to un-
derstand because it can be simultaneously profound, bizarre, and terri-
fying. On one occasion I stayed up all night, wrapped in a bed sheet in
front of my dorm room, posing and gesturing in mannerisms like the
Virgin Mary, and all the while, groundskeepers and students walked by
and proceeded with their day normally. I also became sexually preoccu-
pied and would loudly play pornographic material in the middle of the
day with my doors and windows wide open. I was sure I could smell a
woman’s vagina everywhere I went and would crudely say, “Do you
smell that? I smell pussy!” At times famous athletes or musicians such
as Dwayne Wade or Pitbull would talk to me through the radio or tele-
vision and say, “What’s up, Tino?” or “What’s happening, man?”
Most of all, there was a growing sense of fear and confusion. I re-
member experiencing what felt like my mind beginning to fail at pro-
cessing my environment. One day, I was sitting in class when my brain
could not understand the conversations of my classmates. The words
coming from their mouths became garbled sounds, and their gestures
grew distorted and menacing. As they talked over each other, their con-
versations grew louder and louder, and I became overwhelmed by
what felt like a torrent of environmental stimuli. It felt as if my identity
was beginning to disappear and disintegrate into this chaos. I was un-
able to express what was happening to me, so I left the classroom, feel-
ing confused and disoriented, and found somewhere isolated to smoke
a cigarette. On several nights, when the assault of the senses grew too
intense, I would find a few hours of comfort cradled in the fetal position
in a dorm room shower.
My friends and family were growing increasingly perplexed. Their
observations from this time noted that I began to talk incessantly about
Jesus Christ, and my gaze was fixated toward the sky like the martyr or
saint figures in Counter-Reformation paintings. I would laugh ner-
vously to myself and say, “Ah, good shit, man” in response to most so-
cial situations. My behavior grew increasingly inappropriate, and I
received several conduct violations at school, including an accusation
of having exposed myself to roommates in the dorms. By the end of my
senior year, I was nearly isolated from my college community and in a
state of florid psychotic hallucinations. I was eating meals out of the caf-
eteria trash cans, smoking cigarette butts off the floor, and wandering
the campus at odd hours as I rambled incoherently to myself.
A close family friend I had known since high school, who was also
attending New College, called my mother and said, “Something in Car-
los has changed that isn’t just stress or drug use. You need to speak with
Carlos right away.” My parents came to campus the following day and
we met with my academic advisor, who said, “Carlos, you are an adult,
and you have the right to privacy, and as such we don’t have to discuss
any of the academic or conduct violations that have occurred on cam-
pus.” Seeing the desperation and frustration on my mother’s face, I
said, “With all due respect, Dr. Clark, I have a Cuban mother; I have
never had the right to privacy.” This moment was a turning point that
opened the way for an honest conversation about my mental health
challenges at college.
The Right Diagnosis and Right Treatment

I was asked to leave campus but was allowed to finish my senior-year
thesis at home. I came back home, and my mother and I proceeded to
meet with nearly a dozen mental health professionals. I received several
diagnoses in the process of getting help. One psychiatrist, in his toxic
machismo, simply stated I was fine and needed to cortar caña, or do hard
labor.
During this period, my mother was in contact with a family friend,
Dr. Joseph Gonzalez-Heidrich, who is an Assistant Professor of Psychi-
atry at Harvard Medical School. Joe asked my mom, “Is Carlos still
playing music? How is his academic performance? How is his hy-
giene?” She said my guitar playing had turned into droning, as if I were
getting stuck on a chord or note, and that my hygiene and school per-
formance had deteriorated. I developed the habit of rolling my own cig-
arettes and smoking them down to my fingers, so the tips of my fingers
had turned yellow and orange from nicotine. Trying to get me to sit
down and finish writing my thesis was a source of conflict. Joe didn’t
provide a diagnosis but suggested we see providers for an appropriate
diagnostic workup.
We saw a team of mental health professionals for several months,
but all the while, my behavior was continuing to deteriorate. I had an
incessant manic energy and would exercise for hours at a time. I was
routinely jogging down the streets and singing at the top of my lungs. I
would go to the park to play basketball in the middle of the night, all
the while loudly cursing and laughing to myself. My mom, convinced I
would be arrested, quietly followed behind me in her minivan to be
sure I was really going to the park to play basketball or going for a mid-
night jog. During a fight with my youngest brother, I broke a glass win-
dow with my fist, and he retaliated by throwing broken glass back at
me. My father, in his own state of denial, was starting to call my mom
the crazy one for taking me to find treatment.
Five months into the evaluation process, my mother called the insti-
tution conducting the evaluation one early December day and said that
she would hold them liable if my behavior worsened or if I hurt myself
or somebody else. The next day, roughly 2 weeks shy of my 22nd birth-
day, we received a 12-page clinical evaluation that concluded with the
diagnosis of adult-onset schizophrenia.
Recovery in the Community

I remember seeing my provider after reading the report of my diagno-
sis. The provider was an incredibly accomplished man, with both an
M.D. and a Ph.D. He looked me in the eyes and with complete serious-
ness said, “Carlos, this isn’t good shit, man. We think you have schizo-
phrenia.” I said, bewildered and still in denial, “Doctor, what does this
mean? Will I be able to go to graduate school or work?” He said, “We
don’t know, Carlos. It’s up to you to take your medication and engage
in your recovery to see if your goals are possible.”
I was confused and unsure of what was going to happen next, and I
had my own expectations and prejudices of what it meant to be diag-
nosed with schizophrenia. I thought this meant I would stay at home
collecting disability, smoking cigarettes, and spacing out or talking to
the television. The roller-coaster ride of psychosis took me from the
highs of grandeur, where I thought I was Jesus Christ, to the lows of be-
ing labeled and belonging to the most stigmatized group in society. I felt
as if I had been branded with a scarlet letter that would forever haunt
my life, define who I was, and further incapacitate me.
Dr. Gonzalez-Heydrich, who had suggested that we get the diag-
nostic workup, also suggested that we connect with our local chapter of
the National Alliance on Mental Illness (NAMI). NAMI is the largest
grassroots organization that advocates and supports individuals with
mental illness and their families. My mother encouraged me to attend
the support groups, and at a support group meeting I met Judith Rob-
inson, a mental health advocate with 50 years of experience in Miami’s
mental health system. She took me under her wing and provided much-
needed guidance and direction. On her recommendation, I received
training to facilitate support groups and was encouraged to get in-
volved with the Board of Directors. The NAMI community supported
me as I attempted to make sense of my suffering and experience by
helping others with similar experiences. I was encouraged to share my
story at every opportunity and always felt safe and welcomed in doing
so. The community helped to normalize the experience, and I was able
to form several close friendships with peers and professional mentors
who had had similar adversities. With the support of family, friends,
and my NAMI community, I decided early on that I wanted to become
a mental health professional to work with others going through psycho-
sis or schizophrenia.
In the beginning phases of my recovery, my father would literally
hand me the medication and take me by the hand to enroll in commu-
nity college courses. This required me to get out of the house and navi-
gate my recovery in the community. I had to learn to cope with hearing
voices on the bus and in the classroom. I had to learn how to remain
calm and composed, even with the occasional flare-up of psychotic
symptoms. It felt like I was having to start my life over at 22 years old;
I had to develop a new sense of identity, purpose, and community.
Eventually, my volunteer efforts in the Miami mental health commu-
nity led me to a job interview with Cindy Schwartz from the Jail Diver-
sion Program (JDP) spearheaded by Judge Stephen Leifman. They
earnestly asked me about my lived experience with schizophrenia.
Cindy said, “It’s great that you went to a good school, but tell me about
what you went through. What was it like going through your episode?”
We talked about my experience with psychosis not in hushed or shame-
ful tones but as if it were a valuable asset that I would bring to the table
with future clients of their program. They also employed peer support
specialists and were vocal proponents of the recovery model, rooted in
the notion that when people get the right treatment, recovery is the nat-
ural and expected outcome with mental illnesses. Clients of JDP were
being diverted from criminal justice system involvement and into com-
munity-based treatment with medication, outpatient therapy, case
management, and peer support, and my job was to help to bring in the
federal dollars by helping clients apply for Social Security disability in-
surance. It was wonderful to help people in a practical and concrete
way, but I wanted to keep studying and had greater aspirations, so I en-
rolled in nursing school, with the goal of becoming a psychiatric mental
health nurse practitioner.
I completed an accelerated registered nursing program and began
working the night shift at a maximum-security forensic hospital. I rou-
tinely cared for the psychiatric and medical needs of up to 28 patients
with serious mental illness and pending criminal charges. The hospital
was rife with an undercurrent of violent and racial tension because
many of the patients were poor and minority individuals, and the risk
of assault was a daily reality. It was an eye-opening experience to wit-
ness the sad reality of the treatment of individuals with serious mental
illness in a public system.
I resigned after a coworker took a controlled substance out of the
medication administration system under my name and wouldn’t re-
solve the issue with me. Furthermore, the shift work and long hours
were starting to take a toll on my mental health. On several occasions, I
had been asked to work double shifts of 16 hours because of short staff-
ing and had to administer hundreds of medications and continue to re-
spond to crisis situations between staff or patients. It was an ethically
precarious situation to be part of, and I was complicit in a system that
was profiting from society’s sickest individuals, so I decided to leave
the job and refocus on my initial goal of going to graduate school.
I was experiencing burnout while working the night shift, and my
mother began recognizing another mental health decompensation. She
asked that I speak with Dr. Gonzalez-Heydrich, who had previously
guided us toward a correct diagnosis and NAMI. He said, “You’re go-
ing to start graduate school, and it would help to hunker down, so look
at your medication like this: something that is dynamic in response to
your stressors and workload. You’ve chosen a challenging career as a
fellow clinician, so why not increase the risperidone to 1 mg?” Over a
period of several years, I had weaned down to 0.25 mg of risperidone
to see if I could maintain my recovery on the lowest amount of medica-
tion or whether stopping medication was possible, but I could also rec-
ognize that I was beginning to struggle again. After failing the first
several exams of graduate school, I increased my dosage, and sure
enough, my academic performance, sleeping, and behavior began to
steadily improve once more.
Advocacy and Future Aspirations

I have been able to live my life in a much more productive and fruitful
way since engaging in recovery. I see the need to maintain a low-dose
medication regimen, possibly for the rest of my life, and continue to
check in with therapists and clinicians. Otherwise, I try to lead a gener-
ally normal and healthy life, avoiding drugs and alcohol, staying phys-
ically active, and finding meaning and sense of my experience through
work and helping others. I’m currently a board-certified family nurse
practitioner and practice in a child, adolescent, and adult psychiatric
practice. I treat patients in both English and Spanish and work in a col-
laborative setting with several nurse practitioners, licensed mental
health counselors, psychologists, and psychiatrists. I am pursuing a sec-
ond board certification as a psychiatric mental health nurse practitioner
at the University of Miami so that I may practice at the full extent of my
education and training. Nevertheless, I plan to continue to practice in a
collaborative and team-based approach because this leads to the best
outcomes for patients.
I am currently serving on the Board of Directors for NAMI, both at the
local community level with NAMI-Miami Dade County and in a 3-year
term at the national level. At the local level, we are a growing nonprofit
organization, offering free support groups and education courses for
family members and people with mental health issues. NAMI should
be considered a crucial part of care for people with psychosis because it
provides family support services and a welcoming community. At the
national level, I developed an agenda focused on continuing to change
the conversation surrounding mental health by sharing the stories of
people in recovery and with lived experience, focusing on early inter-
vention with the adolescent and young adult population and develop-
ing an understanding of the financial and policy-related skills necessary
to successfully advocate and create systems-level change.
I continue to share my story with students at local universities and
colleges, police officers in training academy, and health care profession-
als at community events. I hope the sharing of my story in this context
will help inform and shape the narrative surrounding early interven-
tion services for psychosis in some positive and productive way. I hope
to run for a second term with NAMI and build organizational partner-
ships with professional nursing, Latino/Hispanic, and youth organiza-
tions, as well as increase the representation and voice of diverse
perspectives and lived experience with mental illness at the highest

echelons of our society and government.
Embracing my identity as an individual in recovery has helped me
to manage an immensely challenging illness. It took a terrifying diagno-
sis of schizophrenia for me to form a healthy identity and develop a
strong sense of resiliency, but I am now able to find a deep gratification
and purpose in helping others overcome their own struggles with men-
tal illness. My recovery would not have been feasible without the im-
promptu team of people who have supported me along the way. Now
more than ever, we must continue to advocate for funding and services
that surround young people with support and care during the early
phases of this illness. To this end, I intend to pursue further graduate
education in either health policy or public health or to assist communi-
ties and organizations in developing systems for the prevention and
treatment of mental illness in youth. I am filled with gratitude and for-
ever indebted to the friends, family, and community who have sup-
ported me in this journey through recovery and well-being.
My Brother’s Road to Recovery:

A Sister’s Perspective
Chantel Garrett
Note: This narrative was written with the consent of my brother, Nate, who
wishes to be identified by his first name.
I will never forget the day that my brother was diagnosed with schizo-
phrenia. I was 22 at the time, having just started a career in financial ser-
vices in San Francisco. My brother, Nate, 16 months my junior, was in
the Active Marine Corps Reserve program, living on base in San Diego.
After months of concern over strange behavior that our family couldn’t
make sense of, I got a call from my mom at work saying my brother was
in the hospital and had been diagnosed with paranoid schizophrenia.
The mouthful of those two words hung heavy in the space between
us. None of us saw schizophrenia coming. I remember vague images of
movie characters portraying what I thought could have been schizo-
phrenia flashed through my mind. What is it, anyway? Were recreational
drugs to blame? Stress? What will this mean for his health, his future?
How did this happen? And will it happen to me, too?
Nearly 20 years later, even with all of the learning, advocating, and
progress we’ve made as a family, it hasn’t gotten much easier to recount
this story. But the unnecessary isolation and shame bred by the experi-
ence of supporting a loved one through psychosis motivates me to
share our experience. If nothing else, I want mothers, fathers, sisters,

and brothers to know that if their parent, sibling, or child is suffering in
a way that they could never have imagined, they are not alone. This is
our family’s story of navigating the bumpy, winding road of seeking re-
covery alongside my brother.
Growing Up
Nate and I grew up in San Diego with my mom, a single parent for most
of our childhood. The fact that our parents were divorced and lived a
couple of hours from one another was only made more apparent by the
intact family units we observed in our friends’ homes; neither of us can
form a mental picture of our parents in one room together, let alone in
love. In the summer and for a school year or two during our childhoods,
we spent time in the country with my dad and his family, offering us a
diverse set of experiences—being immersed in San Diego’s beach and
surf culture, gaining an appreciation for the performing arts through
our mom’s singing career, and time spent with our dad getting lost on
horses and quad bikes on back country roads.
Nate recently told me that the first time he heard voices he was
about 6 years old. He remembers he and I playing in the living room of
my grandparents’ home and hearing the first clear outsider’s voice
speak to him. It would be another 14 years until changes in his brain
manifested into a full-blown psychotic break. Changes that, unbe-
knownst to him or any of us, had been slowly manifesting since he was
a small child.
Now that I know that early psychosis is highly treatable, I can’t help
but wonder what would have happened had Nate shared his experi-
ences as a child or adolescent. What would have happened if my par-
ents had been aware of what these early experiences could foreshadow,
especially given a family history of psychotic disorders?
Family History
It wasn’t until my brother was diagnosed and I began to learn about
schizophrenia that I began to see my maternal grandmother’s behavior
through a lens of mental disorder. Fragments of hushed-tone conversations
that I had overheard as a child replayed in my mind: a midlife nervous
breakdown...hysteria...commitment to a psychiatric hospital...electric
shock therapy. A picture of my grandma’s struggle as some form of a
psychotic disorder began to take shape. I started to realize that her ex-
treme obsession with microscopic bugs that tormented only her and
that no one else could see was a form of a hallucination. Her intense sus-
picion of neighbors flashing lights in her windows and putting streaks
of water on her driveway were delusions. The elaborate daily system of
combating the bugs over a period of many years and my grandfather’s

unwavering support enabled her to cope with her symptoms. Never in
our upbringing was my grandmother’s mental health addressed or dis-
cussed openly. Even today, I don’t think that many of our extended fam-
ily members understand the depths of her quiet struggle that persisted
for decades.
First Signs
As I look back at our high school years, I can see the first signs of my
brother’s illness. Nate was formerly the wittiest guy in the room, but his
behavior became erratic in his sophomore year and he began to pull
away from his friends. His grades dropped precipitously. He holed
himself up in his room with his guitar, became obsessive about a girl he
had a crush on, and managed to teach himself Portuguese so that he
could speak with her in her native tongue. While he was at it, he became
fluent in Spanish as well. Drugs were definitely part of the equation. I
didn’t know how much, but at the time, I assumed that drugs were the
reason for Nate’s shift in behavior and his disinterest in school. My re-
action was similar to my mom’s: Get your act together!
I was away at my first year of college when Nate abruptly left high
school in his senior year and joined the Marines. It was extremely out of
character and not something he had ever talked about previously. With
the benefit of hindsight, I believe that he could have been trying to find
stability as he found the rigors of high school and the college applica-
tion process more difficult given the deterioration of his mental health
and was navigating an increasingly stressful situation at home.
First Hospitalization
I remember visiting Nate during that first hospitalization. There was
my brother, barely 20 years old. I was relieved that he was safe, that he
seemed less agitated. But where was he? He sat hunched over, a pale
shadow of himself, unable to speak, unable to make eye contact. His left
hand trembled lifelessly along his thigh. He was worn out from the
trauma of being held in the hospital against his best efforts to convince
everyone to let him go, from lack of sleep, and from his brain attempt-
ing to adjust to heavy medication.
His doctors spoke of the grave outcomes we should expect with par-
anoid schizophrenia. His social worker swiftly filed for medical dis-
charge from the military and set him up to receive long-term disability
benefits, referring him to a local group home to live in with other veter-
ans who were disabled by mental illnesses.
Months passed. Nate was no longer in a crisis state but did not show
many signs of improvement. He slept most of his days away. The few
friends he had left slowly faded away. He hated the medication, but it
was the only thing offered to him. There was no ongoing form of treat-
ment or therapy. My mom was told to call 911 if things got really bad,
and Nate would be taken to the hospital by police. A few months later,
that is exactly what happened.
Living With Schizophrenia: The Early Years

Over that first year, without knowing it, I began the process of grieving
the person I’d grown up with. I didn’t tell many people about Nate’s
health because most people appeared visibly uncomfortable by the con-
versation, tripping over comforting words as they looked as confused
as I once was about schizophrenia. This only reinforced how alone I felt
in our family’s suffering, on top of deep sadness and feeling over-
whelmed. Despite going to family education classes and group therapy,
opening up to people outside of my inner circle with relative grace and
confidence would take years of practice.
My brother’s well-being was exhausting to think about when our
family was not in immediate crisis (which was rare in the first few years),
so I tried not to. I went to therapy to try to cope with what felt like a dev-
astating loss and more stress than I could bear. In the first 10 years of his
illness, Nate went through intermittent, sometimes long, periods of opt-
ing not to take medication that took the roughest edges off his symp-
toms but left him feeling that life was not worth living. He regularly
cycled in and out of hospitals—often at the hands of police. He was held
in jail cells for days at a time with no medical attention while every hos-
pital bed was full. After being restrained in hospital beds and injected
with sedatives, it’s no wonder that he once leaped from a moving car in
order to avoid hospitalization. He was kicked out of his church for be-
havior they couldn’t understand. He was routinely the victim of fraud.
He was stolen from and taken advantage of by landlords and room-
mates time and time again.
One of our earliest struggles was that Nate could not live at home
because it was extremely triggering for him; those closest to him were
the root of most of his delusions. Unfortunately, he didn’t do well in
group homes, either. Nate found himself alienated and depressed
against a dreary backdrop. Most of his housemates, all of whom lived
with psychosis, were substantially older than he was. When they
weren’t smoking, they were usually watching TV or sleeping. Nearly all
had been long forgotten by family and friends. A few times each year, a
housemate would quietly pass away, most often decades before the aver-
age expected lifespan for a healthy American man. Within days, a new
veteran in need of supported housing would promptly take his spot. All
of this understandably terrified Nate, a 21-year-old who just 1 year earlier
seemed to have his whole life and full potential ahead of him. Nate de-
cided he was not going to be labeled a castaway disabled Marine who

would eventually be left to die a lonely death alongside his peers.
About 3 years into Nate’s diagnosis, he went missing. When we
found him, he was living in a commune-like setting in rural New Jersey,
in a “natural treatment center” that held the promise to take him off his
medication and replace it with healthy food. To my brother, this
sounded like exactly the miracle cure he had been waiting for. They had
taken thousands of dollars from him—his entire life savings—to fulfill
this promise, which was quickly made impossible when, like clock-
work, he slipped into severe psychosis on stopping his medication and
ended up hospitalized for several months. Despite our pleas and legal
threats, he was never reimbursed for his few weeks of “treatment.” The
paperwork he signed covered the center for all liabilities.
When my dad and I flew out to bring Nate home on hospital dis-
charge, the three of us went for a walk before the return home. I’ll never
forget the conversation I had with Nate that day, seated on a bench on
a glorious spring morning on the Princeton University campus. He told
us that his medication made him feel like he was drowning. He said that
not one doctor had yet attempted to listen to how he felt or offer any
hope of a future that he could envision for himself. He plainly stated
that he would rather be homeless or dead than take the medication or
endure any more treatment. It was the first time I was struck by this re-
ality—and I would be struck by it again and again over the years: as
much as I wanted my brother to be safe, happy, and well, I could not
force him to accept treatment.
It was then that I realized that although we could lead Nate down a
path and provide possibilities, the decision to take control of his well-
ness had to be his. He had to see treatment as valuable—a decision that
was now exceedingly challenging because his association with treat-
ment was painful, disempowering, and even traumatic. All I could do
in that moment was offer him love, compassion, deepest respect, and
even awe because the seemingly endless path of suffering that he had
been walking for the past several years was not something I would ever
understand first hand. I would never know what it was like to hear
multiple voices that try to cut me down throughout the day.
I wondered how we were going to hold on to hope that Nate would
be able to surmount these obstacles. I also felt more driven than ever to
find better treatment and support and show Nate that there was hope.
But I also knew that if it was going to work, he would have to be the one
to forge his path toward recovery.
Turning Point
After about 11 years of cycling in and out of hospitals, my brother fi-
nally surrendered. It did not mean he found a more meaningful life—it
meant that he couldn’t endure hospitalizations anymore, so he bitterly

took his medication every day and resolved to rarely step foot out of his
group home. He suffered long periods of grave depression and har-
bored intense anger at his situation. We especially worried about his
will to keep going during this especially dark time. This went on for an-
other six fairly miserable years, until, through mental health advocacy
work focused on prevention and early intervention that I had begun, I
was introduced to a U.S. Veterans Administration (VA)–based treat-
ment program in San Diego geared specifically toward people living
with psychosis.
The program, a partnership between the University of California,
San Diego and the San Diego VA, has been a game changer for my
brother. The program’s focus is cognitive-behavioral social skills train-
ing, which is exactly what it sounds like—a mix of cognitive-behavioral
therapy and social skills training. It focuses on real-world functional re-
covery, primarily through classes and group therapy aimed at helping
participants learn how to deal with all aspects of living with schizo-
phrenia.
For the first time since his diagnosis, my brother is now in a very
supportive living situation. And for the first time in more than a decade,
he now gets out into the community, is playing his guitar again and
studying online, and is making friends and seeking out things he is pas-
sionate about, like music. He recently told me that he is happier than
he’s been in a very long time, even though he is still frustrated with his
medication. This was surely a sign of breaking new ground; for as long
as I could remember, he had very rarely shared a hopeful or positive
thought about himself.
Reflection
I have often thought about what the past 18 years might have looked
like had Nate been able to access specialty care at the outset of his symp-
toms. Instead, our road was longer, but the impact of family, commu-
nity, and (although late stage) a specialized treatment team supported
Nate into wellness. I would like to believe that part of what led Nate to
finally accept the support of a treatment team was our family’s contin-
ued faith in him, leading him to finally conclude what we had known
all along: that despite illness, he had so much to offer the world and,
likewise, that engaging in the world had a lot to offer him—and that
was worth fighting for. He saw that we believed in him, the treatment
program practitioners and fellow participants believed in him, and his
new “house mom” and roommates believed in him. In the end, it took
a village to remind him of his remarkable strength, his wit, and numer-
ous talents. I have observed this virtuous cycle: his small daily victories
are noticed by others, offering him a motivation boost to step out and
try new things—to show himself that he can do even more. Ultimately,
he had to decide that it was time and make the effort to walk down a
new path. Finally, after 16 years of considerable struggle, he went for it.
Our family’s story is one of hope, endurance, and radical accep-
tance. If nothing else, it reinforces that it is never too late. Recovery is
not a linear path. It takes massive determination, persistence, and inner
strength. It also takes at least one person to not give up on you and keep
being patient and present, even when it seems impossible or hopeless.
Holding on to hope required me to proactively educate myself about
schizophrenia and to learn how to establish a relationship on equitable
terms with my brother. Most of all, it required finding a larger capacity
in myself to love unconditionally, to see myself in his suffering and to
recognize our shared infinite potential. My personal mission through
the nonprofit project I founded, Strong 365, is all about empowering
people with the tools to take that next step, no matter where they are in
their recovery journey.
If I knew at the outset of my brother’s first episode what I know
now, I might have been able to at least question whether changes in my
brother’s behavior were related to changes in his brain, especially given
a well-established history of mental illness in our family (which, as in
most families, was rarely discussed). I might have understood the im-
portance of treatment that aimed beyond simply muting my brother’s
delusions and hallucinations but also focused on regaining cognitive
function and social skills—the things that would have allowed him to
retain his identity, confidence, and independence sooner.
With the current standard of care, we underestimate the major side ef-
fects of antipsychotic drugs and undervalue some of the greatest deficits
that psychosis-bearing illnesses often carry with them: difficulty relating
socially and expressing emotion—core skills necessary for maintaining
relationships and contributing meaningfully to a community. For my
brother, becoming well enough to be discharged from an inpatient unit
meant that he was interested in living and showed fewer outward symp-
toms of psychosis. Hospital discharge also came with heavy doses of
medication that left him feeling numb or, in his words, like he was “con-
stantly drowning” and included no follow-up care or support. It did not
mean he was prepared to go to college, or apply for a job, or regain his
friendships; nor did he believe that these things were possible, as we
were repeatedly told by his many doctors that they were not.
Today, we can offer young people much-improved care focused on
prevention and early intervention. In order to ensure that more young
people can benefit from specialty psychosis care, we must spread
awareness and humanize and destigmatize these experiences.
Advocacy
When I first learned about the promise of early intervention for psycho-
sis, I felt as though I had just been let in on the greatest, most elaborate
secret in health care. How was it possible that early intervention ex-
isted, while families like mine suffered on the rough road to recovery or
never found it at all? The question haunted me, so much so, that I ap-
plied my experience as a corporate marketer to establishing a youth-led
nonprofit project that meets young people where they are (online) to
connect them earlier to mental health treatment and support.
Nearly 20 years after my brother was diagnosed, a lot has changed for
the nine million Americans (Perälä et al. 2007) like my brother who are liv-
ing with serious brain health challenges, but not nearly enough. It is well
understood that mental illness is the chief health issue for teens and young
adults: one in five young adults ages 18–25 are affected by a mental health
condition (National Institute of Mental Health 2017). Psychiatric disor-
ders are the number one disease burden for young people ages 10–24 (Ben-
yamina et al. 2012). Untreated mental health problems put us at risk for a
myriad of life-threatening health issues, including suicide, the second lead-
ing cause of death for 15- to 24-year-olds in the United States (Xu et al.
2016).
Yet only half of teens and young adults get the treatment they need and de-
serve (Substance Abuse and Mental Health Services Administration
2015). My family’s story—and the hundreds of others I have met in do-
ing this work who have walked similar paths—inspires me to be a small
part of changing young lives through early intervention.
KEY CONCEPTS
• It is essential that narratives of individuals with lived experi-
ence of psychosis are shared with consumers, families, and
health care providers. These narratives demonstrate the rich
experience of recovery, represent diverse cultural and eth-
nic experiences, and offer hope to all stakeholders.
• There is need for a team that provides psychosocial ser-
vices in addition to medical care. Although medication is
often necessary, it is not sufficient. Psychosocial services
such as peer support, family education, and supportive
work or school environments get people back into the
community and functioning.
• Advocacy is necessary to ensure reduction of harmful
stigma that keeps young people and their families from
seeking help and to increase funding for services and

research. In addition, it provides a pathway in recovery for
people to help others, create meaning from their experi-
ence, and leverage their lived experience in a career in the
helping profession (e.g., peer support, counselor, clinician).
• The presentation of an acute crisis may be years after the
onset of subtle behavioral changes or even longer from
the onset of neurodevelopmental abnormalities. Early
intervention is crucial for curbing the impact of untreated
psychosis. We must create a pathway to care from a sys-
tems-level perspective so people can engage care before
an acute crisis that disrupts the family and community life.
1. What has been your experience with psychosis or with psy-

chosis of a loved one?
2. How do you draw on this experience in the work that you do?
3. How will you advocate for team-based care and/or care that
incorporates psychosocial services, family, or community in-
volvement in recovery?
4. How is your team equipped to develop and share personal

narratives of recovery?
Suggested Readings
CureSZ Foundation: Schizophrenia Survivors, https://curesz.org/
resources/schizophrenia-survivors
National Alliance on Mental Illness: Early Psychosis and Psychosis,
https://www.nami.org/earlypsychosis
OnTrackNY: www.ontrackny.org/Videos—personal stories of recovery
The Stability Network: Our Stories: Testimony to the Power of Healing,
www.thestabilitynetwork.org/ourstories
Strong 365: www.strong365.org—online resource for information on
early psychosis, treatment, online peer chat and personal stories
Time to Change: www.time-to-change.org.uk/personal-stories—personal
stories of recovery
References
Benyamina A, Blecha L, Reynaud M: Global burden of disease in young people
aged 10–24 years. Lancet 379(9810):29, 2012 22225669
National Institute of Mental Health: Mental illness: prevalence of any mental ill-
ness. Bethesda, MD, National Institute of Mental Health, November 2017.
Available at: www.nimh.nih.gov/health/statistics/mental-illness.shtml#
part_155771. Accessed September 28, 2018.
Perälä J, Suvisaari J, Saarni SI, et al: Lifetime prevalence of psychotic and bipolar
I disorders in a general population. Arch Gen Psychiatry 64(1):19–28, 2007
17199051
Rüsch N, Angermeyer MC, Corrigan PW: Mental illness stigma: concepts, con-
sequences, and initiatives to reduce stigma. Eur Psychiatry 20(8):529–539,
2005 16171984
Substance Abuse and Mental Health Services Administration: Behavioral Health
Barometer: United States, 2014 (HHS Publ No SMA-15-4895). Rockville, MD,
Substance Abuse and Mental Health Services Administration, 2015
Xu J, Murphy SL, Kochanek KD, et al: Deaths: final data for 2013. Natl Vital Stat
Rep 64(2):1–119, 2016 26905861
CHAPTER
6
Engaging Families and

Individuals in Care
Sarah Lynch, LCSW
Rebecca Jaynes, LCPC
PSYCHOTIC disorders, including schizophrenia spectrum and

mood disorders with psychosis, can cause severe functional impairment,
high rates of mortality, and comorbid illnesses, reducing life expectancy
(Breitborde et al. 2017). It is now clearly established that treatment as
early as possible in the course of psychosis is associated with significant
improvement in clinical and functional outcomes (Breitborde et al.
2017). A treatment delay of 1–3 years is common with psychosis onset,
and there is an 80% dropout rate within the first year of treatment
(Dixon et al. 2016). That said, treatment adherence is only the tip of the
iceberg in the world of engagement, which is multifaceted and complex.
The National Alliance on Mental Illness arrived at a definition of en-
gagement that incorporates diverse perspectives: “Engagement is the
strengths-based process through which individuals with mental health
conditions form a healing connection with people that support their re-
covery and wellness within the context of family, culture and commu-
nity” (National Alliance on Mental Illness 2016, p. 6). Engagement
should emphasize these contexts of family, culture, and community,
and we present a three-stage model that ensures engagement at all lev-
els. The three stages of engagement are 1) increasing early detection and
79
intervention by engaging the community with education and outreach;

2) working with participants and families in treatment through a pro-
longed, individualized, and creative engagement phase; and 3) main-
taining active engagement with participants and family members
through all phases of recovery with peer involvement. In Figure 6–1, the
three stages of engagement are pictured in a dynamic, synergistic way
to reflect that the more engaged a community is and the earlier the in-
tervention, the more recovery becomes possible. We recommend that
early intervention for psychosis (EIP) programs use this diagram as a
guiding principle in orienting EIP services toward engagement. More
detailed information and specific strategies can be found in the Sug-
gested Readings at the end of the chapter.
Stage 1: Engaging Communities

Through Outreach Education
The earliest examples of first-episode psychosis programs engaging
communities with comprehensive outreach education were English,
Australian, Danish, and Norwegian initiatives, the most comprehen-
sive being the Early Treatment and Intervention in Psychosis (TIPS)
project in Norway (Joa et al. 2008). Within a comprehensive model of
outreach, the TIPS project was able to show that by combining targeted
outreach and an easy access referral system, the region’s duration of un-
treated psychosis (DUP) was shortened from 114 weeks to 26 weeks,
which equates to a more than 75% reduction in DUP (Johannessen et al.
2001). A follow-up study confirmed that the benefits of community ed-
ucation are maximized when outreach engages the community with
consistent efforts over time, that is, dynamically reiterating the outreach
messages to the targeted audiences (McFarlane et al. 2010).
Adding to the data to support the benefits of outreach education, the
Portland Identification and Early Referral (PIER) program of Portland,
Maine hosted a nationwide study in the United States and in 2016 pub-
lished results that six distinct U.S. sites were able to both reduce stigma
and improve early identification for individuals at risk for psychosis
while adapting outreach efforts to the unique elements of their commu-
nities (Lynch et al. 2016). Furthermore, studies are now making it clear
that outreach and community engagement do not, in fact, require sig-
nificant funding but rather require creative use of current funding
streams to maximize referrals (Baumann et al. 2013). In fact, community
engagement can actually become the backbone of an EIP program’s ac-
tive referral network.
By developing a comprehensive outreach plan, the synergistic effect
of multiple components of outreach education paves the way for EIP
Engaging families and individuals
in care
1. Community outreach and early

detection
• Targeted community outreach
• Create a network of early 1. Community
identifiers in the community outreach and
• Showcase stories of recovery via
program graduates and families
early detection
2. Initial individual and family
engagement
• Create accessible, flexible
program
• Team-based approach
• Participant-driven treatment
2. Initial individual • Family education to engage
natural support
and family • Use of MFGs to strengthen
engagement family and participant
Engagement
engagement
Early intervention
Engaging Families and Individuals in Care
3. Long-term peer and family

engagement 3. Long-term peer
• Foster peer and family and family
connections and support through engagement
MFGs, family education, wellness,
life skills, creative groups
• Develop peer expertise from
within: steering council, speakers
bureau, peer mentors
FIGURE 6–1. Engaging families and individuals in care.

81
Abbreviation. MFGs=multiple-family groups.

programs to operate within an engaged community—one that is aware

and informed of the benefits of early intervention, one that is open and
interested in accessing services across otherwise existing cultural and/
or economic divides, and one that is motivated and engaged to make a
difference to end stigma against mental illness (McFarlane and Jaynes
2017). Within this framework, individuals who are in need of services
are inherently more likely to engage in services. Likewise, their family
members, friends, and professionals who interact with them most often
(e.g., school staff, primary care providers) are more likely to refer (Ruff
et al. 2012).
In 2017, McFarlane and Jaynes from the PIER program developed a
technical assistance manual for the Substance Abuse and Mental Health
Services Administration’s Center for Mental Health Services, which
outlines in greater detail what is defined as a “comprehensive outreach
plan” to engage communities. This is the first manualized guide to walk
program developers and clinicians through full implementation of an
outreach plan, and it is available at the National Association of State
Mental Health Program Directors (NASMHPD) website (McFarlane
and Jaynes 2017). This guide provides an outline and step-by-step tools
to support the seven primary components of a comprehensive outreach
plan, including mapping community strengths and needs, establishing
a steering council, developing and tailoring messages to specific tar-
geted audiences, and other related efforts aimed at ensuring multifac-
eted, continuous community engagement (McFarlane and Jaynes 2017).
A crucial aspect of community engagement is the inclusion, on all
levels, of peer experiences of successful, engaged treatment. Peer stories
and voices illustrate the hope inherent in a successful outreach message
and are the means to both promote early intervention and provide op-
portunities to showcase and engage young people and their families at
all levels of recovery in mental health and wellness. With peer involve-
ment, stories of people who have benefited from early intervention and
are living well with good self-care and experiences of psychosis begin
to go hand in hand with the message of early identification and reduced
stigma. Maintaining these peer connections with program graduates in
this nonclinical outreach/peer role provides incredible opportunities
for wellness and relapse prevention for individuals, keeping them en-
gaged in all phases of their mental health journey. Engagement then
comes full circle—both helping individuals get to services sooner and
helping them stay engaged and active longer in the realm of mental
health and wellness. Young people in recovery benefit personally from
the experience of directly helping others and give authentic voice to a
misunderstood topic. Peer involvement will be discussed in more detail
in stages 2 and 3, increasing and maintaining active engagement with
participant and family members through all phases of recovery.
Engaging Families and Individuals in Care 83
Stage 2: Increasing Engagement in

Treatment for Individuals and Families
The next stage is engaging young people and family members in effec-
tive treatment. In this section, we outline important elements of early
psychosis programming that contribute to strengthening engagement:
a team-based program that is accessible, flexible, and culturally sensi-
tive and offers individualized, person-centered, goal-driven treatment,
with open involvement of family members and other supports identi-
fied by the individual. We also focus on the unique role that peer sup-
port plays with the team.
Creating Accessible, Flexible Programs

for Engagement
Adolescents and young adults with early psychosis are at high risk of
disengagement, with the most influential factors being duration of un-
treated psychosis, symptom severity at baseline, lack of insight, per-
sistent substance abuse, and absence of family involvement and
support (Doyle et al. 2014). Other influences are involvement with the
criminal justice system and lack of youth-friendly services (Becker et al.
2016). It is understandable that individuals experiencing paranoid and
disorganized thinking and fear about their safety may not readily en-
gage in treatment. Therefore, offering a prolonged, individualized en-
gagement period with involvement of family and other natural
supports is critical to successful engagement.
Mental health systems and the rules that dictate treatment guide-
lines often unintentionally create barriers to access and engagement
(Dixon et al. 2018). For example, outpatient treatment clinics often re-
quire multiple steps before engagement in treatment: the adult client
must call a referral line; provide a lot of information, including history
and insurance; attend an orientation appointment; and sometimes be
put on a wait list for the next available intake appointment. If people do
not show for appointments, they are often discharged without follow-
up. Removing these practical barriers to engagement is a key compo-
nent to engagement in EIPs (Dixon et al. 2018).
The timing of engagement is an important factor. A delay in help
seeking can have long-term consequences in terms of the young person’s
insight about symptoms, willingness to engage with providers, treatment
response, and outcomes. It can also increase family stress and negative
family dynamics, which exacerbates symptoms (McFarlane 2016).
Stewart (2013) emphasizes that worsening of psychotic symptoms
and hospitalization can be traumatic and act as a motivation toward re-
covery. Therefore, coordinated specialty care (CSC) team staff meeting

young people in the hospital and assisting with their transition to com-
munity-based care can be a critical opening for engagement. At the
PIER program, it is best practice to have both the clinician and peer sup-
port make a connection with the young person while he or she is in the
hospital and offer the program as voluntary and flexible in meeting the
individual’s needs (Stewart 2013).
Ensuring That Services Are Person Centered

and Goal Driven
Client narratives reveal an early disconnect between what the client
thinks is happening and the actions of family, criminal justice, and
health care systems that may lead to distrust (van Schalkwyk et al.
2015). Treatment providers may focus on symptom levels and behav-
ioral changes, whereas the young person’s goals may be related to rela-
tionships, housing, or school. It is important for the provider to listen to
and validate the experiences and concerns of the young person and be
responsive to his or her perceived concerns.
A literature review about common elements leading to engagement
indicates the importance of comprehensive assessment of the client’s
values and beliefs, goals, race/ethnicity, sexual orientation, religion,
and lifestyle choices (Becker et al. 2016). Cultural sensitivity to meaning
and interpretation of experience are key to trust building. “Providers
who are able to acknowledge cultural differences in how patients con-
ceptualize symptoms, and address how such differences impact pa-
tients’ decisions to follow providers’ recommendations, may have
greater success engaging patients of different cultures and ethnicities”
(Kline and Thomas 2017, p. 75). Given local and cultural differences
within communities, there needs to be some flexibility within evidence-
based practices to individualize and adapt practices to meet the needs
of diverse groups (Kline and Thomas 2017).
Recovery in mental health is broader than symptom reduction or re-
moval. We need to ask service users more about what they value in
terms of recovery. In one study’s exploration of service users’ views of
recovery, four different recovery styles emerged: collaborative support
and understanding, emotional change through social and medical sup-
port, regaining functional and occupational goals, and self-focused re-
covery (Wood et al. 2013). Collaborative support emphasizes positive
thinking, openness to support, and understanding; emotional change
through social and medical support highlights addressing emotional
distress and depression as primary; and regaining functional goals il-
lustrates the importance of reengaging in social and vocational roles.
On the other hand, self-focused recovery is preferred by people with se-
vere and enduring psychosis who may have had negative past experi-
ences with treatment and who focus on the internal process of recovery
(Wood et al. 2013).
EIP programs, such as CSC teams, offer a team-based approach in
which engagement in treatment may occur through different pathways
for different people on the basis of each person’s identified goals. These
pathways include cognitive-behavioral therapy for psychosis (CBTp),
medication management, vocational or educational support, peer sup-
port and family psychoeducation, and group and recovery options. In-
dividualized care driven by the participant’s life goals and the
convenience of “one-stop shopping” with services all on one team and
easily accessible are important elements of engagement for young peo-
ple (Lucksted et al. 2015). In one study, interviews with young people
revealed that the combination of relationships with clinicians who are
client centered and humanistic in addition to peers who have also expe-
rienced first-episode psychosis influenced their decision to stay in treat-
ment (Stewart 2013). Key elements of individual engagement are “staff
flexibility, mobility, patience, warmth, and stamina over time...to navi-
gate ambivalence, illness and life changes” (Lucksted et al. 2015, p. 8).
Using Family Psychoeducation to Engage Family

Families coping with how to help a young person with untreated psy-
chosis experience fear, isolation, and distress (Cairns et al. 2015). With-
out an understanding of psychosis, family members may misattribute
changes to something other than psychosis, causing a delay in help
seeking and leading to a crisis point where symptoms become unman-
ageable and dangerous (Chen et al. 2016; Connor et al. 2016). Addition-
ally, family members’ cultural beliefs can influence their interpretation
of changes, leading them to seek help within their own community
(Connor et al. 2016).
CSC teams providing early intervention in psychosis have a signifi-
cant impact on engagement because they are able to offer education and
proactive outreach not only to the client but to his or her support net-
work as well (Dixon et al. 2018). Comprehensive monthly educational
workshops enable families and community members alike to learn
about psychosis as a spectrum of changes in thinking, perceptions, and
mental processing. These workshops should be made available to any
community member at no cost and include presentations by both peers
with lived experience and professionals with specialized experience
treating first-episode psychosis. The workshops emphasize the rela-
tionship between stressors, the environment, and symptoms and the
important role of family and friends in partnering in treatment. The
message of recovery and hope is key, with a combination of biological,
psychological, and social interventions leading to the best outcomes
(Addington et al. 2013). Offering educational workshops in a classroom
format allows people to gather information before making a commit-

ment to an EIP program.
Using Multiple-Family Groups to Strengthen

Family and Participant Engagement
Family psychoeducation, which is delivered most effectively in a mul-
tiple-family group format (MFG-FPE), is considered an essential evi-
dence-based component of early psychosis CSC treatment (Addington
et al. 2013). The MFG-FPE model addresses the family’s need for infor-
mation, clinical guidance, and ongoing support during the recovery of
their loved one. The model is based on a partnership between the family
(broadly defined as the participant’s trusted supports), the participant,
and the CSC team. At EIP programs, groups are co-facilitated by a com-
bination of disciplines (social worker, employment or education spe-
cialist, peer support, and case manager). The group is always inclusive
of the young person but can benefit the family system with or without
initial involvement from the client.
MFG-FPE is most effective when there is no delay in offering the
group at the beginning of treatment, when the family most needs sup-
port (Fjell et al. 2007). Groups offer ongoing enrollment so newcomers
can benefit from lessons learned by those at later stages of treatment
and experience hope through those further along in recovery. Although
psychoeducation can be provided in a single-family session, we have
found that connecting families with other families is most powerful in
deepening the family and individual’s engagement with treatment.
MFG-FPE addresses common feelings of isolation, stigma, family ten-
sion, and hopelessness in early psychosis by providing community,
normalization, skill building, and hope. Clinicians will need supervi-
sion and coaching on how to present this resource to families because it
is typical for people to refuse groups at the outset (Fjell et al. 2007).
Family Engagement Case Example

Laurence is a young man who describes that he has identified with
ghosts and dark or evil creatures for as long as he can remember and
that this has, in fact, fueled his creative style, identity, and art. At age 17,
Laurence caught the attention of his high school counselor, who was
concerned that he was “over-identifying” with ghosts in his often fright-
ening graphic images and writing. She referred Laurence to the local EIP
program; however, after the intake, his parents encouraged him to de-
cline the program because they felt that early intervention for psychosis
was not a fit. They felt that Laurence’s creative side was being misrep-
resented and misunderstood, and they wanted to protect him from the
stigma of “mental illness.” Laurence’s father was strongest in his reluc-
tance to engage with EIP services and most protective of his son; his
mother was uncertain and agreed to attend a community workshop to

get more information “for future reference.”
About a year later, in the stress of leaving home and transitioning to
college, Laurence said, “I was really stressed and vulnerable. . .then
something inside me just became bad or evil...and I was scared of it.”
Laurence was experiencing very distressing symptoms and was desper-
ate for help. He called his mother, who immediately called the program
to ask if it was “too late” to have Laurence start services. She then
brought both Laurence and his father to another community workshop
to learn more about psychosis. After the workshop, both Laurence and
his parents immediately engaged fully in the program, and, as his father
described, “I had no idea until I got here what this was or how to help
him. I was just doing my best with all I knew as a dad.” Laurence started
learning words to describe his experiences in specific ways to ask for
help from his family to support his recovery and wellness. Importantly,
he also started learning how to let them know when not to worry and
how to not hover too close. Laurence and his parents now regularly at-
tend multiple-family problem-solving groups, which support this pro-
cess openly, alongside other young people and their families who are
having similar questions and struggles. His father jokes about his initial
reluctance about services and how he’s “come around” with the support
of the group, the program, and, most importantly, Laurence.
Stage 3: Maintaining Active Engagement

With the Participant and Family
Members Through All Phases of
Recovery With Peer Involvement
The last phase of engagement gives young people and families an op-
portunity to offer assistance to those in earlier phases of recovery
through peer support, speaking opportunities, an advisory board, or
mentorship, which in turn leads to earlier intervention and ultimately
to social change and reduction of stigma. Similar to the model of peer-
based recovery, we begin our discussion of the role of peer support with
two narrative examples: first, a peer support’s story of immersion into
an EIP team and second, a participant’s story of her experience being
served by an EIP team with peer support.
Peer Narrative: Nyamuon

When I first started with the PIER program in the role of youth support
partner, my goal was to use my own lived experience to help young peo-
ple find a relatable person at the table and feel empowered by seeing
that raw presence partnered alongside their clinical team. Through one-
on-one work, I was able to form authentic connections with young peo-
ple by being nonjudgmental, listening openly, and offering some of my

own journey when relevant. Eventually, the young people learned how
to trust and be honest about their experiences.
At the time of my own first treatment 10 years ago, I had already
been dealing with symptoms and early warning signs of psychosis for
some time. When my first suicide attempt landed me in an inpatient
mental health facility, the stigma, shame, and fear of my mental illness
being discovered by my family and community hindered me from being
honest with the mental health professionals about my experience. Out-
side of the personal shame I had been feeling about the sexual abuse I
believe sparked many of my struggles, I was also carrying the cultural
responsibility to maintain normalcy and uphold my reputation and that
of my family in our East African community. Service providers coming
to the home or reaching out held a stigma in my community that as-
sumed blame was being placed on the parents, finding them unfit to
protect their children. These factors led to barriers in any real or effective
attempts at treatment. I wasn’t able to be honest and open about the
number of symptoms I was having and how they were affecting me day
to day.
As I became a peer support, through training in the components of
CSC (early intervention, community outreach, CBTp, and MFG-FPE), I
gained a deeper understanding of my own story and how long I had
been impacted by trauma and psychosis. This led me to explore not only
my experiences but also my interactions with the mental health system
and providers. In my role as peer support these past 3 years, I have dis-
covered possible engagement tactics that might have proven impactful
for me and beneficial to building my confidence, voice, and ability to ar-
ticulate what I was going through and what “better” would look like for
me. Being able to draw from my story and openly talk about the journey
from a place of strength and hope provides an example and motivation
for others in the program to feel less isolated by their experience and
hopefully be drawn or sparked to become a peer voice in supporting or
encouraging others who follow.
Over time, I have fully integrated into the team and have become an
equal and valued member. I have brought the youth peer support model
training to the PIER team and given the team insight into a different,
and more culturally informed, perspective. I have worked together with
the team to incorporate the peer voice into community outreach presen-
tations, family workshops, and initial meetings with clients and in co-
facilitating a multiple-family group.
Working with many people in the immigrant community, one of the
hurdles that prevents conversation around early detection or intervention
is fear and lack of understanding or ability to relate to the information be-
ing shared about psychosis and other mental health terms. Peer support
can and has acted as a bridge between communities and service providers
in helping to normalize conversations about mental health. The peer sup-
port role offers “lived experience” examples of what clinicians and psy-
chiatrists may discuss in more clinical terms. Peer involvement on a
clinical team can offer a nonclinical, recovery-based perspective that in-
corporates personal wellness, building healthy natural supports in the

community and opening opportunities for youth to establish their voice.
Peer Support Case Example: Helima

Helima, a 19-year-old young woman from an African country, did not
have family involvement because she came to this country on her own.
She was in a temporary living situation and attending high school spo-
radically. She had been hospitalized for suicidal ideation a year prior to
her referral but did not reveal information about past trauma or the ex-
tent of her psychotic symptoms at the hospital. It was not until multiple
emergency department visits with physical complaints that she was re-
ferred to an EIP program. Engaging her was challenging because she
was afraid of being rehospitalized. She was open to EIP staff coming to
her school to meet with her, especially after hearing that they might be
able to support her with her goals of completing school and finding a job
and more permanent housing. The team began to engage with the
school social worker in order to meet Helima at school. There were mul-
tiple attempts because she sometimes did not show. The peer support
and social worker finally were able to meet Helima at a school meeting.
The peer support, Nyamuon, who was also from an African culture,
shared parts of her own story in order to create a safe space and relatable
language to break down barriers of shame. She established a cultural
connection and shared experience with trauma and psychosis.
Nyamuon was the liaison between Helima and the program, enabling
Helima to begin to trust the team. Engagement was still a fluid process,
and the initial focus was on getting Helima into a transitional housing
program, which provided more structure and support. Eventually, she
joined a multiple-family group, accompanied by Nyamuon, and began
to feel more fully integrated with other peers and families in the pro-
gram. She said, “What makes me feel hopeful is helping someone else
and realizing I am not alone in my struggles.”
EIP programs are beginning to incorporate peer and family support,

leadership, and involvement in several aspects of their programs
(Dixon et al. 2018), and a technical assistance manual, “Peer Involve-
ment and Leadership in EIP Services,” is available at the NASMHPD
website (Jones 2016). The manual emphasizes involving peer and fam-
ily members in advisory councils, community mapping of resources
and strengths, and partnering with peer organizations in addition to us-
ing peer and family voices and stories of recovery whenever possible
(Jones 2016). Since 2015, the PIER program has partnered with the
youth-led peer support organization Youth Move Maine to include a
positive peer presence at all outreach opportunities, clinical groups,
family groups, and peer connections (as outlined in the section “Stage
2: Increasing Engagement in Treatment for Individuals and Families”).
Since the late 1990s, the PIER program has been incorporating peer
and family voice and engagement as people have come forth with an in-
terest in giving back and supporting the early intervention movement.

Videos and speakers bureaus allow peer and family voices to guide
community education through hope, recovery, and resilience. In the
PIER program, people tell their stories from the beginning in multiple-
family groups, and over time, their stories emerge and expand as they
make sense of their experiences and deepen their connection to a safe
community. These stories are documented in a peer creative expression
group through videos, stories, artwork, music, or poetry. Participants de-
cide whether their stories are shared only with the group or more broadly.
One of our PIER graduates is now a psychiatric nurse practitioner
and a regular speaker at conferences and in program videos, and she is
influencing the field by providing treatment to others. Another gradu-
ate still comes back to speak to peers and families after 15 years because
it is meaningful for her to offer her story of the ups and downs that ul-
timately shaped who she has become and made her stronger. Now that
peer support has become a critical component of EIP programs, there is
a lot of room for expanding how we involve peer and family voices to
all aspects of engagement, creating social change and breaking down
long-held stigmas and cultural divides.
Conclusion
Disengagement from mental health treatment occurs up to 50% of the
time, with more than 70% of dropout occurring after the first or second
visit (Lal and Malla 2015; Olfson et al. 2009). That said, treatment atten-
dance is a limiting measure of meaningful engagement (Lal and Malla
2015), which we hope to have described in this chapter as a more mul-
tifaceted process. We recommend redefining engagement to include
strengthening individual connections with participants through thera-
peutic alliance and program accessibility, as well as cultivating broader
circles of support with well-engaged peers, families, and communities
as a whole. These circles of engagement then become the cornerstone of
stigma reduction, early intervention, and treatment models rooted in
recovery, strength, and wellness.
KEY CONCEPTS
• Engagement is multifaceted and involves three primary
stages: community outreach, individual and family engage-
ment, and peer and family connections over time in recovery.
• Comprehensive community outreach with peer and family
narratives reduces stigma and increases early detection.
• Communities, individuals, and families are strengthened

when EIP programs are strongly rooted in engagement on
multiple levels with treatment, recovery, and natural and
peer connections.
Key Questions
1. How can EIP programs tailor evidence-based CSC models to

individualized approaches with engagement as the primary
premise?
2. How can CSC programs become more accessible to increase

engagement in early stages?
3. How can we rethink agency policies and processes to incor-

porate engagement-influenced principles?
4. How can programs build in and manage outreach program-

ming and recovery connections in addition to more tradition-
al treatment models?
5. How can we engage youth as peers in nonclinical ways to

maintain involvement over time?
Suggested Readings
Dixon LB, Holoshitz Y, Nossel I: Treatment engagement of individuals
experiencing mental illness: review and update. World Psychiatry
15(1):13–20, 2016 26833597
Jones N: Peer Involvement and Leadership in Early Intervention in
Psychosis Services: From Planning to Peer Support and Evalua-
tion. Rockville, MD, Center for Mental Health Services, July 26,
2016. Available at: www.nasmhpd.org/sites/default/files/Peer-
Involvement-Guidance_Manual_Final.pdf. Accessed September 28,
2018.
McFarlane WR, Jaynes R: Educating Communities to Identify and En-
gage Youth in the Early Phases of an Initial Psychosis: A Manual for
Specialty Programs. Rockville, MD, Center for Mental Health Ser-
vices, 2017. Available at: www.nasmhpd.org/sites/default/files/
DH-Community_Outreach_Guidance_Manual__0.pdf. Accessed Sep-
tember 28, 2018.
McFarlane WR, Lynch S, Melton R: Family psychoeducation in clinical

high risk and first-episode psychosis. Adolescent Psychiatry 2(2):182–
194, 2012
National Alliance on Mental Illness: Engagement: A New Standard for
Mental Health Care. Arlington, VA, National Alliance on Mental
Illness, July 2016. Available at: www.nami.org/About-NAMI/
Publications-Reports/Public-Policy-Reports/Engagement-A-New-
Standard-for-Mental-Health-Care/NAMI_Engagement_Web.pdf.
Accessed September 28, 2018.
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CHAPTER
7
Assessment of People in
the Early Stages of Psychosis
UNLIKE many medical illnesses and despite all the recent advances
in the area of early psychosis research, we still do not have a gold stan-
dard laboratory test to mark the presence of psychosis (McGlashan et al.
2010). Diagnosis of the clinical high-risk phase and the recent-onset
phase of psychosis relies on symptoms that can be observed by others
or symptoms that can be reported by young people themselves, remem-
bering that the young person may be suspicious or may be trying to
hide his or her difficulties. Diagnosis requires a high level of sensitivity
not only to existing symptoms but to the normal course of development
of young people and to the gradual change in their psychosocial func-
tioning. It is crucial for professionals to have an understanding of the
array of presentations of psychotic disorders and the natural history of
a psychotic episode, including the prodromal, active, and recovery
phases, as well as proficiency in performing psychiatric assessment.
Good assessment in early psychosis is an ongoing process, allowing for
the fact that symptoms are fluid and change over time.
It is important to understand that when people seek an early psy-
chosis evaluation, either they are distressed by their symptoms or oth-
ers are noticing a change in their functioning due to these symptoms.
For example, Alan experienced hearing the voice of the devil telling
him to walk barefoot down the middle of the highway. He struggled
against the commands of the devil, which left him distressed and
95
drained of energy. Brenda experienced a cold wave over her body when
she sat at the kitchen table. She reported that she thought this experi-
ence was the ghost of her dead grandmother coming to comfort her.
This did not distress her at all, but she started spending more and more
time sitting at the kitchen table waiting for Grandma rather than going
to school and being with her friends. In Alan’s case, the symptoms were
causing distress, and in Brenda’s case, the symptoms were interfering
with functioning. In both examples, the person needed intervention
and support.
The initial interview is a vital component of early identification and
intervention work. It serves as the principal means for understanding
the client’s experiences and leads to a diagnosis and treatment plan.
More than just taking a history to determine what condition the client
struggles with and how he or she is affected by it, an effective assess-
ment interview starts the therapeutic process. It has been stated that
poor interviews and/or misinterpretation of a client’s presentation can
be critical to that person’s future well-being and subsequent treatment
(UK Essays 2013). For example, when young people present first with
just the negative symptoms of psychosis, they are often misdiagnosed
with other disorders such as major depressive disorder, attention-deficit/
hyperactivity disorder, or even oppositional defiant disorder. They are
started on a course of treatment that not only does not address their to-
tal clinical picture but actually may worsen their existing condition. An
accurate assessment addressing the appropriate warning signs and
symptoms can prevent this from happening.
A component of conducting an effective assessment interview is to
have a framework to help explore potential problem areas and to recog-
nize that the success of an assessment is based on establishing a relaxed,
nonjudgmental atmosphere that promotes a trusting relationship, re-
duces tension, encourages engagement, and starts the therapeutic pro-
cess. Being flexible in how the interview is conducted, respecting the
client’s needs, being empathetic, and engaging in active listening all
contribute to successfully establishing a nonjudgmental atmosphere.
Paranoia and perceptual distortions are often a part of the early phase
of psychosis, and taking time to explain the interview process and what
the client can expect helps to reduce concerns and anxiety associated
with these symptoms. Being clear in defining expectations—what the
young person can expect from the interviewer and what the interviewer
can expect from him or her—reduces tension.
Many young people experiencing psychosis may be younger than
18 years or still living at home, so their parents or other family members
may be attending the assessment with them. For older or more indepen-
dent persons, the interviewer may want to encourage them to have a
parent, spouse, or other relative accompany them to the interview.
These involved family members may be able to provide details about
Assessment of People in the Early Stages of Psychosis 97
the person’s functioning and provide additional and/or collaborative

information about his or her developmental, medical, and educational
history and history of extended family mental health concerns.
With permission from the client, the interviewer works collabora-
tively with family members during the initial stage of the assessment to
help define the family support system. The interviewer clearly defines
the boundaries of confidentiality for everyone, emphasizing the type of
information that cannot be kept private, especially around issues of
self-harm or intent to harm others. Risk assessment, including issues of
neglect, should be a part of every evaluation (Halpin 1995). With
younger persons, these issues usually refer to physical or educational
neglect from their parents, and with older persons, the issues may refer
to neglect of dependents. Assessing for victimization by others applies
to both younger and older persons. Risk assessment should include infor-
mation about past episodes of abuse or neglect, history of self-injurious
behavior, suicide attempts, and all relevant trauma history.
The interviewer should state that he or she will be meeting for a
short time with everyone together and then will complete the majority
of the interview with the client alone. The interviewer explains that he
or she will be asking for information about things that the client might
not be aware of, such as the status of the mother’s pregnancy and deliv-
ery and attainment of developmental milestones. The interviewer helps
the client understand that the interviewer is interested in the client’s
concerns as well as the concerns of family members, acknowledging
that the client’s perspective on things may differ from a family mem-
ber’s perspective and it is helpful for the interviewer to understand
both perspectives. The interviewer works to balance rapport, assess-
ment, psychoeducation, and assistance as he or she navigates through
the interview. Family members are often distressed and anxious about
the changes they see in their loved one, and they appreciate information
and support. The family’s distress, confusion, and denial, if present,
need to be acknowledged. Dismissing presenting problems invalidates
the family’s experience and may impede diagnosis and future treat-
ment for the client.
Family members also provide insight into the nature and culture of
the family. For example, it is not uncommon in American Indian families
for the entire family to accompany the young person to the assessment as
a sign of support. Assessors must do their best to accommodate this prac-
tice, even if it differs from their usual approach. Traditional healers are of-
ten used in American Indian and other cultures, and assessors need to be
familiar with indigenous beliefs and practices and to respect them even
if they differ from their own. A sociocultural framework is needed
during assessment so that diversity of values, interactional styles, and
cultural expectations are all considered. The roles that culture and eth-
nicity or race play in the sociopsychological development of the client—
how they help the client form his or her own identification and how
they impact the client’s beliefs and behavior—are significant factors in
understanding the psychological processes of the client. Asking open-
ended follow-up questions allows clients to frame their experiences in
their own way. This provides insight into the nature and context of the
experiences for the individual and how they impact the client’s percep-
tion of the intensity, frequency, distress, and interference from these ex-
periences. In addition, the American Psychological Association
recommends that all psychologists, regardless of their own ethnic or ra-
cial background, be aware of how their cultural background, experi-
ences, attitudes, values, and biases influence psychological processes
(American Psychological Association 1990).
A good place to start the assessment interview is with the reason for
the referral. It is helpful to establish clients’ understanding of the rea-
son; obtain their insight into how their difficulties are impacting their
day-to-day functioning; learn how they have attempted to cope with
these difficulties; clarify their aspirations, hopes, and goals for the fu-
ture; and evaluate their attitude toward the assessment interview and
their level of cooperation. Understanding whether the client had any
say in the decision to attend the interview can help or hinder how the
interview progresses. It is possible that attendance was not presented as
being optional, and the client may be angry and resentful about being
there. He or she may not cooperate with the interview process. If this oc-
curs, it can be helpful for the interviewer to acknowledge the situation
before moving forward with the interview.
Case Example 1
Carter is a 16-year-old male adolescent who has been struggling in
school, withdrawing socially, and becoming more and more irritable at
home. His teacher recommended that his parents call the clinic to ar-
range an evaluation. Carter’s parents, deeply concerned about their son,
quickly acted on the suggestion and did not spend much time discuss-
ing the reason for the referral or the interview process with him. At the
interview, Carter appeared sullen and withdrawn, and when he was
alone with the interviewer he quickly answered “No” to all of the ques-
tions. The interviewer, without embarrassment or hesitation, acknowl-
edged Carter’s behavior and validated his right to refuse to answer the
questions. The interviewer then explained to Carter that such a refusal
would impede their understanding of his symptoms and the inter-
viewer’s ability to offer suggestions for improving things and would
thus be a waste of time for both of them. Empowering Carter to make
his own decision about participating in the interview allowed him to
move forward with the assessment and obtain help.
Just like their family, young people may be confused and distressed
by their symptoms. The assessment interview provides an opportunity
to help them understand these symptoms and establish a framework

for engagement and compliance with their future treatment. Interview-
ers should take the time to explain to clients that they ask everyone the
same questions and that there are no right or wrong answers because
everyone has different experiences. Many young people have not
shared their symptoms with others, and they mistakenly believe they
are the only ones who experience them. Knowing that others share
these experiences, that there is a connection between psychotic-like ex-
periences and more conventional ones, normalizes their experiences
rather than identifying them as different, reassures the clients, and may
encourage them to share more details of their symptoms and experi-
ences.
Case Example 2
Daniela, a 17-year-old female adolescent, was referred for assessment
because school staff noticed she could no longer pay attention and at-
tend to her schoolwork. She had always been an excellent student, so
this was quite a departure from her normal presentation. Daniela did
not offer any explanation to her teachers or family for this change. When
she arrived at the clinic, the interviewer took the time to show her the
assessment form and to explain to her that the questions they would be
asking were not designed specifically for her experiences but were the
same questions asked of everyone. Halfway through the interview,
Daniela looked at the interviewer with tears in her eyes and asked, “You
mean there are enough kids who experience these things that you have
the questions written out?” The interviewer replied yes. Daniela visibly
relaxed and began to share more details about the voices and intrusive
thoughts that she was experiencing in school on a daily basis. This ad-
ditional information helped the interviewer to understand and commu-
nicate about the change in Daniela’s academic performance. It might
also be helpful to recognize that when discussing a person’s internal ex-
periences, a softer approach provokes less reactivity than a more direct
approach. Statements such as “I’m guessing it might be scary for you
when you hear voices” tend to be accepted more easily than a statement
such as “You get scared when you hear voices.”
The interviewer should also take the time to explain that the pur-
pose of the interview is to increase the client’s understanding of what
he or she is experiencing and to determine what might help the client
feel and do better in his or her daily life. The interviewer should help
the client understand that the interview is not intended to label or judge
him or her but rather to reduce his or her level of stress. The Personal
Assessment and Crisis Evaluation (PACE) Clinic in Melbourne, Austra-
lia acknowledges that young people can be difficult to engage because
of the nature of their symptoms, their lack of familiarity with or stigma
about mental health services, and their ambivalence about their need
for treatment (Thompson 2012). Staff at the PACE Clinic recommend us-
ing excellent communication skills, including active listening and em-
pathy; providing information and education about symptoms; and
working collaboratively with family members with the knowledge and
consent of the young person to help foster engagement. They also rec-
ommend offering the client a choice in where the assessment interview
should take place, which may require the use of mobile outreach teams
to conduct assessments outside the office and outside normal office
hours. Assessments should take place at a location and time that are
suitable and that accommodate the needs and preferences of the client
and his or her family to allow for school and work commitments.
The early identification and intervention model stresses the impor-
tance of assessing the entire spectrum of the client’s well-being (Goldner-
Vukov et al. 2007). This helps to establish the framework for evaluating
potential problem areas and for making an accurate diagnosis regard-
ing prodromal and psychotic symptoms. In addition to the reason for
referral and presenting problems and concerns, the framework should
include many other elements that are based on both interviewing and
observation skills.
Good observation skills allow the interviewer to collect information
that might not be in the client’s awareness. It is important to pay close
attention to the client’s presentation during the entire assessment, taking
note of anything unusual in his or her appearance in terms of self-care,
dress, and makeup. Observing abnormal motor activity, eye contact,
mannerisms, and posture as well as abnormalities in rate, tone, or abil-
ity to express and comprehend language adds important clinical details
to the assessment. The interviewer should also observe whether the cli-
ent attends to the questions and whether his or her thoughts are con-
nected and logical. The interviewer should take notice of untimely or
excessive affect, lack of affect, or affect that does not match thought con-
tent. All of these observations provide information that is vital in mak-
ing a valid assessment and diagnosis.
Other elements of the framework for the assessment are obtained by
directly interviewing the client. The interviewer should keep the client
talking with as little intrusion as possible. This is why open-ended
questions are so valuable. “How so?” or “Can you tell me more about
that?” serve as requests that keep the person talking. “To what extent”
can change any question to an open-ended one. For example, when in-
quiring about the impact of depressive symptoms on a client’s sleep, the
interviewer can ask “To what extent did your sleep change?” instead of
“Did your sleep change?” Phrasing makes a big difference in how ques-
tions are perceived. Instead of “How often have you been hospital-
ized?” the interviewer can say, “Please tell me about your other
hospitalizations.” The interviewer should avoid phrasing questions in
the negative, which implies an expected answer. For example, “You ha-
ven’t been smoking pot regularly, have you?” demands the answer
“No.” Double questions, such as “Have you had problems with your
sleep or appetite?” may be efficient, but they are often confusing, and
the client may respond to one part of the question and ignore the other.
There are also some other techniques that might be helpful with this
process. Experienced interviewers rely on nonverbal encouragements
to keep the client talking. Maintaining continuous eye contact, smiling
or nodding for appropriate responses, and leaning in a little closer all
indicate interest in what the person is saying. This technique increases
rapport and the person’s sense of well-being. Reassurance is a tech-
nique an interviewer uses to increase the client’s level of comfort during
the interview. To be effective, reassurance needs to be sincere, factual,
and specific to the situation. It should not appear forced or fake. The in-
terviewer should avoid generalizations. Because the interviewer cannot
predict the future, stating “I’m sure it will be fine” can seem hollow or
can reduce the interviewer’s credibility with the client.
A technique that encourages continued disclosure is to repeat the
client’s last word. For example, if the client endorses that he or she has
been feeling paranoid recently, the interviewer can respond with “Par-
anoid?” to encourage the client to continue along that same line of
thought. It also helps to briefly summarize what has been said so that
the interviewer and client are on the same page. For example, “As I un-
derstand it, you have been feeling paranoid recently.” There are times
when the client does not need encouragement to give information and,
in fact, may need encouragement to be brief. In this situation, the inter-
viewer must encourage brevity without impairing rapport. It is effec-
tive to state “I really want to hear more about that, but I am aware that
our time today is limited, so I am going to ask you to focus on this spe-
cific question.” The interviewer can nod or smile approval when he or
she gets the brief answer that provides the needed information.
Capturing the client’s medical and psychiatric history is another
piece of the framework addressed through the direct interviewing pro-
cess. It is important to learn about general medical symptoms, previous
diagnoses, previous hospitalizations and medical procedures, and all
prescribed medications or supplements. Medication side effects can
produce a variety of mood symptoms. You may occasionally encounter
a client whose depression was caused by cancer or a psychosis that was
the result of an endocrine disorder. The interviewer should explore all
past psychiatric symptoms and treatment, including hospitalizations,
and treatment compliance for both prescribed medications and thera-
pies. Blood work, physical examinations, and perhaps even a neurolog-
ical consultation may be warranted. Often, a mental status examination
is included in this part of the assessment interview.
Once the interviewer has captured the client’s major areas of diffi-
culty, he or she can explore all the details of the current episode of ill-
ness. This establishes a timeline for how and when the illness began, its
symptoms, the consequences, and possible stressors. The interviewer
should learn as much as possible about the symptoms: Are they con-
stant or intermittent? Are they changing in intensity or frequency? Are
they connected to certain places, situations, or time of day? After first
obtaining a complete educational, occupational, and social history, the
interviewer can query for the changes that have occurred because of
these symptoms. The interviewer should explore for changes in sleep
pattern, weight, energy level, and mood variation. He or she should
also query for the impact the symptoms are having on marital or love
relationships, sexuality and sexual activity, and friendships. The inter-
viewer should explore for any difficulties with impulsivity and any in-
volvement with the police or legal issues, including past arrests or
incarcerations, probation status, and pending court appearances. A his-
tory of past domestic or legal issues can help assess for future risk of vi-
olence and help the interviewer ensure his or her own personal safety.
The interviewer should watch for indicators of potential violence in the
client such as the use of threats or insults, rising pitch in the person’s
voice, aggressive behavior, or significant body language such as agita-
tion or clenched fists. The interview should be conducted in a room that
provides easy access to the exit for both interviewer and interviewee
and that is equipped with an alarm or is within earshot of other profes-
sionals who can provide help if needed.
The interviewer also should probe for information regarding drug
and alcohol experimentation and misuse. Orygen Youth Health approx-
imates that 60%–70% of young people with early psychosis report some
misuse of substances (Crlenjak et al. 2014). This makes screening for
misuse essential in early psychosis programs. The wording of the ques-
tions is important for obtaining honest information. Asking “How often
do you smoke pot in an average week?” as opposed to “Do you smoke
pot?” encourages clients to be open about their use. Further, it is helpful
to let clients know that this question is asked without judgment or prej-
udice and that the information is necessary in order to best understand
the nature of their condition and how to appropriately work with them
in pursuit of their goals. Clients should know that admitting to misuse
of substances is not grounds for termination from treatment so they can
feel comfortable with being more forthcoming. It is important to in-
clude synthetic, over-the-counter, and prescription drugs in the queries.
In addition to identifying the types of substances and the length and
frequency of use, the interviewer should query for the impact the use
has on the person’s day-to-day life and functioning. Substance use can
impact job attendance and performance, family and marital relation-
ships, friendships and social activity, financial status, medical health,
and legal status. Inquiring about the success or failure of any prior sub-
stance misuse treatment is very important in understanding the sever-
ity of the issue for this particular client and its relationship to the
symptoms he or she is experiencing.
Many tools are available to help with the evaluation and diagnosis
of early psychosis. You will find that these tools all share certain inter-
view techniques. Questions are worded in a softer manner that allows
clients to endorse their experiences freely: “Does it seem like your mind
(ears/eyes) is playing tricks on you?” “Do you become confused be-
tween what is real and what is imaginary?” “Do you find yourself feel-
ing mistrustful or suspicious of others?” “Do you feel like you have
special powers or abilities?” “Do you behave without regard to painful
consequences?” Following up these questions with “How so?” “Can
you tell me more about that?” or “What did you make of that when it
happened?” helps the interviewer understand the client’s internal ex-
periences. It is then crucial to inquire whether the experience was cap-
tivating or distressing to the client and whether it had an impact on his
or her behavior or functioning. These are all components of making an
accurate assessment of experiences and of developing the most appro-
priate treatment plan. Some of the assessments, such as the Structured
Interview for Psychosis-Risk Syndromes (SIPS; Miller et al. 2003), are ef-
fective in diagnosing the at-risk phase as well as documenting the onset
of transition to full psychosis, capturing the affective comorbidities and
substance use issues. Professionals should take the time to become fa-
miliar with the most commonly used assessment tools and how they are
suited to meet the needs of the population they serve (Fulford et al.
2014). Familiarity with these tools also helps identify the gaps in proper
assessment in early psychosis and aids in the improvement of existing
tools or the development of new tools. State-of-the-art assessment can
play a pivotal role in ensuring early identification and intervention in
psychosis.
Termination of assessment involves a summary of the client’s partic-
ipation in the process and the outcome of the assessment. Setting a tone
that is optimistic and avoids a deterministic viewpoint of psychosis and
emphasizes hope for recovery is crucial. The amount of information
shared depends on the nature of the outcomes, the state of the client’s
condition, and his or her ability to understand the information and the
recommendations for proposed treatment, further evaluation, or refer-
ral. Brain imaging or neurocognitive testing for memory, attention, ex-
ecutive functioning, language, and visuospatial and motor skills might
be part of the recommendations for future assessment.
It is important to remember that assessment in early psychosis is an
ongoing process and allows for the possibility that the diagnosis may
change over time. If no diagnosis is determined at the time of the initial
assessment, the recommendation might be to have the client return if
symptoms worsen or new symptoms emerge. Persons coming for eval-
uation are experiencing some level of distress from their experiences,
and even if they do not meet criteria for the at-risk or early-onset phase
or another comorbid diagnosis, they are in need of support. Establish-
ing an open discussion regarding the future course of action is import-
ant for the client being assessed. For professionals working in early
psychosis programs, it is important that they continue to enhance their
core skills in assessment and interviewing with additional training and
supervision so they can successfully provide beneficial evaluations.
KEY CONCEPTS
• Making an early psychosis diagnosis is a key component in
determining eligibility for coordinated specialty care services.
• Effective assessment skills of youth presenting with psychotic
symptoms are essential in mental health evaluation.
• Structured interviews are used to support valid and reliable
diagnostic evaluation.
1. How can your team support accurate diagnosis early in the

course of psychosis and how might this effect prognosis?
2. How would you ensure that assessment is culturally in-

formed?
3. What systems are in place, or what might need to be developed,

in your agency to conduct a structured interview reliably?
Suggested Readings
Comas-Diaz L, Griffith EH: Clinical Guidelines in Cross-Cultural Men-
tal Health. New York, Wiley, 1988
Garlikov R: The Socratic method: teaching by asking instead of by tell-
ing, 2012. Available at: http://www.garlikov.com/Soc_Meth.html.
Accessed February 13, 2019.
Miller TJ, McGlashan T, Woods SW, et al: Symptom assessment in
schizophrenia prodromal states. Psychiatr Q 70:273-287, 1991
References
American Psychological Association: Guidelines for Providers of Psychological
Services to Ethnic, Linguistic, and Culturally Diverse Populations. Wash-
ington, DC, American Psychological Association, August 1990. Available
at: www.apa.org/pi/oema/resources/policy/provider-guidelines.aspx.
Accessed October 1, 2018.
Crlenjak C, Ratheesh A, Blaikie S, et al: Let Me Understand: Assessment in Early
Psychosis. Melbourne, Australia, Orygen Youth Health Research Centre,
2014
Fulford D, Pearson R, Stuart BK, et al: Symptom assessment in early psychosis:
the use of well-established rating scales in clinical high-risk and recent-on-
set populations. Psychiatry Res 220(3):1077–1083, 2014 25278477
Goldner-Vukov M, Duska-Cupina D, Moore L, et al: Early intervention in first
episode psychosis: hope for a better future. Srp Arh Celok Lek 135:11–12,
2007 18368910
Halpin S: Assessment in Early Psychosis. New Lambton, NSW, Australia,
Hunter New England Health, 1995. Available at: http://sydney.edu.au/
medicine/psychiatry/workshops/presentations/assess_early_psychosis
(workshop).pdf. Accessed October 1, 2018.
McGlashan TH, Walsh BC, Woods SW: The Psychosis-Risk Syndrome: Hand-
book for Diagnosis and Follow-up. New York, Oxford University Press,
2010
Miller TJ, McGlashan TH, Rosen JL, et al: Prodromal assessment with the struc-
tured interview for prodromal syndromes and the scale of prodromal
symptoms: predictive validity, interrater reliability, and training to reliabil-
ity. Schizophr Bull 29(4):703–715, 2003 14989408
Thompson AD: The Pace Clinical Manual: A Treatment Approach for Young
People at Ultra High Risk of Psychosis. Melbourne, Australia, Orygen
Youth Health, 2012
UK Essays: Ensuring Effective Assessment in Psychiatry and Mental Health
Nursing Essay. Nottingham, UK, UKEssays, November 2013. Available at:
www.ukessays.com/essays/nursing/ensuring-effective-assessment-in-
psychiatry-and-mental-health-nursing-essay.php?cref=1. Accessed Octo-
ber 1, 2018.
CHAPTER
8
Assessment and Targeted

Intervention in Individuals at
Clinical High Risk for
Psychosis
Skylar Kelsven, M.S.
Kristin Cadenhead, M.D.
Case Example
Jane is a 21-year-old Latina college student in the fourth year of a 5-year
structural engineering degree at a top university. She was referred by her
therapist to a local early psychosis treatment center for evaluation of
symptoms indicative of possible prodromal psychosis. She experienced a
number of subsyndromal psychotic-like symptoms over the past 2 years,
but these symptoms had increased in intensity within the last 7 months.
Her psychiatric history was significant for anxiety and mood symptoms
in the context of childhood sexual abuse and neglect. Jane reported ex-
periencing dissociative reactions, hypervigilance, avoidance, and feel-
ings of alienation in response to trauma-related stimuli that had
occurred in childhood. In addition, she reported experiencing periods of
elevated and expansive mood that persisted for 2–3 days, followed by
periods of distinct low mood that lasted for weeks to months. She re-
ported smoking marijuana consistently since age 16 but using no other
drugs. She reported receiving psychotherapy and psychopharmacolog-
ical intervention (sertraline) for posttraumatic stress disorder (PTSD).
She has a family history of PTSD in both parents and bipolar disorder in
her father.
107
Jane was interviewed with the Structured Clinical Interview for

DSM-IV Axis I Disorders, Clinician Version (SCID-CV; First et al. 1997)
and the Structured Interview for Psychosis-Risk Syndromes (SIPS;
Miller et al. 1999). Jane stated that the presenting concerns had been
present for the past 2 years but had worsened significantly within the
past year. She reported multiple unusual, delusional-like beliefs such as
sensing that something was present around her and that she was being
observed. When queried further, Jane shared that the unexplained pres-
ence could be demons or ghosts and revealed that she avoided being
alone for fear of possibly being possessed. She noted that although these
experiences were distressing, she recognized that her ideas were un-
likely. Jane described herself as superstitious and admitted to putting
salt in her windows and hanging crosses. She reported believing she has
some psychic tendencies but was able to spontaneously generate insight
around the reality of this belief.
Jane disclosed that she has started to disassociate more over the past
year, daydreaming often and subsequently losing track of time. Jane
shared that she finds it increasingly difficult to determine reality from
daydreams and that she engages in a lot of “second-guessing” as to
whether or not these experiences are real. She indicated that she has had
these experiences for as long as she can remember. In the past year, Jane
reported that these symptoms could no longer be ignored, caused her to
avoid being around other people, and impacted her concentration in
class. Jane reported feeling hypervigilant of her surroundings and even
mistrustful of her close friends and boyfriend, suggesting suspicious-
ness and emerging paranoia. She explained feeling that others were
thinking about and talking about her negatively but denied being con-
vinced these thoughts were real. Further, Jane reported a number of per-
ceptual changes, including seeing shadows out of the corner of her eye,
accompanied by worries that these shadows might be a demon. Jane re-
ported feeling as though something touched her, which frightened her
and caused her to change locations. Jane also reported hearing a high-
pitched ringing noise and music, with no apparent source, approxi-
mately three times per week.
When asked about possible disorganization of speech, Jane re-
counted having trouble expressing herself to others, indicating that she
mumbled more than she had in the past and that her friends expressed
having difficulty understanding her. Jane stated that she had experi-
enced an increased incidence of losing her train of thought. During the
evaluation, the evaluator had to steer Jane back to the question at hand
and repeat questions. Jane disclosed that prior to the interview, she had
just completed her worst school year to date, with grades dropping
from As and Bs to Cs and Ds. Despite her reported dysfunction and de-
cline in school achievement, Jane reported that she believed herself to be
very intelligent and indicated that with “hard work” she could poten-
tially become a senator or accomplish something that would greatly im-
pact humanity. Jane reported that these grandiose beliefs were present
intermittently.
Individuals at Clinical High Risk for Psychosis 109
Jane met criteria for psychosis-risk syndrome (subtype attenuated

positive symptom syndrome) per the Scale of Prodromal Symptoms
(SOPS; Miller et al. 1999) (see Table 8–3 for a scoring summary). SCID
diagnoses included PTSD and bipolar II disorder. Jane also underwent
brief neuropsychological assessment during her initial clinical visit.
Tests administered included the Hopkins Verbal Learning Test–Revised
(HVLT-R; Benedict et al. 1998) and the Brief Assessment of Cognition in
Schizophrenia–Symbol Coding (BACS-SC; Keefe et al. 2004). Jane’s per-
formance on the HVLT-R was below average (HVLT-R Total Recall raw
score=20), whereas her performance on the BACS-SC was within nor-
mal limits (BACS-SC raw score=61). Comprehensive neuropsychologi-
cal assessment and magnetic resonance imaging were conducted
several days after the clinical interview and did not reveal any abnor-
malities or gross impairments.
Jane’s story is not atypical. If the clinician is unfamiliar with the cri-
teria for psychosis-risk syndrome, it is not uncommon for him or her to
incorrectly assume that this may be an example of acute psychosis or
conceptualize the experiences as better explained by PTSD. Unfortu-
nately, this quandary is far too common, leaving youth at clinical high
risk for psychosis without appropriate diagnosis or intervention. In this
chapter we broadly review the definition and diagnosis of psychosis-
risk syndrome, validated assessment tools for identifying individuals at
clinical high risk for psychosis, and targeted interventions for use in this
population. Jane’s story will be carried throughout this chapter as a
means to illustrate the nuances of assessment and intervention in indi-
viduals at clinical high risk for psychosis.
Definition and Diagnosis
Definition
The term prodrome is derived from the Greek words pro (before) and dromos
(running), with prodromos meaning “precursor.” In contemporary
medicine, the term prodrome is used to describe an early symptom in-
dicating the onset of a disease or illness. Formal diagnosis of a prodro-
mal state is made retrospectively. This means that before a period of
prodrome can be accurately identified, disease onset must occur. Subse-
quently, the period of respective changes during the time leading up to
disease onset is labeled the prodromal state or prodrome.
The psychosis prodrome has been objectively defined in a number
of ways. In 2013, the Diagnostic and Statistical Manual of Mental Disorders,
5th Edition (DSM-5) included attenuated psychosis syndrome in a list of
conditions for future study (American Psychiatric Association 2013).
The Structured Interview for Psychosis-Risk Syndromes (SIPS) defines
it as “prodromal-risk syndrome for psychosis.” The Comprehensive

Assessment of At-Risk Mental States (CAARMS; Yung et al. 2005) terms
it “ultra-high risk for onset of first psychotic disorder.” All iterations of
the term refer to the same set of defined symptoms that we will herein-
after refer to as psychosis-risk syndrome, of which there are three sub-
types: 1) genetic risk and deterioration syndrome, also known as the
vulnerability group; 2) attenuated positive symptom syndrome, also
known as the attenuated psychosis group; and 3) brief intermittent psy-
chotic syndrome, also known as the brief limited intermittent psychotic
symptoms group (Table 8–1). Individuals who meet criteria for one of the
psychosis-risk syndromes are referred to as being at clinical high risk
(CHR) for psychosis or in the prodrome of the first episode of psychosis.
Nomenclature aside, medical treatment intervention and practice
have shifted from an emphasis on curative to preventive care. As a re-
sult, mental health care providers are forced to conceptualize and assess
for pathology in a different way. Such is the case with psychotic disor-
ders, in which the opportunity for intervention and possible prevention
occurs during a nonspecific phase of functional decline and emerging
psychotic-like experiences (i.e., psychosis-risk syndrome).
Diagnostic Features
Compared with psychotic disorders, the symptoms of psychosis-risk
syndrome are less severe and more transient. Diagnosis requires that
symptoms are associated with functional impairment and/or distress
that is of recent onset or worsening. Symptoms are not long-standing trait
pathology; rather, individuals present with marked changes in their men-
tal state, evidenced through reports from self and concerned others. Fur-
ther, insight remains largely intact (Table 8–2). Affected individuals
maintain reasonable cognitive flexibility regarding psychotic-like experi-
ences and generally appreciate that altered perceptions and/or unusual
thought content are not real. Insight may be expressed spontaneously, or
the interviewing clinician may need to probe overtly for insight. Al-
though establishing the presence of insight is not emphasized in pro-
posed DSM-5 diagnostic criteria for attenuated psychosis syndrome, it
appreciably discriminates between psychosis risk and frank psychosis
(Box 8–1). For further reading on attenuated psychosis syndrome, see
DSM-5 (American Psychiatric Association 2013, pp. 783–786).
Box 8–1. DSM-5 proposed diagnostic criteria for attenuated

psychosis syndrome
A. At least one of the following symptoms is present in attenuated form,
with relatively intact reality testing, and is of sufficient severity or fre-
quency to warrant clinical attention:
1. Delusions.
2. Hallucinations.
3. Disorganized speech.
B. Symptom(s) must have been present at least once per week for the past
month.
C. Symptom(s) must have begun or worsened in the past year.
D. Symptom(s) is sufficiently distressing and disabling to the individual to
warrant clinical attention.
E. Symptom(s) is not better explained by another mental disorder, including a
depressive or bipolar disorder with psychotic features, and is not attributable
to the physiological effects of a substance or another medical condition.
F. Criteria for any psychotic disorder have never been met.
Source. Reprinted from American Psychiatric Association: Diagnostic and Statistical

Manual of Mental Disorders, 5th Edition, Arlington, VA, American Psychiatric Associa-
tion, 2013. Copyright © 2013 American Psychiatric Association. Used with permission.
Risk and Prognostic Factors

Psychosis-risk syndrome typically emerges in mid to late adolescence
or early adulthood. Preceding development can be normal, or the pres-
ence of impaired cognition, impaired social development, and negative
symptoms may be observed. Specific subtypes of psychosis-risk syn-
drome are identified through a formal structured clinical interview and
are differentiated through individual risk factors, as discussed in the
next section. Broadly, risk factors for psychosis-risk syndrome include
presence of attenuated positive symptoms, negative symptoms, cogni-
tive impairment or cognitive decline, decline in social and/or role func-
tioning, and family history of psychosis.
Assessment
A number of structured interviews have been developed for evaluation of
psychosis-risk syndrome. The selected assessment tools for identification
of CHR individuals reviewed in this section show excellent overall prog-
nostic accuracy and interrater reliability in trained raters (Fusar-Poli et al.
2015; Miller et al. 2003). The use of these tools in non-help-seeking indi-
viduals from the general population is not recommended because these in-
struments were developed for and validated in help-seeking populations.
Structured Interview for Psychosis-Risk Syndromes

SIPS is a diagnostic semistructured interview designed to be used with
an accompanying severity scale, the Scale of Prodromal Symptoms
112
TABLE 8–1. Psychosis-risk syndrome diagnostic subtypes
CHR subtypes
SIPS CAARMS SIPS diagnostic features CAARMS diagnostic features
Genetic risk and Vulnerability group 1. The person has met criteria for 1. The person has met criteria for schizotypal
deterioration schizotypal personality disorder, now personality disorder, now or in the past, and/or
syndrome or in the past, and/or the person has a the person has a first-degree relative with a
first-degree relative with a psychotic psychotic disorder.
disorder. 2. The person has experienced a 30% drop in
2. The person has experienced at least a SOFAS (Goldman et al. 1992; Yung et al. 2005)
30% drop in GAF score compared with within the past year, occurring within the past
1 year ago, sustained over the past month and sustained for at least a month, or
month. SOFAS score is ≤50 over the past 12 months or
longer.
TABLE 8–1. Psychosis-risk syndrome diagnostic subtypes (continued)
CHR subtypes
Attenuated positive Attenuated 1. The person scored 3–5 on one or more Subthreshold intensity
symptom syndrome psychosis group of SOPS items P1, P2, P3, P4, or P5. 1. Global score: unusual thought content 3–5,
2. The symptoms are not better nonbizarre ideas 3–5, perceptual abnormalities
accounted for by a DSM-5 disorder. 3–4, and/or disorganized speech 4–5
3. The symptoms occurred at an average 2. Frequency score: unusual thought content,
frequency of at least once per week in nonbizarre ideas, perceptual abnormalities, and/
the past month. or disorganized speech 3–6 for at least a week or
2 on more than two occasions, with symptoms
occurring during the last year
Subthreshold frequency
1. Global score: unusual thought content 6,
Individuals at Clinical High Risk for Psychosis
nonbizarre ideas 6, perceptual abnormalities

5–6, and/or disorganized speech 6
2. Frequency score: unusual thought content,
nonbizarre ideas, perceptual abnormalities,
and/or disorganized speech 3, with symptoms
occurring during the past year
3. The person has experienced a 30% drop in
SOFAS within the past year, occurring within
the past month and sustained for at least a
month, or SOFAS score is ≤50 over the past
113
12 months or longer.
114
TABLE 8–1. Psychosis-risk syndrome diagnostic subtypes (continued)
CHR subtypes
Brief intermittent Brief limited 1. The person scored 6 on one or more of 1. Global score: unusual thought content 6,
psychotic syndrome intermittent SOPS items P1, P2, P3, P4, or P5. nonbizarre ideas 6, perceptual abnormalities
psychotic 2. Symptoms are not better explained by 5–6, and/or disorganized speech 6
symptoms group a DSM-5 disorder. 2. Frequency score: unusual thought content,
3. Symptoms are not seriously nonbizarre ideas, perceptual abnormalities,
dangerous or disorganizing. and/or disorganized speech 4–6, with
4. The person does not meet DSM-5 symptoms occurring during the past year
criteria for a psychotic disorder. 3. For each episode, symptoms are present for less
5. The symptoms currently are present than 1 week, and symptoms spontaneously
for at least several minutes per day remit on every occasion.
(not more than 1 hour) at least one 4. The person has experienced a 30% drop in
time per month, up to an average SOFAS within the past year, occurring within
frequency of several minutes per day 4 the past month and sustained for at least a
days per week over 1 month. month, or SOFAS score is ≤50 over the past
12 months or longer.
Note. P1–P5 refer to positive symptom domains.
Abbreviations. CAARMS= Comprehensive Assessment of At-Risk Mental States; CHR= clinical high risk; GAF=Global Assessment of Functioning;
SIPS=Structured Interview for Psychosis-Risk Syndromes; SOFAS=Social and Occupational Functioning Assessment Scale; SOPS=Scale of Prodromal
Symptoms.
TABLE 8–2. Determining the presence of insight in psychosis
Definition of insight Clinical considerations
Awareness of or acknowledgment that • Does the individual spontaneously

one’s thoughts and behaviors are the report awareness that his or her
result of mental illness, with experiences or beliefs are not real or
recognition of the need for treatment are the product of his or her own
and/or questioning of the reality of mind? If yes: insight intact.
one’s beliefs or experiences • Can doubt about the reality of
delusional thinking or hallucinatory
experiences be induced by others or
by contrary evidence? If yes: insight
intact.
• Despite contrary evidence, does the
individual remain fully convicted
that his or her beliefs or experiences
are real? If yes: loss of insight.
(SOPS), as well as the Criteria of Prodromal Syndromes (COPS) to op-

erationalize the definition of psychosis-risk onset (Miller et al. 1999).
The goal of these integrated tools is to 1) systematically identify the
presence or absence of a prodromal-risk state (SIPS interview), 2) mea-
sure the severity of prodromal symptoms cross-sectionally and longitu-
dinally (SOPS ratings), and 3) operationalize the threshold of psychosis
(COPS diagnosis). For further reading on symptom assessment, see
Miller et al. (1999).
The SOPS includes four symptom constructs measured through 19
specific items and subscales: 1) positive symptoms, 2) negative symptoms,
3) disorganization symptoms, and 4) general symptoms. The positive
symptom construct is measured through five subscales (see Table 8–3).
Two different severity scales are used for quantifying symptoms on the
SOPS. The positive symptom items are rated on the following scale:
0=absent, 1=questionably present, 2=mild, 3=moderate, 4=moderately
severe, 5=severe but not psychotic, and 6=severe and psychotic. A score of
6 indicates the presence of a positive symptom that is at a psychotic
level of intensity, whereas a score of 3–5 is considered to be not psy-
chotic but subsyndromal. Further, positive symptoms rated as a 3 de-
note that symptoms reoccur meaningfully but the individual functions
mostly as usual despite this increase in symptom frequency. Positive
symptoms rated a 4 denote that some degree of distress, confusion, be-
wilderment, or unease occurs in conjunction with symptom presenta-
tion. Positive symptoms rated a 5 denote that the symptoms have
become so distressing that behavioral changes occur in the individual
116
TABLE 8–3. COPS scoring summary for Jane
SOPS positive symptom domain
P1: Unusual thought P4: Perceptual

content and P2: Suspicious and abnormalities and P5: Disorganized
delusional ideas persecutory ideas P3: Grandiosity hallucinations communication
Severity rating 4 3 4 4 4
Description of Sense that ideas, experi- Concerns that people are Notions of being Illusions or momen- Circumstantial speech
symptom ences, or beliefs may untrustworthy and/or unusually gifted, tary formed halluci- (i.e., eventually get-
domain be coming from out- may harbor ill will powerful, or spe- nations that are ting to the point)
side oneself or that Sense of unease and need cial; has exagger- ultimately recog- Difficulty directing
they may be real but for vigilance (often ated expectations nized as unreal but sentences toward a
doubt remains intact unfocused). Person may be can be distracting, goal
Distracting and Mistrustful expansive but can curious, and unset- Sudden pauses
bothersome Recurrent (yet redirect to the tling Can be redirected with
May affect functioning unfounded) sense that everyday on own May affect occasional questions
people might be functioning. and structuring
thinking or saying
negative things about
him or her
Onset “For as long as I can 1 year ago “For as long as I can “For as long as I can 1 year ago
remember” remember” remember”
Increase 1 year ago NA 1 year ago 1 year ago NA
TABLE 8–3. COPS scoring summary for Jane (continued)
SOPS positive symptom domain
P1: Unusual thought P4: Perceptual

content and P2: Suspicious and abnormalities and P5: Disorganized
delusional ideas persecutory ideas P3: Grandiosity hallucinations communication
Better Not likely Not likely Rule out bipolar Not likely Not likely
explained by disorder (manic
another DSM episode)
disorder?
Diagnosis achieved using above criteria: attenuated positive symptom syndrome.
Note. P1–P5 refer to positive symptom domains.
Abbreviations. COPS= Criteria of Prodromal Syndromes; NA=Not applicable; SOPS=Scale of Prodromal Symptoms.
Individuals at Clinical High Risk for Psychosis
117
in response to the symptom occurrence. Positive symptoms rated as a 6

imply that insight is completely lost and that the symptoms are experi-
enced with full conviction, potentially affect the person’s behavior, and
are experienced as bothersome or distressing. The fundamental differ-
ence between ratings of 3–5 versus 6 is insight. Insight into the reality of
symptoms remains intact for severity ratings of 3–5. Rating an item at
the level of 6 marks that the symptom is experienced with full convic-
tion and there has been a total loss of insight.
For positive symptom items rated at a severity level of 3 or higher,
symptom onset, symptom worsening, symptom frequency, and whether
or not the symptom is “better explained by another DSM disorder” are
also recorded. Symptom onset refers to the date at which the positive
symptom rating achieved a score of between 3 and 6 for the first time.
This could be a retrospective rating and requires careful probing by the
interviewer to elicit information from the individual regarding when he
or she first noticed the symptom meaningfully occur. Finally, the likeli-
hood that positive symptoms rated as 3 or higher are “better explained
by another DSM disorder” is indicated. If the co-occurring disorder has
been present continuously throughout positive symptom presentation,
then it must be differentiated whether or not the symptoms are more
characteristic of a psychosis-risk syndrome or of the co-occurring disor-
der. In the example of Jane, her feelings of frank superiority occur only
in the context of mania and are therefore “likely” better explained by
mania rather than psychosis-risk syndrome.
Negative, disorganized, and general symptoms items are rated on a
similar SOPS scale ranging from 0 (absent) to 6 (extreme); however,
these symptom ratings are not used for making a psychosis-risk diag-
nosis on the COPS. Instead, these ratings are useful in providing both
descriptive and quantitative estimates of the diversity and severity of
accompanying negative, disorganized, and general symptoms.
The COPS operationalizes three psychosis-risk syndromes: 1) ge-
netic risk and deterioration syndrome, 2) attenuated positive symptom
syndrome, and 3) brief intermittent psychotic syndrome. Genetic risk
and deterioration syndrome is defined by a combined genetic risk for a
psychosis spectrum disorder and a recent history of functional decline.
Attenuated positive symptom syndrome is defined by the presence of
attenuated positive symptoms of sufficient severity and frequency.
Brief intermittent psychotic syndrome is defined by the presence of
frank psychotic symptoms that are brief or intermittent when current
psychotic syndrome can be ruled out because sufficient frequency, du-
ration, and urgency criteria have not been met. Positive symptoms ex-
perienced at a level of psychotic intensity (i.e., unusual thought content,
suspiciousness, or grandiosity with delusional conviction; perceptual
abnormalities of hallucinatory intensity; and/or speech that is incoher-
ent or unintelligible) that occur for at least 1 hour per day at a minimum
average of at least 4 days per week and/or are seriously disorganizing

or dangerous are considered to be indicative of a psychotic syndrome,
not psychosis-risk syndrome. For specific scoring criteria, refer to Table
8–1. Figure 8–1 models onset of psychosis-risk symptoms using associ-
ated assessment criterion from the SIPS and CAARMS.
Using the information from the case example, Jane meets the crite-
ria for attenuated positive symptom syndrome. Her symptoms are de-
scribed as recurrent and distressing. Over the past year, the symptoms
became more frequent, started to affect her behaviors, and impacted
her social functioning, as well as her academic achievement. Insight
into the reality of these symptoms remained intact, as evidenced by ei-
ther spontaneously divulged doubt or doubt induced by further ques-
tioning. Table 8–3 breaks down the scoring of Jane’s symptoms using
the SIPS-associated COPS criteria.
Comprehensive Assessment of At-Risk

Mental States-Brief
The Comprehensive Assessment of At-Risk Mental States-Brief
(CAARMS-B) is a semistructured interview designed for use by mental
health professionals in Australia to identify the prodrome of a first psy-
chotic episode using validated criteria and reliable methodology (Yung
et al. 2005). Its function is to assess psychosis-like pathology and deter-
mine whether an individual meets criteria for being at ultra-high risk for
onset of first psychotic disorder. CAARMS-B is designed for repeated use
over time, from monthly to biyearly. CAARMS-B aims to 1) determine if
an individual meets the criteria for an at-risk mental state, 2) rule out or
confirm acute psychosis, and 3) map a range of psychopathology and
functioning factors over time in young people at ultra-high risk of psy-
chosis. CAARMS-B ratings are completed on a range of subscales that
target different areas of psychopathology and functioning. From these
ratings it is then possible to extract information relating to these aims.
The following constructs are used to evaluate presence and severity of
psychopathology and functional impairment: 1) disorders of thought con-
tent, 2) perceptual abnormalities, 3) conceptual disorganization, 4) motor
changes, 5) problems with concentration and attention, 6) problems with
emotion and affect, and 7) subjectively impaired energy and impaired tol-
erance to normal stress. The severity of each of these constructs is rated us-
ing a global rating scale score as follows: 0=never/absent, 1=questionable,
2=mild, 3=moderate, 4=moderately severe, 5=severe, and 6=psychotic
and severe. Ratings for each of the CAARMS-B subscales are anchored
with content-specific benchmarks (as with the SIPS); however, several se-
verity rating themes exist throughout the scale. A severity level rating
of 2 indicates that the person is “not concerned/ worried about the ex-
perience.” A severity level rating of 4 indicates that the symptom “does
120
FIGURE 8–1. Model of psychosis risk onset.

Abbreviation. BLIPS=brief limited intermittent psychotic symptoms.
Source. Adapted from Fusar-Poli et al. (2013).

not result in a change in behavior but may be associated with mild dis-
tress.” A severity level rating of 5 indicates that the symptom “may re-
sult in some minor change in behavior and may be frightening or
associated with some distress.” A severity level rating of 6 indicates that
the symptom “may have marked impact on behavior and may be very
distressing” (Yung et al. 2005). As previously discussed with the SIPS,
a rating of 6 on the CAARMS-B subscales distinguishes frank psychotic
symptoms (full conviction with no insight) from the psychosis-like ex-
periences (doubt remains intact and insight is either spontaneously di-
vulged or can be induced given contrary evidence from others) that are
indicated in the 1–5 range.
Onset and offset dates, frequency and duration of occurrence, pat-
tern, and level of distress are also recorded. Symptoms rated as a 6 that
last for more than a week at a time are considered to be above the psy-
chosis-risk threshold and should instead be considered evidence for
presence of frank psychosis. Frequency and duration are rated through
a frequency scale score ranging from 0 (absent) to 6 (continuous). Pat-
tern of symptoms is used to determine whether or not the presenting
symptoms are accounted for by the use of alcohol or illicit substances in
order to denote whether there is a relation between symptoms and sub-
stance use. Finally, level of distress experienced by the symptom is rated
on a scale of 0=not at all distressed to 100=extremely distressed.
CAARMS-B operationalizes three groups of ultra-high-risk individ-
uals: 1) the vulnerability group, 2) the attenuated psychosis group, and
3) the brief limited intermittent psychotic symptoms group. The vulner-
ability group is defined as young people at risk of psychosis due to the
combination of a trait risk factor and a significant deterioration in men-
tal states and/or functioning. The attenuated psychosis group is de-
fined as young people at risk for psychosis due to a subthreshold
psychotic syndrome, in which the experienced symptoms do not reach
a threshold level for psychosis because of either subthreshold intensity
(not severe enough) or subthreshold frequency (occurrence not often
enough). The brief limited intermittent psychotic symptoms group is
defined as young people at risk of psychosis due to a recent history of
frank psychotic symptoms that resolved spontaneously (without anti-
psychotic intervention) within 1 week. For specific scoring criteria, refer
to Table 8–1 and Figure 8–1. For further reading on this assessment mea-
sure, see Yung et al. (2005).
Again, using the information from the case example, Jane would
meet CAARMS-B criteria for attenuated psychosis group: subthreshold
intensity. Her symptoms are recurrent and have increased in intensity
over the past year. However, insight remains intact and Jane is able to
generate insight into the reality of these experiences. Table 8–4 breaks
down the scoring of Jane’s symptoms using the CAARMS-B-associated
criteria.
122
TABLE 8–4. CAARMS-B scoring summary for Jane
CAARMS-B symptom domains
Unusual thought Perceptual

content Nonbizarre ideas abnormalities Disorganized speech
Global rating 5 4 4 4
Description of Unusual thoughts that Clearly idiosyncratic beliefs Much clearer hallucinatory Clear evidence of mild
symptom domain contain completely that, although possible, experiences that are more disconnected speech
original and highly have arisen without logical external to self (more severe and thought patterns
improbable material evidence (more severe than a than a rating of 3, in which Links between ideas are
Person can doubt these rating of 3, in which belief may they are described as tangential; person
thoughts (i.e., thoughts be supported by some logical “distortions,” “illusions,” or experiences an
not held with delusional evidence and is not entirely “indistinct murmurs”) increased feeling of
conviction) or does not implausible) Examples: hear name being frustration in
believe them all the time May include thoughts that called, phone ringing conversations
May result in some minor others wish the person May be fleeting or transient
change in behavior, but harm (without logical Person is able to give
this change is minor evidence) or thoughts of plausible explanation for
May be frightening or having special powers experiences, but they may
associated with some Beliefs may be easily be associated with mild
distress dismissed by individual but degree of distress
associated with mild degree
of distress
Frequency score 3 2 3 2
Diagnosis achieved using above criteria: attenuated psychosis group

Abbreviations. CAARMS= Comprehensive Assessment of At-Risk Mental States.
Risk Calculator
Using data from more than 500 individuals determined to be at clinical
high risk for psychosis, the North American Prodrome Longitudinal Study
(NAPLS) Consortium developed a diagnostic algorithm that can ascertain
the probability of conversion to psychosis in CHR youth (Cannon et al.
2016). This risk calculator combines a unique set of demographic (age,
family history of psychosis), clinical (unusual thought content and suspi-
ciousness), neurocognitive (verbal learning and memory, speed of process-
ing), and psychosocial (traumas, stressful life events, decline in social
functioning) predictor variables to generate a specific number representing
an individual’s probability of transitioning to psychosis within 1–2 years.
The calculator is available online at http://riskcalc.org/napls.
The risk calculator performs well, with a concordance index (C-index)
of 0.71. This index score is comparable to that of established calculators
used for the identification of recurrence risk in cardiovascular disease
and cancer (C-index values ranging from 0.58 to 0.81). The calculator as-
sumes that the ratings and scores input into the algorithm are obtained
by a clinician or health professional. In addition, a SIPS-based diagnosis
of a prodromal risk syndrome must be established because the calcula-
tor is not operational without this information. Use of this calculator in
non-help-seeking, nondistressed individuals from the general popula-
tion is not recommended. For further reading, see Cannon et al. (2016).
If the above criteria are satisfied, the following information is then in-
put into the calculator: 1) age in years (range of 12–35), 2) Brief Assess-
ment of Cognition in Schizophrenia (BACS) symbol coding total raw
score, 3) Hopkins Verbal Learning Test–Revised (HVLT-R) total raw
score, 4) undesirable life events raw score (obtained through the Research
Interview Life Events Scale), 5) number of types of trauma observed (ob-
tained through the Childhood Trauma and Abuse Scale), 6) sum of re-
scaled SIPS ratings for positive symptom domains P1 and P2 (unusual
beliefs and suspiciousness subscales), 7) change in global social role
functioning over the past year (measured using the Global Functioning:
Social Scale and calculated by subtracting the individual’s lowest score
in the past year from the highest score in the past year), and 8) family
history of psychosis in first-degree relative (yes or no) (Cannon et al.
2016). SIPS scores on P1 and P2 are rescaled such that scores 0–2 on the
original scale are redefined as 0, scores 3–5 on the original scale are re-
defined as 1–3, respectively, and score 6 on the original scale is rede-
fined as 4.
As an example, the following information was input into the calcu-
lator for Jane (Figure 8–2): 1) age=21 years, 2) BACS symbol coding to-
tal raw score =61, 3) HVLT-R total raw score=20, 4) undesirable life
events raw score=21, 5) number of types of trauma observed=6, 6) sum
of rescaled SIPS ratings for P1 and P2=3, 7) change in global social func-
tioning over the past year=3, and 8) family history of psychosis=no.
This profile yielded a 1-year probability of conversion to psychosis

of 26.5% and 2-year probability of conversion to psychosis of 33.9%
(Figure 8–3).
Prodromal Questionnaire-Brief
The previously discussed semistructured interviews have established
validity and reliability for identifying individuals who are at the high-
est risk for developing psychosis. However, these interviews are time
consuming, typically requiring 1–2 hours to administer and score by a
trained clinician. Because of the cumbersome nature of these structured
interviews, screening tools have been developed for the purpose of dis-
tinguishing between individuals who might benefit from further psy-
chosis-risk assessment and those who would not. One such screening
tool is the Prodromal Questionnaire-Brief (PQ-B; Loewy et al. 2011). Use
of the PQ-B can limit the costs associated with unnecessarily adminis-
tering lengthy interviews in clinical settings where time is a limited re-
source. The PQ-B is a 21-item self-report scale. It has established
concurrent validity in differentiating between individuals who will
qualify for a psychosis-risk diagnosis from those who do not meet cri-
teria. The PQ-B consists of 21 yes or no questions; questions receiving a
yes answer are followed by distress ratings on a scale of 1 (strongly dis-
agree) to 5 (strongly agree). This yields two composite scores: total score
(range 0–21) and distress score (range 0–105). For total score, a cut-off
≥3 has 89% sensitivity and 58% specificity, and for distress score, a cut-
off ≥6 has 88% sensitivity and 68% specificity. Using these cut-offs, the
PQ-B has been established as a reliable and valid way of differentiating
individuals who may qualify as having psychosis-risk syndrome and/
or psychotic syndrome from individuals with no diagnosis, thereby re-
ducing costs associated with administering lengthy structured inter-
views to individuals who will likely not meet criteria for psychosis-risk
syndrome.
It is important to emphasize that the PQ-B is not meant to replace
traditional structured interviews for diagnosing a psychosis-risk syn-
drome. It is not a diagnostic tool. The PQ-B is meant to serve as the first
step in a two-step process of identifying help-seeking individuals who
may benefit from further in-depth assessment in the form of a struc-
tured interview (i.e., SIPS or CAARMS).
Cultural Considerations in Assessment

and Diagnosis
In assessment and diagnosis of mental disorders, it is critical that pro-
viders consider the complexity of culture in presenting symptoms.
FIGURE 8–2. Risk calculator input.
There have been attempts to look at the impact of culture on experience

and development of psychosis-risk syndrome, but more research is
needed to provide definitive recommendations regarding the impact of
culture on the diagnosis and treatment of psychosis risk. Despite this,
Risk 26.5% Risk 33.9%
FIGURE 8–3. Risk calculator output: Jane’s 1-year and 2-year probabil-
ities of conversion to psychosis.
This calculator was based on a Cox proportional hazards regression model that was de-
veloped from a cohort consisting of 596 clinical high-risk participants from the second
phase of the North American Prodrome Longitudinal Study.
we can refer to several particularly robust cultural considerations re-

vealed through research on the impact of culture in early psychosis.
During assessment, clinicians must differentiate between culturally
sanctioned response patterns and persistent abnormal experiences. For
example, an individual may report hearing voices during a religious
ceremony, but if these voices are not experienced as persistent or dis-
tressing and are not considered abnormal by other members of that re-
ligious community, then the symptom should not be considered
pathological. Religious background must be taken into account, espe-
cially when assessing for delusional beliefs or perceptual abnormalities.
Other considerations include socioeconomic status, narrative expres-
sion and language, emotional expression and posturing, race, and eth-
nicity. Clinicians need to rule out linguistic variation and language
barriers when assessing for disorganized speech and alogia. Differences
in style of emotional expression, eye contact, and body language should
not be mistaken for negative or disorganized symptoms.
Ideas that might be considered delusional in one culture, such as
witchcraft, voodoo, or nonmedical healing, may be commonly accepted
in another culture; therefore, the etiology of beliefs must be assessed.
Several specific cultural concepts of distress should be considered in as-
sessment of psychotic-like symptoms. Ataque de nervios, nervios, maladi
moun, and taijin kyofusho are all examples of culture-bound syndromes
that may better account for symptoms such as depersonalization, per-
ceptual abnormalities, or overvalued beliefs (see “DSM-5 Glossary of
Cultural Concepts of Distress,” American Psychiatric Association 2013,

pp. 833–837).
Stigma associated with the diagnostic label of psychosis-risk syn-
drome is another domain of cultural consideration. The interpretation
of this diagnostic label may vary between cultures or languages for in-
dividuals and their families. Research in the area of stigma and diag-
nostic labeling of psychosis-risk syndrome is ongoing. Of note, studies
involving Chinese individuals with psychosis-risk syndrome and
Latino CHR individuals indicate that current diagnostic labeling may
be stigmatizing and associated with reduced help-seeking behaviors
(Lee et al. 2017; Tsai et al. 2015). For some individuals, the assignment of
a diagnosis may be experienced as relieving, reducing confusion and un-
certainty regarding the meaning of symptoms, as well as increasing hope
through recommendations for treatment. For others, the understanding
of this label may result in feelings of hopelessness, loss of independence,
or increased isolation. When the cultural interpretation of diagnostic la-
beling is of concern for individuals, it may be appropriate to disclose di-
agnostic information in terms of symptoms rather than diagnostic
labeling (Mittal et al. 2015). Guiding individuals through the meaning
of and treatment recommendations for psychosis-risk syndrome may
be particularly important. Risk for does not equate to certainty of a psy-
chotic disorder developing. Clients should be well informed of the lim-
its to diagnostic accuracy of psychosis-risk syndrome, as well as the
benefits of intervening early to prevent further impairments.
Treatment
As will be discussed in later chapters, there are many targeted interven-
tions shown to be effective in reducing or improving social, cognitive,
and functional impairments in first-episode or early psychosis. The
search for effective treatment interventions for psychosis-risk popula-
tions is ongoing. Research that focuses explicitly on vulnerability for
psychosis risk not only brings the field closer to understanding the
causal processes and mechanisms that need to be therapeutically ad-
dressed once psychosis occurs but also aids in preventing the onset of
psychosis or, at least, attenuating the duration and intensity of symp-
toms and accompanying functional impairments.
Cognitive-behavioral therapy, social skills training (CBSST), cogni-
tive therapy, family-focused therapy, and supportive contact have all
shown low to moderate effect sizes for reducing risk of a psychotic dis-
order and improving symptoms as well as overall functioning. Addi-
tional randomized controlled trials are under way to evaluate the
effectiveness of these psychosocial interventions and characterize long-
term outcomes of such treatments in psychosis-risk syndrome (CBSST
trial in CHR youth ongoing; Cadenhead et al. 2018). Current treatment

guidelines of attenuated psychosis syndrome proposed by the Ameri-
can Psychiatric Association recommend “careful assessment and fre-
quent monitoring” (Woods et al. 2010). Low-risk, nonpharmacological
interventions are recommended over the use of drug treatment for psy-
chosis-risk syndromes, and treatment recommendations are based
largely on presenting symptoms and co-occurring disorders. Comorbid
disorders should be treated simultaneously while psychotic-like symp-
toms are being monitored. If frank psychotic symptoms emerge, the use
of antipsychotic medication should be considered.
Receiving psychosis-risk-specific treatment is correlated with lower
risk of psychosis at 1-, 2-, and 3-year follow-up (Fusar-Poli et al. 2013).
Preventive interventions in psychosis-risk youth are feasible and valu-
able to improving prognosis. Early intervention is associated with de-
creased duration of untreated psychosis (DUP). Longer DUP has been
associated with poor prognostic outcomes, high costs, and reduced
functioning (Allott et al. 2018; Fusar-Poli et al. 2017).
In the case example, Jane received treatment for symptoms of PTSD
but chose not to engage in treatment specific to psychosis-risk syndrome.

One year after the initial interview, Jane presented at a university-based
psychosis evaluation clinic to complete a follow-up SIPS assessment. Her
symptoms had increased to include stable persecutory and grandiose de-
lusions and fully formed auditory and visual hallucinations, as well as
disorganized appearance and behavior. These symptoms had reportedly
increased during the preceding month and were experienced at a level of
full conviction; insight into these symptoms was no longer intact and
could not be induced. Jane was ultimately diagnosed with schizoaffective
disorder, bipolar type. Careful monitoring of Jane’s symptoms allowed
for immediate detection of psychosis, intervention with psychotherapy,
and initiation of mood stabilizer and antipsychotic medication. Ulti-
mately, repeated psychosis-risk assessment and careful monitoring facili-
tated early detection and intervention, thereby reducing Jane’s DUP.
KEY CONCEPTS
• The concept of preserved insight is one of the key features
in differential diagnosis of psychosis-risk syndrome versus
full psychotic disorders and refers to the awareness or
acknowledgment that one’s thoughts and behaviors are
the result of mental illness, with recognition of the need
for treatment, and/or questioning of the reality of one’s
beliefs or experiences.
• One of the Conditions for Further Study in DSM-5, attenu-

ated psychosis syndrome involves the presence of psycho-
sis-like experiences that are below the threshold for a full
psychotic disorder. As compared with the symptom crite-
ria for full psychotic disorders, symptoms of attenuated
psychosis syndrome are more transient and less severe
and involve greater preservation of insight.
• Duration of untreated psychosis (DUP) is the period of
time from onset of frank psychosis to initiation of ade-
quate treatment. Longer DUP is associated with poorer
prognosis in individuals with psychosis.
• Criteria of Prodromal Syndromes identifies three psychosis-
risk syndrome subtypes:
1. Genetic risk and deterioration syndrome (GRDS)—Criteria

are met if an individual 1) has a first-degree relative
with a psychotic disorder and/or has ever met DSM-5
schizotypal personality disorder criteria and 2) demon-
strates a 30% or greater drop in Global Assessment of
Functioning within the past year. GRDS is similar to the
vulnerability group from the Comprehensive Assess-
ment of At-Risk Mental States-Brief (CAARMS-B).
2. Attenuated positive symptom syndrome (APSS)—
Symptoms are experienced as unwilled, not easily
ignored, confusing, bothersome, or distressing to
affected individuals and may affect an individual’s daily
functioning. APSS is similar to the attenuated psychosis
group from CAARMS-B.
3. Brief intermittent psychotic syndrome (BIPS)—Criteria
are met if frank psychotic symptoms occur for at least sev-
eral minutes a day at a frequency of at least once per
month; preservation of insight is typically lost during
symptom occurrence. BIPS is similar to the brief limited
intermittent psychotic symptoms group from CAARMS-B.
1. In what way is insight a clinically relevant diagnostic feature

in psychosis-risk syndrome?
2. Structured assessments classify three distinct subtypes of

psychosis-risk syndrome. What are these subtypes? How do
the criteria for each subtype differ?
3. In assessment of psychosis-risk syndrome, clinicians must

differentiate between culturally sanctioned response patterns
and persistent abnormal experiences. Additionally, culture
must be considered when assigning diagnostic labels. Why is
this of particular importance for psychosis-risk syndrome?
4. Even though research on effective intervention in psychosis

risk is ongoing, what treatment options should be considered
after identifying psychosis-risk syndrome? Why is early in-
tervention important in psychosis risk?
Suggested Readings
American Psychiatric Association: Conditions for Further Study: Atten-
uated psychosis syndrome, in Diagnostic and Statistical Manual of
Mental Disorders, 5th Edition. Arlington, VA, American Psychiatric
Association, 2013, pp 783–86
American Psychiatric Association: Glossary of cultural concepts of dis-
tress, in Diagnostic and Statistical Manual of Mental Disorders, 5th
Edition. Arlington, VA, American Psychiatric Association, 2013, pp
833–837
Cannon TD, Yu C, Addington J, et al: An individualized risk calculator
for research in prodromal psychosis. Am J Psychiatry 173(10):980–
988, 2016 27363508
Fusar-Poli P, Borgwardt S, Bechdolf A, et al: The psychosis high-risk
state: a comprehensive state-of-the-art review. JAMA Psychiatry
70(1):107–120, 2013 23165428
Loewy RL, Pearson R, Vinogradov S, et al: Psychosis risk screening with
the Prodromal Questionnaire–Brief version (PQ-B). Schizophr Res
129(1):42–46, 2011 21511440
Marshall M, Lewis S, Lockwood A, et al: Association between duration
of untreated psychosis and outcome in cohorts of first-episode pa-
tients: a systematic review. Arch Gen Psychiatry 62(9):975–983, 2005
16143729
Miller TJ, McGlashan TH, Woods SW, et al: Symptom assessment in

schizophrenic prodromal states. Psychiatr Q 70(4):273–287, 1999
10587984
Yung AR, Yuen HP, McGorry PD, et al: Mapping the onset of psychosis:
the Comprehensive Assessment of At-Risk Mental States. Aust N Z
J Psychiatry 39(11–12):964–971, 2005 16343296
References
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and neurocognitive functioning in first-episode psychosis: a systematic re-
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Disorders, 5th Edition. Arlington, VA, American Psychiatric Association,
2013
Benedict RHB, Schretlen D, Groninger L, Brandt J: The Hopkins Verbal Learning
Test-Revised: normative data and analysis of interform and test–retest reli-
ability. Clin Neuropsychol 12:43–55, 1998
Cadenhead K, Addington J, Cornblatt B: Cognitive behavioral social skills train-
ing for youth at clinical high risk for psychosis: Recovery Through Group
(ReGroup). Presented at International Conference on Early Intervention in
Mental Health, Boston, MA, October 2018
Cannon TD, Yu C, Addington J, et al: An individualized risk calculator for research
in prodromal psychosis. Am J Psychiatry 173(10):980–988, 2016 27363508
First MB, Spitzer RL, Gibbon M, Williams JBW: Structured Clinical Interview
for DSM-IV Axis I Disorders, Clinician Version (SCID-CV). Washington,
DC, American Psychiatric Press, 1997
Fusar-Poli P, Borgwardt S, Bechdolf A, et al: The psychosis high-risk state: a
comprehensive state-of-the-art review. JAMA Psychiatry 70(1):107–120,
2013 23165428
Fusar-Poli P, Cappucciati M, Rutigliano G, et al: At risk or not at risk? A meta-
analysis of the prognostic accuracy of psychometric interviews for psycho-
sis prediction. World Psychiatry 14(3):322–332, 2015 26407788
Goldman HH, Skodol AE, Lave TR: Revising Axis V for DSM-IV: a review of mea-
sures of social functioning. Am J Psychiatry 149(9):1148–1156, 1992 1386964
Keefe RS, Goldberg TE, Harvey PD, et al: The Brief Assessment of Cognition in
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Loewy RL, Pearson R, Vinogradov S, et al: Psychosis risk screening with the
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46, 2011 21511440
Miller TJ, McGlashan TH, Woods SW, et al: Symptom assessment in schizophrenic
prodromal states. Psychiatr Q 70(4):273–287, 1999 10587984
Miller TJ, McGlashan TH, Rosen JL, et al: Prodromal assessment with the struc-
tured interview for prodromal syndromes and the scale of prodromal
symptoms: predictive validity, interrater reliability, and training to reliabil-
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try 39(11–12):964–971, 2005 16343296
CHAPTER
9
Medical Workup for

First-Episode Psychosis
Agnieszka Kalinowski, M.D., Ph.D.
PSYCHIATRY is in the midst of an explosion in scientific and techni-

cal advances that are beginning to explain complex behavioral phenom-
ena in ways never before possible. With these advances, we are better
able to understand the core pathophysiology that links disparate symp-
toms and better explain complex syndromes throughout medicine.
Schizophrenia is, and has been, a diagnosis of exclusion, yet patients with
psychosis are often given only cursory medical evaluation. Psychiatrists
then bear the burden of not missing a reversible condition, especially
early in the disease course when families may be perplexed and seeking
explanations for the sudden change in their loved one’s behavior.
Given the wide range in presentations of early psychosis, psychia-
trists are often called on to lead a medical workup. Consider the follow-
ing vignette:
Case Example 1
Abraham is a 19-year-old former honors student who has experienced a
significant loss of functioning, including needing nearly full assistance
with activities of daily living, over the past 3 years and is nearly unable
to talk. At the time of his initial presentation, he reported hearing voices
telling him that he was stupid and had a new-onset germ phobia requir-
ing him to wash his hands frequently. He developed many other rituals
133
as well that he had not demonstrated previously. Abraham started tak-

ing an antipsychotic medication but showed minimal response, and his
functional decline continued. After several antipsychotic trials, Abra-
ham started taking clozapine, but it was also ineffective for his symp-
toms. Electroconvulsive therapy and benzodiazepine treatments were
tried to help with catatonia, but there was no change in Abraham’s level
of cognition or other symptoms despite high doses. Ultimately, he was
admitted to a psychiatric unit for closer observation and consideration
of a medical washout. A panoply of specialty consults and tests were
performed, yet there were no notable findings. At the suggestion of
rheumatology staff, an empirical trial of steroids was considered. After
3 days of taking high doses of methylprednisolone, Abraham began to
speak in partial sentences and was able to start performing activities of
daily living for the first time in 2 years. Although an ultimate diagnosis
is elusive for Abraham, steroid-responsive autoimmune encephalitis is
most likely. However, there was never a seropositive test to confirm the
focus of an autoimmune condition. Abraham continues to receive po-
tent anti-inflammatory treatment and continues to slowly regain the
abilities that were lost over the course of his illness.
Although Abraham’s case includes an unusual presentation and a

dramatic outcome, with media streaming with information about new
possible causes of psychosis, psychiatrists and other mental health pro-
fessionals may often feel compelled to do more extensive medical work-
ups. These more comprehensive workups are discussed in the literature
(Coleman and Gillberg 1997; Freudenreich et al. 2009; Golomb 2002),
and the list of possible etiologies (e.g., autoimmune, postinfectious,
paraneoplastic) keeps growing. Disagreement exists as to what extent
these workups are able to identify a potentially reversible cause of psy-
chosis, but a study from 1987 showed that up to 3% of cases have iden-
tifiable causes other than a primary psychiatric disorder, many of which
are reversible if identified in a timely manner (Johnstone et al. 1987).
Extensive medical workups are typically not pursued when the pa-
tient’s age and duration of onset of symptoms, types of symptoms (pre-
dominantly paranoia and auditory hallucinations), and level of social
and occupational functioning match a generally understood canonical
pattern that most medical professionals would agree is likely to be due
to a primary psychiatric condition (Freudenreich et al. 2009). On the
other hand, there can be substantial variability in symptom presenta-
tion, and finding a reversible cause early in the disease course is clearly
worthwhile. Delineating a prudent balance between testing for all pos-
sible causes of psychosis, including the long list of rare disorders, com-
pared with minimal testing focused on finding the most common
disorders, is often unclear. Furthermore, although an argument can be
made for an extensive workup for a person in the first episode of psy-
chosis, the feasibility may be challenging in many practice settings be-
cause of cost and unavailability of resources.
Medical Workup for First-Episode Psychosis 135
The American Psychiatric Association (APA) guidelines for initial

medical workup of first-episode psychosis were published in 2004
(Lehman et al. 2004), with an update provided in 2009 (Dixon et al. 2009;
see also Freudenreich et al. 2009); these suggested baseline tests are pre-
sented in Table 9–1. The updated guidelines added routine testing for
HIV, even without risk factors and urine toxicology, as recommended
by the Centers for Disease Control and Prevention. Current guidelines
for a medical workup for people with onset of psychosis are grounded
in the idea that if there is an alternative medical explanation, then the
foundational history and/or physical examination should provide an
initial clue to guide further workup (Table 9–2). Often, this may be the
case—seizures in a young woman suggesting limbic encephalitis, an
abnormal neurological examination suggesting stroke, or tachycardia
occurring in a patient with thyrotoxicosis.
TABLE 9–1. Baseline medical evaluation of patients with first-

episode psychosis
Type of test Test
Physical • Vital signs

examination • Complete physical examination, including detailed
neurological examination
• Weight, height, and body mass index
• Clinical assessment of extrapyramidal symptoms and
abnormal movements
Laboratory and • Fasting blood glucose and/or hemoglobin A1c
ancillary tests • Lipid panel
• Prolactin level
• Electrocardiogram for QTc monitoring and cardiac status
• Pregnancy test (for women of child-bearing age)
However, what may be unsettling is the idea that there may be in-
stances when psychosis is truly the only indication of illness, yet a med-
ical cause can still be present. A study published in 2011 in which
lumbar punctures were performed on 155 consecutive people who pre-
sented with new-onset psychosis found an alternative medical cause
that changed the clinical management in 5 (3%) of the patients (Kranas-
ter et al. 2011). These alternative diagnoses included herpes simplex en-
cephalitis, neuroborreliosis, multiple sclerosis, and two cases of chronic
inflammation of the central nervous system of uncertain origin. Haunt-
ingly, the authors stated that the patients in these 5 cases did not differ
in their clinical presentation from the other patients with psychosis, and
their history and physical examination were unremarkable.
TABLE 9–2. Suggested workup for medical causes of

psychosis
Type of test Test
Tests for common, • Complete blood count

treatable causes
• Basic metabolic panel
• Liver function tests
• Urine toxicology screen
• Thyroid function tests
• HIV screen
• Urine heavy metals
• Vitamin B12
• Antinuclear antibodies test
• Test for syphilis (fluorescent treponemal
antibody absorption preferred)
Tests for conditions that • Magnetic resonance imaging of the brain with
should be considered if and without contrast
history or the physical • Electroencephalogram
point to a possible
positive finding • Hepatitis B and C screen
• Lumbar puncture (or peripheral blood) for
infectious and paraneoplastic antibodies
• Ceruloplasmin, serum copper
• Quantiferon and/or chest X-ray
• Erythrocyte sedimentation rate and C-reactive
protein
• Neuropsychological and/or cognitive testing
Specialty consultations • Genetics workup (e.g., karyotype, fluorescence
in situ hybridization, sequencing)
• Neurology for workup of demyelinating
disorders, seizure, or encephalitis
• Neurosurgery if potential tumor or other
structural brain abnormalities are seen
• Immunology for workup of autoimmune or
postinfectious disorders
• Endocrinology if consideration for significant
hormonal abnormalities
• Rheumatology for workup of autoimmune
concerns or vasculitis
Because of the burgeoning delineation of paraneoplastic syndromes,

pediatric acute-onset neuropsychiatric syndrome (PANS), and other
postinfectious syndromes, along with increased access to genetic test-
ing, psychiatrists are in the uncomfortable position of wading through
an onslaught of complex information in hopes of finding an identifi-
able, reversible etiology that can be treated and saving their patient
with new-onset psychosis the concerning future of chronic schizophre-
nia. Navigating this information is challenging, even for clinicians in
well-resourced medical centers and teaching hospitals. Clear guide-
lines, epidemiology, and even “typical” clinical phenotypes do not yet
exist. At the same time, glimpses of hope are on the horizon with each
new discovery and successful treatment. Table 9–3 is an assembly of the
medical causes that are known to be related to or to cause psychosis. It
is based on Freudenreich and Golomb’s lists (Freudenreich et al. 2009;
Golomb 2002), with more recent additions, particularly in the autoim-
mune encephalitis category. The same principle of starting with a thor-
ough history and physical examination applies in approaching this
comprehensive differential diagnosis.
Questions often arise about what sorts of tests should be included in a
standard or expanded workup. For example, should a lumbar puncture
(LP) be a part of the standard medical workup? We propose that consider-
ation be made for the likelihood of a positive finding and whether or not
there will be a likely change in clinical management based on the outcome
of the test. If those standards are sufficiently met, LP should be offered to
patients and their family as an option, and if the procedure is desired but
not feasible within the practice where the patient is being seen, a referral
should be considered. This is also how we would suggest approaching
other invasive or expensive diagnostic testing such as magnetic resonance
imaging, electroencephalography, neuropsychological testing, and send-
out blood tests. Although it is generally unlikely that any one test will un-
cover a consequential finding, there can be a rationale for obtaining these
tests if there is an increased index of suspicion for a positive finding and the
tests are available. More easily, common conditions that are potentially re-
versible should be routinely evaluated through screening for thyroid func-
tion, HIV, vitamin B12 deficiency, and presence of heavy metals. In the
following subsections, we review and suggest updates to the available
guidelines for working up the first presentation within the heterogeneous
category of early psychosis, while providing a logical and accessible frame-
work for psychiatrists and other personnel working with patients to follow.
Where to Start
The most current guidelines from the APA regarding the initial workup
of first-episode psychosis were published in 2004 and updated in 2009
TABLE 9–3. Medical causes of psychosis

Neurological disorders
• Epilepsy
• Head trauma
• Neuropsychiatric diseases: Huntington’s disease, Wilson’s disease,
Parkinson’s disease, familial basal ganglia calcification, Friedreich’s ataxia
• Dementias: Alzheimer’s disease, frontotemporal dementia, Lewy body disease
• Space-occupying lesions and structural brain abnormalities: primary brain
tumors (e.g., meningiomas), secondary brain metastases, brain abscesses
and cysts, tuberous sclerosis, midline abnormalities (e.g., corpus callosum
agenesis, cavum septi pellucidi), cerebrovascular malformations (e.g.,
involving the temporal lobe), hydrocephalus
• Demyelinating diseases: multiple sclerosis, leukodystrophies (e.g.,
metachromatic leukodystrophy, X-linked adrenoleukodystrophy,
Marchiafava-Bignami disease), Schilder’s disease
• Narcolepsy
• Stroke
Autoimmune diseases
• Rheumatological diseases: systemic lupus erythematosus, rheumatic
arthritis, myasthenia gravis, Hashimoto’s thyroiditis, steroid-responsive
nonvasculitis autoimmune inflammatory meningoencephalitic syndrome
• Paraneoplastic diseases: Morvan’s syndrome; limbic encephalitis, including
but not limited to antibodies against Hu, Ma2, CV2/CRMP5, amphiphysin,
anti-AMPAR, NMDAR, NR1, NR2, voltage-gated potassium channel
antibody syndrome, GlyR, D2RA, GABAR, metabotropic glutamate receptor
antibody, or IgLON5
• Postinfectious disease: pediatric acute-onset neuropsychiatric syndrome
Infections
• Viral: HIV, viral encephalitis (e.g., herpes simplex, measles, cytomegalovirus,
rubella, Epstein-Barr, varicella)
• Bacterial/fungal: neurosyphilis, neuroborreliosis (Lyme), tuberculosis,
Cryptococcus infection
• Other: prion disease (e.g., Creutzfeldt-Jakob disease), central nervous
system–invasive parasitic infections (e.g., cerebral malaria, toxoplasmosis,
neurocysticercosis), sarcoidosis
Endocrinopathies
• Hypoglycemia, Addison’s disease, Cushing’s syndrome, hyperthyroidism
and hypothyroidism, hyperparathyroidism and hypoparathyroidism,
hypopituitarism
TABLE 9–3. Medical causes of psychosis (continued)

Nutritional deficiencies
• Magnesium deficiency, vitamin A deficiency, vitamin D deficiency, zinc
deficiency, niacin deficiency, vitamin B12 deficiency
Toxic and metabolic diseases
• Amino acid metabolism: Hartnup disease, homocystinuria, phenylketonuria,
urea cycle disorders, hyperornithinemia-hyperammonemia-homocitrullinuria
syndrome, isovaleric acidemia
• Storage disorders: GM2 gangliosidosis, Fabry’s disease, Niemann-Pick
disease type C, Gaucher’s disease–adult type
• Porphyrias (acute intermittent porphyria, porphyria variegate, hereditary
coproporphyria)
• Heavy metals: lead, mercury, Wilson’s disease
Chromosomal abnormalities
• Fragile X syndrome, 22q11 deletion syndrome (velocardiofacial syndrome,
DiGeorge syndrome), Klinefelter’s syndrome, XXX syndrome, metachromatic
leukodystrophy
(Dixon et al. 2009; Lehman et al. 2004). The APA clearly suggests a com-
plete medical history; physical examination; and basic blood tests, such
as complete blood count, electrolyte and liver function tests, and thy-
roid testing (thyroid-stimulating hormone [TSH]). Questions regarding
travel history, developmental history, and infectious and environmental
exposures are particularly important in the initial history taking. Fur-
ther, if the patient’s medical history includes a history of neurological
or infectious illnesses, then the workup may prompt further testing in
those directions. Family history of immigration (especially from under-
developed nations), infections, developmental disorders, cancers, or en-
docrine disorders should be evaluated. Although many metabolic
disorders are screened for during routine prenatal screening, this may not
always be done in underdeveloped countries. The history should include
a clear time course for the development of the index episode of psychosis,
including a search for a clearly identifiable prodromal period.
In this initial stage it is also crucial to include a primary care physi-
cian on the team of people working with the individual experiencing
symptoms. Although many people with the first episode of psychosis
will be referred by pediatricians or adult primary care providers, team-
ing up to work in concert on the workup is essential. Obtaining a more
thorough history and physical, or a second look at the existing history
and examination results, may help to pick up subtle clues that could
change the index of suspicion for different potentially affected systems
or disorders. Typical mimickers of schizophrenia such as amphetamine

abuse, hyperthyroidism, and pituitary tumor should be considered as a
part of the initial differential diagnosis and ruled out by standard labo-
ratory testing and examination.
High-Yield Conditions for Consideration

in Initial Workup
The most common possible conditions other than schizophrenia spec-
trum disorders that need to be ruled out in all individuals at the first ep-
isode of psychosis include infectious diseases, paraneoplastic and
autoimmune disorders, toxic-metabolic disorders, endocrine disorders,
neurological disorders, and genetic disorders. Although not an exhaus-
tive list of potential causes (see Table 9–3), these high-yield conditions
should be considered in all initial workups.
Infectious Diseases
Psychosis can be the initial presentation in patients with HIV, and all
patients should be considered for an HIV test as part of their initial eval-
uation. In a recent study out of South Africa, where HIV is highly prev-
alent, researchers looked at 159 consecutive individuals who presented
to an academic emergency department with a first episode of psychosis
(Laher et al. 2018). Of these, 40% had HIV as at least a comorbidity. Be-
yond the contribution of HIV to the likelihood for developing psycho-
sis, 84% of HIV-positive subjects had further underlying medical
conditions considered to be potentially causative in the development of
the psychotic symptoms. These other conditions included infections,
such as meningitis, tuberculosis, or fungal pneumonia; renal or hepatic
dysfunction; or stroke. In those first-episode patients who were HIV
negative, 35% were found to have an underlying medical condition,
such as epilepsy, ischemic stroke, or meningitis, that was considered
most likely responsible for the psychotic symptoms.
Rates of infectious agents and availability of treatment vary
throughout the world and are an important factor in history taking.
Country of origin and/or history of immigration from underdeveloped
countries should also lead to consideration of potential causes of psy-
chosis that are less common in more developed countries. For example,
many providers may not be accustomed to seeing psychosis as a mani-
festation of malaria, which should be considered in patients who have
immigrated from or traveled to malaria-infected areas. Similarly, ter-
tiary syphilis, neurocysticercosis, and other infectious complications
may give risk to psychosis in someone from an underdeveloped or un-

der-resourced area.
Along with the manifestations of acute infections, our understanding
of the impact of previous infectious exposures is evolving at a rapid rate.
PANS refers to a panoply of symptoms that are often associated with prior
streptococcus or other infections. Although PANS is a rare condition, it can
be striking to see a precipitous and rapid decline in function, often over
only several days, occur in a previously healthy young person. In people
experiencing these syndromes, there is typically a sudden onset of symp-
toms, often with an initial presentation of psychosis in conjunction with ob-
sessive-compulsive behaviors, change in intellectual function, and tics
(Chang et al. 2015). Testing for PANS is challenging, and referral to an in-
stitution with specific expertise in this area is important when symptoms
match this pattern and time course (Frankovich et al. 2015).
Paraneoplastic and Autoimmune Disorders

Paraneoplastic syndromes have received more attention since journalist Su-
sannah Cahalan wrote about her experience of anti-N-methyl-D-aspartate
(anti-NMDA) receptor encephalitis in the book Brain on Fire (Cahalan
2012). Under the general category of autoimmune encephalopathies, the
first symptoms tend to be psychiatric, describing a process by which an
autoantibody targets the brain and disrupts function or causes inflam-
mation. Delirium, catatonic features, anterograde amnesia, personality
change, rapid progression of symptoms, fluctuating symptoms, and
seizures may occur in conjunction with elevated inflammatory markers
such as erythrocyte sedimentation rate and C-reactive protein (Oldham
2017). Recent viral illnesses are seen in more than half of patients with
anti-NMDA receptor encephalitis and often co-occur with gonadal tu-
mors. Similarly, smokers with small cell lung cancer can manifest with
paraneoplastic encephalomyelitis.
Autoimmune encephalitis can occur in the context of systemic auto-
immune disorders such as antiphospholipid antibody syndrome;
Sjögren’s syndrome; polymyositis; vasculitis syndrome; and large, me-
dium, or small vessel vasculitis. Unusual accompanying symptoms, such
as arthralgias or unexplained hypoventilation, could also be helpful in
tipping the clinician toward evaluation of the patient for autoimmune en-
cephalopathy. Unfortunately, peripheral blood antibodies do not seem to
be sufficient to rule out the disorder, and false positives occur in the nor-
mal population, so only antibody testing from cerebrospinal fluid is con-
clusive (Gaughran et al. 2018).
Numerous autoimmune disorders are associated with psychosis,
and many times, psychosis is the first presenting symptom. A patient
with systemic lupus erythematosus may present with psychosis up to
2%–3% of the time (Kosmidis et al. 2010; Patten et al. 2005); thus, a test
looking for the antinuclear antibody is recommended in people with a

first episode of psychosis. There are increasing numbers of autoanti-
bodies associated with psychosis to varying degrees, as well as other
neuropsychiatric manifestations (Ho et al. 2016). In addition, comorbid
rheumatological and autoimmune disorders occur at increased rates in
patients with schizophrenia (Chen et al. 2012).
Toxic-Metabolic Disorders
Many potential environmental or toxic exposures, such as heavy metal
toxicity, can contribute to the risk for psychosis. When taking an initial
history, it is important to survey for potential lead exposure. Lead may
contribute to numerous neuropsychiatric symptoms, including poor
concentration and low IQ, but at sufficient levels can also contribute to
psychosis (Vorvolakos et al. 2016). Although lead exposure is less com-
mon now because of the reduction of lead-containing pipes, paints, and
gasoline, there is still potential for exposure in old buildings and/or for
people with a prior exposure in an underdeveloped country.
In addition to environmental exposures, there can also be issues
with the metabolism or storage of heavy metals in the body. Wilson’s
disease is a copper storage disorder manifested most commonly by
tremors; hepatic dysfunction; and psychiatric symptoms, including de-
pression or psychosis (Zimbrean and Schilsky 2014). Elevated liver en-
zymes or unusual tremor, especially if the patient is particularly
sensitive to extrapyramidal symptoms from antipsychotic medication,
should prompt an investigation into Wilson’s disease.
B12 and folate deficiencies can manifest with fatigue, personality
changes, or psychosis. Historical clues to such deficiencies include a
vegetarian diet, alcohol abuse, or oral contraceptive use. In the case of
B12 deficiency, patients may also complain of parasthesias or fatigue.
Similarly, pellagra or B3 (niacin) deficiency can lead to psychosis, typi-
cally in patients with chronic alcoholism.
Endocrine Disorders
Derangements in cortisol have well-known psychiatric manifestations.
For example, elevated cortisol levels can manifest with lability, irritabil-
ity, mania, or psychosis with associated cognitive slowing and poor
short-term memory, which may overlap with clinicians’ expectations
for schizophrenia. Cushingnoid features such as upper-body obesity
with thin arms and legs, bruising, purple striae, menstrual irregulari-
ties, vertigo, hyperglycemia, “moon” facies, fluid retention, thin skin,
and high blood pressure are other clues that may prompt testing. How-
ever, an estimated 50% of patients will present with psychiatric symp-
toms prior to physical signs or symptoms (Rasmussen et al. 2015). Low
cortisol levels, on the other hand, typically result in fatigue, weight loss,
malaise, memory impairment, and confusion.
Assessing for changes in thyroid function is typically part of routine

testing on initial medical evaluations because it is well known that in-
dividuals with thyroid disease can present with psychiatric complaints.
Classically, hyperthyroidism manifests with elevated heart rate, dia-
phoresis, and anxiety, but at especially high levels of circulating thyroid
hormone, people may present with psychotic symptoms (Brownlie et
al. 2000). Often referred to as a thyroid storm, this extreme form of thy-
rotoxicosis is a life-threatening emergency and requires urgent hospital-
ization if evident.
In contrast to the thyroid storm, people with hypothyroidism may
also present with psychosis. At extremely low levels of circulating thy-
roid hormone, and consequently significantly elevated TSH, patients
may develop myxedema and can present with psychotic symptoms.
The psychotic symptoms correlate with a significant slowing of metab-
olism, and fatigue, depression, weight gain, and confusion often pre-
cede the psychotic symptoms (Heinrich and Grahm 2003).
Neurological Disorders
People with structural abnormalities such as chronic subdural hemato-
mas, cerebral contusions, glial cell tumors, and meningiomas that com-
press underlying cortex and impair processing may present with
psychotic symptoms (Kar et al. 2015). Similarly, ischemic strokes or
brain metastases have been documented in people who present with
psychosis. Associated neurological signs and/or symptoms that sug-
gest structural brain abnormalities require follow-up with brain imag-
ing (Khandanpour et al. 2013). Notably, a typical brain imaging pattern
for a person with schizophrenia includes reduction in gray matter; pau-
city of axons and dendrites in the cortex; compensatory enlargement of
the lateral and third ventricles; and volumetric loss, especially in the
temporal lobes. On positron emission tomography, there is often de-
creased activity in the frontal lobe. Suspicion for a structural neurolog-
ical condition would increase if the onset of psychosis is acute or
subacute, if there are other neurological symptoms such as weakness or
change in coordination, if there are concurrent or historical comorbid
cancer diagnosis and treatment, or if the psychosis has atypical features
such as nonauditory hallucinations.
Seizures, specifically temporal lobe epilepsy (TLE), may manifest
initially with depression and behavioral changes that may be confused
with schizophrenia (Kandratavicius et al. 2014). Classically, people with
TLE may experience delusions that they are dead that occur paroxys-
mal with the ictal activity. Additionally, patients with a history of sei-
zures have an increased risk for developing a psychotic illness. This is
particularly true for patients with TLE (7%), which may lead to scarring
of the hippocampus, a structure implicated in the pathophysiology of
schizophrenia (Kandratavicius et al. 2014). A clear time course for the

seizures, including periods of confusion and urinary incontinence,
should be assessed in the history. Because latency in response is a com-
mon manifestation of a psychotic process, psychosis can be confused
with potential partial-complex seizure activity. Long-term electroen-
cephalogram monitoring may be required to identify seizure activity.
Identifying a seizure disorder is important not only for assessment; it
may also guide antipsychotic selection because antipsychotic medica-
tions variably lower the seizure threshold.
Genetic Disorders
Velocardiofacial syndrome, or 22q11 deletion syndrome, has an inci-
dence of 1:2,000–4,000 in the population, has wide variability in presen-
tation, and can often be missed. Identification is important because it
may suggest alternative treatment approaches (Carandang and Schol-
ten 2007) and provide the patient and family with another community
for potential engagement and support. Typical co-occurring symptoms
include a submucosal cleft palate, learning disorder in childhood, and
short stature (McDonald-McGinn et al. 2015). Seizures, renal agenesis,
and cardiac and immune abnormalities may also be present. Testing is
best done in consultation with medical geneticists.
Conclusion
Expanded workup should be pursued when there is indication after the
basic workup that an underlying reversible condition may exist. In
these cases, one must consider the index of suspicion for various causes
and target the workup in the direction that seems most likely. Not all of
the testing reviewed here would be indicated in most patients, and, in
fact, many cases will warrant investigation in only one of these catego-
ries, if any. However, when history, physical, family history, and/or
other telltale signs point in the direction of another potential cause or
contributor to onset of psychosis, a targeted workup should be com-
menced.
A word of caution about pursuing medical workups is warranted.
The following vignette illustrates a common story within our clinic.
Case Example 2
Tyler is a 19-year-old who presented with 2–3 months of delusions and
obsessive-compulsive symptoms. He was previously a high school
honor student and had been accepted by an elite university but had to
drop out of school after one quarter because of the onset and worsening
of his psychiatric symptoms. He had numerous physical complaints,
and initial laboratory workup showed unexpected levels of inflamma-
tion and insulin resistance. This prompted further workup with endo-
crinology to understand whether there was a hormonal connection to
the insulin resistance and with immunology and rheumatology to ascer-
tain potential causes of the inflammation. Despite a thorough workup
from these services, including several visits and numerous tests, a deci-
sion was made by an outside consultant to try empirical treatment with
intravenous immunoglobulin (IVIg). Although Tyler’s parents initially
felt that he improved from the IVIg, the effect was short lived. Discus-
sion of options for further pursuit of a medical cause of his psychosis
continued, and his parents often focused much of the clinical sessions
on asking about further consultations throughout the medical center.
Tyler’s treatment team recognized that pursuit of alternative explana-
tions was interfering with effective treatment of his ongoing psychosis.
After several months, his parents agreed to a referral for Tyler to see one
of the team’s psychologists to begin cognitive-behavioral therapy for
psychosis. At this point, despite seeking further medical workup, Tyler
and his family began to understand the nature of his experience, and Ty-
ler achieved tremendous symptomatic improvement. He was able to
join a book club and participate in regular volunteer work in a capacity
beyond what he had been capable of for the previous 2 years.
In Tyler’s case, when looking at how the process unfolded, it is clear

that time was lost in pursuit of the medical workup at the expense of en-
gaging in effective psychiatric treatment. This example demonstrates
the importance of setting reasonable expectations at the onset of a de-
tailed medical workup for psychosis, as well as a plan for initiating care
to achieve relief and begin healing as the workup proceeds. In some
cases, as the psychiatric diagnosis becomes clearer and/or the search
for medical causes becomes more remote, patients and families may be-
come desperate to deepen the search. This understandable reaction can
shift attention away from initiation of evidence-based therapies for psy-
chosis. For example, when there is concern for infectious causes such as
Lyme disease, there may not be objective markers to guide treatment. It
is helpful to delineate with patients and families what tests you agree to
run to rule out a suspected condition and what you will do with the re-
sults, as well as the limits of those tests. To continue to pursue a lengthy
medical workup when the likelihood of a primary psychotic disorder is
becoming clear can be a disservice to both patients and families.
On the other hand, mental health providers must also be fierce ad-
vocates for patients as they enter the general medical system. Too often,
elements of the physical examination or history are overlooked, written
off as psychiatric, and not given the attention they deserve. Further,
people with psychotic disorders may misattribute somatic sensations,
leading to further misunderstanding. For example, a patient might de-
scribe feeling unusual body sensations and suggest that they may be a
result of body control due to hallucinations, when in fact he or she may
be experiencing the onset of a neurological condition. Mental health

professionals must insist on the appropriate workup and testing when
the circumstances dictate and not settle for simple explanations in com-
plex situations without careful consideration of what is being excluded.
KEY CONCEPTS
• Approach workup of psychosis methodically, starting with
the basics: history, physical examination, and routine labo-
ratory tests.
• Consider additional testing as your index of suspicion
increases in a particular direction. There should be a ratio-
nale for ordering more invasive tests.
• Assemble a team. The workup may be complex and often
requires outside consultation from specialty providers.
Make sure to include primary care in the earliest stage of
the workup if not already involved.
• Remember the patient and family in the process while pur-
suing medical workup. Work with families to set expecta-
tions for the workup and remember to focus on providing
treatment while a workup is pending.
1. What resources in your area can you use to provide a com-

plete workup for a person who comes to you in a first episode
of psychosis?
2. How will you work with families to understand the road

map and limitations of the medical workup? What can you
do to manage expectations?
3. How might you respond to a family who asks for more exten-
sive workup than you judge to be warranted? How can you
maintain a therapeutic connection with the patient and fam-
ily while setting appropriate limits on the medical workup?
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Freudenreich O, Schulz SC, Goff DC: Initial medical work-up of first-
episode psychosis: a conceptual review. Early Interv Psychiatry
3(1):10–18, 200921352170
Kandratavicius L, Hallak JE, Leite JP: What are the similarities and dif-
ferences between schizophrenia and schizophrenia-like psychosis
of epilepsy? A neuropathological approach to the understanding of
schizophrenia spectrum and epilepsy. Epilepsy Behav 38:143–147,
201424508393
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CHAPTER
10
Assessing and Treating

Trauma in Team-Based
Early Psychosis Care
Rachel L. Loewy, Ph.D.
Tara Niendam, Ph.D.
Paula Wadell, M.D.
IN this chapter, we address the assessment and treatment of posttrau-

matic stress within the framework of team-based treatment of early psy-
chosis. First, we discuss the prevalence of trauma exposure in psychosis,
highlighting different types of trauma that are particularly relevant to
first-episode psychosis (FEP) and briefly discuss models of the relation-
ship between trauma and psychosis. Next, we propose universal screen-
ing for trauma exposure and posttraumatic stress symptoms in early
psychosis services and describe assessment tools and best practices for
assessment procedures. Then we explain how trauma-informed care
(TIC) can be applied to early psychosis programs. Finally, we review ev-
idence-based trauma-specific interventions that can be used by early
psychosis teams, including cognitive-behavioral therapy (CBT), family
interventions, and medication management. We also provide a case ex-
ample to illustrate how each component of care can apply to an individ-
ual presenting with trauma and psychosis. Given the relative lack of
attention to trauma in early psychosis work and the hesitation that
many providers express regarding addressing trauma with their clients,
we hope that this chapter gives both novice and experienced early psy-
151
chosis team members more confidence that they can safely and effec-
tively treat traumatic experiences and symptoms to promote resilience
and recovery.
Case Example
Maria, a 25-year-old woman, was referred to the FEP program by her
older sister, Sarah, who was concerned about Maria’s recent hospitaliza-
tion after a 3-month period of homelessness. Sarah reported that Maria
experienced periods of depression, anxiety, strange thoughts, and un-
usual behaviors. Maria presented to the clinic for the clinical intake with
her sister. Maria reported periods of chronic depression since childhood
that worsened after high school graduation. She reported that she
worked odd jobs after graduation, but nothing ever seemed to stick. In
the fall of the previous year, Maria reported that she began to hear whis-
pers coming from the vents in her apartment. At first, she wondered if
they were the voices of angels or demons. Sarah reported that the family
lost touch with Maria at this time until they received a call from the local
psychiatric hospital. Maria had been evicted from her apartment after
she smashed the walls looking for “the demons” and trying to release
“the angels.” She had painted her walls with crosses and said that she
had been chosen by God to save the world. After being evicted, Maria
was homeless and lived in her car. Police brought her to the hospital be-
cause she was yelling at people in a parking lot and threatening to hurt
them. Maria reported that she felt others were noticing her “brown
skin” and that they had hostile intentions toward her, including want-
ing to hurt her. In the past month, Maria reported that her new medica-
tions had helped to quiet the whispers, but she still felt unsafe when
walking in public. She also reported periods of suicidal ideation, won-
dering if death would be better than burdening her family. When asked
about their early history, Maria and Sarah reported they were adopted
as children from Guatemala, noting that their biological parents died in
1992 during the civil war. Maria was 9 and Sarah was 12 at the time of
their adoption. Sarah reported that their biological father had a history
of drinking too much and would often get angry and hit his family to
“get them in line.”
Trauma Types and Prevalence
Trauma in Early Psychosis

Exposure to traumatic events is, unfortunately, quite common in psy-
chosis, occurring at much higher rates than in the general population
(Varese et al. 2012). History of trauma exposure is related to a variety of
poorer outcomes, including more severe symptoms, worse social func-
tioning, substance use, homelessness, and risk for suicide. The relation-
ship of trauma and psychosis is likely reciprocal; early trauma may
Assessing and Treating Trauma in Early Psychosis Care 153
contribute to later risk for psychosis, and young people with psychosis
are at increased risk for bullying and interpersonal victimization (see
Figure 10–1). Traumatic experiences can shape the form of psychotic
symptoms, such as suspiciousness, and many people experience psy-
chotic symptoms, such as auditory hallucinations, in the context of
posttraumatic stress disorder (PTSD). Finally, psychotic symptoms can
themselves be frightening and experienced as traumatic, as can hospi-
talizations and involuntary restraint. Furthermore, compared with the
general population, people with psychotic disorders are at higher risk
for revictimization.
Childhood Trauma
A meta-analysis of psychosis and adverse childhood events (sexual
abuse, physical abuse, emotional/psychological abuse, neglect, paren-
tal death, and bullying) reviewed 36 studies in three categories of re-
search: 1) case-control studies that compared individuals with
psychosis to those without psychosis and those with childhood trauma
exposure to those without a childhood trauma history; 2) prospective
cohort studies that followed people with and without childhood
trauma over time, and 3) cross-sectional cohort studies that examined
the relationship of trauma to psychotic-like experiences in the general
population (Varese et al. 2012). Varese and colleagues found significant
relationships between childhood trauma and psychosis across all three
types of studies and concluded that childhood adversity is strongly as-
sociated with increased risk for psychosis.
Bullying and Interpersonal Victimization

People with psychosis may have experienced bullying by peers in
childhood during the prodrome or pre-psychotic phase of their disorder
or after onset of their first psychotic episode. In some cases, these expe-
riences meet narrow definitions of trauma, such as interpersonal vio-
lence or verbal threat of harm, and in others, they represent a painful
pattern of verbal abuse and rejection that can nonetheless be stressful
and psychologically traumatizing, especially in childhood and adoles-
cence. These kinds of experiences can often affect mood and social func-
tioning and influence the form of psychotic symptoms through
mistrust, paranoid delusions, and hallucinations.
Community, Intergenerational, and

Identity-Based Trauma
In addition to direct experiences of trauma, individuals with FEP may
be exposed to violence in their families and communities that must be
154
GENETIC
VULNERABILITY
INCREASED TRAUMA ALTERED

VULNERABILITY DEVELOPMENTAL
TO FUTURE TRAJECTORY
TRAUMA
Hypervigilance and reactivity to threat Poor emotional regulation and coping skills
Affirmed faulty cognitions Negative global views of self and others
Increased cognitive impairment Aggression and poor social functioning
(e.g., executive control, social cognition) Impaired cognition
Increased high-risk behaviors Changes in brain structure and function
(e.g., substance use, crime) Increased stress sensitivity and vulnerability
Poor social and role functioning
Decreased treatment adherence and participation
Reduced social support
Comorbid conditions
(e.g., mood/anxiety disorders, PTSD)
PSYCHOTIC-LIKE
EXPERIENCES
FIGURE 10–1. Cycle of trauma, psychotic-like experiences, and vulnerability.

Abbreviation. PTSD=posttraumatic stress disorder.
Source. Reprinted from Mayo D, Corey S, Kelly LH, et al.: The role of trauma and stressful life events among individuals at clinical high risk for psychosis:
a review. Frontiers in Psychiatry 8:55, 2017. Used with permission.
accounted for in treatment of their psychosis. This can impact treatment

when family members, seen as important sources of support in FEP
care, are either perpetrators or themselves victims of assault, abuse,
and/or neglect. In communities with high levels of ongoing violence,
perceived threat must be examined in the context of reality-based
threats. Furthermore, discrimination based on personal identity or
characteristics (e.g., sex, race, ethnicity, sexuality, religion, intersection-
ality) and historical or institutionalized discrimination must be
thoughtfully included in conceptualization and treatment of trauma
and psychosis. Careful discussion in assessment and treatment from a
cultural humility approach can differentiate these elements rather than
assuming that symptoms are psychotic or, alternatively, assuming that
they are nonpsychotic responses to discrimination.
Temporal Characteristics of Trauma

Trauma may be a single event, or it may be chronic abuse and victim-
ization. It also can be experienced in multiple domains. This can affect
the severity of posttraumatic stress (PTS) as well as the presentation of
symptoms in response to a single time-limited event or complex PTSD
as a result of prolonged periods of victimization. Complex PTSD can
carry higher levels of risky behaviors and self-harm, as well as addi-
tional symptoms of changes in perceptions of self, others, and relation-
ships that may be misdiagnosed as personality disorders. Additionally,
past traumatic experiences are treated differently from ongoing abuse
or victimization, which requires establishing current safety first and
foremost. FEP programs should have established policies on reporting
abuse communicated clearly to clients and families at the outset of pro-
gram participation, with every effort made to deal with reporting as col-
laboratively as is legally allowed.
Assessment

During the initial evaluation, the examiner asked Maria to complete the
Posttraumatic Stress Disorder Checklist for DSM-5 (PCL-5), a brief self-
report screening questionnaire for trauma experiences and symptoms
(Weathers et al. 2013a). On this measure, Maria endorsed experiencing
physical abuse by her father, observing the physical abuse of other fam-
ily members, experiencing the sudden death of a family member, and
being around war. She also reported that she had quickly left a neigh-
borhood when a number of U.S. Immigration and Customs Enforce-
ment trucks appeared in the street, noting that she was terrified that she
could be deported because of her undocumented status. She reported

that the experience of abuse by her father was the most distressing of
these experiences. In response to this abuse, she endorsed multiple
trauma symptoms, including hypervigilance, re-experiencing, blaming
herself, and feelings of low self-worth and avoidance. The examiner also
completed a semistructured interview about Maria’s trauma experi-
ences and symptoms. Maria met criteria for PTSD, according to the Di-
agnostic and Statistical Manual of Mental Disorders, 5th Edition (DSM-5;
American Psychiatric Association 2013).
Trauma Screening
Universal screening for both exposure to traumatic events and related
PTS symptoms should be part of every initial evaluation for FEP ser-
vices. Although we appreciate that an extensive intake process can be
burdensome to clients, families, and clinicians, attention to trauma is
critical for 1) differential diagnosis and 2) collaborative treatment plan-
ning. Because of feelings of shame and avoidance, many people will not
report trauma unless specifically asked about it. Compassionate trauma
screening can make someone feel understood and “seen” as a whole
person, with a full life history, rather than a constellation of psychotic
symptoms. However, repeated screening may be necessary because
some people will be more comfortable reporting trauma after the ther-
apeutic relationship develops over time. High levels of distress related
to PTS can interfere with engagement and must be addressed. In fact,
many individuals with FEP may identify relief from PTS as a primary
treatment target that is more important to them than first targeting hal-
lucinations or delusions.
Trauma Measures
Several validated measures for assessing trauma and PTS that can be used
in FEP programs are discussed in this subsection and are listed on the web-
site for the National Center for PTSD (www.ptsd.va.gov/professional/
index.asp). In some cases, programs may be required by their operating
agency, municipality (city, state, or county) or funding organization
(e.g., Substance Abuse and Mental Health Services Administration
[SAMHSA]) to use a specific measure. If the measure recommended for
general mental health programs is insufficient for the FEP service, we
encourage programs to negotiate with the relevant parties. The FEP ser-
vice should consider whether it is important to have one measure that
can be used across a wide age span, such as from adolescence to adult-
hood. Some measures are self-report, whereas others are semistruc-
tured interviews. Some options can offer client self-report and caregiver
or provider versions to allow multiple informants to contribute to the
assessment.
Although the gold standard for diagnosis of PTSD is a semistructured

interview such as the Clinician-Administered PTSD Scale (CAPS-5;
Weathers et al. 2013b) or the Structured Clinical Interview for DSM-5®
Disorders—Clinician Version (SCID-5-CV; First et al. 2016), the choice
of the correct tool may be based on the population served by the FEP
program as well as the resources available. For example, the Life Events
Checklist (LEC; Gray et al. 2004, Weathers et al. 2013c) can be used to
evaluate the presence of traumatic events. The PTSD Checklist for
DSM-5 (PCL-5) is a 20-item self-report screen that can be combined with
the LEC to assess associated PTS. This combination can be used to de-
termine whether additional assessment is warranted and to monitor
change in symptoms in response to treatment. In children, the Child
and Adolescent Trauma Screen (CATS; Sachser et al. 2017) provides the
ability to examine traumatic events and associated symptoms in a man-
ner that is parallel to the PCL-5 with LEC. The Traumatic Events Screen-
ing Inventory for Children (TESI-C; Ippen et al. 2002; Ribbe 1996) is a
semistructured interview that includes child and caregiver self-report
versions to screen for traumatic events and assesses PTS related to each
event. The National Center for PTSD provides excellent free resources
for assessment of trauma experiences and symptoms for children and
adults (see Recommended Resources).
Differential Diagnosis
A very common referring question posed to early psychosis (EP) ser-
vices who provide diagnostic evaluations is differential diagnosis of
PTSD versus a primary psychotic disorder. In many cases this is a false
dichotomy because the same individual can present with both PTS and
psychotic symptoms. Although prevalence rates vary, one large study
estimated that 16% of people with schizophrenia spectrum disorders
meet formal diagnostic criteria for PTSD (de Bont et al. 2015). Sub-
threshold PTS symptoms are measured less often but occur at even
higher rates, and psychotic-like symptoms are common enough in
PTSD that there has been debate about whether there is actually a psy-
chotic subtype of PTSD.
In terms of clinical presentation, hallucinations must be distin-
guished from vivid memories, flashbacks, and dreams that occur as re-
experiencing of traumatic events. Details of the symptoms and their
explanation are important. Both types of symptoms can be upsetting,
but one has a known source, whereas the other may be experienced as
unrelated to the trauma or being of unknown origin (e.g., the perpetra-
tor’s voice vs. an unidentified voice). Paranoia must be differentiated
from exaggerated suspiciousness and mistrust that does not reach delu-
sional severity. Here, the level of conviction may be helpful (e.g., “I am
sure he wanted to hurt me” vs. “I think he wanted to hurt me, but it’s
possible that was my imagination”). Dissociation must be differentiated

from delusional experiences (e.g., “I felt as if I was not present in my
body” vs. “Another being took over control of my body”). These cases
can be complex and often require consultation, supervision, or group
discussion to reach a consensus regarding the differential diagnosis.
Further complicating factors include the triggering effect of stress in ex-
acerbating both types of symptoms and the high rates of substance use
to cope with PTS, which can trigger or induce psychosis. Finally, some
EP services may not accept PTSD with psychotic features as an eligible
diagnosis for services, whereas others do accept it.
Cultural Factors
A variety of cultural factors can influence an individual’s exposure to
trauma, as well as that person’s ability to access appropriate care. The
DSM-5 Cultural Formulation Interview (American Psychiatric Associa-
tion 2013) could be useful as the clinician works to understand how an
individual’s cultural experience impacts his or her experience of symp-
toms related to psychosis, trauma, or other domains. In the case of Ma-
ria, her lived experience as a survivor of a civil war was not seen by her
as the most significant traumatic experience in her life. Additionally,
her identification as Latina was associated with increased fear of depor-
tation and a perception of others as being hostile toward her. These
fears and concerns are not wholly inaccurate, and it is important for the
clinician to consider these factors when attempting to determine which
experiences are treatment targets. Language, religion, racial and ethnic
identity, gender and sexual identity, and acculturation represent some
of the cultural areas that must be explored with clients as part of the
treatment planning process to ensure accurate identification of treat-
ment targets for both psychosis and trauma symptoms.
Treatment Approaches to Trauma

in Early Psychosis

During the first meeting with her clinician, Maria was provided with
feedback about the results of her intake evaluation. The clinician dis-
cussed Maria’s experiences of depression, auditory hallucinations, and
delusions as well as her experiences of trauma and the associated symp-
toms. At first, Maria was surprised at being asked to discuss her painful
childhood memories when she was seeking care for her psychosis. The
clinician took time providing education about the relationship between
stress and symptoms, noting that traumatic experiences are one form of
stress that can impact recovery. The clinician then laid out a plan for
care, in which education about psychosis, depression, and trauma
would be provided along with skills to improve Maria’s ability to cope
with stress and reduce her symptoms. The clinician asked Maria’s per-
mission to share this information with Sarah and their adoptive parents,
who wanted to be active participants in Maria’s care because she was
now living at home with them. Maria reported that she was primarily
concerned about her depression and hearing the voices, so the clinician
agreed to target those symptoms first. As those experiences improved,
the clinician stated that they would re-evaluate Maria’s depression, psy-
chosis, and trauma symptoms to determine which direction to take next.
Trauma-Informed Care
Although there are different models of TIC, their primary aim is to help
survivors resolve trauma rather than be retraumatized by their interac-
tions with services and systems. These approaches promote awareness
of the signs and effects of trauma and support trauma-sensitive interac-
tions by educating staff at all system levels—from the phone or front
desk administrative staff who first interact with clients, through front-
line providers, to the financial billing staff and upper management.
Trauma-sensitive policies and procedures are integrated throughout
the organization. SAMHSA has developed a number of TIC resources
based on six core principles:
1. Safety: making physical and psychological safety of all clients and

staff a priority
2. Trustworthiness and transparency: conducting all operations and mak-
ing decisions with transparency and the goal of building and keep-
ing trust with those served
3. Peer support: promoting trauma recovery through use of peers
4. Collaboration and mutuality: sharing power and decision making be-
tween clients and staff and also between all staff members in differ-
ent roles
5. Empowerment, voice, and choice: promoting empowerment and resil-
iency for clients and staff through respectful, shared decision-making
6. Cultural, historical, and gender issues: moving past stereotypes and bi-
ases to offer culturally sensitive and responsive services
Although we are unaware of a formalized approach to integrating

TIC into EP services in the published literature, many organizations
that receive SAMHSA funding or provide an array of services have
used a trauma-informed approach, as have some stand-alone EP clinics.
The TIC principles defined above overlap substantially with many as-
pects of coordinated specialty care models, although TIC may also have
particular challenges that require attention in integration, as summa-
rized in Table 10–1. For example, all programs working with this popu-
lation should have clear procedures in place to ensure the physical
safety of all clients and staff, communicated with transparency to all.
Sensitivity to suspiciousness and paranoia, much like trauma, means
checking in with clients frequently to gauge their sense of psychological
safety.
Collaborative decision making is a hallmark of many EP programs,
which offer a variety of services tailored to the needs and goals of indi-
viduals. Peer staff in EP programs are often individuals with lived ex-
perience of psychosis, who, given the high rates of trauma experienced
by individuals with psychosis, are often also trauma survivors. Training
and supervision of peers should focus on experiences of trauma and
how they may interact with psychosis. Prioritizing self-care for staff in
EP clinics can reduce workforce turnover by addressing vicarious
trauma and burnout. Shifting the power balance between staff and cli-
ents and between different staff members may be more of a challenge
for EP programs embedded in medical models and systems. As we
have discussed previously, ensuring staff members’ knowledge of and
sensitivity to identity-related trauma and discrimination, as well as his-
torical trauma, is necessary to understand clients’ experiences and pro-
mote recovery from both psychosis and trauma.

Maria felt very unsafe in public and, at times, felt very uncomfortable in
the clinic waiting room. To help with this fear, she checked in with the
clinic coordinators on arriving at the clinic, and the peer case manager,
Kevin, went out to the lobby to sit with her. Maria liked Kevin, so this
helped her feel safer and more relaxed while she waited. Consistent
with TIC, the team prioritized Maria’s sense of safety, and Kevin helped
level the balance of power by interacting with her as a supportive peer
with his own recovery experience rather than as a doctor in a position
of authority.
Cognitive-Behavioral Therapy
The use of cognitive-behavioral approaches to treating psychosis allows
for easy integration of specific trauma approaches based in CBT in order
to address both trauma and psychosis. Evidence-based treatments for
trauma, such as trauma-focused cognitive-behavioral therapy (TF-CBT)
for youth and prolonged exposure (PE) or eye movement desensitization
therapy (EMDR) for adults, have a foundation in cognitive-behavioral
theory. In a recent review, Cragin et al. (2017) found studies that demon-
strated the effectiveness of these trauma treatments in individuals with
established psychosis and PTSD; however, the authors’ survey of EP
TABLE 10–1. Elements of trauma-informed care and coordinated specialty care for first-episode psychosis
TIC principle CSC compatibility Potential integration challenges
1. Safety • Clear guidelines should be communicated to All staff, not just individual providers, require
clients, family members, and staff for training in assessing fearfulness and safety.
assessing and ensuring physical safety of
clients, family, and staff, including abuse, SI/
HI reporting, and evaluations for
hospitalization.
• Attention should be paid to the client’s
perceived threat in the moment in clinic and
other situations.
• Flexibility is key in offering services in clinic,
at the client’s home, or in neutral community
spaces.
2. Trustworthiness and • A team-based approach that honors Organizational transparency requires particular
transparency contributions of all team members is required. attention in busy, complex team-based programs.
• Patience and flexibility are needed in
Assessing and Treating Trauma in Early Psychosis Care
establishing trust when clients feel suspicious.

3. Peer support • Peers and family partners often work in CSC Additional training in disclosure and support of
programs. trauma may be required for peers and family
partners.
161
162
TABLE 10–1. Elements of trauma-informed care and coordinated specialty care for first-episode psychosis (continued)
TIC principle CSC compatibility Potential integration challenges
4. Collaboration and mutuality • Treatment planning is characterized by shared Organizations need to be thoughtful in leveling
decision making, including defining specific power differences between staff in programs with a
treatment goals and selecting CSC elements medical model orientation.
with particular clients and families.
5. Empowerment, voice, and • There should be a focus on strengths-based Programs should be responsive to varying levels of
choice perspectives, resilience, and recovery goals for achievement, particularly in supported
orientation. education or employment models that may have
traditionally focused on lowered expectations.
6. Cultural, historical, and • Cultural or contextual sensitivity is often built Attention to these issues can lapse when training and
gender issues into clinical assessment and conceptualization supervising staff in multiple evidence-based
of psychosis. approaches.
• Identity issues often are important for
transitional-age youth.
Abbreviations. CSC=coordinated specialty care; SI/HI=suicidal ideation/homicidal ideation; TIC=trauma-informed care.
program providers indicated uncertainty regarding how to address

trauma symptoms in early psychosis.
Within an integrated trauma-psychosis cognitive-behavioral frame-
work, the clinician and client collaboratively develop a conceptualiza-
tion of how the trauma experiences and psychosis symptoms are being
maintained and contribute to current distress. The clinician provides
psychoeducation around both psychosis and trauma, such as informa-
tion on how stress can lead to the exacerbation of both psychosis and
trauma symptoms. Information about the rates of certain traumatic
events or types of trauma symptoms can also be provided. The clinician
and client work to develop a set of coping skills to manage symptoms
and distress. Measuring distress regularly through subjective distress
ratings and addressing it directly and early in the therapy with coping
skills are critical to giving clients an early positive experience of the
treatment and to providing them coping skills to support later exposure
practices. Coping skills can address relaxation, awareness of affect, and
regulation as well as cognitive coping skills.
Relapse and safety planning are essential for maintaining stability in
an outpatient setting. At this point, it would be important to reassess
the severity of trauma and psychosis symptoms to determine the focus
of subsequent treatment. If psychosis is stable, trauma treatment would
suggest that exposure—through creation of a trauma narrative—would
be the next step. Such a narrative would be shared with a caregiver in
the case of a TF-CBT approach or the clinician in the case of PE or
EMDR. As noted by Cragin and colleagues (2017), exposure is an essen-
tial component in the treatment of trauma symptoms in individuals
with psychosis and should not be avoided in cases where psychosis
symptoms are stable. If psychosis symptoms are not stable, ongoing
psychoeducation around trauma and enhancement of coping skills to
manage trauma-related symptoms would be appropriate in the context
of treatment that focuses on psychosis symptom reduction. Regardless
of whether the client’s level of trauma symptoms warrant exposure to
trauma history, CBT for psychosis would use exposure as one method
for addressing psychosis symptoms. For example, a client and provider
may walk around public places, identify times when the client feels
strangers are looking at him or her (or not), and use cognitive skills (e.g.,
“Catch it, check it, change it”) to evaluate the client’s belief that people
are out to get him or her.

As Maria engaged in EP services, her depression and auditory halluci-
nations improved; however, she continued to feel very unsafe in public.
As part of the treatment conceptualization, Maria had learned that part
of her anxiety was related to experiences of trauma and realistic con-
cerns about her immigration status, whereas another piece was associ-
ated with potentially unrealistic beliefs that other people judged or

persecuted her because of the darker color of her skin. As part of her
treatment, Maria and her clinician developed a hierarchy of anxiety-
provoking experiences so that they could analyze and examine her
thoughts in real time. Maria realized that she often felt afraid when
walking in her neighborhood, worrying that someone might assault her
because of her skin color. To address this fear, as part of her treatment,
Kevin took walks with Maria in her neighborhood, allowing them to ac-
tively record her thoughts and try alternative thoughts (cognitive cop-
ing) while measuring her emotional response (assessing distress).
Family Involvement
CSC for early psychosis sees family involvement as a core component in
supporting understanding and recovery. Family members who actively
support the client should also receive psychoeducation on psychosis and
trauma. Family can support use of effective coping skills when the client
is in the community and provide feedback to the clinician about their ef-
fectiveness in reducing distress in the real world. TF-CBT incorporates
sharing of the trauma narrative with a nonoffending caregiver as part
of the exposure process. If this is appropriate for the EP client, it could
also be included in the integrated trauma-psychosis treatment ap-
proach. However, this may or may not be appropriate for adult clients.
In general, sharing the trauma narrative with someone other than the
clinician should be discussed with the client to determine the best ap-
proach. Overall, family members or other loved ones should be seen as
natural and ongoing supports for youth and adults with psychosis, and
EP care should strive to enhance these supports through education and
collaboration, regardless of the symptoms that are being targeted.

Maria actively participated in individual and group treatment. Bi-
weekly family sessions included her biological sister, Sarah, and their
adoptive parents. Maria was encouraged to share information on psy-
chosis and trauma symptoms with her family, with the support of her
clinician. She also shared her favorite coping skills, which included
deep breathing and meditation, and asked her family to prompt her to
use her skills when she is upset. Maria was able to identify family argu-
ments and large crowds as triggers for her anxiety. Specifically, she re-
ported that she was often overwhelmed by Sarah’s critical comments
and tendency to yell when upset. The clinician reflected that both Maria
and Sarah had experienced verbal and physical abuse by their biological
parents and noted that both of them could benefit from improved cop-
ing and communication skills. Sarah and Maria agreed. Maria asked her
family to participate in an upcoming communication skills group for
families so they could improve their communication as a family. They

expressed appreciation for the help with understanding more about
Maria’s experiences and how they could be more supportive. They were
also impressed by how much knowledge Maria had gained. Sarah re-
ported that she was pleased to have Maria participate in a recent family
barbecue, noting that it was nice to see her enjoy being with family
again.
Medication Management
There are currently no guidelines for the psychopharmacological treat-
ment of comorbid trauma and psychosis. Generally, the treatment of co-
morbidity should be modeled on the evidence for each disorder.
Antipsychotic medications are the appropriate treatment for psychosis
and have all been shown to be more effective than placebo (Schatzberg
et al. 2010). Antipsychotic medications have also been studied in the
treatment of PTSD. Studies of risperidone, olanzapine, and quetiapine
demonstrated some efficacy, with the greatest impact seen on reduction
of intrusive traumatic ideation and hypervigilance (Ahearn et al. 2011;
Carey et al. 2012). The most widely studied medications for the treatment
of PTSD are the selective serotonin reuptake inhibitors, with paroxetine
and sertraline both having specific U.S. Food and Drug Administration
approval.
All other medications used in PTSD are off label. Randomized placebo-
controlled treatment studies have shown some efficacy in the reduction
of symptom severity with a range of other antidepressants, including
fluoxetine, amitriptyline, imipramine, mirtazapine, nefazodone,
phenelzine, and venlafaxine (Ipser and Stein 2012). There are data re-
garding the use of antidepressants in schizophrenia because of the fre-
quent presence of depressive symptoms in first-episode clients (Koreen
et al. 1993; Tapp et al. 2001), but studies have suggested that depressive
symptoms may resolve with antipsychotic medication, and therefore
initial treatment with an antipsychotic alone is generally recommended
to minimize medications and potential side effects (Robinson et al.
2014). Data supporting the use of other medication classes in PTSD are
limited and show conflicting evidence (Raskind et al. 2018). The only
class considered relatively contraindicated is the benzodiazepines,
which can worsen symptoms in PTSD (Guina et al. 2015).
Training and Consultation

As with all evidence-based interventions, implementing trauma-informed
care and trauma-specific interventions requires allocated resources
from finances, administrative planning, and staff time for training and
ongoing supervision and consultation. Although these approaches are

compatible in many ways with team-based early psychosis programs
and can build on skills and elements already in place, they do require a
long-term commitment from program leadership for successful integra-
tion. There are a number of resources available for training and consul-
tation, starting with online resources and toolkits and including expert
consultation on both the organizational changes required and specific
clinical supervision. Many care systems are asking all organizations to
include trauma-informed approaches and may offer free trainings,
workshops, and technical support. The resource list provided at the end
of this chapter includes several organizations that can respond to re-
quests for training and technical assistance.
Conclusion and Future Directions

Given the very high rates of trauma seen in EP populations, team-based
EP care must include assessment and treatment of trauma. Treatment
should include both trauma-informed practices throughout the service
and evidence-based psychotherapy for trauma; neither is a sufficient
approach on its own. Staff providing medication management should
also be familiar with treating both psychosis and PTS, with particular
attention to how benzodiazepines are used. Clinicians are often con-
cerned that addressing trauma with clients with EP may exacerbate psy-
chotic symptoms, similar to the long-held but erroneous view that talk
therapy is contraindicated for psychosis. Without training in evidence-
based assessment and treatment of trauma, many clinicians hesitate to
address the trauma, inadvertently contributing to retraumatization or
client disengagement and withholding chances for full recovery. Iden-
tifying when a client has sufficient coping skills to tolerate exposures
and when PTS is a priority for treatment is a decision to be made in col-
laboration with the client and with good clinical supervision and con-
sultation. Although EP care already requires intensive training in
evidence-based practices and additional training may initially feel bur-
densome to teams, a focus on trauma will actually help clinicians be
more effective with some of their most distressed clients and will help
staff understand their own reactions to working with this population,
with a focus on self-care to address vicarious trauma. The relative lack
of attention to trauma in psychosis until more recently leaves many av-
enues in need of further research to help guide EP teams. However, we
hope we have made a sufficient argument for attention to trauma in EP
care, with the ultimate goal of supporting the whole person and pro-
moting recovery from both psychosis and trauma.
KEY CONCEPTS
• Trauma occurs at high rates in the first-episode psychosis
population, including childhood trauma, bullying and vic-
timization, intergenerational trauma, and traumatic hospi-
talization experiences.
• Assessment of both trauma exposure and posttraumatic
stress symptoms is important for every client and may
need to be repeated over time as the therapeutic relation-
ship develops.
• Trauma treatment can be safe and effective for individuals
with psychosis.
1. How do you assess trauma exposure and symptoms in your

program?
2. How might a trauma history affect a client’s perceptions and

expectations of treatment for psychosis?
3. How could a trauma-informed perspective inform the oper-

ation of your program, from the first contact to the last?
4. How should each member of the treatment team approach

trauma issues with clients and their families?
5. How can therapists integrate trauma-specific interventions

into their treatments for clients with psychosis?
Recommended Resources
Frontiers: Trauma, Psychosis, and Posttraumatic Stress Disorder. Available
at www.frontiersin.org/research-topics/4761/trauma-psychosis-
and-posttraumatic-stress-disorder. Accessed December 4, 2018.
National Association of State Mental Health Program Directors Center
for Trauma-Informed Care: www.nasmhpd.org/content/national-
center-trauma-informed-care-nctic-0
National Center for PTSD: www.ptsd.va.gov/professional/index.asp
National Child Traumatic Stress Network: www.nctsn.org
Substance Abuse and Mental Health Services Administration: SAMHSA’s

Concept of Trauma and Guidance for a Trauma-Informed Ap-
proach. Pub ID SMA14-4884. Rockville, MD, Substance Abuse and
Mental Health Services Administration, 2014. Available at: https://
store.samhsa.gov/product/SAMHSA-s-Concept-of-Trauma-and-
Guidance-for-a-Trauma-Informed-Approach/SMA14-4884.html.
Accessed December 4, 2018.
TF-CBT Therapist Certification Program: https://tfcbt.org
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CHAPTER
11
Intervening Early
A TEAM-BASED APPROACH
Iruma Bello, Ph.D.
Debra R. Hrouda, Ph.D.
SPECIALIZED multi-element early intervention services for the treat-

ment of first-episode psychosis (FEP) have been in existence for at least
two decades in both Australia and parts of Europe and Canada. Research
studies have consistently found that individuals who receive these ser-
vices early in their illness trajectory demonstrate short-term positive out-
comes (Gafoor et al. 2010; Grawe et al. 2006). More recently, studies in the
United States have obtained similar positive results (Dixon et al. 2015;
Kane et al. 2015; Srihari et al. 2015). A recent meta-analysis by Correll and
colleagues (2018) also found that individuals receiving early intervention
services had better outcomes than those receiving treatment as usual.
These research findings have led to a broad implementation effort of spe-
cialized early intervention services across the United States that have come
to be known as coordinated specialty care (CSC) services.

CSC is an early intervention treatment approach for young people expe-
riencing a first episode of nonaffective psychosis. It consists of a multidis-
ciplinary team with specialized training to deliver assertive care
171
management, individual or group psychotherapy, supported employ-

ment and education services, family education and support, appropriate
pharmacotherapy, and primary care coordination. The program philoso-
phy emphasizes the delivery of person-centered, recovery-oriented, cul-
turally competent care using shared decision making (Heinssen et al.
2014). The National Institute of Mental Health defined CSC on the basis
of the national and international body of research focused on early psy-
chosis; the positive findings of the Recovery After an Initial Schizophre-
nia Episode (RAISE) studies conducted in the United States provided
further support for CSC (Azrin et al. 2016).
There are several types of CSC programs that are being imple-
mented throughout the United States, including Navigate, OnTrackNY,
the Early Assessment and Support Alliance (EASA), FIRST Coordi-
nated Specialty Care, and Specialized Treatment Early in Psychosis
(STEP). Although all of these programs have comparable key elements,
there are some differences in the way the teams are structured or the
way in which the services are provided and the level of manualization
associated with each approach. Nonetheless, they all share the philoso-
phy that the nonspecifics related to delivery of CSC services (including
team members’ attitudes, youth orientation, flexibility, team collabora-
tion, and recovery orientation), which can convey to participants and
families a sense of compassion, warmth, and hope for the future, are
paramount for ensuring the successful implementation of CSC and
helping young people attain good outcomes.
The ability to connect with young people experiencing FEP in a col-
laborative and productive way that respects their personal values and
keeps them at the center of the team’s efforts is fundamental for being
able to deliver the CSC interventions. Therefore, in most of this chapter
we focus on describing 1) the specific interventions delivered across
CSC teams, using a time-limited framework for service delivery, 2) the
important factors associated with working within a multidisciplinary
treatment team, and 3) the underlying clinical concepts that drive all of
the evidence-based practices delivered under CSC. A vignette is used
throughout to illustrate the implementation of each of these compo-
nents. In the final section of this chapter, we provide guidance on adap-
tations that should be considered when implementing CSC services in
rural settings.
Case Example
Jasmin is a 19-year-old Latina living with her mother, aunt, uncle, and
two younger siblings. Jasmin’s father lives in the Dominican Republic,
and she visits him regularly. When Jasmin was 10 years old, her mother
brought her and her siblings to live in the United States with Jasmin’s
maternal uncle and his wife to provide them with better educational op-
portunities. Jasmin’s mother works at a bank, and the aunt and uncle
Intervening Early 173
have their own small business selling jewelry. Jasmin’s relationship with
her family is close but marked by discord related to their differing views
on religion.
Throughout her childhood, Jasmin was a good student interested in
the sciences. She was accepted to an out-of-state college with a scholar-
ship. During the first semester of her sophomore year, Jasmin began tak-
ing courses related to her engineering major and began experiencing
school as increasingly stressful. Her GPA declined, which further in-
creased her stress level because she feared she might lose her scholarship.
She also started spending more time drinking with friends during the
weekends as a way to cope. She was arrested for public intoxication once.
By the end of the semester, Jasmin became increasingly distressed. She
stopped sleeping and ate very little, spending most days at the library
studying for finals. She also started experiencing auditory and visual
hallucinations and started believing that her teachers were plotting to
get her expelled from school. Jasmin’s friends noticed the change in her
demeanor, hygiene, and thinking and decided to take her to the school’s
counseling center. This resulted in her first hospitalization, where she
was prescribed antipsychotic medication.
On discharge from the hospital, Jasmin returned to live with her fam-
ily and took a medical leave from school. Although she was experiencing
fewer voices and visual hallucinations and no longer believed that her
professors were plotting against her, Jasmin felt apathetic, refused to meet
with friends, barely interacted with her siblings, and spent a lot of time
alone in her room watching television. Jasmin’s mother searched for ap-
propriate mental health services online and contacted a local CSC pro-
gram. Once evaluated by the team, Jasmin was found to be eligible and
was offered services, and she agreed to enroll in the program.

Interventions
CSC programs provide a suite of evidence-based practices that have
been shown to be effective in treating individuals diagnosed with
schizophrenia. At a minimum, services offered include care manage-
ment, individual and family therapy, supported employment and edu-
cation services, medication management, and coordination with
primary health care. Some teams offer enhanced services such as peer
support services for participants and for family members, treatments
for cognitive health, cognitive-behavioral therapy for psychosis
(CBTp), occupational therapy, and supported housing. Interventions
are delivered using a phased, time-limited framework that typically
lasts 2–3 years. Within the CSC model, participants are not required to
engage in any of the interventions in order to maintain enrollment, al-
though everyone is connected to a primary provider who serves as the
point person for the participant and family members. It is the partici-
pant’s and family’s ability to engage with the team in a flexible way that
allows the interventions to be tailored specifically to each individual
and his or her set of circumstances to promote achievement of school,
work, and relationship goals.
At the outset of treatment, teams focus on forging highly collabora-
tive and engaging alliances with participants and family members
through the use of specific assertive outreach and engagement strate-
gies (Bennett et al. 2017). For instance, successful teams are able to re-
main proactive in connecting with participants and family members
throughout all phases of treatment, which might include the use of var-
ious forms of communication (phone, texting, e-mail, and in-person
meetings). The time and location of sessions are flexible and responsive
to the needs of the participants and family members (e.g., in the home,
community, or clinic, with increased or decreased frequency as needed).
Considerations of transportation, work schedules, and other caregiving
are critical, especially in areas that are geographically spread out where
public transportation may not be readily available. The flexibility of
team members to be creative in communication and scheduling is es-
sential in developing a solid working alliance.
Teams provide important information for participants to consider
all relevant treatment choices rather than dictating treatment recom-
mendations, which helps ensure that treatment decisions are guided by
pressing concerns expressed by participants and family members—not
the priorities of the team. Providers maintain a flexible and consistent
stance toward treatment, which allows them to respond sensitively and
practically to the range of situations that might arise on an as-needed
basis. At the same time, they focus on demonstrating to the participant
and family members that the team will remain a consistent presence by
behaving in a reliable manner and offering support, empathy, and trust-
worthiness (Bennett et al. 2017). This therapeutic alliance usually serves
to ensure that treatment engagement remains across time and serves as
the foundation for introducing and delivering the pharmacological,
psychosocial, and other treatments offered. Teams typically have the
flexibility to keep the participant’s file open in the program for longer
periods of time than in traditional clinical settings, even when there is
little contact with the participant.
Once rapport has been established and the team is able to gain a
more in-depth understanding of the individual and his or her natural
supports, preferences, values, and worldview, interventions can be tai-
lored accordingly and delivered as intensely as necessary to promote re-
covery. The final phase of treatment is focused on transitioning the
individual from the team on the basis of his or her continued needs and
preferences. Some options might include a CSC step-down program if
available, regular outpatient clinic care, or other less traditional sup-
ports offered through school or the community.

When Jasmin arrived at the CSC clinic, she was surprised at how youth-
friendly and nontraditional the environment felt. She noticed that there
were other younger individuals like herself in the waiting room, the de-
cor was warm and appealed to her, and there was even a computer
room where several young people were congregating and seemed to be
discussing a computer game. Jasmin and her mother met with Martha,
her assigned primary therapist. Unlike other providers Jasmin had en-
countered at the hospital, Martha did not start by asking Jasmin about
her diagnosis or whether she was taking her medications as prescribed.
The meeting did not feel rushed, and Jasmin felt heard and involved in
the process. Jasmin quickly got the impression that Martha wanted to
really get to know her as a person and understand her point of view.
Initially, Martha spent time discussing with Jasmin and her mother
the services the team could provide and how these services would be fo-
cused on helping Jasmin achieve her personal goals, which included fin-
ishing her engineering degree. Martha described the various ways in
which the team had worked with other participants and introduced Jas-
min and her mother to the various team members. Martha maintained
a curious stance, which conveyed support, reassurance, and hope. She
offered to communicate with Jasmin via text and to visit her at home to
get to know the rest of the family who were unable to make it to the
clinic. Martha spent several meetings both at the clinic and at the fam-
ily’s home learning about Jasmin’s needs and concerns as well as those
of her family members.
At first, Jasmin conveyed that she did not want to meet with any
other team members. However, over time, as Martha got to know Jas-
min and her family and the things they found to be important, she was
able to make individualized recommendations about how working
more closely with other team members might be beneficial. Together,
they settled on the plan that Jasmin would benefit from receiving CBTp
in their sessions to help cope with the symptoms she continued to expe-
rience and would also start meeting with the team psychiatrist to dis-
cuss medication side effects.
Because Jasmin continued to express the goal of completing her en-
gineering degree, she and Martha decided that Jasmin would meet with
the supported employment and education specialist, Scott, to start to
figure out how to get back on track. Martha recommended that Jasmin
also meet with the peer support specialist for added support and per-
spective. At first, Jasmin was hesitant, but after one meeting with Paul,
the peer specialist, she agreed that it was helpful to interact with and get
the perspective of someone who had experienced similar symptoms
and shared how he pursued his goals with the support of mental health
services. Throughout her treatment with the team, Jasmin at times
would meet with specific team members more frequently, particularly
when she needed more support or when she was struggling with an in-
crease in symptoms. However, she appreciated being able to decrease
the frequency of these meetings and meet with fewer team members
during those times when she was feeling more stable and was busy pur-
suing her educational goals. The fact that she did not feel pressured to
follow a regimented treatment schedule allowed her to remain working
with the team for 2 years.
Working Within a Multidisciplinary

Treatment Team
One of the central elements of providing CSC services is the effective use
of a multidisciplinary treatment team. CSC teams are composed of a va-
riety of providers. Most commonly, these include a team leader, who pro-
vides administrative and supervisory oversight, and licensed therapists
(e.g., psychologists, social workers, mental health counselors, occupa-
tional therapists) able to provide therapeutic interventions. These inter-
ventions might include individual and group evidence-based
psychosocial treatments such as CBTp, social skills training, motivational
interviewing, harm reduction, and family education and support. The
team also includes medical providers (e.g., prescriber, nurse) able to de-
liver medication management, health and wellness interventions, and
primary care coordination and trained employment or education support
specialists who provide community-based support for attaining school
and work goals based on the individualized placement and support
model. Some teams may also include additional care managers, peer spe-
cialists for participants, and peer specialists for family members.
The number of providers necessary to fulfill all of these roles some-
times depends on the configuration of the specific CSC model being fol-
lowed (e.g., OnTrackNY vs. Navigate vs. EASA), the available resources
within a specific agency, and the size of the cohort being served. It is
common for team members to hold multiple roles. For example, in ad-
dition to having administrative and supervisory responsibilities, the
team leader might also deliver individual psychotherapy to a group of
participants. The roles of primary therapist and care manager might be
combined, with the primary therapist also in charge of managing refer-
rals and performing eligibility evaluations, or the primary therapist
might work primarily to provide family education and support. Al-
though most teams have four to six providers (some part time and some
full time) serving 30–35 participants, the number of team members is
less important than the amount of effort devoted by each provider to
working on the CSC team and ensuring that all the roles are covered.
Team collaboration is another essential element for delivering effec-
tive CSC treatment. This is accomplished by having weekly team meet-
ing attended by all team members where providers have an
opportunity to at least briefly discuss each individual with whom they
are working, provide feedback, and review progress toward treatment
goals. These meetings can also serve as a platform for team members to
strategize about how they might work together to help each participant
achieve his or her goals, process and troubleshoot challenges they
might be encountering with specific participants and family members,
and ensure that the team’s culture remains recovery oriented and per-
son centered.

During a particular team meeting, Martha noted that she noticed Jasmin
decompensating during the past month after she stopped taking her
medication, which was leading Martha to believe that Jasmin was not
ready to take a course at her local college next semester. Paul reminded
Martha that the term decompensating is not recovery oriented and en-
couraged Martha to instead describe in detail the behavioral changes
she has noticed and how these changes are affecting Jasmin and her
family so that the team could strategize together. Additionally, Paul said
that he would share aspects of his recovery story during his next meet-
ing with Jasmin to see if he could provide her with added support.
Scott shared that there is a zero exclusion principle for engaging in
work and school, which means that the team should support individu-
als in their work and school goals without presuming readiness or their
ability to succeed. He shared how he has worked with many partici-
pants whose symptoms seem to decrease when they are able to actively
work on their goals, and taking a class might be just what Jasmin needs
at this moment to help her feel better. He offered to work with Jasmin
on her preferences to determine good next steps.
This discussion allowed Martha to feel supported by her team on
several levels. Jasmin’s care was now based on multiple perspectives,
which provided a more optimistic outlook and helped relieve some of
Martha’s concerns. On a practical level, other team members with ex-
pertise in their respective areas developed a plan to help support Jasmin
and her family.
Clinical Concepts That Drive

Coordinated Specialty Care Treatment
Four clinical concepts and practices lie at the core of all services pro-
vided by CSC teams: health, home, purpose, and community. Providers
within CSC teams are expected to deliver recovery-oriented, person-
centered, culturally competent services that are guided by a framework
of shared decision making regarding treatment options. Teams that are
recovery oriented ascribe to the definition of recovery promoted by the
Substance Abuse and Mental Health Services Administration: “A pro-
cess of change through which individuals improve their health and
wellness, live a self-directed life, and strive to reach their full potential”
(Substance Abuse and Mental Health Services Administration 2011). A

CSC team might implement the four dimensions of recovery as follows:
1. Health: The team works with service participants and their families
to make informed decisions to assist individuals in managing symp-
toms and to support physical and mental health.
2. Home: The team helps individuals and their families with concrete
case management services, including assistance with insurance, en-
titlements, and a stable and safe place to live.
3. Purpose: All members of the team work with the service participant in
order to clarify and meet personal goals around work and/or school.
4. Community: The team is responsive to participants’ preferences re-
garding their desired level of interaction with family and friends. Si-
multaneously, the team also encourages the development of such
relationships, including involvement in community groups that
may foster support, friendship, and hope.
When working from a recovery perspective, providers convey a

sense of hope and focus on individual strengths and resiliency rather
than symptoms and impairment. Participants view the process of re-
covery as one that is nonlinear and progresses over time, allowing them
to achieve important life goals (Bennett et al. 2017).
Person-centered care works alongside a recovery philosophy be-
cause it positions the participant at the center of the team, collaborating
with all of the providers regarding the person’s care. The individual’s
life goals, aspirations, and ambitions drive treatment planning. Further-
more, the individual has a voice and a choice in deciding which treat-
ment is best and what are considered good treatment outcomes
(Bennett et al. 2017). It is important that providers allow a space for dis-
cussions to occur regarding what participants are experiencing and
how they are making sense of their FEP, what it means in the context of
their identity and life goals, and how to be part of the solution, instead
of attempting to convince them of a diagnosis.
Normalizing the existential questions that program participants
may be asking themselves while demonstrating humility about the pro-
viders’ ability to predict course and outcomes is important. It is not un-
common for young people to attribute the experience of FEP to many
different factors, question whether it is a one-time event or lifelong
change, and remain skeptical that the services provided by the CSC
team are actually what they need (Bennett et al. 2017). As such, when
providers are able to walk alongside participants in this journey, using
an inquisitive and open stance regarding the individual’s and family’s
understanding about what is happening, participants and families tend
to feel respected and valued and are able to build an alliance with the
team that allows for better treatment.
Developing culturally competent practices enhances the team’s abil-

ity to facilitate this process of finding common ground and sustaining
an alliance throughout the time that the young person is receiving CSC
treatment. Culture can be defined as an evolving process of meaning
making that all individuals undergo on the basis of their background
and experiences. Multiple aspects of people’s social backgrounds can
provide a basis for their cultural orientation, including their age, class,
race or ethnicity, gender, sexual orientation, geographic culture (urban,
suburban, or rural), occupation, language, and, for some, immigration
and acculturation (Lewis-Fernandez et al. 2018).
With regard to FEP, culture is important because it guides how an in-
dividual and family understand the illness and what steps should be
taken. Therefore, it is important that teams spend time developing an
understanding of the cultural framework for each participant as well as
how the culture of the team shapes the care that is provided. In doing
so, the team becomes responsible for developing practices that incorpo-
rate relevant knowledge, skills, and attitudes that convey an apprecia-
tion for the role of the person and the family as experts on their own
experiences and interpretation. The team should elicit the individual’s
preferences and terms that should be used to describe aspects of the
young person’s identity (Lewis-Fernandez et al. 2018). An important
tool that can help with obtaining some of this information is the Cultural
Formulation Interview in the Diagnostic and Statistical Manual of Mental
Disorders, 5th Edition (DSM-5; American Psychiatric Association 2013).
The key is genuinely understanding participants’ self-identification and
interpretation. The team should not presume that just because partici-
pants are of a specific race or religion they ascribe to the beliefs and
norms associated with that culture.
Shared decision making then becomes the vehicle for putting together
all of these concepts and practices because it provides a systematic frame-
work for making treatment decisions that prioritize what matters most to
participants and families by deliberately shifting the power dynamics be-
tween providers and participants. In essence, it consists of a process of
deliberation whereby providers share their knowledge and the range and
strength of the evidence on which their recommendations are based,
while at the same time emphasizing how this knowledge aligns with the
individual’s preferences and values (Elwyn et al. 2017). At the center of
shared decision making reside the principles of collaboration: an ability
to share information in an accessible format that details all available op-
tions relevant to the decisions that program participants find important
to make, inclusivity, and active listening to promote participation in
treatment decisions.
Enacting shared decision making transcends being aware of or sen-
sitive to what matters most to participants. It requires the use of specific
steps to ensure that participants feel heard and are receiving all of the
information needed to make informed choices. Shared decision making

consists of a three-step process of shared decision making and details
what should be happening at each step. The first step, team talk, con-
sists of setting the framework for the collaborative approach, commu-
nicating support, and exploring an individual’s goals. The second step,
option talk, consists of describing the available options with all of the
related evidence in an accessible format that allows for deliberation re-
garding the pros and cons of each option. The third step, decision talk,
allows the individual to develop and share informed preferences and
make a treatment decision (Elwyn et al. 2017). It is important to note
that this process is not linear or final but rather cyclical as individuals
progress through treatment and the need for various decisions to be
made arises.

When working with Jasmin, the team was able to keep her goal of re-
turning to school at the forefront of her treatment. The team worked
closely with Jasmin and her family while providing a hopeful message
to help her find the best way to pursue her goal of becoming an engi-
neer. Therefore, discussion around medications, therapy, and supported
employment and education always connected back to how these treat-
ments were instrumental in allowing Jasmin to pursue the life she
wanted for herself.
Another important part of the treatment consisted of offering Jasmin
and her family support and developing an understanding of their world-
view. Jasmin’s family is devout Christian, and it was important to them
that Jasmin attend church and have the fellow parishioners pray for her
recovery through prayer circles. This was something that Jasmin did not
feel comfortable participating in, which led to frequent arguments. The
team worked to develop a trusting relationship with Jasmin’s supports.
With Jasmin’s permission, Martha attended a service and had an oppor-
tunity to have a discussion with the church’s pastor, who has a close re-
lationship with the family. Using the framework of shared decision
making, Jasmin, her family, and the rest of the team were able to find
some common ground around ways to incorporate other supports into
her treatment that are important in the rest of the family’s life and whose
advice they value. Everyone discussed the options of attending church,
meeting with the pastor, or going to a prayer circle and deliberated on
the pros and cons of each. Jasmin decided that although she did not feel
comfortable going to prayer circles or attending weekly services, she
was willing to meet with her mom and the pastor on a more regular basis.
Jasmin thought this would demonstrate respect toward her mother’s cul-
tural beliefs while also providing the pastor with information that could
better help the family deal with Jasmin’s difficulties and symptoms.
Thus far in this chapter, we have demonstrated the key components

and the various ways in which a high-fidelity CSC program can work
to provide services to young people and their families. At the same

time, it is important to acknowledge that as the dissemination of CSC
programs becomes more far reaching, adaptations will be necessary in
order to meet the demands of specific communities and to work within
the context of sometimes limited resources. This has become evident
when services are implemented in rural settings.
Implementing Coordinated Specialty

Care Services in Rural Settings
It is important to consider that distance and variability in available re-
sources and infrastructure might inform the implementation of CSC ser-
vices across geographic settings. This will impact several factors: 1) team
training and functioning, 2) outreach activities, and 3) service delivery.
The following subsections include recommendations for useful adapta-
tions that can be implemented in each of these categories to help support
the success of CSC teams delivering services in more rural areas.
Team Training and Functioning

As described earlier, CSC teams contain a very specific configuration of
team members who require specialized training and support to help
bolster their competencies in delivering specialized care. This can prove
to be challenging in rural and underresourced areas where there is less
access to financial resources, infrastructure, and workforce. Training a
CSC team requires protected time and commitment, which can be diffi-
cult for agencies with staff who have multiple responsibilities with as-
sociated productivity requirements and that lack financial resources for
engaging in training.
Creativity and flexibility go a long way toward overcoming some of
these barriers. For example, one approach is to schedule trainings
during times that are convenient for team members while taking into
consideration whether this will lead to decreased productivity or affect
their ability to perform other duties. Some organizations develop spe-
cial productivity codes to account for the necessary training, consulta-
tion, and supervision time; others incentivize participation in these
activities. In addition, the organization needs to plan resources for re-
imbursing travel and other costs associated with attending training,
consultation, and supervision activities—especially when these activities
are at a time or location when the team is not usually together. Conduct-
ing these activities face to face, with the entire team, helps to build collab-
orative relationships while providers acquire knowledge and skills.
Considerations about infrastructure are also necessary for facilitat-
ing learning during the training activities, particularly if done remotely.
Measured application of distance learning can be extremely useful. Or-

ganizations need to ensure that staff members have the proper equip-
ment (e.g., computer, Web camera, microphone, speakers) to access the
training materials. In addition, when using video technology, organiza-
tions need to ensure that Internet connections are robust enough to al-
low a smooth signal for uninterrupted interactions. Having a video
freeze during a training or consultation session can break up the flow
and interfere with learning.
A similar creative approach should be employed when considering
team functioning. Rural and underresourced areas sometimes lack psy-
chiatric providers; therefore, CSC teams should make an effort to attract
and retain clinicians who are motivated to work with FEP and practice
in a recovery-oriented framework. In addition, there are often logistical
issues that might impede effective team functioning, such as when team
members are not colocated. Teams may need to be flexible in the format
of team meetings—either scheduling early enough in the day so that
team members can spend the rest of the time in the community or using
video or teleconferencing technologies. It takes extra effort to work as a
team when members are not physically in the same place; however, it is
not impossible.
Outreach Activities
Some of the most important activities performed by CSC teams are
those associated with outreach because this helps to ensure appropriate
and rapid referrals to the program. In rural and underresourced areas,
it is vital that outreach activities are tailored to meet the individual
needs of the community and its culture. When outreach activities are
performed by staff members who are from the community and are
keyed into the local network, their understanding of the culture, stake-
holder priorities, and important relationships can help obtain buy-in
from referral sources as well as more effectively engage potential par-
ticipants. If, on the other hand, the team member performing outreach
is not local, it is recommended that he or she take the time to develop
effective working relationships with stakeholders within and outside
typical health care settings (e.g., hospitals, schools, jails, chamber of com-
merce, Rotary Club, Knights of Columbus, faith-based organizations).
Service Delivery
The delivery of the CSC model can also require several adaptations and an
added layer of flexibility and creativity in order for the team to effectively
work with participants and their supports in rural and underresourced
communities. One important consideration is that the number of partic-
ipants being served by each team member and productivity expecta-
tions (if they exist) need to account for the additional time required to
travel, sometimes long distances, to home or community sites where
participants choose to meet with team members. Organizations need to
recognize the additional time and effort needed by team members in or-
der to adequately reach, engage, and work with participants and their
families. This is especially relevant in rural areas where public transpor-
tation may not be readily available and the ability of team members to
demonstrate flexibility in communication and scheduling is critical to
developing a solid working alliance. Some recommendations include
lowered productivity expectations to account for nonbillable travel
time and adequate reimbursement for mileage or access to organiza-
tion-provided vehicles.
When some team members are not able to meet in the community and
participants are unable to get to the office, telehealth can be a useful tool.
In fact, some younger people are more used to electronic communication
and thus are more open to telehealth and other technology-associated
communications. In addition to allowing for prescribers who are not co-
located to serve participants, telehealth can also facilitate consultation
and liaison between providers at the CSC program and others with ex-
perience and expertise in treating FEP.
However, as with other aspects of CSC, technology is useful only
when it is consistent and reliable. Participants may not have reliable cel-
lular service or Internet access where they live. Similarly, Internet ser-
vice may be slow and may not support full video. Here again, flexibility
and creativity are in order. Some organizations partner with resources
closer to where participants live as a workaround. Having appoint-
ments at places such as recreation centers, libraries, businesses, or other
health care providers or systems combines convenience, comfort, and
the availability of more reliable Internet or cellular service. This serves
the double task of providing reliable, convenient locations for partici-
pants and family members to receive services and building awareness
and collaborative relationships with key community resources.
Conclusion
CSC is a treatment model for delivering team-based care for young peo-
ple experiencing their first episode of psychosis, which has been
demonstrated to improve outcomes. Although there are several varia-
tions for configuring this multi-element, multidisciplinary team ap-
proach, CSC includes several evidence-based practices that should be
offered to individuals and families, including individual and group
psychotherapy, family education and support, evidence-based psycho-
pharmacology and wellness strategies, supported employment and ed-
ucation, and care management. It is important to remember that it is not
solely the distinct interventions delivered but rather the process

through which team members collaborate with each other and the un-
derlying messages of hope, recovery, and empowerment that the team
conveys to participants that seems to make a difference in young peo-
ple’s lives. Furthermore, it is important to note that even when adapta-
tions to the model are needed, employing creativity and flexibility and
appropriately adapting the implementation to meet the needs of the
community being served ultimately lead to the success of the program
and its participants.
KEY CONCEPTS
• Coordinated specialty care is an evidence-based multi-
element early intervention treatment approach for young
people experiencing a first episode of nonaffective psy-
chosis. It is a time-limited intervention delivered by a team
that has received specialized training.
• CSC provides participants with a suite of evidence-based
practices that include individual and group psychotherapy,
assertive care management, supported employment and
education services, family education and support, and
wellness and primary care coordination. Some teams pro-
vide additional services such as peer support.
• Recovery is viewed as a nonlinear “process of change over
time through which individuals improve their health and
wellness, live a self-directed life, and strive to reach their
full potential” (Substance Abuse and Mental Health Ser-
vices Administration 2011). Recovery for many individuals
means learning to manage symptoms effectively and to
use wellness strategies in order to achieve the things that
matter in life: love, work, and community contribution.
• CSC relies on shared decision making, an approach to set-
ting goals and making treatment decisions that relies on
techniques such as decision aids, discussion of options,
decisional balance exercises, comparing parallel ratings,
and negotiating compromises. Shared decision making
aims to increase knowledge, increase the individual’s par-
ticipation in and commitment to treatment, enhance the
professional’s understanding of the individual’s values and
preferences, and strengthen the therapeutic alliance.
• Professional practice providers are responsible for devel-

oping cultural competency, which is grounded in cultur-
ally relevant knowledge, skills, and attitudes.
1. What are some of the advantages associated with starting a

CSC program in your community for both providers and
young individuals experiencing FEP?
2. Given the range of services provided by CSC teams, what

might be some ways in which an agency can support putting
together this multidisciplinary treatment team?
3. Team collaboration is an important component of delivering

effective CSC treatment. What are some concrete strategies
that promote team collaboration and communication?
4. How might teams encourage and promote participant engage-

ment with the treatment team across time? Are there any cre-
ative strategies that are unique to your community?
5. What steps can team members take to ensure that they remain
recovery oriented and hopeful and that they are actively us-
ing formal shared decision-making steps?
Suggested Readings
Bennett M, Lee R, Watkins L, et al: OnTrackNY Team Manual. New
York, Center for Practice Innovations, 2017. Available at:
www.ontrackny.org/Resources. Accessed October 5, 2018.
Crisanti AS, Altschul D, Smart L, et al: Implementation of Coordinated
Specialty Services for First Episode Psychosis in Rural and Frontier
Communities. Albuquerque, NM, University of New Mexico, 2015.
Available at: www.nasmhpd.org/sites/default/files/Rural-Fact
Sheet-_1.pdf. Accessed October 5, 2018.
Dixon LB, Goldman H, Srihari V, et al: Transforming the treatment of
schizophrenia in the United States: the RAISE initiative. Annu Rev
Clin Psychol 14:237–258, 2018 29328779
Heinssen RK, Goldstein AB, Azrin ST: Evidence-Based Treatments for First
Episode Psychosis: Components of Coordinated Specialty Care. Rock-
ville, MD, National Institute of Mental Health, 2014. Available at:
www.nimh.nih.gov/health/topics/schizophrenia/raise/nimh-
white-paper-csc-for-fep_147096.pdf. Accessed October 5, 2018.
Mueser KT, Gingerich S: NAVIGATE Team Members’ Guide. Bethesda,
MD, National Institute of Mental Health, 2014. Available at: http://
navigateconsultants.org/manuals. Accessed October 5, 2018.
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CHAPTER
12
Psychopharmacology for
People in Early Psychosis
Jian-Ping Zhang, M.D., Ph.D.
Pharmacotherapy in First-Episode
Psychosis
Antipsychotic medications are the mainstay of pharmacotherapy for peo-
ple with schizophrenia and are also a key component of first-episode
treatment. Because research has shown that duration of untreated psy-
chosis (DUP) is correlated with worse outcome, successful treatment of
the first psychotic episode is crucial for minimizing the cascading effects
of social and vocational deterioration. In general, both typical, or first-
generation, antipsychotics (FGAs) and atypical, or second-generation,
antipsychotics (SGAs) are effective in improving positive symptoms.
However, not all antipsychotics are created equal. Large clinical trials
among people with first-episode psychosis (FEP) and meta-analyses
have demonstrated that some antipsychotics are more efficacious than
others. There are also significant differences in each medication’s side-
effect profile. Therefore, careful evaluation of a patient’s symptomatol-
ogy, family history, and prior medication exposure is the key to tailoring
treatment to each individual in order to maximize efficacy and mini-
mize potential side effects.
187
Although we can find guidance in the general schizophrenia treat-

ment literature, it should be noted that randomized controlled trials
(RCTs) of people with chronic schizophrenia have several limitations.
These include confounding effects of prior medication use, potential
overrepresentation of partially responsive or treatment-nonadherent
patients, and a tendency to recruit patients with low pre-study func-
tioning levels in whom ongoing illness and treatment effects might re-
duce overall treatment response. Conversely, some trials might enroll
more responsive patients who are eligible for and willing to consent to
participation in RCTs, thereby, again, potentially washing out differ-
ences between medications that would be apparent in more heteroge-
neous, real-life samples. Therefore, the results of large FEP clinical trials
such as the European Union First Episode Schizophrenia Trial (EUFEST;
Kahn et al. 2008), Comparison of Atypicals in First Episode of Psychosis
(CAFE; McEvoy et al. 2007), and the Center for Intervention Develop-
ment and Advanced Research (CIDAR) clinical trial (Robinson et al.
2015) provide useful information as to how we can best treat people in
their first episode. These studies point to several issues that are unique
to pharmacotherapy in FEP and should be considered in initial treat-
ment planning and follow-up care.
Compared with treatment of individuals with chronic schizophrenia,
treatment of first-episode patients is generally characterized by higher re-
sponse rates, lower effective antipsychotic doses, and a higher sensitivity
to drug-induced adverse effects. Hence, studies in first-episode popula-
tions offer the unique opportunity to examine the effectiveness and side
effects of antipsychotics in patients who are more representative of the
entire schizophrenia population and in whom important initial treat-
ment effects can be observed. Furthermore, prior therapeutic and ad-
verse response patterns to antipsychotics are largely unknown in
individuals with FEP, so treatment recommendations must be based on
information other than past treatment history.
Selection of an Antipsychotic Drug

to Treat First-Episode Psychosis
The goal of antipsychotic treatment for people in FEP is to achieve sig-
nificant treatment response, which will facilitate symptom remission
and recovery from the illness and minimize drug-induced side effects,
which will help treatment adherence and long-term treatment success.
Unlike medication selection for patients with chronic illness, for whom
selection of antipsychotic drugs can be guided by past treatment his-
tory, the choice of the first agent for patients in FEP needs to be based
on evidence provided by clinical trials.
Psychopharmacology for People in Early Psychosis 189
More than 20 published randomized clinical trials have been pub-

lished comparing antipsychotic medications in people with FEP. One
comprehensive meta-analysis examined the relative efficacy and toler-
ability of individual SGAs versus individual FGAs in 13 head-to-head
trials with more than 2,500 patients (Zhang et al. 2013). Although there
was no significant difference in overall efficacy between the two anti-
psychotic classes, SGAs had slight advantages in treating negative
symptoms and improving cognitive function. Olanzapine seemed to
outperform the FGA comparators in several outcome measures, but the
effect sizes were relatively small (i.e., Hedges’ g=0.1–0.3). SGAs were
significantly better than FGAs in maintaining patients in treatment with
lower all-cause discontinuation rate. As a class, FGAs caused more ex-
trapyramidal effects (EPS) and tardive dyskinesia than SGAs, whereas
SGAs were generally associated with more weight gain and cardiomet-
abolic changes. In summary, SGAs, including olanzapine, risperidone,
and quetiapine, may have a slight advantage over FGAs in treatment ef-
ficacy and persistence, although they are more likely to cause weight
gain and metabolic side effects.
Recently, our group conducted another comprehensive meta-analytic
review to compare the efficacy and side effects of various SGAs in treat-
ing FEP (Zhang et al. 2016). Twenty-two randomized acute treatment
trials with more than 3,600 individuals in FEP using seven SGAs (olan-
zapine, risperidone, quetiapine, ziprasidone, aripiprazole, clozapine,
and amisulpride) were included. Clozapine and amisulpride were used
in only one study each, so the meta-analytic findings were based mostly
on the other five drugs. Although there were no differences in treatment
response rate and all-cause discontinuation, olanzapine and risperi-
done significantly outperformed quetiapine and ziprasidone in reduc-
ing overall symptoms as well as positive symptoms, with effect sizes
ranging from 0.20 to 0.85 (all P values<0.05). Aripiprazole also had a
slight advantage over quetiapine in total symptom reduction, but the
difference was only approaching statistical significance. All drugs were
similar in treating negative symptoms, except that in one study, aripip-
razole was better than risperidone in treating negative symptoms such
as avolition, apathy, asociality, and anhedonia (Robinson et al. 2015).
Consistent with clinical experience, olanzapine caused significantly
more weight gain than other drugs. Risperidone caused more EPS than
olanzapine, whereas aripiprazole was more likely than quetiapine to in-
duce akathisia.
On the basis of the meta-analytic findings and results from large FEP
clinical trials, and after efficacy and side effects are carefully weighed, it
seems that SGAs, especially risperidone and aripiprazole, should be con-
sidered as a first-line drug choice in treating people in FEP. Although
olanzapine is as efficacious as risperidone, its weight gain liability and
potential metabolic side effects make it less suitable as a first-line drug.
Quetiapine and ziprasidone may be considered as second-line drugs.

Haloperidol and other FGAs may also be considered if a patient has
failed or cannot tolerate first-line or second-line drugs. The evidence on
using clozapine in FEP is limited. However, clozapine is certainly the
drug of choice for patients whose illness proves to be treatment refrac-
tory, and there may be advantages to starting clozapine within the first
year of illness when needed (Ballon et al. 2018). In addition, several
newer antipsychotic medications, such as lurasidone, asenapine, and
cariprazine, have shown relatively good tolerability in people with
schizophrenia, a desirable characteristic in first-line medication. How-
ever, no clinical trials have been conducted to test the efficacy and tol-
erability of these medications in individuals with FEP.
Treatment Response Rate and

Drug Dosing
The definitions of treatment response vary among medication treat-
ment studies. Most studies use a percentage of total symptom score re-
duction, measured by either the Positive and Negative Symptoms Scale
(PANSS; Kay et al. 1987) or the Brief Psychiatric Rating Scale (Woerner
et al. 1988), or other equivalent instruments. RCTs among patients with
chronic schizophrenia tend to use a 20% reduction of symptoms,
whereas FEP trials usually use more stringent criteria, such as 40% or
50% reduction. It is generally agreed that patients in FEP need to have
clinically significant symptom improvement to promote functional re-
covery; therefore, 50% or more reduction in total symptoms is more ap-
propriate and a reasonable target for a substantial proportion of
patients to achieve. A few studies have used even more stringent crite-
ria, such as mild or lower rating on PANSS items and Clinical Global
Impressions scale scores (Guy et al. 1976) of much improved or very
much improved, which is close to the definition of symptom remission.
Table 12–1 shows the average medication dose, response rate, definition
of treatment response, and all-cause discontinuation rate (a measure of
treatment effectiveness) in modern medication trials for FEP.
Overall, short-term treatment response rate in FEP clinical trials
ranged widely from 9.1% to 76.2%, largely due to variations in medica-
tion used, treatment duration, and definition of treatment response. Av-
eraging across multiple trials, risperidone, olanzapine, and aripiprazole
had slightly higher response rates (44.8%, 45.1%, and 46.8%, respec-
tively) than haloperidol and quetiapine (38.7% and 39.5%), with ziprasi-
done in between (41.2%). These numbers are slightly higher than the
average response rate in people with chronic schizophrenia. Leucht and
colleagues (2009) found in a meta-analysis of drug registration trials
TABLE 12–1. Medication used in large first-episode psychosis (FEP) clinical trials, dose, response rate, and all-cause
discontinuation rate
Short-term Discontin- Time to Long-term

Trial Medication/ response Response Time to uation rate discontin- response
Trials N duration mean dose rate criteria response (all-cause) uation rate
Emsley and 183 6 weeks Haloperidol 56% ≥50% reduction NR 31.0% NR NR

Risperidone 5.6 mg on PANSS
Working
Group 1999
Risperidone 63% 20.2%
6.1 mg
Lieberman et 160 52 weeks Clozapine 400 mg NR ≥50% reduction 8 weeks 10% NR 81%
al. 2003a on BPRS +
CGI-S ≤3 + ≤3
on BPRS
positive
Psychopharmacology for People in Early Psychosis
symptoms
(defined as
“remission”)
Chlorpromazine 12 weeks 11% 79%
600 mg (12 weeks)
(12 weeks) (15% and
22.5% at
52 weeks)
191
192
discontinuation rate (continued)

Lieberman et 263 104 Haloperidol 46% ≥30% reduction 8.4 weeks 46% 230 days 67.2%
al. 2003b weeks 4.4 mg on PANSS+
CGI-S ≥4+
mild or lower
ratings of
positive
symptoms
Olanzapine 55% 7.9 weeks 32% 322 days 59.9%
9.1 mg (12 weeks) (within (12 weeks) (2 years)
(12 weeks) 12 weeks)
Early 555 104 Haloperidol 76.2% >20% reduction 22 days 22.4% 218 days 77.8%
Psychosis weeks 2.9 mg (12 weeks) on PANSS
Global (9.1% for
Working >50%
Group; reduction
Schooler et al. on
2005 PANSS)

Risperidone 73.6% 26 days 22.3% 192 days 75.5%

3.3 mg (12 weeks) (12 weeks) (12 weeks) (2 years)
(10.6% for (for 2 years:
>50% 36.5%,
reduction 42.1%)
on
PANSS)
PAFIP; 172 6 weeks Haloperidol 57.1% >40% reduction 4.32 weeks 57.1% 7.9 months 96.4%
Crespo- 5.4 mg on BPRS
Facorro et
al. 2006
Risperidone 52.5% 4.85 weeks 43.9% 9.6 months 92.1%

4.0 mg
Olanzapine 63.6% 4.36 weeks 32.7% 10.0 months 98.2%
15.3 mg (1 year) (1 year) (6 months)
193
194

Robinson et 112 16 weeks Risperidone 54.3% Mild or lower of 10.4 weeks 26.7% 12.1 weeks NR
al. 2006 3.9 mg SADS-C+PD
positive
symptoms+
CGI-I ≤2
Olanzapine 43.7% 10.9 weeks 28.3% 11.5 weeks
11.8 mg
CAFE; 400 52 weeks Risperidone NR ≤3 on all PANSS NR 71.4% 25 weeks 65%
McEvoy et al. 2.4 mg items+CGI-S
2007 ≤3
Olanzapine 68.4% 28 weeks 64%
11.7 mg
Quetiapine 506 70.9% 25 weeks 58%
mg
EUFEST; 498 52 weeks Haloperidol 34.0% ≥50% reduction NR 72% 0.5 months 37%
Khan et al. 3.0 mg on PANSS
2008

Amisulpride 52.9% 40% 5.3 months 67%

451 mg
Olanzapine 46.7% 33% 6.3 months 67%
12.6 mg
Quetiapine 44.2% 53% 1.2 months 46%
499 mg
Ziprasidone 37.8% 45% 1.1 months 56%
107 mg
TEOSS; 119 8 weeks Molindone 50% ≥20% reduction NR 39% 5.9 weeks NR
Sikich et al. 59.9 mg on PANSS+
2008 CGI-I ≤2
Olanzapine 34% 53% 5.9 weeks

11.4 mg
Risperidone 46% 33% 6.4 weeks
2.8 mg
195
196

German 289 8 weeks Risperidone 49.3% >30% reduction 41.0 days 38.5% 50.8 days NR
Research 3.8 mg on PANSS+
Network; CGI-S
Möller et al. ≤4+mild or
2008 better ratings
of positive
symptoms
Haloperidol 49.6% 38.6 days 54.1% 44.0 days
3.7 mg
Cuesta et al. 100 26 weeks Olanzapine NR >50% reduction NR 45.5% 12.7 weeks 70.5%
2009 10.2 mg on SAPS
Risperidone 50.0% 11.7 weeks 76.8%
6.0 mg
San et al. 2012 114 52 weeks Haloperidol 19% >50% reduction NR 85.7% 125 days NR
5.8 mg on PANSS
Olanzapine 40% 40.0% 260 days
16.2 mg

Risperidone 36% 56.5% 187 days

5.1 mg
Quetiapine 26% 64.0% 206 days
672 mg
Ziprasidone 30% 80.0% 143 days
117 mg
Zhang and 254 52 Paliperidone NR NR NR 22.2% NR NR
Dai 2012 weeks 6.4 mg
Aripiprazole 21.1%
14.5 mg
Ziprasidone 16.9%
65.3 mg
197
198

PAFIP; 202 12 weeks Aripiprazole 61.1% ≥50% reduction NR 23.1% 5.3 weeks NR
Crespo- 16.8 mg in BPRS
Facorro et
al. 2013
Ziprasidone 36.5% 37.1% 5.1 weeks
87.7 mg
Quetiapine 50.0% 61.8% 5.1 weeks
358.3 mg
Ou et al. 2013 260 6 weeks Ziprasidone NR NR NR 8.5% NR NR
138.2 mg
Olanzapine 14.6%
19.0 mg

CIDAR trial; 198 12 weeks Aripiprazole 62.8% Mild or lower 8.0 weeks 37.9% 8.3 weeks NR
Robinson et 14.8 mg of 4 BPRS
al. 2015 positive
symptoms+
CGI-I ≤2
Risperidone 56.8% 8.2 weeks 43.9% 8.2 weeks
3.2 mg
Pagsberg et 113 12 weeks Aripiprazole 23% ≥30% reduction NR 35% 9.3 weeks NR
al. 2017 14.6 mg in PANSS and
CGI-I ≤2
Quetiapine ER 23% 22% 10.4 weeks
451.8 mg
Abbreviations. BPRS=Brief Psychiatric Rating Scale; CAFE=Comparison of Atypicals in First Episode of Psychosis; CGI-I=Clinical Global Impres-
sions—Improvement; CGI-S=Clinical Global Impressions—Severity; CIDAR=Center for Intervention Development and Advanced Research;
CNFEST=Chinese First-Episode Schizophrenia Trial; EUFEST=European Union First Episode Schizophrenia Trial; NR=not reported; PAFIP=Programa
Atención Fases Iniciales de Psicosis; PANSS=Positive and Negative Symptoms Scale; SADS-C=Schedule for Affective Disorders and Schizophrenia—
Change; SAPS=Scale for the Assessment of Positive Symptoms; TEOSS=Treatment of Early-Onset Schizophrenia Spectrum Disorders.
Source. Adapted from Zhang et al. 2013.
199
(mostly in patients with chronic schizophrenia) that the average re-

sponse rate was 41% for SGAs and 29% for haloperidol. In one large
clinical trial comparing olanzapine and haloperidol (Lieberman et al.
2003b), 45% of patients with chronic schizophrenia (n = 1,913) re-
sponded to olanzapine, compared with 67% of patients in their first ep-
isode (n=83) using the same criteria for response. Given the fact that
many FEP trials used more stringent criteria to define treatment re-
sponse, the response rate would have been much higher in patients
with FEP than in patients who had had multiple episodes if the same
criteria had been applied to both type of studies.
In contrast, effective doses of antipsychotic drugs used in individu-
als with FEP are relatively lower than in chronic patients. Across the
large FEP clinical trials summarized in Table 12–1, the average daily
dose is 4.0 mg for risperidone, 13.0 mg for olanzapine, 497 mg for que-
tiapine, 15.2 mg for aripiprazole, and 103 mg for ziprasidone. The aver-
age daily dose for haloperidol is 4.4 mg. Almost all of the FEP studies
used a flexible dosing strategy. Therefore, these relatively lower doses
were achieved while balancing efficacy and side effects. Many young
people in FEP are sensitive to antipsychotic drugs because of lack of
prior exposure, so they are more susceptible to developing side effects
such as EPS, akathisia, and sedation. Rapid weight gain in young pa-
tients who are treated with antipsychotic drugs is very problematic, not
only for metabolic health consequences but also for patients’ self-image
and social acceptance. Severe side effects from antipsychotic drugs may
give patients a bad experience during their first treatment episode, which
may lead to treatment nonadherence and worse long-term outcomes.
Therefore, slow dose titration and close monitoring of drug-induced side
effects are critical when treating a patient with FEP to ensure that pa-
tients will stay in treatment and obtain maximum benefits from treat-
ment (Ballon et al. 2018).
Duration of Treatment
Clinicians treating patients with FEP will want to address the question
of when improvement will be seen with both patients and their family.
There is a large variation in how quickly a patient’s psychosis responds
to antipsychotic treatment. Unless psychosis is induced by substance
use, which may quickly remit once the triggering substance is discon-
tinued, it usually takes weeks for a patient’s psychotic symptoms to im-
prove. In studies listed in Table 12–1, the average time to response
ranged from 4 to 11 weeks, with more studies in the range of 7–9 weeks.
Patients will start to improve within the first 1–2 weeks of initiating
treatment, often within days, but it is reasonable to estimate that many
patients will need about 2 months of treatment to achieve significant
improvement. In people with chronic schizophrenia, several studies have

found that the amount of symptom improvement after 2 weeks of taking
antipsychotic drugs is predictive of treatment response after 3 months.
However, this phenomenon has not panned out in individuals with
FEP. One study found that patients continued to improve week after
week, up to 16 weeks of treatment, regardless how much they improve
after 2 weeks (Gallego et al. 2011).
Note that these data resulted from monotherapy with a single anti-
psychotic medication. In clinical practice, clinicians often face pressure
from health insurers and family members to get patients better quickly.
Frequently, patients are treated with their first antipsychotic medication
for 2–4 weeks, then switched to another if they do not improve fast
enough. This practice may increase the chance of drug-induced side ef-
fects without actually helping patients improve faster. We recommend
that patients continue to take their first antipsychotic medication for at
least 8 weeks as long as they are able to tolerate it and show some response
to treatment.
After significant improvement in psychosis with treatment (many
individuals may have complete remission of all positive symptoms af-
ter their first episode), patients and their families often ask when they
can stop taking medications. It is common for patients who have been
hospitalized during their first psychotic episode to be taking high doses
of multiple medications at discharge and experiencing significant, un-
familiar side effects. Patients may become nonadherent to the medica-
tion regimen, sometimes with the support of their family. In clinical
trials conducted in North America and Europe, all-cause discontinua-
tion rate within the short-term acute treatment phase (6–16 weeks)
ranged from 20% to 57% (Table 12–1). The rate increased to 33%–81%
within 1–2 years of treatment.
The question often arises whether a patient can be taken off medica-
tion without any further psychotic relapse, and if not, how soon a pa-
tient will have a relapse after stopping antipsychotic medication. Data
on relapse after the first episode of psychosis are relatively scarce com-
pared with data on treatment efficacy. However, both clinical experi-
ence and limited research data demonstrate that patients will be more
likely to relapse into another psychotic episode when they are not tak-
ing antipsychotic medication than when they are. One study showed
that after achieving responder status during the first year of treatment
for psychosis, patients who adhered to their medication regimen had an
11.2% relapse rate, compared with a 26.9% relapse rate among patients
who did not adhere to their medication regimen or stopped medication
treatment (Crespo-Facorro et al. 2011).
Naturalistic follow-up studies of people with FEP up to 5 years after
treatment commencement have suggested a progressive increment in
the cumulative rate for relapse, from 16.2% at 1-year follow-up to 81.9%
at 5-year follow-up for a first episode of schizophrenia, and the top predic-
tor of relapse is medication nonadherence (Robinson et al. 1999). Tiihonen
and colleagues (2018) recently confirmed higher rates of treatment fail-
ure in patients who stop compared with those who continue antipsy-
chotic medication following a first episode of schizophrenia in a large
population sample across Finland with up to a 16-year follow-up; the
study authors also found that time on medication prior to discontinua-
tion is not protective against relapse. Therefore, it seems that the chance
of relapse is substantial when a patient stops taking antipsychotic med-
ication.
Preventing the second psychotic episode and helping individuals
and families understand the risks of relapse and disease progression
should be a large part of maintenance treatment. With each subsequent
psychotic relapse, the risk of developing persistent psychotic symp-
toms increases. Recurrent psychotic episodes are associated with pro-
gressive loss of gray matter that may mediate cognitive impairment and
treatment resistance. Moreover, relapse is likely to interfere with the so-
cial development and networks of young people suffering from psycho-
sis, which may have a significant impact on long-term psychosocial and
vocational functioning. The second edition of the American Psychiatric
Association treatment guideline for schizophrenia, published in 2004
(no longer considered to be current), recommends indefinite antipsy-
chotic drug treatment or, after at least 1 year of complete symptom re-
mission, discontinuation of drug therapy with close follow-up and a
plan of antipsychotic reinstitution with symptom recurrence (Lehman
et al. 2004; see also Dixon et al. 2009 for update).
There are certainly controversies about the potential consequences
of long-term antipsychotic use, but the general consensus is that for
most people with first-episode psychosis, continued antipsychotic
treatment will lower risks of relapse. However, regardless of practice
guidelines and empirical evidence, many patients will attempt at least
one trial of medication discontinuation after psychosis remission. For
these individuals, it is critical that the treating clinician work closely
with other members of the treatment team, the patient, and the patient’s
family on supervised medication discontinuation, perhaps first care-
fully tapering the medication to the lowest effective dose for mainte-
nance to minimize side effects. When a patient chooses to stop
medication, ensuring a slow tapering schedule with continuing engage-
ment in other components of treatment and carefully monitoring for
signs of relapse is advisable. Personalized early warning signs of re-
lapse should be identified with the patient and family. Finally, it is also
important to maintain an as-needed prescription after medication dis-
continuation so the patient can restart antipsychotic medication imme-
diately on the first indication of relapse.
Shared Decision Making in

Antipsychotic Drug Treatment
Successful treatment of FEP and complete recovery from the illness are
not only critical to patients’ long-term prognosis but also have signifi-
cant impact on future treatment and relapse prevention (Kane et al.
2016). As discussed previously, many young people with FEP recover
quickly, and thus, they frequently question whether they need to keep
taking medications. Antipsychotic medications are not benign and
carry multiple tolerability challenges. In addition, many people with
FEP have used substances such as marijuana and may attribute their
psychosis to substance use. They may hope that as long as they stop or
control their substance use, they will not have another episode of psy-
chosis. Developmentally, transition-age youth operate in a short time
horizon and commonly underestimate risks. As such, lack of a disease
framework for understanding their experience of psychosis can under-
mine logical recognition of need for treatment. Research has shown that
lack of understanding regarding the nature of their illness is a predictor
of treatment nonadherence and poor prognosis. Unless this is ad-
dressed effectively, treatment persistence is a significant problem for
people after FEP.
Interestingly, medication refusal may at times serve patients’ need
for autonomy. Clinicians traditionally provide specific medical advice
by consulting the biomedical literature and considering what is in the
best interest of the patient. However, this approach to medical decision
making may be experienced as paternalistic and does not take into ac-
count the perspective or preferences of the patient. Nonadherence may
result from lack of patient input in medical decision making and dissat-
isfaction with the treatment relationship. A shared decision-making ap-
proach, in which clinicians and patients (as well as families and other
support network members) work together to arrive at medical deci-
sions after careful education about decision parameters and options
and inclusion of patients’ perspectives, values, goals, and preferences
for treatment, is optimal. Research has shown that use of shared deci-
sion making in treatment of people with schizophrenia leads to higher
patient satisfaction, resulting in better medication adherence and im-
proved symptom regulation. Other studies have shown that shared de-
cision making results in better quality of life, fewer unmet needs, and
greater satisfaction with treatment.
Shared decision making is particularly relevant in treatment of peo-
ple during and after their first episode of psychosis because of their un-
familiarity with their disorder, their developmental stage, and their
sensitivity to medication-induced side effects. Antipsychotic medica-
tions are not easy to take. Bothersome side effects can quickly lead to a
negative experience of medication, thereby affecting long-term percep-

tions of medication treatment. Cultural attitudes toward Western med-
icine and medication taking must be considered and addressed as well.
There is little research specifically evaluating the effectiveness of shared
decision making in first-episode treatment. However, clinical experi-
ence in our early psychosis programs suggests that shared decision
making does help build therapeutic relationships with patients, in-
crease treatment engagement of patients and their families, and de-
crease treatment dropout rate. Using a shared decision-making model
to work with patients in FEP usually involves the following steps:
1. Provide psychoeducation to patients and family regarding the na-

ture of the illness, role of medication treatment, and possible long-
term outcomes.
2. Discuss treatment options with various antipsychotic medications
and explain benefits and efficacy and potential risks and side effects
associated with each recommended option. Conduct a risk-benefit
analysis with an emphasis on achieving and maintaining remission.
3. Listen to what the patient and family say regarding their needs and
wishes for treatment and their cultural preferences and answer any
questions that they may have about medications, other treatment,
diagnosis, and prognosis.
4. Enter principled negotiation with the patient regarding medication
choice, dosing, follow-up interval, laboratory tests, and other related
issues, taking into account the patient’s needs and requests.
5. When a patient chooses to stop taking medication, encourage him or
her to stay in treatment and closely monitor for signs of relapse col-
laboratively to reduce risk for periods of untreated psychosis.
The goal of the shared decision-making approach is to keep patients

engaged with a strong sense of ownership over their treatment choices
and the relative merits of each option. Compromise is necessary at
times to meet the patient where he or she is and to increase patient sat-
isfaction with treatment. This give-and-take occurs at every follow-up
visit, and the collaborative relationship between the clinician and the
patient continues when the clinician is evaluating treatment outcomes
and dealing with emerging issues in treatment. When a patient arrives
at a treatment decision after considering risks, benefits, and alternatives
with the help of the treating clinician, he or she is more likely to adhere
to the treatment choice, thus improving long-term outcomes.
Case Example
Dave was a 24-year-old graduate student when he experienced onset of
paranoia, ideas of reference, confusion, and disorganized thinking and be-
haviors. He was treated with olanzapine during an acute hospitalization.

On referral to our early psychosis clinic, he was experiencing residual
ideas of reference and fear of things getting out of control, as well as seda-
tion and weight gain. Olanzapine had already been tapered from 20 mg to
5 mg nightly by his prior provider. After reviewing the rationale for
maintenance antipsychotic treatment to prevent relapse and available
medication options, we agreed to try switching to risperidone 1 mg
nightly to address Dave’s concern about the side effects he was experi-
encing. He returned reporting improvement in energy and normaliza-
tion of appetite, but he was having difficulty falling asleep some nights
as well as experiencing increased anxiety. We agreed to add risperidone
0.5 mg prn that Dave could take when he was having difficulty with
anxiety or getting to sleep.
Dave responded well to psychotherapy and a physical exercise rou-
tine and rarely required the as-needed medication. His remaining symp-
toms faded, and his confidence improved over several months. When
Dave obtained a full-time job, he found that subtle daytime sedation
seemed to limit his cognitive performance at work. Because he was as-
ymptomatic, we agreed to taper his scheduled risperidone dose to 0.5 mg
and eventually 0.25 mg daily with resolution of cognitive impairment.
After about a year, Dave began to ask about whether continuing
medication was necessary. His job was going well, and he had married
his longtime partner. He reported no medication side effects, but he did
not like the idea of taking medication. After reviewing risks of relapse
and potential impact on life course, Dave chose a carefully monitored
trial of medication discontinuation. We agreed that he could restart
medication at any point and that he would call if there were any ques-
tions. At next visit he noted that suspiciousness, ideas of reference, and
feelings of unease had developed within a week of stopping medication,
so he had restarted risperidone and preferred to continue taking it to en-
sure his stability. He has remained in remission since.
Conclusion
Antipsychotic medication therapy is an essential component of first-
episode psychosis treatment. Choosing an appropriate medication,
carefully dosed on the basis of research evidence and individual char-
acteristics to maximize efficacy and minimize side effects, is critical in
helping patients to improve symptoms and maintain long-term stabil-
ity. Risperidone and aripiprazole seem to have a balanced profile of ef-
ficacy and side effects and thus should be considered first-line
medications for treatment of FEP. Other antipsychotics with a high mar-
gin of safety are reasonable alternatives and deserve specific evaluation
in people with FEP. Treatment nonadherence and early discontinuation
of medications are common, and using a shared decision-making ap-
proach in an integrated treatment team setting may help patients en-
gage with and stay in treatment and achieve long-term recovery.
KEY CONCEPTS
• Antipsychotic medication treatment is central to early inter-
vention for people with schizophrenia spectrum disorders.
• First-line treatments should ideally provide high tolerability
with reasonable efficacy.
• Antipsychotic medications are typically difficult to tolerate
and may constrict functioning but provide well-established
protection against relapse, requiring careful shared deci-
sion making around acute and ongoing use.
• When people choose to stop taking antipsychotic medica-
tion after onset of psychosis, continued engagement in
treatment and careful monitoring can minimize risks for
relapse and ensure rapid response.
1. How do you educate people experiencing a first episode of
psychosis (and their family) about duration of untreated psy-
chosis, prevention of progression, and remission?
2. How do you discuss the role of antipsychotic medication

treatment in preventing progression of psychosis?
3. How can you use shared decision making to address com-

mon side effects of antipsychotic medication?
4. How do you work with patients who have experienced a first

episode of psychosis on optimizing their health, well-being,
and long-term recovery?
5. How do you discuss ambivalence about treatment and desire

to stop taking antipsychotic medications with patients (and
families) in early psychosis?
Suggested Readings
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clinical practice guidelines for early psychosis. Br J Psychiatry Suppl
187(48):s120–s124, 2005
McGorry PD, Killackey E, Yung AR: Early intervention in psychotic dis-

orders: detection and treatment of the first episode and the critical
early stages. Med J Aust 187(7 suppl):S8–S10, 2007
Tiihonen JA, Tanskanen A, Taipale H: 20-year nationwide follow-up
study on discontinuation of antipsychotic treatment in first-episode
schizophrenia. Am J Psychiatry 175(8):765–773, 2018
Yung AR, Killackey E, Hetrick SE, et al: The prevention of schizophre-
nia. Int Rev Psychiatry 19(6): 633–646, 2007
Weller A, Gleeson J, Alvarez-Jiminez M, et al. Can antipsychotic dose
reduction lead to better functional recovery in first-episode psycho-
sis? A randomized controlled-trial of antipsychotic dose reduction.
The reduce trial: study protocol. Early Interv Psychiatry Nov 29,
2018 [Epub ahead of print]
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AZ, June 2016
CHAPTER
13
Psychotherapeutic
Interventions for Early
Psychosis
Kate V. Hardy, Clin.Psy.D.
Yulia Landa, Psy.D., M.S.
Piper Meyer-Kalos, Ph.D.
Kim T. Mueser, Ph.D.
PROVIDING psychotherapy is a core component of early psycho-

sis services. Only relatively recently has the contribution of psychother-
apies in supporting recovery from psychosis been recognized. This
change is due in part to a shift in our understanding of psychosis and
the recognition of the stress-diathesis model (Zubin and Spring 1977) as
an explanatory model for psychosis. The recognition of stressors in the
model as a contributing factor to the development, and maintenance, of
psychotic symptoms encouraged mental health professionals to de-
velop interventions designed to help individuals with psychosis learn
more adaptive coping strategies for managing potential stressors and
distress. Additionally, the recognition that psychosis exists on a contin-
uum (and is not a discrete entity as previously posited) allowed for in-
creased normalization of psychotic symptoms and an understanding of
psychosis within a recovery framework that facilitated more frank dis-
cussion of these symptoms.
211
Psychotherapy and Early Psychosis

Psychotherapy has been included as a core component of early psycho-
sis service provision since the inception of these service packages. Two
primary models of psychosocial interventions for psychosis have
emerged that are frequently implemented in coordinated specialty care
(CSC) services for first-episode psychosis (FEP) in the United States:
cognitive-behavioral therapy for psychosis (CBTp) and individual resil-
iency training (IRT). These two models will be referred to collectively as
psychotherapies, and both are described in detail in this chapter. Key ele-
ments of these interventions are consistent with the overarching princi-
ples of early intervention in psychosis (Table 13–1). Both approaches are
evidence-based and, as all psychotherapeutic models do, rely on the de-
velopment of a collaborative relationship to support the intervention.
Both approaches recognize the potentially stigmatizing nature of a
mental health diagnosis and address this through normalization and
psychoeducation. In addition, the problems and goals that the young
person identifies are prioritized in treatment with the aim of supporting
functioning and resiliency, and both approaches can be adapted in re-
sponse to cultural needs. However, there are also key differences be-
tween the CBTp and IRT models that will be highlighted in this chapter.
TABLE 13–1. Comparison of early intervention principles and key

elements of psychotherapy interventions
Early intervention
principlesa Psychosocial interventions
Provide interventions with Evidence-based approach

demonstrated efficacy
Provide services that actively Collaborative approach (the “collaborative
partner with young people fence”)
(shared decision making)
Challenge stigmatizing and Normalization and psychoeducation
discriminatory attitudes
Generate optimism and Problem list and goals
expectation of positive Focus on functional recovery and resiliency
outcomes and recovery Development of skills and tools to support and
maintain recovery
Wellness planning
Culturally sensitive services Individualized formulation
aBased on values and vision elaborated by Bertolote and McGorry (2005).
Psychotherapeutic Interventions for Early Psychosis 213
Frequently, talking therapies are provided in an outpatient setting

by a single provider. However, within a CSC model, both CBTp and IRT
are offered within the team setting, and providers of these models are
integrated into the team approach. The core clinical competencies re-
quired for delivering these models are similar and are predicated on the
principles of recovery orientation, respectful communication, collabo-
ration, and shared decision making. Roth and Pilling (2013) describe
competencies required for providers to effectively work with individu-
als with psychosis and highlight the need for knowledge of the present-
ing problems and diagnostic criteria of people presenting with
psychosis; general therapy skills, including assessment, intervention,
and collaboration; and comfort with metacompetencies, which they relate
to “an ability to implement ‘procedural rules’—using clinical judgment
to decide when, how, and whether to carry out a particular action or set
of actions...” (Roth and Pilling 2013, p. 25). In line with these core com-
petencies is the need to ensure that providers are trained appropriately
in the chosen intervention. However, it has been routinely observed
that training alone is not sufficient to support the implementation of a
practice, so it is important that trained clinicians have access to ongoing
consultation with an expert in the model, where continued learning
takes place, and that the consultation include review of taped examples
of clinical interactions and provision of feedback on the competency of
the individual clinician.
Psychotherapies in a Team Setting

Because CBTp and IRT for early psychosis are most often delivered in
the context of a CSC team, the clinician collaborates extensively with
the other members of the team to integrate psychotherapy as part of a
comprehensive treatment. Weekly team meetings facilitate this collabo-
rative process, although additional communication is often also neces-
sary. Table 13–2 describes potential interactions between the clinician
providing psychotherapy and the other team members related to com-
mon issues. However, this list is not exhaustive, and there are numerous
creative ways in which a clinician may collaborate with other team
members to provide holistic and integrated treatment for the young
person.
Ideally, the clinician has the sole focus of providing psychotherapy,
either CBTp or IRT, to the young person. However, in smaller teams
with fewer resources, it may be necessary for the provider to hold the
dual role of case manager and therapist. In this case, supervision should
focus on this dual role and supporting the clinician to navigate the chal-
lenges associated with integrating these approaches.
TABLE 13–2. Examples of team collaboration with psychotherapy

clinician
Possible collaboration with

Provider psychotherapy provider
Medication management provider • Address medication adherence and

medication options through
examination of beliefs about
medications
• Discuss timeline of development of
symptoms and early warning signs
of relapse to support medication
planning
Supported education and • Identify and address motivational
employment provider and personal organizational barriers
to following through on school or
work leads.
Peer specialist • Engage around normalization of
symptoms.
• Support young person to put in
action skills discussed in therapy.
Family worker • Develop wellness plan with family.
Cognitive-Behavioral Therapy
for Psychosis
Cognitive-behavioral therapy for psychosis is an approach to improv-
ing symptoms and functioning in individuals with psychotic disorders.
CBTp was adapted from cognitive-behavioral therapy (CBT) methods
developed by Dr. Aaron T. Beck and used primarily for the treatment of
depressive and anxiety disorders (Beck et al. 1979, 1985). Although the
first documented application of CBT to psychotic symptoms was by
Beck in the early 1950s and preceded most of the CBT applications to
depression and anxiety (Beck et al. 2009), findings from standardized
treatment programs (Chadwick et al. 1996; Kingdon and Turkington
1994; Morrison et al. 2004) and rigorous clinical trials of CBTp (Sensky et
al. 2000) did not begin to be published until more than 40 years later by
several different clinical research teams in the United Kingdom. Currently,
more than 50 randomized controlled trials and multiple meta-analyses of
the research literature on CBTp have been published documenting its
beneficial effects on a range of symptoms and functional outcomes
(Burns et al. 2014; Turner et al. 2014).
The goal of CBTp is to improve individuals’ functioning and overall

life satisfaction by reducing the distress and disability caused by delu-
sions, hallucinations, negative symptoms, and thought disorder. An es-
sential component of CBTp is its focus on the personal meaning of
symptoms and anomalous experiences and on changing appraisals of
these experiences in order to reduce distress. The key elements of CBTp
include a shared understanding (or formulation) of psychosis between
the client and therapist, identification of targeted symptoms that cause
distress or interfere with the individual’s functioning, and development
of cognitive and behavioral strategies to cope with these symptoms.
The therapeutic process of CBTp includes the following core compo-
nents: 1) engagement, 2) identification of goals, 3) assessment and for-
mulation, 4) interventions, and 5) relapse work.
Engagement
In CBTp, the development of a strong therapeutic alliance is essential to
the success of the treatment. The therapist engages the client with em-
pathy and normalizing and works to understand the problem as the cli-
ent sees it. Rather than using an authoritative, directive, or expert style,
the therapist uses what is called Columbo style (after the famous televi-
sion detective) to gently help clients describe their experiences, how
they arrived at their conclusions, and how they developed their specific
beliefs. Engagement continues throughout the therapeutic relationship
but can be thought of as the first step in the therapeutic process.
Identification of Goals
CBTp treatment starts with identification of the client’s goals. The client
generates a list of problems. The goals are based on the problem list and
are usually written down so that each goal corresponds to a specific
problem. Goals are specific, positive, realistic, achievable, measurable,
and time limited.
After the problems and goals are identified, the therapist and client
collaboratively decide which goal to address first. The factors consid-
ered in making certain goals a priority are the level of urgency, which is
usually related to the level of distress caused by a problem, and the like-
lihood that the problem could be quickly and successfully resolved. The
latter can provide the client with the experience of resolving problems
successfully and therefore a sense of hope for treatment.
Assessment and Formulation

The individual’s strengths and vulnerabilities and the possible effects of
stress are discussed to develop a formulation—a model that explains the
psychological mechanisms that underline the client’s psychotic symp-
toms and related difficulties. This assessment is done in an empathic

manner in which maintaining rapport with the client overrides the ther-
apist’s need to gain information. This formulation is developed collab-
oratively with the client and incorporates information about the
cognitive, behavioral, affective, and physiological components of the
individual’s psychotic experiences. Cognitive components include in-
formation about cognitive intrusions (e.g., voices, visions, negative in-
trusive thoughts) and appraisal and interpretations of these intrusions,
as well as cognitive biases (e.g., jumping to conclusions, attention to
threat, externalizing). The client’s life experiences that contributed to
the formation of his or her current beliefs are also explored and inte-
grated into the formulation. A narrative approach, constructing a story
of what has been happening collaboratively with the client, is used
when developing a formulation.
Interventions
Once the formulation is developed, therapist and client work collabora-
tively to identify appropriate interventions based on the client’s goals.
Interventions in CBTp can include exploring the evidence the client uses
to support his or her delusional beliefs, verbal exploration of beliefs
through discussion, and testing the validity of the beliefs. Verbal explo-
ration of beliefs could involve looking for alternative explanations for
the experiences that contributed to the formation of specific beliefs and
comparing which explanations (beliefs) are better supported by evi-
dence. Testing the validity of beliefs can involve encouraging the client
to engage in specific behavior for the purpose of testing the belief, setting
predictors for external events so that outcomes serve as tests of these
predictors, and reviewing the outcomes. For example, an individual is
more likely to be distressed by voices and to comply with command hal-
lucinations if he or she believes that those voices have power or control
over him or her. Clients are encouraged to explore alternative explana-
tions of anomalous experiences (such as voices) that are less threatening,
helped to engage in behavioral experiments to test out their belief about
the power of auditory hallucinations, and helped to develop a more nor-
malizing rationale for making sense of such experiences.
Similar to the IRT model, the stress-vulnerability model (Zubin and
Spring 1977) is used to help individuals make sense of and normalize
psychotic experiences. According to the stress-vulnerability model, vari-
ous genetic predispositions and life events (e.g., early trauma, physical
illnesses) make us vulnerable to developing certain symptoms (e.g., para-
noia, hearing voices), and we tend to experience these symptoms when
we are under stress. Thus, the stress-vulnerability model serves to high-
light the relationship between stress and symptoms as well as to help nor-
malize psychotic experiences by illustrating that at different levels of
distress all people are capable of having such experiences. The therapist
also helps the client become aware of whether or not his or her current
coping behaviors are helping and develop better ways of coping. For ex-
ample, a therapist could help identify strategies of coping with the voices
that could diminish their frequency and intensity (e.g., talking to some-
one, reading aloud, listening to music, using earplugs). During the course
of the treatment, the therapist and client collaboratively evaluate the ef-
fectiveness of these interventions. If the interventions are not successful,
new interventions are tried until the treatment goal is achieved. CBTp is
considered to be culturally responsive in that the influence of cultural
background is integrated into the formulation, which aids the develop-
ment of culturally responsive interventions (Rathod et al. 2015).
Relapse Prevention
Once both client and therapist decide that the goals of the treatment
have been achieved, then relapse prevention is discussed. In the same
manner in which the formulation of the client’s difficulties is assessed
and developed, the therapist assesses the relapse triggers and cogni-
tions, and relapse prevention interventions are designed collabora-
tively with the client. CBTp treatment is intended to be provided
weekly for at least 6 months. The treatment can also take longer de-
pending on the client’s symptomatology (e.g., it takes about 40 sessions
to successfully work with systematized delusions). Once the treatment
is complete, it is recommended that the client attend booster sessions
(once a month, and then once in 3 and then 6 months) to reinforce the
coping skills and cognitive strategies learned in therapy.
Case Example 1
Julio is a 20-year-old young man who was referred to CBTp after being
hospitalized for FEP due to paranoia. Julio was afraid of being killed by
the Mafia. He grew up in an Italian neighborhood in the Bronx in New
York City, where he often felt unsafe. His father left when he was very
young. He had witnessed several violent incidents at school and was
hurt by older boys during one of these incidents, and as a result, he often
felt vulnerable and unprotected. After Julio graduated from high school,
he began working as a waiter in an Italian restaurant in his neighbor-
hood. Around the same time, following the lead of his friends, he began
using cannabis.
Initially, the CBTp therapist used empathy and a normalizing ap-
proach to understanding Julio’s problems as Julio saw them in order to
develop a therapeutic alliance and to begin to work collaboratively on
formulating Julio’s therapy goals. Julio wished that the Mafia “would
leave me alone” and that he would be able to go out without the debili-
tating fear, make friends, and maybe even have a girlfriend. Rather than
using an authoritative, directive, or expert style, the therapist used the
“Columbo style” of gently asking Julio to describe his experiences and

how he arrived at his conclusion that the Mafia was out to kill him.
The therapist worked with Julio to better understand his experi-
ences, thoughts, and feelings and to come up with a historical formula-
tion—a model of symptom formation and maintenance (Figure 13–1).
Julio’s earlier life experiences contributed to his beliefs that he was
worthless and weak, that people are dangerous, that he cannot trust
anybody, and that paranoia is useful because it kept him on his toes.
Growing up, Julio had also developed a tendency to personalize (to as-
sume that what people are saying or doing relates to him), to jump to
conclusions with little evidence, and to selectively pay attention to
threatening information—thinking styles that contributed to the forma-
tion of delusional paranoid beliefs. The formulation also included infor-
mation about a particular event that made Julio believe that the Mafia
was after him: He had been working in the restaurant for several days
and was getting little sleep in order to make more money. The restaurant
owner made a negative comment about Julio’s chatting with a customer,
who turned out to be the restaurant owner’s daughter. Julio then went
to a party where he smoked cannabis and watched The Godfather, the
classic tale of a Mafia family. On the way back home, Julio continued
thinking about the restaurant owner’s comment. He thought that the
owner must belong to the Mafia and that he was mad at him for chatting
with his daughter and might want to eliminate him. Suddenly, Julio
heard loud sounds that he thought were gunshots. He began to think
that these were warning messages for him sent by the Mafia. He became
terrified and admitted himself to the hospital to escape. He continued
hearing strange sounds, which he kept interpreting as gunshots by the
Mafia to threaten him.
CBTp interventions were based on the formulation and Julio’s goals.
They included working with Julio to identify and reduce daily triggers
of thoughts about the Mafia, including his use of cannabis. As part of the
interventions, Julio’s therapist provided education on cognitive distor-
tions and thinking styles that contribute to the formation of delusions
(including personalizing and jumping to conclusions) and taught him
reasoning skills. She also worked with Julio on core beliefs contributing
to paranoia (e.g., “I am helpless,” “People are dangerous”) and auto-
matic thoughts of the same nature.
Throughout the treatment, the CBTp therapist continued to engage
Julio, made efforts to protect and enhance his self-esteem, and explored
the reasons Julio concluded that the Mafia was after him. She helped Ju-
lio question and reevaluate this belief by using a collaborative empiri-
cism approach, in which she and Julio worked together to explore
different possible explanations for his experiences and examined the ev-
idence supporting or refuting each explanation (including those on
which his beliefs were based). Julio’s level of conviction that the Mafia
was after him dropped from 99% to 5%. This enabled him to feel less
scared and stressed, and he began to go out. As he went out and experi-
enced being safe, he gradually stopped believing that the Mafia was af-
ter him.
After 20 sessions of CBTp, Julio decided that he had achieved his

goals. Julio and his therapist discussed his thoughts about the possibility
of relapse (the return of the debilitating fear of being killed by the Mafia),
discussed relapse prevention, and formulated a plan. For 3 months, Julio
continued to attend monthly booster sessions to reinforce skills learned in
time-limited CBTp. After completing therapy, Julio met and moved in with
a girlfriend, went to a culinary school, and opened his own restaurant.
Individual Resiliency Training

Individual resiliency training is a broad-based individual psychothera-
peutic intervention that is part of the NAVIGATE program, a compre-
hensive treatment program for people recovering from a first episode of
psychosis (FEP; Mueser et al. 2015). The NAVIGATE program was de-
veloped to be implemented by a five-person team of clinicians who pro-
vide four different interventions: 1) individualized medication
management, 2) the family education program, 3) supported education
and employment, and 4) individual resiliency training. The treatment
philosophy of the program is based on a core set of clinical competen-
cies that are cultivated among all the team members and are thought to
be critical to the successful implementation of the program, including
shared decision-making skills, a focus on strengths and resiliency, mo-
tivational enhancement, psychoeducational skills, and collaboration
with natural supports. More information about NAVIGATE can be
found in the article by Mueser et al. (2015).
The IRT program was designed as a psychotherapeutic approach
aimed at achieving the following goals:
1. Establish personal goals of the client and make progress toward

those goals over the course of the program
2. Support self-determination, build resiliency skills, and create posi-
tive emotional experiences in order to facilitate clients’ ability to
spring back from the adversity of FEP and regain control over their
lives
3. Help individuals process the often-traumatic experience of FEP and
reduce self-stigmatizing beliefs about mental illness that may ac-
company the episode
4. Teach basic information about FEP and the principles of its treat-
ment in order to enable clients to participate in informed decision
making about treatment for their disorder
5. Teach skills to clients for improving the management of their psychi-
atric disorder
6. Teach skills for improving clients’ social relationships, leisure time,
and health behaviors
220
These are gunshots–

Hearing loud warning messages
sounds sent by the Mafia
Physiology Panic attacks
Automatic Feelings/
Antecedents Terrified
thoughts emotions
Behavior Hides and

isolates
Underlying
Childhood and Strategies
assumptions/
earlier life events core beliefs
Lived in Bronx; did not • I am weak

feel safe; father left them • Personalization bias
• People are dangerous
very early; had violent • Jumps to conclusions
incidents in school; was • I cannot trust anybody
• Paranoia is useful and • Hypervigilance
experimenting with
drugs (cannabis) keeps me on my toes
FIGURE 13–1. Historical formulation: making sense of Julio’s beliefs and experiences.
In IRT, people learn skills and strategies to manage their psychosis

and take steps toward recovery. IRT is focused on helping people learn
information and skills to address common concerns and problem areas
such as substance use, social skills and interpersonal connections, neg-
ative feelings, and healthy lifestyles. IRT is tailored to meet individual
needs by helping people identify personally meaningful goals at the be-
ginning of treatment. Several unique considerations are embedded in
IRT to address specific features of FEP, such as an awareness of devel-
opmental milestones in adolescence and early adulthood and a lack of
experience with symptoms and treatment. IRT materials use plain lan-
guage to increase engagement of persons with low insight and a brief
history of psychosis.
In addition, responses to psychosis can be traumatic and stigmatiz-
ing and can lead to a syndrome of posttraumatic stress disorder (PTSD)
symptoms (Mueser et al. 2010). IRT incorporates an approach designed
to emotionally process upsetting and traumatizing experiences related
to FEP and to address stigmatizing beliefs that clients may have about
psychosis and their ability to achieve personal goals. IRT is inclusive of
different cultural beliefs and traditions. An individualized assessment
and treatment formulation allows for the integration of culture into per-
sonal definitions of recovery, individual goals, and illness management
strategies and skills. Finally, to strengthen the focus of resilience in IRT,
there are specific activities adapted from positive psychology interven-
tions included throughout the intervention to increase positive emo-
tions. These IRT elements are interwoven with client strengths and
goals to help clinicians increase choice, respond flexibly to a person’s
concerns, and strengthen engagement.
Theoretical Underpinnings of IRT

The development of IRT was influenced by four general theories: theo-
ries of well-being, the stress-vulnerability model, the psychiatric reha-
bilitation model, and the theory of reasoned action. FEP is typically
preceded by a gradual decline in psychosocial functioning, followed by
a gradual worsening that occurs after the onset of psychosis but before
the person is engaged in treatment, which traditionally focuses on ad-
dressing pathology and deficits rather than improving functioning and
well-being. In order to reduce the demoralizing effects of this loss in func-
tioning, and the impact of being diagnosed with a mental illness, IRT
draws on theories of well-being, which posit that the cultivation of positive
emotions and experiences leads to improvements in well-being, de-
creases in negative feelings, and a greater capacity to thrive despite the
presence of adversity (Seligman 2012). For example, the broaden-and-
build theory posits that experience of positive emotions leads to a broad-
ening of one’s personal and social resources and strengths, which can
then be deployed in the service of achieving personal and functional

goals (Fredrickson 2009). IRT adopted a specific focus on individual
strengths (Rapp and Goscha 2006) while also incorporating specific strat-
egies designed to enhance resiliency and positive emotional experiences.
The stress-vulnerability model of schizophrenia was used to guide the
teaching of information and skills in IRT related to the management of
psychosis and improving its long-term course (Zubin and Spring 1977).
This model hypothesizes that psychosis, and its course, are influenced
by the dynamic interplay between biological vulnerability, stress (in-
cluding trauma), personal resources, and the social environment. On
the basis of this model, a variety of factors can influence both biological
vulnerability and stress, such as taking medication and minimizing
substance use to reduce biological vulnerability and improving coping
strategies and social support to reduce the effects of stress. More recently,
this model has been modified to incorporate recovery skills as another
personal factor that can influence the course of the illness, such as knowl-
edge of psychosis and its treatment, involvement in treatment planning,
and developing a relapse prevention plan (Mueser et al. 2013).
Psychiatric rehabilitation approaches were integrated into IRT to ad-
dress the problem of impaired psychosocial functioning that is already
prominent because of the FEP. Psychiatric rehabilitation directly targets
improved psychosocial functioning through a combination of two broad
approaches: teaching skills for achieving interpersonal and instrumental
goals and providing environmental supports to facilitate optimal func-
tioning and attainment of goals (Corrigan 2016). Skills training methods
were incorporated into IRT to help participants achieve social goals (e.g.,
social skills training), and the provision of environmental supports is a
primary focus of both the Family Education Program and Supported Em-
ployment and Education components of NAVIGATE.
Last, the theory of reasoned action was used as a general guide in IRT to
understanding motivation to change one’s behavior (Hale et al. 2002). This
theory posits that the intention to engage in a behavior is the strongest de-
terminant of behavior, and that intention is based on the expected out-
comes of the behavior. Thus, people are more inclined to change their
behavior when they view such change as in their own best interest. In IRT,
the process of identifying and collaborating with clients on achieving per-
sonal goals creates natural opportunities to explore how improved illness
self-management skills could help the individual achieve his or her goals,
thereby harnessing motivation to actively participate in treatment.
Clinical and Technical Influences

on the Development of IRT
The IRT program also drew on several previous interventions for the FEP
or similar populations. The structure and organization of IRT informa-
tion and skills training content into discrete modules, as well as the role
of goal setting and tracking throughout the program and the teaching of
illness self-management information and skills, was based on the Illness
Management and Recovery program (McGuire et al. 2014). IRT also was
modeled after the Graduated Recovery From Initial Psychosis (GRIP)
program for people recovering from an FEP. GRIP is a flexible modular-
based cognitive-behavioral therapy intervention that also includes goal
setting and teaching of illness self-management skills (Penn et al. 2011).
The two resiliency modules in IRT were based on positive psychother-
apy (Seligman et al. 2006) and the Positive Living intervention for people
with schizophrenia (Meyer et al. 2012). Behaviorally based exercises from
Positive Living were included in IRT to help people generate more positive
emotions and incorporate these strategies into their daily lives.
Finally, the IRT program adopted the same basic session structure
used in cognitive and behavioral therapies, including setting agendas,
reviewing homework, teaching specific information and skills, and col-
laboratively developing home assignments to practice skills and foster
generalization. Furthermore, many of the specific strategies used in
cognitive and behavioral approaches were incorporated into the differ-
ent IRT modules. For example, with respect to CBTp, the strategy of
normalizing psychotic symptoms was incorporated into the Education
About Psychosis module, the teaching coping strategies were incorpo-
rated into the Coping With Symptoms module, and cognitive restruc-
turing was incorporated into the Processing the Psychotic Episode and
Dealing With Negative Feelings modules. Similarly, social skills train-
ing strategies were incorporated into the Having Fun and Developing
Good Relationships modules of IRT.
Structure and Organization of IRT

In IRT, clinicians (preferably with at least a master’s degree) meet
weekly to help people make progress toward a personally meaningful
goal, learn illness management skills and information, and learn skills to
build resiliency. IRT clinicians work closely with the other NAVIGATE
team members to collaboratively develop treatment plans, enhance en-
gagement in treatment, and practice IRT strategies.
The IRT manual is divided into 14 modules, each of which focuses
on a specific topic area. The first 7 modules comprise the standard mod-
ules that target typical needs of persons with FEP and are designed to
be delivered to everyone. Three IRT modules (Orientation, Education
About Psychosis, and Relapse Prevention Planning) are coordinated
with the Family Education program in NAVIGATE to encourage collab-
oration with family members and other supportive persons to ensure
that family members are learning the same information and to offer flex-
ibility on where people can learn illness management strategies and ed-
ucation. The individualized modules include an additional 7 modules
that address special topics specific to persons with FEP. After the stan-
dard modules are completed, a decision is made by the client and clini-
cian to focus on individualized modules that could help reduce distress
or help the person achieve his or her goals. Usually, people complete the
standardized modules before moving to the individualized modules,
but the clinician has the option of teaching individualized modules at
any point during IRT when the need arises (e.g., when significant sui-
cidal ideation, co-occurring substance use, or distressing hallucinations
are present and require immediate attention).
The IRT materials for each module include clinical guidelines that
outline the goals of the module, teaching strategies, and strategies to
solve common problems. The clinical guidelines are designed to help
clinicians with varying levels of experience deliver IRT. Each set of clin-
ical guidelines is accompanied by a set of worksheets that the IRT clini-
cian uses in session to interactively discuss and practice skills and
strategies. The IRT worksheets include discussion questions to elicit in-
dividual examples, opportunities to demonstrate and practice skills,
and suggestions for home practice.
The IRT program relies on a core set of teaching strategies, including
motivational, educational, and cognitive-behavioral methods. These
strategies are used throughout the program to stimulate clients’ interest
and desire to learn information and skills related to the management of
their psychosis and the attainment of personal goals, to teach critical in-
formation, and to help individuals acquire new skills and to transfer
those skills to their daily lives.
Case Example 2
Ana, a 23-year-old woman, was referred to the NAVIGATE team after
being hospitalized for wandering around her aunt’s neighborhood
screaming about the FBI monitoring the street with hidden cameras.
Ana had moved in with her aunt in a small town about 3 months before
being hospitalized because she had not been getting along with her
grandmother, with whom she lived in a major metropolitan city. At the
time that Ana was enrolled in NAVIGATE, she was often confused by
what people were saying and had trouble putting together a full sen-
tence. After being hospitalized, Ana described hearing voices talking to
her, and her aunt said that she would stay in her room for several hours
at a time.
Ana was introduced to Celia, the IRT clinician, when the NAVIGATE
director, Terry, was enrolling her in the program. A week later, Ana
started the Orientation module with Celia. In the beginning of IRT, Ana
was hesitant to talk to her therapist. Celia focused on teaching and prac-
ticing relaxed breathing in session with Ana. Eventually, Celia worked
with Ana to set small positive goals. In the beginning, Celia met with
Ana twice a week for shorter sessions until she was more comfortable
meeting weekly for 1 hour. Over the first 3 months of IRT, Ana shared
her recent experiences at the hospital, including how uncomfortable she

was with her voices and how she struggled with organizing her
thoughts.
After completing module 2 (Assessment and Goal Setting), Ana
identified her strengths as love of learning, kindness, gratitude, zest,
and honesty. She started working on small goals such as earning some
spending money to buy video games and to help her aunt with buying
groceries. At the end of the Assessment and Goal Setting module, Celia
reintroduced Ana to the supported employment and education special-
ist, Lin, in an IRT session to discuss how Lin could help Ana find short-
term work to earn extra money.
When Celia started module 3 (Education About Psychosis) with Ana,
she slowed down and broke each handout into two sessions because Ana
needed to review the symptoms of psychosis and the stress vulnerability
model in small chunks. After completing a relapse prevention plan in IRT,
Ana shared the plan with her aunt in the family education meeting. Ana
and Celia discussed completing module 5 (Processing the Episode) be-
cause Ana had repeatedly brought up how the hospitalization had up-
set her. After discussing the rationale with Ana, Celia decided to see if
module 5, “Processing the Episode.” could help Ana put together what
had happened before she was hospitalized. During the completion of
module 5, Ana identified “I will never recover” and “People will always
believe I am dangerous” as self-stigmatizing beliefs that were very dis-
tressing to her. After telling her story of her experience with symptoms
and being hospitalized for the first time, Ana updated her belief about her
recovery, stating, “I had a difficult time, but I have family members who
support me, and I am working hard to help my family and do things I en-
joy.” By the end of module 6, “Resiliency—Part 1,” Ana had tried new
ways to use her top five strengths in her daily life and had written down
the good things that had happened to her at the end of every day.
Celia and Ana met collaboratively at the end of the standard mod-
ules to discuss Ana’s progress to date and next steps for the individual-
ized modules. In that session, Ana revealed to Celia that she had a new
goal: she wanted to move back to the city to live with her grandmother
so she could find a job and reconnect with her friends. On the basis of
their discussion, Celia and Ana decided to move to module 8 (Dealing
With Negative Feelings) to help Ana reduce her social anxiety, then re-
view module 11 (Having Fun and Developing Relationships) to allow
Ana to practice new skills to meet new people and reconnect with her
friends when she returned to live with her grandmother.
CBTp and IRT: Comparing the Models

Table 13–3 summarizes the core components of psychotherapy for FEP
and indicates how CBTp and IRT address each of them. Although there
is significant overlap between the two approaches in terms of session
structure, orientation toward goal attainments, and wellness and recov-
ery, there are key differences as well. IRT is a highly manualized ap-
proach with extensive educational and worksheet materials in the form

of handouts for clients and clinicians, whereas CBTp is less standardized
and structured and consequently requires stronger clinical skills and ex-
perience to implement, offering greater flexibility for the experienced cli-
nician. IRT is prescriptive in the sessions that are offered (with flexibility
depending on the needs of the client), allowing for a consistent and sys-
tematic approach to treatment, whereas CBTp draws heavily on the col-
laboratively developed formulation to inform the direction of
intervention, resulting in each client receiving different interventions.
Clients (and clinicians) may variably respond positively to one ap-
proach over the other in terms of preference for a structured, manual-
ized treatment or a more flexible idiosyncratic process. IRT provides a
strong psychoeducational basis to support treatment, thus ensuring the
client has an understanding of psychotic symptoms. When clients are
reluctant to engage in discussion regarding the experience of their psy-
chotic symptoms, IRT encourages clinicians to use normalizing lan-
guage consistent with the terminology being used by the client and to
explore the client’s understanding of his or her experiences. In addition
to this approach, CBTp also encourages the clinician to sit on the collab-
orative fence, drop assumptions, and explore explanations other than
an illness model or diagnosis to explain the distressing experiences.
This does not preclude psychoeducation, but it does offer an additional
way of engaging the individual who may not be initially open to con-
sidering his or her experiences within a mental health framework.
Common Challenges in Conducting

Psychotherapeutic Interventions
in Early Psychosis
Although psychotherapeutic interventions are routinely integrated into
coordinated specialty care, there are a number of potential challenges in
offering this approach to individuals with early psychosis. The impor-
tance of team coordination should not be underestimated, but it should
also be recognized that this approach can be challenging in terms of re-
sources and communication. Ensuring that there is protected time each
week in the form of a case conference or team meeting may aid this pro-
cess, and the use of remote teleconferencing capacity may be necessary
to ensure that clinicians in remote geographical locations are able to be
connected to the team virtually.
The clinician may also face challenges if a young person does not
want to engage in services. Typically, both CBTp and IRT offer an alter-
native means of engaging a young person who may not be ready to dis-
cuss medications, and in some cases, the therapist may be the first point
TABLE 13–3. Goals, structure, organization, and methods of cognitive-behavioral therapy for psychosis (CBTp) and
individual resiliency training (IRT)
Dimension CBTp IRT
General focus, structure, and format
Target population All persons with FEP All persons with FEP
Aims of intervention • Improve quality of life • Increase strengths, resiliency, and self-
• Reduce distress and prevent future determination
distress • Teach information and skills to facilitate
• Elicit hope in recovery informed decision making about
• Assist the maintenance of a client’s treatment and illness self-management
capacity to make informed decisions • Teach information and skills and provide
about his or her life support for achieving personally
• Help the client, over the course of therapy, meaningful goals
work toward becoming his or her own
therapist
Session frequency and intervention duration Frequency: adapted to the client’s needs Frequency: weekly or biweekly
Psychotherapeutic Interventions for Early Psychosis
and speed of learning Duration: 9–24+ months, depending on

Duration: termination should include need
planning for long-term maintenance of
gains after treatment
227
228
individual resiliency training (IRT) (continued)
Dimension CBTp IRT
Organization • Engagement Curriculum-based program with

• Development of problem list and shared goals information and skills organized into 14
• Assessment (exploration of symptoms) different modules (or topic areas):
• Development of collaborative formulation • 7 standard modules provided to all
• Identification and implementation of clients
cognitive and behavioral skills • 7 individualized modules provided on
• Consolidation of skills the basis of client need and interest
• Relapse prevention (taught whenever needed; do not require
• Booster sessions completion of standard modules)
Structure of sessions • Session structure and content should be Usual flow of sessions:
decided jointly between client and • Set agenda
therapist • Review previous session
• Client should be encouraged to prioritize • Review home practice
items on the agenda • Follow up on goals
• Major brief summaries should occur at • Teach new material
the beginning and end of each session • Summarize
• Set new home practice
Materials for clinicians Numerous manualized CBTp interventions Manual and guidelines for teaching each
module
Dimension CBTp IRT
Materials for clients Worksheets from manuals (may be included or Educational handouts for each module,
may be developed idiosyncratically to meet including the following:
needs of client) • Information about topic area
• Prompt questions to facilitate discussion
• Suggestions for in-session practice of skills
• Tables completed in session
• Suggestions for home assignments
Specific methods used and topic areas covered
Befriending and engagement • Engage the client in the therapeutic Emphasize engagement from the
relationship and take into account the beginning of IRT in module 2
client’s perspective and world view (Assessment and Goal Setting) when
• Explain the rationale of CBT to the client developing a definition of recovery and
and demonstrate its use discussing different areas of life
• Use client feedback to inform
interventions
• Encourage clients to express positive and
negative reactions regarding therapy
• Ensure consistent collaboration
throughout sessions
• Use collaborative feedback to engage the
client
229
230
Dimension CBTp IRT
Assessment • Careful and collaborative exploration of • Brief Strengths Test

current experiences through nonjudgmental, • Satisfaction With Areas of My Life
open questioning • Psychosocial history
• Exploration facilitated by ability of clinician • Additional questions about medications
to sit on the “collaborative fence” and substance use
• Symptom-specific measures used to track
outcomes
• Assessment of presenting
symptomatology, past experiences of
services, and cultural or family issues in
engagement
Team formulation Formulation is used as part of team meetings IRT clinician participates in the weekly
and case consultation to support coordination team meeting and regular treatment
around complex cases planning meetings to provide feedback
on goals, strengths, and challenges
Goal setting and tracking • Initial problem list • Comprehensive review of life domains to
• Development of SMART goals relating to set personally meaningful goals
problem list • Breakdown of long-term goals into
• Prioritization of goals based on need shorter-term goals and steps
• Tracking of goals over time to assess progress • Use of a goal-tracking sheet to
operationalize goals and track progress
over time
Dimension CBTp IRT
Resiliency skills training Exploration of strengths and existing coping • Covered in two modules (1 standard
skills to support change module and 1 individualized module)
• Includes skills to identify character
strengths and practice gratitude,
mindfulness, and other positive
emotions
Psychoeducation about FEP and its treatment • Psychoeducation is incorporated as needed • Covered in Education About Psychosis
(providing standard information about but is not made a priority module (standard)
disorder in an interactive, flexible way to • Clinician remains open to pursuing • Clinician maintains focus on
facilitate comprehension) alternative ways of understanding psychosis understanding client’s experience of
in a manner that allows reduced distress and psychosis
increased functioning • Clinician incorporates client’s language
• Clinician normalizes psychotic symptoms to describe symptoms
to reduce stigma and improve
engagement
231
232
Dimension CBTp IRT
Shared formulation and processing the Idiosyncratic formulation is developed for all Formulation is covered in Processing the
psychotic episode clients: Episode module (standard):
• Incorporates historical understanding of • Develop a narrative account of the
formation of psychotic symptoms and how episode
client has reacted to them • Identify and challenge self-stigmatizing
• Informs interventions beliefs about mental illness
Formulation includes maintenance based in the
here and now and a longitudinal formulation,
to understand formation of psychosis
symptoms:
• A balanced conceptualization should
highlight the client’s strengths
• Conceptualization should draw together
current concerns, vulnerabilities, and
precipitating and perpetuating factors
• A cognitive-behavioral maintenance
cycle should be devised and used to set
targets for intervention
• For effective CBT to occur, the
conceptualization must be appropriate
and shared
Dimension CBTp IRT
Relapse prevention training (developing a plan Wellness plan should be developed before Covered in Relapse Prevention Planning
to prevent future relapses) terminating therapy module (standard)
Enhancement of coping strategies (systematic Idiosyncratic coping strategies should be Covered in Coping With Symptoms
enhancement of strategies for coping with identified through the formulation and module (individualized):
problematic symptoms and teaching new implemented as a behavioral intervention • Address broad range of symptoms
coping strategies) (psychotic symptoms, negative
symptoms, depression, anxiety)
• Incorporate behaviorally based coping
strategies
Cognitive restructuring (teaching thought- • Identify unhelpful thoughts and beliefs Briefly covered in Processing the Psychotic
feeling-behavior triad, recognizing thoughts through the formulation, including Episode module (standard) and Dealing
underlying negative feelings, evaluating examination of their impact on actions and With Negative Feelings module
evidence for thoughts and changing when emotions (individualized):
inaccurate) • Implement cognitive strategies to address • Address any negative feelings, including
unhelpful thoughts those related to psychotic symptoms,

• Address core schema depression, suicidal thinking, anxiety,
and PTSD symptoms (due to traumatic
life events, psychotic symptoms, or
coercive treatments)
• Teach cognitive coping strategies
233
234
Dimension CBTp IRT
Interpersonal skills training (teaching social Training incorporated as a behavioral Covered in Having Fun and Developing
skills via breaking down skills, modeling, role intervention as needed on the basis of Good Relationships module
play practice, feedback, home practice) individualized formulation (individualized)
Substance use problems (education about Interventions related to substance abuse Covered in Substance Use module
substances and effects, motivational incorporated as needed on the basis of client’s (individualized)
interviewing, decisional balance about using, goals and formulation
plan for cutting down or preventing relapses)
Health issues (education about healthy Interventions related to healthy living Covered in Making Decisions About
lifestyles, guidance on changing habits) incorporated as needed on the basis of client’s Smoking, Nutrition, and Exercise
goals and formulation module (individualized)
Note. CBTp column is based on Morrison and Barratt 2010. Italics indicate content added by chapter authors.
Abbreviations. FEP=first-episode psychosis; PTSD=posttraumatic stress disorder.
of contact with the team. These approaches allow a focus on personal

goals and recognition of strengths and resiliencies that may be far re-
moved from the presenting symptoms of psychosis. For a young person
who is beginning to disengage with services, both approaches allow for
a return to initial befriending and a focus on the therapeutic relation-
ship to support ongoing continuation of care. Where a young person ex-
periences an exacerbation of symptoms, it may also be necessary to
return to rapport building, communicate concerns to the team, and li-
aise with other team members regarding appropriate support for the
young person. Alternatively, when a young person is doing well and
identifies that he or she needs less support, the provider, as well as the
team, might want to engage the young person in shared decision mak-
ing about the frequency of sessions potentially dropping to less fre-
quent booster session contacts.
CBTp or IRT: Which Is the Best Fit?

CBTp and IRT are the two most common psychotherapy approaches for
early psychosis used in the United States, although neither is broadly avail-
able. The structure of IRT sessions is grounded in cognitive-behavioral
theory, offering a manualized approach to delivering psychoeducation
and key skills, whereas CBTp may be seen as an extension of the tradi-
tional CBT model, emphasizing idiosyncratic formulation to inform in-
tervention. At present, no formal guidance exists to support agencies in
determining which of the two approaches is the most appropriate for
their service. However, there are several principles that provide direction
to agencies looking to train staff in psychotherapy approaches for this
population. IRT was initially created in recognition of the need to support
rapid workforce development in the provision of specialized psychother-
apy for psychosis. Unlike other countries where early intervention in
psychosis has been implemented, the United States lacks a training infra-
structure that ensures clinicians are qualified in basic CBT for depression
or anxiety on completion of postgraduate training. IRT offers a structure
to support novice clinicians in providing key therapeutic interventions
in a manualized manner, ensuring that clients are exposed to a range of
interventions specific to early psychosis while also training the clini-
cians in the basic principles of CBT. IRT training assumes that clinicians
may have a range of past experiences of CBT (including no previous ex-
posure to CBTp) and supports the clinician in demonstrating fidelity to
the approach through tape review and consultation. IRT materials may
be used by novice and expert clinicians alike, with expert clinicians
demonstrating greater flexibility in their use of the modules and in-
creased familiarity with the materials.
In contrast, CBTp training typically assumes clinicians have at least

an intermediate understanding of CBT and are comfortable with the
core components of a CBT session, including agenda setting, collabora-
tion, and homework development. This grounding in CBT is taken as a
foundation on which CBTp is then built, supporting clinicians to learn
the key skills specific to CBTp, including psychosis-specific formula-
tion, normalization, and working from the collaborative fence. Training
in CBTp may be aimed at the intermediate-level CBT practitioner, with
consultation and tape review ensuring that clinicians develop compe-
tence in this approach.
Given the different orientations of these approaches in terms of the
intended target audience of trainees, we recommend that services con-
sider the skill level of their clinicians prior to engaging in training. For
services in which clinicians lack significant experience either providing
CBT or working with persons with psychosis, IRT offers a structured in-
troduction to evidence-based practice. For agencies where clinicians are
experienced in providing CBT and have at least several years’ experi-
ence working with people with psychosis, CBTp may offer additional
skills and insights to support the collaborative understanding of the cli-
ent’s presenting symptoms. In some cases, clinicians with extensive ex-
pertise in working with individuals with psychosis (but with less
exposure to CBT) may be trained to competence in CBTp.
It is important that agencies considering training in these ap-
proaches conduct a thorough assessment of the strengths, skills, and
needs of their staff team and consult with training experts regarding the
best fit. In keeping with the current recommendations for tiered psy-
chotherapy interventions for psychosis (Ince et al. 2016), an integrated
approach in which both IRT and CBTp are available from clinicians
trained to competence in both approaches may be warranted. For teams
considering integrating both approaches at services where clinicians
are unfamiliar with CBT or working with psychosis, we recommend
initial training in IRT followed by CBTp training once IRT competence
is achieved. The benefits of an integrated approach include the oppor-
tunity for clinicians to offer a range of services that match the needs of
the client and for increased choice of services available to the client, thus
further supporting shared decision making. Further investigation of the
benefits and challenges of this integrated approach is justified.
Conclusion
Individual psychotherapy is a core component of early psychosis care
and should be made routinely available to young people experiencing
first episode of psychosis. Cognitive-behavioral therapy for psychosis
and individual resiliency training are two evidence-based interventions
that can be implemented within a team setting. Although there is over-

lap between these two approaches, each model also brings unique
strengths, and the best fit for the service will be determined on the basis
of resources, previous staff training, and overall service ethos.
KEY CONCEPTS
• Psychotherapy is a core intervention in early psychosis
intervention.
• Individual resiliency training and cognitive-behavioral ther-
apy for psychosis are two models of psychotherapy that have
been integrated into coordinated specialty care services.
• Both models support recovery from psychosis through the
development of key skills.
• Services considering implementing individual psychother-
apy need to assess clinician skill and client preference.
1. How oriented is the staff team to providing evidence-based

psychotherapeutic interventions for psychosis?
2. What is the skill level and training background of the clini-

cians in the service in relation to providing psychotherapy for
psychosis?
3. What resources are in place to support training and consulta-

tion in evidence-based psychotherapeutic interventions for
psychosis?
Suggested Readings
French P, Morrison A: Early Detection and Cognitive Therapy for Peo-
ple at High Risk for Psychosis: A Treatment Approach. New York,
Wiley, 2004
Hardy KV: Fact sheet: Cognitive behavioral therapy for psychosis
(CBTp). SAMHSA/CMHS, 2018. Available at: www.nasmhpd.org/
sites/default/files/DH-CBTp_Fact_Sheet.pdf. Accessed October 9,
2018.
Kingdon D, Turkington D: Cognitive Therapy of Schizophrenia. New

York, Guilford, 2005
Penn DL, Meyer PS, Gottlieb J, et al: Individual resiliency training (IRT).
April 1, 2014. Available at: http://raiseetp.org/StudyManuals/
IRT%20Complete%20Manual.pdf. Accessed October 9, 2018.
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CHAPTER
14
Substance Use and Early

Psychosis
Jeffrey D. Reed, D.O.
Mary F. Brunette, M.D.
Case Example
James, a 19-year-old young man, went to his local emergency depart-
ment with severe anxiety and the conviction that his family was in grave
danger. His parents (with whom he lived) related that he became in-
creasingly irritable about 3 months ago. He reported “weird thoughts”
that his family was going to be murdered, that he was responsible for
the misfortunes of others, and that strangers could “see” his thoughts of
guilt. During the past month he slept poorly, was exhausted, and was
distracted at his cashier job.
When asked about substances, James said he had been using mari-
juana for about 4 years, increasing his use in the past year to a “few bong
hits with friends” each day. He realized that he felt more paranoid after
he smoked pot and said his supervisor was criticizing his work. Al-
though he last used 2 weeks ago, he was now even more distressed.
While in the hospital, James started taking risperidone 0.5 mg each
evening for psychosis and melatonin 3 mg at bedtime for sleep. He and
his family met with his treatment team to discuss information about
psychosis and substance abuse, as well as options for care. His sleep and
distress from paranoia improved by 50% within 2 days. James stated
that his goals were to “get back to normal and to be able to go to work.”
His team recommended continued medication, avoidance of alcohol
and marijuana, and counseling to work on skills to “do reality checks”
and manage anxiety and stress.
241
Following discharge, James attended monthly appointments with a

psychiatrist and twice-monthly appointments with a therapist. His
paranoia, irritability, and thought broadcasting progressively im-
proved.
James’s use of substances is similar to many individuals who are ex-

periencing their first episode of psychosis. About half of people with
early psychosis have recently used substances, and up to one-half of
people with schizophrenia will develop a substance use disorder over
their lifetime, a rate that is three to five times higher than general pop-
ulation rates (Addington et al. 2014; Brunette et al. 2018a). Although
many people with schizophrenia report subjective pleasant effects with
substance use, they also experience exacerbated psychotic symptoms
(D’Souza et al. 2005). Persistent substance use or substance use disorder
is associated with poorer treatment outcomes and worse course of ill-
ness in people with early psychosis (Hadden et al. 2018).
Given the adverse impact of substance use on an individual’s symp-
toms and progress in treatment, in what ways can clinicians best sup-
port people who are in the early stages of psychotic illness and also
using substances? The goals of this chapter are to 1) review facts about
co-occurring early psychosis and substance use, 2) discuss how to
screen and assess for substance use disorders and distinguish between
early psychosis with co-occurring substance use disorders and sub-
stance-induced psychosis, and 3) describe stage-wise psychosocial and
pharmacological interventions to treat people with early psychosis with
co-occurring substance use disorders
Consequences of Substance Use

in People with Early Psychosis
Among people with early psychosis, cannabis, tobacco, and alcohol use
are particularly prevalent, and use of substances tends to follow the pat-
tern seen in the general population, although people with schizophre-
nia are less likely to engage in heroin and other opioid abuse compared
with the general population (Chiappelli et al. 2018). Heavy cannabis use
in early adolescence has been shown to increase the risk of later devel-
oping schizophrenia (Murray et al. 2017); thus, cannabis likely precipi-
tates schizophrenia in people who are at risk for developing the
disorder.
When using substances, most people with a psychotic illness expe-
rience pleasant, relaxed, and “high” feelings and may also experience a
sense of heightened sociability. These same individuals also experience
transient increases in psychotic symptoms, despite taking antipsychotic
medications. For example, in one study, about 70% of people with
Substance Use and Early Psychosis 243
schizophrenia developed transient increases in psychotic symptoms af-

ter a single dose of a stimulant (Berman et al. 2009). Other studies have
demonstrated that acute and chronic cannabis use exacerbates psy-
chotic symptoms (D’Souza et al. 2005). Some reports have indicated that
developing a substance use disorder is associated with higher levels of
impulsivity, mood lability, and hostility in people with first-episode
psychosis, which may place them at higher risk for unsafe behavior and
legal problems (Brunette et al. 2018a). In people with schizophrenia,
substance use disorder is related to more severe symptoms, reduced ad-
herence to antipsychotic and psychological treatments, more relapses
and hospitalizations, and lower levels of functioning (Drake et al. 2008).
Many clinicians ignore tobacco use disorder in individuals with
first-episode psychosis because it does not appear to impede function-
ing or worsen symptoms in the way that alcohol and drugs do. How-
ever, people with psychosis are more likely to initiate smoking and have
a higher level of dependence than smokers without psychosis (McClave
et al. 2010). The problem with smoking is that it directly contributes to
heart disease, lung disease, diabetes, and cancers—smoking is the lead-
ing preventable cause of these diseases in the United States. People with
schizophrenia die 20–30 years earlier than the general population, and
smoking is responsible for 50% of those deaths (Callaghan et al. 2014).
Clinicians can provide information and resources to help clients cut
down and quit smoking. A majority of young people with psychosis re-
port a desire to quit smoking and will take steps to quit if provided clin-
ical support (Brunette et al. 2017).
Distinguishing Between
Substance-Induced Psychosis
and First-Episode Psychosis
In the acute treatment setting, when an individual presents with both
new psychosis symptoms and recent drug or alcohol use, the clinician
will need to determine over time whether the client is experiencing a
first episode of a primary psychotic illness, such as schizophrenia, or
whether he or she is experiencing a substance-induced psychosis. Psy-
chosis spurred by substance use may indicate an increased risk for ad-
ditional psychotic episodes in the context of substance use or a more
chronic psychotic illness. Providers and families should know that un-
certainty exists and that close, longitudinal monitoring is necessary to
distinguish between substance-induced and first-episode psychosis. In
order to distinguish between substance-induced and primary psycho-
ses, clinicians should consider whether the psychosis symptoms are
consistent with the type of substances being used, the time course of the
substance use and psychotic symptoms, and the person’s personal and
family history of substance abuse and psychosis (see Table 14–1).
Some substances of abuse are known to produce psychotic states in
nonpsychotic people, especially when used in large amounts for long
periods of time. Substance-induced psychosis is the presence of psychotic
symptoms in the context of intoxication by or withdrawal from a sub-
stance that are not otherwise accounted for by a non-substance-related
psychotic disorder (e.g., schizophrenia spectrum illness, affective disor-
ders with psychotic features, delirium). People with substance-induced
psychosis may also experience mood symptoms, abnormal behavior,
disorganized speech, and impaired cognition. Substance-induced psy-
chosis is most likely to develop in polysubstance users.
A number of abused substances can precipitate psychotic symptoms
through intoxication or withdrawal in people with and without a psy-
chotic disorder (Table 14–2). Stimulants and cannabis are the most com-
monly abused agents known to cause psychotic symptoms. For
example, abuse of stimulants increases the risk of developing psychotic
symptoms up to 11 times the risk in the non-using population (McKetin
et al. 2006). Psychosis can also occur in the context of abusing phency-
clidine, other hallucinogens, and inhalants. Psychosis symptoms typi-
cally seen with substance use, as well as other signs and symptoms
associated with intoxication and withdrawal, are shown in Table 14–2.
If a substance-using individual presents with psychosis symptoms that
are not consistent with the substance, the clinician may be more con-
cerned about the presence of a first episode of schizophrenia, but the di-
agnosis becomes clearer over time (Drake et al. 2011).
In the United States, many states are legalizing cannabis as medical
marijuana and/or for recreational use, leading to more favorable atti-
tudes and increased use of cannabis. Tetrahydrocannabinol (THC), the
main psychoactive agent in naturally occurring cannabis and in syn-
thetic cannabinoids (e.g., Spice, K2), can cause psychotic symptoms and
exacerbate psychosis in people with schizophrenia who are taking anti-
psychotics (D’Souza et al. 2005), whereas cannabidiol (CBD), also in
naturally occurring cannabis, may have calming, antipsychotic, and an-
algesic effects (D’Souza et al. 2016; Hahn 2018; Murray et al. 2017). The
concentration of THC in cannabis has increased over the last 40 years.
Some strains of high-THC cannabis precipitate psychotic symptoms
among many people who use them. Cannabis-induced psychosis may
be transient and remitting, but studies have reported that approxi-
mately 41% of people with cannabis-induced psychosis converted to
having chronic schizophrenia (Starzer et al. 2018). Additionally, regular
cannabis use causes changes in cognition (e.g., deficits in memory, dis-
organized thinking) as well as amotivation and impaired expression of
affect.
TABLE 14–1. Distinguishing between first-episode psychosis and substance-induced psychosis
First-episode psychosis without First-episode psychosis

substances triggered by substances Substance-induced psychosis
Urine or blood Negativea Likely positive (stimulants, Likely positive (stimulants,

toxicology cannabis, alcohol, sedatives, cannabis, alcohol, sedatives,
phencyclidine, other phencyclidine, other
hallucinogens, opioids)a hallucinogens, opioids)a
Psychosis onset Gradual or sudden and not coinciding with Sudden onset during periods of Usually sudden during periods of
substance usea acute substance use acute or chronic substance use or
withdrawala
Substance Use and Early Psychosis
Resolution Psychosis is nonremitting (may reduce in Psychosis may or may not remit Psychosis resolves during periods
severity or resolve with antipsychotic during periods of abstinencea of abstinence or following
medication)a withdrawal from acute or
ongoing substance usea
Symptoms Positive symptoms: mood incongruent Symptoms may be characteristic Dependent on substance of abuse
hallucinations, delusions, thought disorder, of substance of abuse. May (see Table 14–2)
agitationa overlap with symptoms
Negative symptoms: avolition, apathy, consistent with schizophreniaa
reduced affect, poverty of speech, impaired
cognitiona
245
246
TABLE 14–1. Distinguishing between first-episode psychosis and substance-induced psychosis
First-episode psychosis without First-episode psychosis

substances triggered by substances Substance-induced psychosis
History May have personal or family history of May have personal or family May have personal or family
primary psychotic illnessa history of substance use history of substance use disorder
disorder, primary psychotic or substance-induced psychosisb
illness, or substance-induced
psychosis
Acute treatment Antipsychotic medications, education, Antipsychotic medications, Reducing stimulation, reassurance
family engagement, ensuring safe reducing stimulation, and supportive care with close
environment, close monitoring, sleep providing reassurance and monitoring, antipsychotic and/
regulation, abstinence from substances supportive care, education, or sedative-hypnotic
close monitoring, sleep medications (if behavior is
regulation dangerous)c
aAmerican Psychiatric Association 2013.
bBrady et al. 1995.
cMcIver et al. 2006.
TABLE 14–2. Signs and symptoms of acute intoxication and withdrawal for commonly abused substances
Exacerbates
psychosis in
Psychotic schizophrenia
Psychotic symptoms symptoms with spectrum
Substance Acute intoxication Acute withdrawal with intoxication withdrawal disorders?
Alcohol and • Depression • Increased heart • Visual and tactile • Visual and tactile Sometimes
sedativesa,b,c • Problematic behavior rate hallucinations hallucinations
• Slurred speech • Tremor • Auditory, visual, and • Auditory, visual,
• Poor coordination • Insomnia tactile illusions and tactile
• Impaired cognition • Nausea or illusions
• Stupor vomiting
• Hallucinations or
illusions
• Restlessness
• Anxiety
• Seizures
247
248
TABLE 14–2. Signs and symptoms of acute intoxication and withdrawal for commonly abused substances (continued)
Exacerbates
psychosis in
Cannabisa,b,c,e • Problematic behavior • Irritability • Paranoid delusions No Yes

• Euphoria • Anxiety • Auditory and visual
• Impaired learning and • Insomnia hallucinations and
memory • Decreased illusions
• Red or injected eyes appetite
• Increased appetite • Restlessness
• Dry mouth • Depression
• Increased heart rate • Physical
complaints
Stimulantsa,b,f • Heart rate • Depression • Paranoid delusions No Yes
abnormalities • Fatigue • Auditory, visual, and
• Blood pressure • Vivid dreams tactile hallucinations
abnormalities • Insomnia or
• Pupillary dilation hypersomnia
• Sweating • Increased appetite
• Nausea or vomiting • Motor slowing or
• Weight loss agitation
• Restlessness
• Seizures and coma

Exacerbates
psychosis in
Opioidsa • Euphoria • Depression No No Unknown

• Apathy • Nausea or
• Pupillary constriction vomiting
• Drowsiness and coma • Diarrhea
• Impaired cognition • Muscle pain
• Pupillary dilation
• Sweating
• Piloerection
• Yawning
• Insomnia
249
250
Exacerbates
psychosis in
Phencyclidine • Impulsivity • Headaches • Paranoid and other No Unknown

(PCP)a,g • Aggression • Increased appetite delusions
• Abnormal balance • Fatigue • Auditory, visual, and
• Restlessness • Depression tactile hallucinations
• High blood pressure or
heart rate
• Reduced response to
pain
• Seizures
• Sensitivity to sound
and volume
Exacerbates
psychosis in
Other • Pupillary dilation Unknown • Ideas of reference Persisting Unknown

Hallucinogena,g • Palpitations • Depersonalization hallucinations
• Sweating • Derealization consistent with
• Blurred vision • Auditory, visual, and those experienced
• Tremor tactile hallucinations during
• Poor coordination • Illusions or intoxication

synthesthesias
aAmerican Psychiatric Association 2013.
bOuellet-Plamondon et al. 2017.
cNoordsy et al. 1991.
dD’Souza et al. 2005.
eSherif et al. 2016.
fBerman et al. 2009.
gNational Institute on Drug Abuse 2018.
251
To determine whether psychosis symptoms occur independent of sub-

stance use, clinicians can help clients draw a timeline of psychosis symp-
toms alongside a timeline of substance use, including type, frequency, and
severity. If psychotic symptoms continue during periods of abstinence, a
primary psychotic illness is likely. Clinicians may need to monitor individ-
uals prospectively for symptoms and substance use to observe whether
psychosis persists during periods of abstinence, taking into account that
when clients are taking antipsychotic medication, psychosis may be con-
trolled or in remission, and it may take months for psychosis to recur once
people are no longer taking medications. People with substance-induced
psychosis can be advised that they may develop a chronic psychotic disor-
der and should be provided appropriate monitoring and treatment.
Management of Acute Substance-

Induced Psychosis
People with an acute episode of substance-induced psychosis may re-
quire reassurance and a calm, quiet, low-stimulation, supportive envi-
ronment. Those with substantial psychological or behavioral agitation
may require oral or intramuscular sedative-hypnotic or sedating anti-
psychotic medications. Individuals with psychotic symptoms that are
substantially distressing or disruptive should be treated with antipsy-
chotic medications, with or without sedative-hypnotic medications
(McIver et al. 2006). Once the crisis is stabilized, clients and their fami-
lies can be provided education, monitoring, and additional intervention
as described below. If psychotic symptoms occur solely with substance
use and resolve completely with abstinence from substance use, taper-
ing off of antipsychotic medication may be indicated.
Screening and Evaluation of Substance

Use Disorder in People With Psychosis
All clinicians treating individuals with psychosis can screen for sub-
stance use initially, periodically evaluate them for substance use disor-
ders, and provide basic education about the impacts of substance use.
The National Institute on Drug Abuse (NIDA) offers a “quick screen”
(https://www.drugabuse.gov/publications/resource-guide-screening-
drug-use-in-general-medical-settings/nida-quick-screen), including the
NIDA-Modified ASSIST (https://www.drugabuse.gov/sites/default/
files/pdf/nmassist.pdf), that systematically assesses the type and fre-
quency of substances used. The NIDA-Modified ASSIST, which is
based on the World Health Organization’s Alcohol, Smoking and Sub-
stance Involvement Screening Test (ASSIST), obtains a more detailed

history of all substance use and severity of use. As in the case of James,
obtaining an initial comprehensive history of substance use and pres-
ence of use disorder relative to the onset of psychotic symptoms is an
important part of the initial and ongoing evaluation.
Clinicians can ask clients whether they have ever used alcohol,
street drugs, or tobacco and also whether they have used prescribed
medications or medical marijuana to relax, deal with stress, or get high.
Among those who have used, clinicians can then ask about recent use
(we recommend past year) of each substance, including amount,
method of use, frequency of use, and context of use (e.g., people,
places), in a curious and nonjudgmental fashion. The clinician should
assess perceived benefits and consequences of use, such as inclusion in
peer groups; anxiety reduction; impacts on school or work and family
relationships; and legal problems. Such an evaluation should be com-
pleted at the time of initial contact and periodically thereafter. Because
people generally underreport substance use, obtaining information
about substance use from family, friends, clinicians, and other supports is
also important. Many clinics obtain urine drug screens when behavior
suggests that substance use may be contributing to a person’s illness.
Peer Influences on Substance Use

in Psychosis
In addition to direct genetic and environmental effects on substance use
in young people, peer substance use is influential, both through selec-
tion (choosing to be with people whose behavior is similar to one’s
own) and via direct influence (creating or changing perceptions and ex-
pectancies, facilitating access, using social modeling, and other mecha-
nisms) (Edwards et al. 2016). Given the importance of peer influence on
behavior in young people, including peers in team care may increase
engagement and acceptability of interventions for people with early
psychosis (Deutsch et al. 2017).
Integrated Stagewise Treatment for

Substance Use Disorders in Early
Psychosis: Assessing Motivation
for Recovery
Integrated treatment consolidates components of treatment for early psy-
chosis and treatment for substance use disorders into a single setting and
team (Addington et al. 2014; Drake et al. 2008). This approach ensures
that all clients receive a consistent message about how substance use im-
pacts their psychotic symptoms and also ensures access to both treatments
and individualization of these treatments to best fit the needs of the client
(Drake et al. 2008; Mueser et al. 2003). Ideally, treatments are tailored to
an individual’s level of motivation to change and recovery goals.
Stagewise substance use treatment for people with schizophrenia
yields functional improvements over time (Xie et al. 2005). This ap-
proach employs Osher and Kofoed’s (1989) Model of Recovery Sup-
ports applied strategically for individuals at each level of motivation
(Mueser et al. 2003):
1. For clients who are in precontemplation, interventions focus on en-

gagement. Engagement interventions include developing a thera-
peutic relationship, providing practical help, assessing substance
use and related problems, and providing education on risks of sub-
stance use and effects on psychiatric symptoms.
2. For clients who are in contemplation, interventions are encom-
passed by the term persuasion. In this phase, clinicians continue with
education, provide motivational interventions, help clients set
meaningful personal goals, and then help them identify the pros and
cons of substance use and how substance use may affect their ability
to attain these goals.
3. For clients who are in the action stage of change, clinicians provide
active treatment interventions. Active treatment includes helping peo-
ple learn skills to reduce and stop substance use and to cope with
symptoms and stress. Most people in this phase still need motiva-
tional support.
4. For clients in the relapse prevention phase, clinicians help them avoid re-
lapse and maintain recovery. During this phase, clinicians provide as-
sistance in learning skills to maintain sobriety and expand recovery to
other areas of life, such as school, fitness, social networks, and work.
Interventions for Substance Use

Disorders in Early Psychosis
Psychosocial Interventions
Individuals entering treatment for a first episode of early psychosis
need intensive supports to stabilize their psychosis, as described in the
second half of this book (see Chapters 10–20). Early on, clinicians pro-
vide engagement-stage interventions, assessing level of substance use
and whether a substance use disorder is present. Clinicians educate all
clients and families about psychiatric symptoms and prognosis and
provide an overview of treatment as described in Chapter 6 (“Engaging

Families and Individuals in Care”) and Chapter 17 (“Implementing
Peer Support in Early Psychosis Programs”), as well as about the nega-
tive impact of substance use on psychosis recovery. Individuals who
persist in using substances and experience negative consequences from
using after the first 3–6 months of coordinated specialty care for psycho-
sis may need additional treatment for substance use disorders.
Motivational interviewing is a form of counseling in which clinicians
help clients increase their interest in making change (Miller and Rollnick
1991). It can focus on substance use, antipsychotic medication, or any
behavior. Among individuals who are misusing substances, brief moti-
vational interviewing can help them use skills to reduce their substance
use in the early stages of psychotic illness (Kavanagh et al. 2004).
Among others, it may simply increase a client’s willingness to engage
in counseling to learn new skills to cut down and stop using substances.
Incorporating families into motivational counseling may enhance the
efficacy of this approach (Horsfall et al. 2009).
Cognitive-behavioral therapy (CBT) is a type of counseling that involves
teaching people skills to cope with urges to use substances, avoid high-risk
situations, manage social interactions effectively, and engage in replace-
ment activities such as hobbies and sports. This action-stage intervention
can be provided to individuals, families, and groups of individuals.
Among clients who are motivated to change their substance use, CBT can
be tailored to help clients manage both their psychosis and their substance
use disorder (see Chapter 13, “Psychotherapeutic Interventions for Early
Psychosis”). CBT provided in groups offers the advantage of developing
and practicing social skills with peers, access to peer feedback about sub-
stance use, and exposure to peer role models who have been able to take
positive steps forward (Mueser et al. 2003).
Contingency management combined with psychosocial interventions
such as community reinforcement therapy is an effective approach to
addressing addiction (Sigmon 2007). Contingency management in-
volves providing agreed-on reinforcers for behaviors such as absti-
nence based on clear evidence of that behavior (e.g., drug-free urine)
(Horsfall et al. 2009; Sigmon 2007). For example, effective contingent re-
inforcers could include small and increasing amounts of cash, gift cards
for movies or meals, or drawings for prizes based on negative urine
drug screens, treatment attendance, or both. Teams can work with cli-
ents and their families or representative payees to provide such incen-
tives using money from the person's social security benefits in
situations where other resources are not available for incentives (Ries et
al. 2004). Recent evidence supporting use of this strategy shows success
in treating alcohol use disorder and tobacco use disorder in people with
schizophrenia and other severe mental illnesses (Brunette et al. 2018b;
McDonell et al. 2013).
Medication Management
Medications are important preparation-, action-, and maintenance-
stage interventions for people with early psychosis and substance use
disorders. Antipsychotic medications reduce or eliminate psychosis
symptoms, enabling people to participate in school and work; engage
in naturally rewarding, healthy activities; and participate in substance
use disorder treatment if needed. Addiction treatment medications aim
to reduce craving and reduce substance use. In the following subsec-
tions, we review the impact of antipsychotic medications and other
medications on substance use in schizophrenia.
ANTIPSYCHOTICS AND SUBSTANCE USE DISORDERS

Antipsychotic medications are targeted at psychosis but may have dif-
ferential impacts on substance use behavior (Akerman et al. 2014).
Maintaining good control of psychotic symptoms is important for peo-
ple with co-occurring substance use disorder because this enables them
to participate in substance use disorder treatment. However, drugs with
strong dopaminergic blockade, such as high-potency typical antipsy-
chotics (e.g., haloperidol), have been associated with worse outcomes,
worsening substance use in patients with co-occurring disorders, per-
haps due to reduced brain reward circuit function (Green 2007). Drugs
with partial dopaminergic blockade, such as aripiprazole, or with a rela-
tively low level of dopamine D2 receptor blockade and stronger α2-adren-
ergic receptor antagonism and noradrenergic reuptake inhibition, such as
clozapine and quetiapine, may reduce substance use, perhaps by improv-
ing brain reward function. More research is needed to establish whether
one medication provides clear advantage over another for people with
co-occurring schizophrenia and substance use disorder.
Long-acting injectable (LAI) formulations of antipsychotics simplify
medication for patients and enable clinicians to be aware of when pa-
tients discontinue antipsychotic medications. Several studies indicate
that people with chronic schizophrenia assigned to receive LAI risperi-
done or paliperidone had better substance-related outcomes than those
assigned to receive oral medications (Green et al. 2015; Lefebvre et al.
2017). Long-acting injectable antipsychotics are an important option for
patients who have difficulty taking oral medications.
MEDICATIONS USED TO TREAT SUBSTANCE USE

DISORDERS
In this subsection, we discuss medication options in the treatment of
substance use disorders and, where data are available, in the treatment
of people with co-occurring psychosis (Akerman et al. 2014).
Alcohol use disorder. The first-line pharmacological treatments for

alcohol use disorder include naltrexone and acamprosate, which reduce
craving for alcohol and are appropriate for people with heavy drinking
(Lyon 2017). These medications may be used safely in combination with
antipsychotic medication. Naltrexone has been shown to have a prom-
ising impact on reducing drinking in people with schizophrenia and al-
cohol use disorder (Petrakis et al. 2004).
Disulfiram is a medication that blocks metabolism of alcohol, result-
ing in aversive and potentially dangerous side effects if a person drinks.
Anticipating these effects can be a deterrent to drinking. This medica-
tion is most effective when its use is monitored daily by family or clini-
cians of motivated patients (Mueser et al. 2003). Varenicline has been
shown to reduce drinking in people with alcohol use disorder (Litten et
al. 2013). One small trial was promising in people with schizophrenia
and alcohol use disorder, but the effectiveness was limited by low toler-
ability (primarily abdominal pain) (Meszaros et al. 2013).
Cannabis use disorder. N-acetylcysteine may offer some positive ef-

fects in reducing cannabis use in adolescents with cannabis use disorder
(Deepmala et al. 2015), but it has not been studied in people with
schizophrenia and cannabis use disorder. Oral THC as a replacement
therapy does not reduce cannabis use in people with cannabis use dis-
order (Haney et al. 2008); however, early research indicates that the
combination of high doses of THC and CBD in nabiximols combined
with motivation enhancement therapy and CBT may be helpful (Trigo
et al. 2018). Early research has shown that CBD reduces symptoms of
psychosis in people with schizophrenia (Hahn 2018), but it is not clear
whether CBD alone has an impact on cannabis use in individuals with
cannabis use disorder.
Tobacco use disorder. Three U.S. Food and Drug Administration–

approved treatments for tobacco use disorder have all been shown to be
safe and effective in people with schizophrenia: varenicline (Chantix),
bupropion (Zyban), and nicotine replacement therapy (nicotine gum,
patch, lozenge, or inhaler) (see Cather et al. 2017 for review). Current
treatment guidelines recommend providing cessation counseling with
the use of varenicline or bupropion alone or with nicotine replacement
therapy in smokers with schizophrenia. Continued maintenance treat-
ment with counseling and medications may also reduce relapse in this
population.
Opioid use disorder. Medication-assisted treatments dramatically

improve outcomes and reduce overdose deaths for people with opioid
use disorder. The current recommended opioid agonist therapies in-
clude buprenorphine, which can be prescribed by office-based provid-
ers, and methadone, available only from licensed clinics. These
medications occupy brain opioid receptors, preventing people from

getting high when they use opioids, thus reducing drug-seeking behav-
ior and enabling people to engage in treatment and recovery activities.
Naltrexone occupies opioid receptors without agonism, also preventing
intoxication. This medication has lower rates of success than buprenor-
phine and methadone in the general population. These medications
have not been studied in people with schizophrenia and opioid use dis-
order, but their use is safe and should be encouraged (American Society
of Addiction Medicine 2015). Close monitoring and avoiding medica-
tion interactions, such as with benzodiazepines, enhances safety and
adherence.
Maintenance Treatment, Relapse

Prevention, and Recovery
Once individuals with early psychosis and substance use disorder are
managing symptoms of psychosis and are abstinent or without symp-
toms of substance use disorder, preventing relapse is the primary goal
of treatment (Drake et al. 2008). Relapse prevention skills training helps
clients identify triggers—situations, people, and places that may in-
crease risk for relapse—and to develop a plan to address them.
People with psychosis and co-occurring substance use disorders are
better able to maintain sobriety when they have stable housing in a sup-
portive environment, are socially connected with abstinent peers, and
have adopted self-monitoring attitudes around their substance use and
mental health. Regular structured activities, such as school, exercise,
and paid or volunteer work, are key to developing a meaningful life as
young people maintain their recovery. Involvement in self-help groups
such as Alcoholics Anonymous may provide support and an avenue for
developing a social network that does not involve substance use.

A few months after James’s discharge, he returned to work. There, he re-
connected with friends and started smoking marijuana with them. A
week later, he stopped his medication. Over the next few weeks, he be-
came increasingly anxious. With his therapist, he explored the pros and
cons of smoking marijuana in relation to being with his friends and in
relation to anxiety and paranoia. They also explored the pros and cons
of using antipsychotic medication in relation to James’s symptoms and
his ability to function at work. Additionally, he talked with his doctor
about weight gain—he had gained 20 pounds. His newly stated per-
sonal goals were to look good in order to get a girlfriend, to avoid feel-
ing anxious, and to be able to keep his job so he could have money. After
reviewing these goals, James realized he probably should use medica-
tion to keep the anxiety low. He agreed to restart an antipsychotic with

lower risk for weight gain and developed a plan for regular exercise.
James noticed feeling calmer within a few days of starting the medi-
cation. He decided he would commit to taking the medication for a year.
After a month of ongoing discussions with his therapist about whether
smoking marijuana “was worth it,” especially related to his work perfor-
mance, James decided to avoid smoking pot and to focus on one friend at
work who did not smoke marijuana. Over the next 12 months, James
worked his way up to an assistant manager position at his place of em-
ployment.
Conclusion and Recommendations

Many people with early psychosis experiment with stopping medica-
tions and trying substance use again after a period of abstinence.
James’s presentation demonstrates the challenges that can be worked
through to engage and treat clients with co-occurring disorders. His
treatment team continued to regularly assess for substance use and en-
gage in therapeutic work to rebuild motivation to manage psychosis
symptoms and avoid using substances. They supported him in finding
sober peers, listened to his concerns about his psychiatric treatment,
and worked with him to find a tolerable medication that would enable
him to make progress toward his personal goals.
A team-based approach that involves client-centered psychosocial
and medical interventions enables assessment, prevention, and man-
agement of substance use disorders in individuals with early psychosis.
Teams deliver the following treatment components to help clients effec-
tively manage their substance use:
• Early and accurate identification of psychosis and psychosis-risk

syndromes
• Psychoeducation for clients and families that promotes understand-
ing of psychosis and substance use and their interactions
• Screening for substance use and diagnosis of use disorders
• Stagewise psychotherapeutic interventions to increase motivation
and skills to reduce and stop substance use
• Peer support to improve social connectedness and model responsi-
ble substance use and abstinence
• Careful medication management that targets both psychosis and
substance use
With these treatment components in coordinated specialty care, cli-

ents can develop the skills needed to manage both their substance use
and psychosis to better meet their personal goals and achieve recovery.
KEY CONCEPTS
• Substance use is common in people presenting with early
psychosis, with bidirectional interactions.
• Longitudinal observation is often required to distinguish
substance-induced psychosis from early psychosis trig-
gered by substance use.
• Ongoing substance use is associated with lower likelihood
of remission from psychosis and worse outcomes.
• Integrated treatment for psychosis and substance use
within a coordinated specialty care framework is recom-
mended in order to improve outcomes.
1. Why might diagnostic uncertainty between substance-induced

psychosis and primary psychosis be a good prognostic sign?
How would you discuss this with families eager to know the
diagnosis?
2. Why would degree of reduction in positive and negative

symptoms in response to antipsychotic medication and absti-
nence be helpful in clarifying diagnosis?
3. How could discussion of long-term functional goals facilitate

motivation for treatment of substance abuse? For treatment
of psychosis?
4. Why might integration of substance abuse treatment into the

coordinated specialty care team have advantages?
Suggested Readings
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Drake RE, O’Neal EL, Wallach MA: A systematic review of psychosocial
research on psychosocial interventions for people with co-occurring
severe mental and substance use disorders. J Subst Abuse Treat

34(1):123–138, 2008 17574803
Mueser KT, Noordsy DL, Drake RE, et al: Integrated Treatment for Dual
Disorders: A Guide to Effective Practice. New York, Guilford, 2003
Ziedonis DM, Smelson D, Rosenthal RN, et al: Improving the care of in-
dividuals with schizophrenia and substance use disorders: consen-
sus recommendations. J Psychiatr Pract 11(5):315–339, 2005 16184072
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CHAPTER
15
Role of Aerobic Exercise

in the Treatment of
Early Psychosis
Luz H. Ospina, Ph.D.
David Kimhy, Ph.D.
MOST psychotic disorders, including schizophrenia spectrum disor-

ders, begin with a prodromal period characterized by attenuated posi-
tive and negative symptoms as well as altered functioning before the
onset of a full psychotic episode (Yung et al. 2004). These subthreshold
symptoms differ from symptoms associated with full psychotic epi-
sodes in their intensity, frequency, and/or duration. Nevertheless, these
symptoms, in combination with additional risk factors, may increase
the likelihood of developing a psychotic disorder and may predict clin-
ical severity and general functional outcome. For example, deficits in
neurocognition (e.g., memory, attention, executive functioning, percep-
tual processes) appear during the prodromal stage and remain present
throughout illness progression and may represent a core feature of psy-
chosis-related disorders (Rund 1998). Furthermore, cognitive impair-
ments remain after psychopharmacological intervention (Keefe et al.
2007) and symptomatic stabilization (Bilder et al. 2000) and have been
shown to be a main predictor of functional outcome in individuals with
early and chronic psychosis (Green et al. 2004). Additionally, negative
clinical symptoms such as anhedonia, blunted affect, avolition, and ap-
265
athy occur during the high-risk period and remain persistent through-
out the course of illness, and these symptoms typically respond poorly
to psychopharmacological intervention (Hasan et al. 2012). These clini-
cal and affective impairments negatively influence individuals’ disabil-
ity levels and ability to function in all areas of daily life, including social
and occupational areas, and do not appear to be treatable using tradi-
tional antipsychotic medications (Hasan et al. 2012).
Although pharmacological intervention is widely used in psychotic
disorders and may treat specific symptoms (such as hallucinations or
other positive symptoms), very few, if any, interventions exist that reli-
ably improve neurocognition and functioning in this population. There-
fore, it is imperative to develop intervention strategies that target
neurocognitive deficits in people experiencing early psychosis, which
may subsequently improve general functional outcome. One recent inter-
vention that targets these factors for both chronic and early psychosis in-
cludes using the benefits of increased physical activity or exercise.
Exercise refers to structured, planned, and repetitive physical movement
to maintain or improve one or more mechanisms of physical fitness. In
this chapter, we detail the potential benefits of physical activity, primarily
aerobic exercise interventions, for cognitive and negative symptoms in
people with psychotic disorders.
Impact of Physical Exercise on

Cognition in Early Psychosis
Although a significant number of studies have assessed the influence of
exercise on cognition in individuals with chronic psychosis, few studies
have examined this relationship in individuals with early psychosis, in-
cluding individuals with first-episode psychosis (FEP) and persons at
clinical high risk (CHR) of psychosis. An early meta-analysis by Dauwan
et al. (2016) of individuals with chronic psychosis (29 studies with 1,109
schizophrenia spectrum patients) found no reliable effect of general ex-
ercise on neurocognition. However, the large heterogeneity in the re-
sults suggested that type, frequency, and intensity of exercise may
differentially influence cognitive performance. Addressing this issue, a
subsequent review and meta-analysis by Firth et al. (2017) of 10 trials
with 385 individuals diagnosed with schizophrenia indicated that aer-
obic exercise improved global cognition, demonstrating a moderate-
level effect size and no statistical heterogeneity. Exercise was found to
improve specific cognitive domains, including working memory, social
cognition, and attention/vigilance—domains typically known to be de-
ficient in people with psychotic disorders. No significant benefits were
shown for processing speed, verbal and visual memory, and reasoning
and problem solving. Also, a greater amount of exercise (in minutes per
Aerobic Exercise in Treatment of Early Psychosis 267
week) and exercise interventions supervised by physical activity pro-

fessionals were associated with greater global cognitive improvements
(Firth et al. 2017). Evidence from other studies indicated that intensity
of aerobic exercise also predicted cognitive improvement (Kimhy et al.
2016). Overall, meta-analytic results suggest that exercise of moderate
to vigorous intensity confers the greatest benefits on mental and physi-
cal health, as well as aspects of neurocognition.
Studies examining potential benefits of physical exercise on cogni-
tion in individuals with early psychosis have generated similar results
(see Table 15–1). One early study including 14 individuals with FEP
compared groups on the basis of low or high physical activity levels
(without an exercise intervention) on brain volume, cortical thickness,
and cognitive performance (McEwen et al. 2015). The results showed
that individuals with FEP and low physical activity presented with re-
duced brain volume and cortical thickness, as well as a trend-level ten-
dency toward poor social cognition (using the MATRICS Consensus
Cognitive Battery), when compared with individuals with FEP and
high physical activity.
In another study, Lin et al. (2015) implemented aerobic exercise and
yoga therapy of 12 weeks duration to 124 women diagnosed with
schizophrenia spectrum disorders (within 5 years of onset) to deter-
mine possible improvements in cognition. Both yoga and aerobic exer-
cise conditions demonstrated enhancement in working memory, with
moderate to large effect sizes, in comparison with the control group.
Additionally, the yoga group also displayed significant improvements
in attention and verbal acquisition.
Firth and colleagues also conducted a number of aerobic exercise in-
tervention studies to assess the effects of exercise on cognition, particu-
larly in people with FEP. In their feasibility study, Firth et al. (2018a)
administered a 10-week exercise program to 31 individuals with FEP;
their exercise regimen aimed to achieve at least 90 minutes of weekly
moderate to vigorous activity using aerobic and resistance training
(e.g., treadmills, rowing, cycle ergometers). Cognitive results indicated
the greatest change for verbal memory scores, with moderate improve-
ments in social cognition, processing speed, executive functioning, and
inhibitory control. Firth et al. (2018b) conducted a subsequent longitu-
dinal study assessing the effects of their previously described exercise
program on cognition at 6-month follow-up. Although improved scores
in processing speed were maintained at 6-month follow-up, verbal
memory had reverted to baseline performance at 6-month assessment.
This finding is supported by prior literature, which suggests that exer-
cise-induced enhancements in verbal memory persist only when phys-
ical activity is maintained (Bowie et al. 2014); in Firth et al.’s (2018b)
longitudinal study, only 55% of the sample continued to exercise inde-
pendently after termination of the study.
268
TABLE 15–1. Studies assessing effects of exercise on cognition in early psychosis
Sample characteristics Exercise intervention
Exercise Control Mean age Duration and Cognitive

(n) (n) (years) Population Activity frequency domains
Lin et al. 31 (aerobic) 33 24.56 Onset within 60 minutes of either 12 weeks, 3 Verbal memory
2015 38 (yoga) waitlist 5 years yoga therapy or times per Working memory
aerobic exercise week Attention
(i.e., walking or Executive function
cycling)
McEwen et 7 7 23.35 FEP Low and high — Processing speed
al. 2015 physical activity Attention/
according to the vigilance
IPAQ Working memory
Verbal learning
Visual learning
Reasoning/
problem solving
Social cognition
TABLE 15–1. Studies assessing effects of exercise on cognition in early psychosis (continued)

Firth et al. 31 7 25.85 FEP 45–60 minutes of 10 weeks, 2 Processing speed

2018a TAU moderate to times per Verbal memory
vigorous activity week Executive function
using aerobic Inhibitory control
(e.g., treadmill, Motor function
rowing, cycle Social cognition
ergometer) and
resistance
exercises
Firth et al. 28 — 26.96 FEP Longitudinal 10 weeks, 2 Verbal memory
Aerobic Exercise in Treatment of Early Psychosis
2018b follow-up of times per Processing speed

previous study week Executive function
6 months later Inhibitory control
Social cognition
269
270

Nuechterlein 7 (with CT) 9 22.65 FEP 150 minutes/week 10 weeks, 4 Processing speed
et al. 2016 CR of moderate to times per Attention/
vigorous aerobic week vigilance
exercise (i.e., Working memory
calisthenics) in Verbal learning
conjunction with Visual learning
CR Reasoning/
problem solving
Social cognition

Dean et al. 12 — 19.42 CHR Two exercise 12 weeks, 2–3 Processing speed
2017 conditions: times per Attention/vigilance
1) moderate (65% week Working memory
intensity 2 days/ Verbal learning
week) or Visual learning
2) vigorous (85% Reasoning/problem
intensity 3 days/ solving
week), including Social cognition
treadmill, bikes,
and elliptical
Aerobic Exercise in Treatment of Early Psychosis
machines
Abbreviations. CHR=clinical high risk; CR=cognitive remediation; CT=cognitive training; FEP=first-episode psychosis; IPAQ=International Physical
Activity Questionnaire; TAU=treatment as usual.
271
Finally, Nuechterlein et al. (2016) conducted a combined 10-week in-

tervention pilot study examining the effects of aerobic exercise in con-
junction with cognitive training, compared with cognitive training
alone, in individuals with FEP. For the first 5 weeks, neurocognitive
training consisted of computerized exercises aimed at improving per-
ceptual processing and verbal learning and memory; the remaining
weeks focused on social cognitive training exercises to improve cogni-
tive processes underlying social and emotional interactions. The com-
bined intervention group also completed a concurrent aerobic exercise
training program, which consisted of a series of calisthenics for a total
of 150 minutes over 4 days per week. Results indicated that persons in
the combined exercise and cognitive training condition improved nota-
bly more (with large effect sizes) than did individuals in the cognitive
training alone group, with the largest increase in scores for social cogni-
tion, working memory, processing speed, and attention/vigilance do-
mains. The combination of cognitive training and physical exercise may
allow for the beneficial effects of aerobic exercise training by enhancing
improvements yielded from cognitive training alone, which has been
previously demonstrated (Wykes et al. 2007). Therefore, these results
suggest possible improvements in cognition as a result of moderate-in-
tensity (i.e., aerobic) exercise in individuals with early psychosis.
To date, only one study has used an exercise intervention in persons
at CHR for psychosis. In Dean et al.’s (2017) pilot study, 12 CHR indi-
viduals were assigned to one of two aerobic exercise regimens: 1) a
moderate-intensity program, exercising twice per week at 65% intensity
of their maximal oxygen consumption for 12 weeks (n=7), or 2) a vigor-
ous-intensity program, exercising 3 days a week at 85% intensity of
their maximal oxygen consumption for 12 weeks (n=2). Both groups
were given the choice to use treadmills, stationary bikes, or elliptical
machines, and each session lasted approximately 30–45 minutes. Re-
sults indicated considerable improvement in cognitive performance for
both groups, specifically, working memory, verbal learning, visual
learning, processing speed, attention/vigilance, and reasoning and
problem solving (with moderate to large effect sizes). There was also a
significant increase in the cognitive composite score after completion of
the intervention.
One possible explanation for the positive effects of exercise on neu-
rocognition relates to increases in brain volume, particularly in the hip-
pocampus. The hippocampus has been largely implicated as a major
brain region impaired in psychosis and plays a significant role in con-
trolling both the physiological stress response and higher-order cogni-
tion (Harrison 2004). A number of studies using physical exercise
programs have demonstrated increases in hippocampal volume in indi-
viduals with schizophrenia (Pajonk et al. 2010). Similarly, studies in in-
dividuals with early psychosis have also shown concurrent increases in
brain volume and improved neurocognitive scores, particularly volu-

metric increases in hippocampal and prefrontal cortex, in response to
physical exercise. Also, reduced cortical brain thickness in the prefron-
tal cortex has been evidenced in individuals with FEP with low physical
activity (McEwen et al. 2015). Finally, one study assessing functional
connectivity in CHR individuals showed increased functional connec-
tivity between the left hippocampus and occipital cortex after a 12-week
aerobic exercise intervention (Dean et al. 2017).
Another possible explanation for the beneficial effects of physical
exercise on neurocognition relates to brain-derived neurotrophic factor
(BDNF), a neural growth factor that is highly expressed in the hippo-
campus and is associated with facilitating neurogenesis, synaptic plas-
ticity, memory, and learning (Gomez-Pinilla et al. 2008). Although no
studies to date have assessed changes in BDNF expression in response
to an exercise intervention in individuals with early psychosis, one
study did demonstrate a significant relationship between BDNF upreg-
ulation and improved neurocognition in people with chronic schizo-
phrenia. Using a 12-week moderate-to-vigorous aerobic exercise
intervention in 33 people with schizophrenia, Kimhy et al. (2015) found
significant improvement in neurocognitive scores, particularly social
cognition and visual learning. Additional regression analyses also de-
termined that increases in BDNF and enhancement in aerobic fitness
significantly predicted neurocognitive improvement. Taken together,
these results suggest that aerobic exercise upregulates the production of
BDNF, which is believed to be associated with brain neuroplasticity and
neurogenesis, thereby promoting growth of specific brain regions, such
as the hippocampus, that are critical for neurocognitive performance
(Vakhrusheva et al. 2016).
Impact of Physical Exercise on

Positive and Negative Symptoms
in Early Psychosis
A number of meta-analyses and reviews have examined the influence
of physical activity on positive and negative symptoms in individuals
with chronic schizophrenia spectrum disorders. In Firth et al.’s (2015)
early meta-analysis, 16 out of 17 studies monitored the effects of exer-
cise on overall mental health, focusing on positive and negative symp-
toms. Although low-intensity exercise did not affect change scores for
clinical symptom assessments, moderate to vigorous exercise exhibited
a strong effect on total psychiatric symptoms, with significant reduc-
tions in both positive and negative scales. Dauwan et al.’s (2016) review
also demonstrated reductions in total symptom severity, although their
results had high heterogeneity. Their analysis of positive symptoms (15

studies, N=641), negative symptoms (18 studies, N=765), and general
symptom severity (10 studies, N=436) indicated significant reductions
in overall clinical symptoms as a result of exercise, specifically yoga and
aerobic interventions, compared with control groups. Finally, a review
by Tarpada and Morris (2017) included eight intervention studies
(N=301) using the Positive and Negative Syndrome Scale (PANSS) as
the outcome measure; physical activity regimens included yoga, dance,
and aerobic exercises and resistance training. They discovered that
physical activity significantly improved total and positive PANSS
symptom scores when compared with control groups. Also, there was
a trend for improvement in PANSS negative symptom scores, although
this finding did not achieve significance.
Most studies assessing exercise and symptom severity in early psy-
chosis also demonstrated improvements in positive, negative, and total
symptom scores. In one early study, Mittal et al. (2013) examined 29
CHR individuals and 27 matched controls on physical activity (using
actigraphy monitors), clinical symptoms, and brain structure. They
found that CHR individuals engaged in less physical activity than did
the nonclinical control group. Furthermore, physical activity was ob-
served to correlate significantly with bilateral parahippocampal gyrus
volumes and occupational functioning. However, Mittal and colleagues
did not detect any relationship between physical activity level and clin-
ical symptoms.
Regarding exercise intervention studies, Lin et al. (2015) showed im-
provement of overall symptom severity in response to 12-week yoga and
aerobic exercise interventions. Interestingly, negative symptoms de-
creased for those in the yoga condition, whereas positive symptoms did
not improve for either the yoga or aerobic exercise groups. Also, Firth et
al. (2018a) demonstrated a significant reduction in PANSS scores, partic-
ularly for negative and general symptoms, for individuals with FEP as-
signed to a 10-week aerobic exercise program, compared with a control
(treatment as usual) group. Similarly, positive symptoms in the exercise
group did not decrease and were statistically similar to symptoms in the
control group. Results for Firth et al.’s (2018b) follow-up longitudinal
study suggested that individuals who continued to exercise on a
weekly basis after completion of the intervention study continued to
show symptomatic reductions in PANSS total scores, compared with in-
dividuals who ceased exercising after supervised intervention. In fact,
non-exercisers’ total PANSS scores increased (i.e., worsened) after the in-
tervention period. Finally, Dean et al.’s (2017) aerobic exercise interven-
tion in 12 CHR individuals exhibited significant medium-to-large
decreases in positive symptoms and a small-to-medium decrease in
negative symptoms at termination of the 12-week trial. Overall, these
results implicate potential beneficial effects of physical exercise on
symptoms, particularly negative and total symptom scores, in individ-

uals with early psychosis.
Although the specific mechanisms by which physical activity may af-
fect positive and negative symptoms in early and chronic psychosis re-
main unclear, a number of hypotheses attempt to explain this relationship.
One frequently proposed explanation includes enhanced synaptic neuro-
plasticity due to upregulation of BDNF. As mentioned in the previous
paragraph, BDNF is related to neurogenesis and neuroplasticity. One
meta-analysis (Green et al. 2011), which included 16 studies, demon-
strated moderately reduced blood BDNF levels (Hedges’ g=–0.458) in
drug-naïve and medicated patients with schizophrenia, both male and
female. Neurodevelopmental models of schizophrenia (van Haren et al.
2008) suggest that reduced BDNF underlies the core behavioral signs
and symptoms of the disorder; as such, upregulation of BDNF as a re-
sult of physical activity may lead to reductions in many of the clinical
symptoms associated with psychosis.
Most studies in individualindividuals with early and chronic psy-
chosis reflected reductions in negative and total symptoms, with one
study (Dean et al. 2017) including CHR individuals showing reductions
in both negative and positive symptoms. Although it remains unclear
why physical activity specifically reduces negative symptoms more
than positive symptoms, this observation is important given that prior
studies have revealed significant associations between negative symp-
toms and functional outcome, whereas positive symptoms are less
strongly correlated with overall functioning in schizophrenia spectrum
disorders (Ventura et al. 2009). Therefore, reducing negative symptoms,
which may partially mediate the association between neurocognition
and general functioning, may improve both neurocognition and func-
tional outcome in individuals with early and chronic psychosis.
Impact of Physical Exercise on Affective

Symptoms in Early Psychosis
Studies assessing the impact of physical activity on affective symptoms
in both chronic and early psychosis are limited. Regarding chronic pa-
tients, Firth et al.’s (2015) meta-analysis demonstrated that physical ex-
ercise decreased depressive and anxiety scores within broader mental
health assessments in 3 of 17 trials, although only in relation to baseline
scores and not comparison groups. Dauwan et al.’s (2016) review pre-
sented overall significant reductions in depressive symptomatology,
with a large effect size (Hedges’ g=0.71), in response to exercise inter-
ventions. Finally, one recent study examining factors that motivate and
sustain exercise in schizophrenia spectrum patients who were already
independently and regularly exercising (n=14) showed 7%–11% aver-
age decreases in anxiety and depressive symptoms in response to indi-

vidual exercise sessions (Dahle and Noordsy 2018). Therefore, physical
exercise interventions also appear to confer beneficial reductions in af-
fective, particularly depressive, symptoms, in chronic psychosis.
Exercise studies in individuals with early psychosis also generally
demonstrate potential improvements in clinical affective symptomatology.
For example, Lin et al. (2015) showed a significant decrease in depressive
symptoms for both yoga and aerobic exercise groups after a 12-week in-
tervention; importantly, these effects on affective symptoms remained
stable at 12-month follow-up. Also, in the study by Firth et al. (2018b), re-
sults exhibited trend-level reductions in depressive and anxiety symp-
toms after a 10-week moderate-to-vigorous aerobic exercise intervention.
Although evidence for the effects of physical exercise on affective
symptoms in psychosis is scant, numerous studies have assessed these
effects in depressive disorders. In individuals with depression, exercise
has been observed to lead to physiological changes such as increased re-
lease of specific neurotransmitters that have been linked to enhanced
mood (e.g., serotonin and endorphins) (Ströhle 2009). Other possible
mechanisms for the beneficial effects of physical activity on affective
symptomatology and mental health in individuals with psychosis in-
clude changes in psychological factors such as increased social support
and improved perceptions of self-efficacy, competence, and autonomy
(Gorczynski and Faulkner 2010).
Impact of Aerobic Exercise on Functional

Outcome in Early Psychosis
Studies in chronic psychosis have overwhelmingly demonstrated the
beneficial effects of physical activity, particularly moderate to vigorous
aerobic exercise, on functional outcome. The meta-analysis by Firth et
al. (2015) showed significant improvements in functional disability and
quality of life in two trials that used moderate- to vigorous-intensity ex-
ercise, and two studies that used low-intensity exercise demonstrated
mild improvements in social functioning. Similarly, Dauwan et al.’s
(2016) review also suggested that exercise improves global functioning
scores, with a moderate effect size (Hedges’ g =0.32). In individuals
with early psychosis, various types of exercise have been associated
with enhanced global functioning and quality of life. Results from Lin
et al. (2015) demonstrated greater physical and psychological health as
a result of both yoga and aerobic exercise programs.
Other studies have demonstrated beneficial effects of moderate- to
vigorous-intensity physical exercise on specific aspects of functioning,
such as socio-occupational functioning, in individuals with FEP as well
as CHR individuals. Furthermore, one longitudinal study (Firth et al.
2018b) assessing follow-up 6 months after an exercise intervention con-

tinued to show improvements in socio-occupational functioning after
the intervention had ended, regardless of exercise adherence after su-
pervised intervention. A combined aerobic exercise and cognitive train-
ing pilot study (Nuechterlein et al. 2016) revealed enhanced functional
outcome, specifically in such domains as independent living, family
network relationships, and working productivity, above and beyond
improvements elicited in individuals who received cognitive training
alone. Finally, physical exercise of moderate to vigorous intensity has
also been observed to improve both social and role functioning in CHR
individuals (Dean et al. 2017). Similar to explanations of exercise’s en-
hancing effects on affective symptoms, theories attempting to explain the
beneficial effects of physical activity on functional outcome relate to psy-
chological improvements in self-esteem and confidence, which may lead
to further engagement in the world and better well-being (Vancampfort
et al. 2011).
Conclusion
Overall, numerous studies have found beneficial effects of physical activ-
ity, particularly moderate to vigorous aerobic exercise, on cognition and
negative symptoms, as well as functional outcome in early and chronic
psychosis. Importantly, studies have found that physical exercise inter-
ventions improved cognition, attenuated psychotic symptoms, amelio-
rated negative symptoms, decreased depressive symptoms, and
improved social and role functioning. A number of biological markers
may partially explain these enhancement effects, including increased re-
lease and upregulation of BDNF, which may subsequently promote neu-
rogenesis and neuroplasticity, leading to volumetric increases in key
brain regions (such as the hippocampus) associated with cognition. Al-
though most studies implicate the importance of moderate- to vigorous-
intensity level of exercise in order to maximize benefits, a few studies do
suggest that lower-intensity training, such as yoga, may also ameliorate
symptoms and improve neurocognition and functioning. Additional
studies are necessary to ascertain the specific mechanisms by which var-
ious forms of physical exercise improve cognition, symptoms, and func-
tioning in early and chronic psychosis.
KEY CONCEPTS
• Aerobic exercise training has been observed to improve
cognitive functioning and clinical symptoms in individuals
with psychosis disorders.
• Preliminary results suggest that aerobic exercise training may

also improve cognition, clinical and affective symptoms, and
overall functioning in individuals at high risk for psychosis.
• Neurobiological studies associate aerobic exercise with the
increased release and upregulation of brain-derived neuro-
trophic factor, a neural growth factor, in specific brain
regions related to neurocognition and functioning.
1. Most studies have assessed the effects of aerobic exercise on
cognition and clinical symptoms in individuals with psycho-
sis disorders. Would other types of exercise (strength train-
ing, high-intensity interval training, yoga, or stretching)
confer similar effects on aspects of cognition or clinical symp-
tom severity? If so, what are the possible neurobiological
mechanisms for such enhancement effects?
2. Psychosis disorders that are treated early during illness pro-

gression (i.e., during the first psychotic episode) have better
illness prognosis. Would this phenomenon also occur when
using an aerobic exercise intervention? What would the
course of illness look like for individuals with a psychosis
disorder who engaged in aerobic exercise treatment during
their first episode?
Suggested Readings
Firth J, Rosenbaum S, Stubbs B, et al: Motivating factors and barriers to-
wards exercise in severe mental illness: a systematic review and
meta-analysis. Psychol Med 46(14):2869-2881, 2016
Rosenbaum S, Lederman O, Stubbs B, et al: How can we increase phys-
ical activity and exercise among youth experiencing first-episode
psychosis? A systematic review of intervention variables. Early Interv
Psychiatry 10(5):435-40, 2016
Stubbs B, Rosenbaum S (eds): Exercise-Based Interventions for Mental
Illness. London, Academic Press, 2018
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2004 14984872
CHAPTER
16
Supported Employment and

Education for People in Early
Psychosis
Deborah R. Becker, M.Ed., CRC
EMPLOYMENT and education are normal and expected life activ-

ities for adolescents and young adults. Young people with a first epi-
sode of psychosis desire to fit into society like their peers in the general
population. Furthermore, holding a job and/or going to school—once
thought to be goals for people after a lengthy stabilization period fol-
lowing early psychosis—are paths to recovery from behavioral health
disorders. Work and school provide opportunities for young people to
use their skills, meet people, earn income, have a positive identity and
social status, and be like other young people. Team members of coordi-
nated specialty care teams that serve young adults with early psychosis
provide the hope and support for these individuals to secure functional
roles as workers and/or students.
The most effective vocational intervention for people with behav-
ioral health conditions, including people with first-episode psychosis,
is evidence-based supported employment, also known as individual
placement and support (IPS; Drake et al. 2016; Marshall et al. 2014). Ser-
vice delivery systems sometimes use the term supported employment dif-
ferently, and therefore the term IPS is used to clearly differentiate the
evidence-based practice, which includes the strongest research base,
implementation manuals, a fidelity scale and manual, and an interna-
281
tional network of providers. More than 25 randomized controlled trials

of IPS conducted worldwide by different investigators have demon-
strated that IPS is more effective than any other vocational intervention
(for more information, see www.ipsworks.org).
We use the term IPS specialist (rather than employment/education
specialist) to identify clearly the person who directly provides these ser-
vices. Although the initial focus of IPS in the late 1990s was on people
with serious mental illness and therefore mostly on competitive em-
ployment, IPS is now provided to people with early psychosis as well
as to transitional-age youth with mental health conditions. When serv-
ing a young population, IPS includes support for education and further
schooling as part of building a career path (Swanson et al. 2017). By
helping young adults return to functional roles (i.e., worker, student),
IPS services help divert people from a life of disability.
IPS uses a strengths-based approach by drawing on the person’s
skills, talents, interests, and previous experiences. Although the IPS
specialist takes the lead on providing employment and education sup-
port, other members of the coordinated specialty care team support the
participant’s efforts toward building a career path. They ask questions
that help young people consider employment or furthering their edu-
cation: “What job would you like the most? What skills do you have
that would transfer to that type of work? What about that job interests
you?” Team members focus on what the person can do rather than on
limitations. Through a strengths-based approach, practitioners demon-
strate their belief in the person’s capabilities and resilience.
Engaging People With Early Psychosis

in Work and School
The IPS specialist on the coordinated specialty care team engages peo-
ple when they say they are ready to think about going to work or school.
They build rapport on the basis of each person’s level of interest. The
rapid job search principle helps in this regard; participants do not want
to be delayed by lengthy assessments. IPS specialists ask program par-
ticipants how often they want to meet, where they want to meet, and for
how long: “What are we working on that you find helpful? What else
could we be doing that would be helpful to you? What would you like
to be doing in 3 or 4 years? What would be a good first step in reaching
that goal?” People are more likely to stay in services when the focus is
on their strengths and their interests (Maraj et al. 2019).
When engaging young people, IPS specialists limit the amount of
time completing paperwork and forms. They have discussions that fo-
cus on jobs, schooling, and careers and minimize talking about mental
health problems. IPS specialists build credibility with the people they
Employment and Education for People in Early Psychosis 283
serve when they demonstrate knowledge of the local labor market and
educational institutions. In order to maintain engagement and a work-
ing relationship, IPS specialists are flexible to changes in direction that
the person may present. They may spend small amounts of time talking
about other topics and interests as part of relationship building but al-
ways return to the topics of employment, education, and careers.
Technology provides various ways to communicate and maintain
engagement with young people. Many young people respond more
quickly to texts, instant messaging, and e-mails rather than by phone.
By using modern technology, IPS specialists can connect with young
people frequently and reach out when they miss appointments.
Including Family Support for

Employment and Education
With permission from the young person, the IPS specialist invites fam-
ily members to their meetings. Family is defined broadly and may in-
clude immediate family, friends, and other supporters. The IPS
specialist should ask whether the young person would like a friend to
be part of one of the meetings to talk about work and career plans. To
expand the pool of people who are important to the individual, the IPS
specialist may ask who would the person want to tell if he or she just
became employed or aced a test in school.
Family members are an important resource for information about
the person’s skills, interests, and experiences that may relate to work
and career goals. Family members want to be involved and to know
about the services and plans. The IPS specialist educates the family that
young people often try several jobs that last brief periods of time before
settling into a job. Young people change their minds frequently about
their plans, and team members and family members may sometimes be
frustrated by this uncertainty. IPS specialists help young people explore
options of employment and schooling, continue to engage them during
periods of uncertainty, and support family in adjusting expectations in
terms of career plans (Table 16–1).
Snapshot of IPS Services
Team-Based Approach
The IPS specialist is the primary team member of the coordinated specialty
care team who provides direct employment and education support. The
IPS specialist attends all team meetings to encourage consideration of work
and/or school for all participants, to report on each participant’s progress
TABLE 16–1. Core principles of IPS supported employment and

education
Principle Description
Zero exclusion for eligibility All young adults with early psychosis who
are interested in work and school are
eligible, regardless of symptoms, substance
use, or other characteristics.
Mainstream competitive The focus is on regular jobs and mainstream
employment and education educational programs that are available to
people on the basis of their qualifications
rather than disability status or participation
in social services.
Individual preferences and Services are based on participants’
strengths preferences and choices rather than
providers’ judgments.
Integrated services Team members provide employment and
educational support through a team
approach. IPS specialists participate in team
meetings to review and coordinate client
progress.
Rapid job/school search Rapid job search and career/educational
exploration begin soon after entry into IPS.
Job development IPS specialists meet employers to learn about
their business needs and hiring practices.
They may give the information to job
seekers or directly introduce qualified job
seekers to employers, depending on the job
seeker’s preference.
Individual and time-unlimited Team members provide individualized job
supports and educational supports as long as needed
and desired by program participants.
Personalized financial Young adults are referred for personalized
counseling counseling to learn how earned income
affects entitlements and how to finance their
education.
in his or her return to work or school, and to ask about those who are not
pursuing work or school: “How are they spending their time? What do
they want to be doing in 2 years? What are their interests?”
During the intake assessment, the team asks participants about their
work history, interest in working, education background, and interest
in furthering their education. The team supports and nurtures partici-
pant goals in part because they are related to functional outcomes.

Young adults often value work or school above addressing problems re-
lated to low energy, social relations, confusion and poor concentration,
and symptoms and side effects. In addition, having school and work in-
terests leads to greater work or school participation 12 months later (de
Waal et al. 2018).
Young people who express an interest in support around employ-
ment and/or education are referred directly to the IPS specialist. The
IPS specialist meets with participants individually to learn about their
interests, build relationships, review their history, and develop a plan.
All team members should attend to the person’s interests and goals and
view structured activity as vital to illness management by providing an-
chors to keep attention away from symptoms. Team members gently
encourage vocational planning and provide support to individuals who
are actively seeking employment and to those who have gained employ-
ment. Some young people may want to postpone pursuing employment
and/or education. Team members have brief discussions with them over
time to keep the topic of conversation current and demonstrate that they
can pursue these goals in the future.
During team meetings, team members provide input about each
person’s skills, experiences, and preferences that may relate to an indi-
vidualized job search or support plan. For example, a social worker
might say to the IPS specialist, “I learned from Sharon’s mother that
Sharon loves to bake. Have you thought about exploring a job related
to baking?” Team members may offer information about the type of en-
vironments where the young person feels comfortable and other as-
pects of the person’s preferences that could transfer to a work setting.
For example, a psychiatrist might say, “Matthew is less preoccupied
with symptoms when he has structured time. A job may help him dis-
tance from symptoms.” Team members may have leads for potential
employers and can recommend specific job types and locations that are
a fit for specific individuals.
Team members provide suggestions for problem solving and re-
mind participants of individualized coping strategies to use in stressful
situations at work or school. Medication prescribers tailor medications
to best fit the needs of a young person’s functioning at work and/or
school. The peer specialist on the team may provide motivation by tell-
ing how he or she moved forward in his or her recovery through work
or school and may accompany the participant to increase comfort and
confidence (e.g., on a visit to the campus where the young person will
attend classes). Team members help with socialization and communica-
tion skills in the context of work and/or school and provide general en-
couragement.
Many participants are likely to have current alcohol or drug use (see
Chapter 14, “Substance Use and Early Psychosis”). The team helps
these young people reflect on how their use may impact employment
and learning at school. They help to identify a job type and work envi-
ronment that will support recovery. Money is often a trigger for alcohol
and drug use; therefore, the IPS specialist helps to develop a plan for
managing paychecks. Many young people with early psychosis experi-
ence cognitive difficulties that may interfere with learning, and sub-
stance use can further complicate education experiences. Over time,
interest in school and/or a job that they find rewarding can provide mo-
tivation to reduce alcohol and drug use for many young people with
early psychosis.
Career Profile and Employment and Education Plan

Case Example 1
Jack is a 19-year-old who developed a psychotic illness just as he was
finishing high school. As he recovered, he thought about college but
was certain that he was not ready. Talking with his IPS specialist, Zeke,
Jack decided he would like to find a job instead, but he had no idea what
kind of job. They discussed lots of options, but Jack kept coming back to
the theme that he liked playing music with his friends in a local band
and spending time with his dog. Jack decided to continue meeting his
friends in the evening for “jam sessions” and to find a job during the day
working with dogs. Zeke and the team checked with veterinary clinics
and pet stores before one team member talked with a friend of his who
had a business as a dog walker. This friend needed an assistant to ex-
pand his business and was delighted to hire Jack soon after he met him.
The two of them walk dozens of dogs each day, and Jack makes a good
salary for 4 hours of work each day. He naps in the afternoon and plays
with his band in the evening.
The IPS specialist begins meeting right away with the young person
who has expressed interest in employment and/or school to gather in-
formation about the person’s interests, goals, hobbies, experiences, and
transferable skills. The information is documented in the career profile
or other similar assessment tool. During these meetings, the IPS special-
ist builds a collaborative relationship with the participant. The IPS spe-
cialist assesses the participant’s tolerance for these discussions and
makes adjustments accordingly. Sometimes the meetings are brief and
geared to other interests of the participant. Occasionally, IPS specialists
use interest inventories to help identify career choices. The IPS special-
ist and job seeker use the information along with suggestions from the
family and team members to develop ideas for jobs, types of preferred
work environments, number of work hours, and interest in further ed-
ucation and training.
Information from the career profile is the foundation for building an
employment and/or education plan. The young person’s short- and
long-term goals are documented on the plan in his or her own words.
Steps and timeframes to reach the goals are outlined, as well as the peo-
ple who will provide supports to help achieve the steps. The IPS spe-
cialist and participant share the plan with the team and family members
in order to build support and collaboration.
Conducting an Individualized Job Search

The IPS specialist and the participant begin to explore job possibilities
from the employment plan within 30 days. They explore jobs quickly,
which demonstrates to participants that the IPS specialist and coordi-
nated specialty care team are honoring their goals and taking action.
The IPS specialist makes at least six in-person direct employer contacts
with hiring managers per week to learn about their business and hiring
practices. They develop relationships with employers who have posi-
tions that are consistent with the skills and interests of people they are
serving.
Prior to the start of the job search, the IPS specialist explains to the
participant how he or she contacts employers to learn about hiring
practices and positions. If the IPS specialist speaks to an employer
about a specific job seeker, the job seeker needs to agree to disclosure be-
forehand. Through discussions about disclosure and confidentiality, the
young person weighs the advantages and disadvantages of an em-
ployer having information about his or her needs and the job support
team. For example, many people feel that there is a stigma about having
a mental health condition and fear they will be treated differently by
employers. The participant decides what if any information may be dis-
closed to an employer. If the participant does not wish to disclose infor-
mation about his or her mental health condition, the IPS specialist does
not contact employers directly but instead gives information about po-
sitions and hiring practices to the job seeker. With this information, the
job seeker can apply for positions independently without the IPS spe-
cialist.
In addition to discussions about disclosure, the IPS specialist offers
participants access to a trained benefits counselor who explains infor-
mation about possible entitlements such as Social Security disability
benefits. Family members or clinicians may consider applying for ben-
efits if they fear that work is too stressful and will exacerbate symp-
toms, but participants and family need to know that securing disability
benefits may have unintended consequences. For some people, disabil-
ity benefits may be helpful in the short term but harmful over the long
term. In any given year, less than 0.5% of Social Security Disability In-
surance and Supplemental Security Income (SSI) beneficiaries leave the
disability rolls and return to work. Monthly SSI checks are below the
poverty level, so the team should encourage participants to consider
jobs and careers, avoiding the path of dependence on the mental health
system and poverty. If the young person is interested in applying for
benefits, team members help the individual consider the advantages
and disadvantages. For example, the peer specialist may explain his or
her choice of employment over disability benefits. If the participant
then chooses to apply for benefits, the team should continue to encour-
age education and work to build a path to independence.
People with early psychosis may have little or no work experience.
They may have never gone on a job interview and might be unfamiliar
with expected work behaviors. Some people know what they want to
do, but others will want to explore different options. The IPS specialist
and job seeker may visit job sites to learn about different types of jobs
and interview people in those positions to help make decisions about
work. Young people explore the world of work in different ways that
sometimes include volunteer work, internships, certificate programs,
and additional schooling. When the individual expresses interest in an
internship, the IPS specialist should suggest options that are related to
the person’s job goals. The IPS specialist listens carefully to all of the
person’s ideas and supports trying different opportunities.
IPS specialists also help young people with criminal justice back-
grounds apply for jobs. IPS specialists coach job seekers on how to de-
scribe their skills and characteristics in relation to the position. Because
most employers conduct a background check that reveals a person’s le-
gal history, job seekers are encouraged to prepare a brief statement ex-
plaining regret for past actions and commitment to corrected ways to
encourage employers to consider hiring them. In these situations, some
employers consider having a support team to be an advantage.
Providing Job Supports

The IPS specialist and the rest of the coordinated specialty care team
provide individualized supports when participants start working. The
IPS specialist coaches the employee about going to work on time, how
to get to work, what to wear, and other matters for the first day on the
job. Recently hired employees need to know when they will receive
paychecks and for what time period. The new employee and the IPS
specialist develop a support plan that will help the person be a success-
ful worker. Team members help workers with communication skills
with their fellow employees and supervisor. Family members and other
members of the coordinated specialty care team provide support and
encouragement as well.
The IPS specialist and coordinated specialty care team members
provide ongoing support to enable successful work experiences. Some-
times, when young people start jobs, they no longer see the need for
continued support. They are striving for independence and may want
to disengage from services, believing that they have recovered from

their problems. In these situations, the IPS specialist may reduce the
number of contacts but should maintain some engagement to give sup-
port until the person has demonstrated the ability to stay employed.
Advancing Careers
The IPS specialist helps people end jobs and provides support to start
new jobs. Most young people work multiple jobs over time as they are
developing a career path. When someone wants to leave a job, the IPS
specialist counsels the worker to give advanced notice to the employer
and to include the work experience on his or her resume. The IPS spe-
cialist reviews the positive and negative aspects of the job experience:
“What did you learn about yourself as a worker and your preferences
for the future? What will you do differently on the next job?” New
short-term or long-term job goals are incorporated into career plans,
and the IPS specialist should ask the young person whether he or she
wants further education or training to gain skills and knowledge to ad-
vance his or her career.
Supported Education
Case Example 2
Rebecca is a 20-year-old who became ill during her sophomore year of
college. After a brief hospitalization, she returned to her hometown,
where she joined an early psychosis program. Meeting with her IPS spe-
cialist, Lucia, Rebecca insisted that her only goal was to return to college
as a full-time student. Together with Lucia, she explored the local com-
munity college and filled out an application for the next term. Following
admission, Rebecca signed up for a full course load and declined any
disclosure with the college’s academic services office. One month into
the term, however, she realized she was unable to concentrate in class,
was falling behind, and was headed for disaster. She asked Lucia for
help. Lucia and Rebecca rapidly negotiated with the college academic
dean to reduce Rebecca’s course load to one class and with the academic
services office to allow her to tape lectures and have extra time for tests.
Lucia also helped Rebecca find a quiet place to study in the college li-
brary. After these accommodations, Rebecca did well in her first class
and decided to increase her college workload gradually.
Education is developmentally appropriate for adolescents and

young adults and therefore is an important part of IPS. Some young
people, particularly those with attenuated symptoms, are in high school
when they first experience psychosis (see Chapter 8, “Assessment and
Targeted Intervention for Individuals at Clinical High Risk for Psycho-

sis”). Others are in postsecondary education or are considering educa-
tion or vocational skills training to develop careers.
Just as IPS specialists develop relationships with employers in the
community, they also learn about different educational institutions and
training programs in the local area. The IPS specialist should tour col-
lege campuses to see where students attend classes, study, and gather
socially. The IPS specialist makes appointments to meet with guidance
counselors and staff from offices for special services who can help to ar-
range accommodations if needed. In addition, the IPS specialist should
learn about vocational certificate training programs (e.g., pharmacy
technician, home health aide) that are offered in community colleges
and other educational resources such as short-term training programs
(e.g., graphic design programs, culinary programs).
IPS for Students in High School

Level of education relates to employment and financial security over
time; therefore, the team should always encourage young people to
complete high school or obtain the equivalent certificate. To earn the
certificate, students must pass four general educational development
(GED) tests in the areas of language arts, math, science, and social stud-
ies. Students may attend free classes to prepare for the test. The IPS spe-
cialist may talk with an instructor to find out about a student’s progress
and help the student structure ways to study. For high school students,
the IPS specialist may contact a school counselor to obtain guidance on
how to support the student. IPS specialists never fill the role of a tutor,
but they may help students develop good study habits. If a tutor is in-
dicated, the IPS specialist may help to make arrangements.
In the United States, high school students with a disability that affects
their ability to learn may be eligible for an Individualized Education Pro-
gram (IEP). Special education teachers, parents, the student, and others
(e.g., a school psychologist or other specialist) develop a written plan that
includes academic and functional goals and objectives, the student’s
strengths, and possible accommodations to help the student succeed. On-
going meetings occur to discuss the student’s progress, and the plan is
updated at least yearly. If the student is determined ineligible for an IEP,
he or she may request a 504 plan, which has less restrictive eligibility re-
quirements and includes opportunities for accommodations and services
to enhance learning and school performance.
Postsecondary Education
The IPS specialist helps the young person identify a course of study
based on the young person’s ideas about careers. How does the career
choice fit with the person’s interests, strengths, and preferred work en-
vironment? The IPS specialist can help the young person meet people
working in the field, observe them working, and interview them about
their job. What do they like about the work? What skills are needed?
Young people need to consider their options carefully. Making deci-
sions about which classes to enroll in after high school is important be-
cause time and financial resources are invested in education. The IPS
specialist helps the young person identify possible universities or com-
munity colleges, visit the schools, and learn about financial alternatives
to pay for school and can accompany the young person to appoint-
ments with guidance counselors and academic advisors. IPS specialists
are flexible when working with young people and understand that
changing directions is normal for most young people.
The IPS specialist coaches the young person about college applica-
tions, which are typically online, and may accompany the young person
to meetings with financial counselors and help with federal student aid
applications if financial support is needed. The IPS specialist helps the
young person with class registration and discusses the course load. Many
young students are eager to take a full course load, but starting with a re-
duced course load allows the person who has been away from school for
an extended period to adjust to the student role. Students who experience
onset of psychosis in high school or college may use a reduced course
load to support staying in school. Student support groups such as Stu-
dents With Schizophrenia (www.sws.ngo) may also be helpful.
Providing Education Supports

The IPS specialist and the student develop an education plan, which
outlines the student’s goals and steps to achieve the goals. Because
many young people complain of poor attention, the team should focus
on ways to optimize cognitive function to support learning by address-
ing medications, substance use (see Chapter 14), exercise (see Chapter
15, “Role of Aerobic Exercise in the Treatment of Early Psychosis”), nu-
trition, cognitive skills training, and technology supports (see Chapter
20, “Using Technology to Advance Early Psychosis Intervention”). The
team helps the student identify stressors, individualized coping tech-
niques, and potential accommodations. Other members of the team as
well as family members support the student and provide encourage-
ment, and family members are reminded to refrain from having high
expectations too soon.
IPS specialists ensure that students have a system for keeping track
of homework assignments and test dates and may suggest using a cal-
endar to keep track of due dates as well as time devoted to completing
homework. They help students develop good study skills and an indi-
vidualized plan for learning. For example, a student who has difficulty
with concentration may plan to focus for 15 minutes, take notes, and
take a break. The student and IPS specialist discuss places to study that
will minimize distractions. Postsecondary schools have offices for stu-
dents with disabilities where students who have disabilities may re-
quest accommodations to help them succeed in school. Documentation
of the disability is required prior to receiving approval for an accommo-
dation. Examples of accommodations include extra time on tests; extra
breaks during classes; tutoring; permission to record lectures; preferen-
tial seating, such as sitting at the front of the room to minimize distrac-
tions; help with notetaking; extended deadlines for projects; and
receiving an incomplete grade to finish coursework late because of a
hospitalization. Additionally, an IEP from high school may carry over
to postsecondary education to address specific learning issues.
Supported Employment and

Supported Education
Case Example 3
Dwight is a 21-year-old who developed a psychotic illness during his
first year of college. He returned home and tried several jobs, but they
were short-lived because of arguments with his coworkers and supervi-
sors. Dwight joined an early psychosis program knowing that he would
have help with employment. He was introduced to the team’s IPS spe-
cialist, Nick, who asked him about his interest in work, previous work
experiences, schooling, how he spends his time, and other background
information. They discussed opportunities to use Dwight’s computer
skills and the possibility of taking a computer course at the local com-
munity college. Members of the treatment team also talked with Dwight
about his alcohol and marijuana use and the possible impact of this use
on work and school. Dwight and Nick identified several entry-level
computer positions and practiced job interviewing. At his second inter-
view, Dwight received a job offer. The job was a good fit for him, and af-
ter 4 months he registered for a computer course with Nick’s help.
Dwight was excited about building his skills to prepare for a more ad-
vanced computer job in the future.
The IPS specialist, other team members, and family support stu-
dents as they gain knowledge and skills to advance their careers. Young
people may take time off from school and return when they feel ready
to continue their studies. They may go back and forth between employ-
ment and education. For some young people, short-term certificate pro-
grams give them the opportunity to advance with technical skills. Each
young person makes decisions about how best to build his or her career
path as part of recovery from early psychosis.
Conclusion
People who work a job or take a class are moving forward in their re-
covery. The whole coordinated specialty care team supports their ef-
forts and continues to provide hope and support during difficult
periods. The team helps the young person learn from missteps at work
and/or school to improve his or her next experiences. For people with
early psychosis, work and school provide the opportunity to gain con-
fidence and control of their life. A major responsibility of coordinated
specialty care teams is to help people with early psychosis to experience
opportunity, develop their aspirations, and build successful careers.
Employment and education are central areas to address in supporting
young people with early psychosis in achieving recovery.
KEY CONCEPTS
• Work and school are important to young adults in early
psychosis.
• Early psychosis programs engage young adults in employ-
ment and school using a strengths-based approach.
• Family members are included in supported employment
and education to expand support.
• Key elements of supported employment and education
include a team-based approach, developing an employ-
ment and/or education plan, conducting an individualized
search, providing supports, and advancing careers.
• All members of coordinated specialty care teams support
people in work and school as part of their care.
1. Why are work and school important to young adults with

early psychosis?
2. How might the vocational and education needs of a teenager

with attenuated psychosis syndrome differ from those of a
young adult with schizophrenia?
3. How might you help a young person who has unrealistic

school goals? How might you help a young person who has
no job experience?
4. How might you help a young person who uses marijuana

and wants to seek employment?
Suggested Readings
Bond GR, Drake RE, Luciano A: Effectiveness of individual placement
and support for young adults. Epidemiology and Psychiatric Ser-
vices 24(5):446–457, 2015
Corrigan PW: The disabling effects of mental illness on my education.
Psychiatr Serv 69(8):847–848, 201829716448
Di Capite S, Upthegrove R, Mallikarjun P: The relapse rate and predic-
tors of relapse in patients with first-episode psychosis following
discontinuation of antipsychotic medication. Early Interv Psychia-
try 12(5):893–899, 201827734591
Dixon LB, Goldman HH, Bennett ME, et al: Implementing coordinated
specialty care for early psychosis: The RAISE Connection Program.
Psychiatr Serv 66(7):691–698, 201525772764
Kane JM, Robinson DG, Schooler NR, et al: Comprehensive versus usu-
al community care for first-episode psychosis: 2-year outcomes
from the NIMH RAISE early treatment program. Am J Psychiatry
173(4):362–372, 201626481174
References
de Waal A, Dixon LB, Humensky JL: Association of participant preferences on
work and school participation after a first episode of psychosis. Early In-
terv Psychiatry 12(5):959–963, 2018 29052948
Drake RE, Bond GR, Goldman HH, et al: Individual placement and support ser-
vices boost employment for people with serious mental illness, but funding
is lacking. Health Aff (Millwood) 35(6):1098–1105, 2016 27269028
Maraj A, Mustafa S, Joober R, et al: Caught in the “NEET trap”: the intersection
between vocational inactivity and disengagement from an early interven-
tion service for psychosis. Psychiatr Serv Feb 5, 2019 [Epub ahead of print]
30717644
Marshall T, Goldberg RW, Braude L, et al: Supported employment: assessing
the evidence. Psychiatr Serv 65(1):16–23, 2014 24247197
Swanson SJ, Becker DR, Bond GR, et al: The IPS Supported Employment Ap-
proach to Help Young People with Work and School: A Practitioner’s
Guide. Lebanon, NH, IPS Employment Center at the Rockville Institute,
2017
CHAPTER
17
Implementing Peer Support

in Early Psychosis Programs
Megan Sage, M.S.W., LCSW
Tamara Sale, M.A.
Nybelle Caruso, B.S., PSS
Michael Haines, QMHA, PSS
Ryan Melton, Ph.D.
Ally Linfoot, PSS
ALTHOUGH professional peer support has not traditionally been

a part of all early psychosis programs, it is rapidly evolving as a core
discipline within early psychosis teams. Fortunately, this addition is in-
formed by a large history and thriving peer support movement. Peer
support specialists play essential roles in all aspects of program service
delivery and decision making, and effective inclusion of peer support
helps organizations to become truly recovery oriented. The combina-
tion of lived experience as a source of relevant knowledge along with
scientific inquiry enables early psychosis programs to create more effec-
tive, humane, and relevant responses to their participants.
Marcus’s Story
Our story begins with Marcus, a peer support specialist in the local
early psychosis program, as he makes a presentation for Mental Health
295
Awareness Week at the local library. As part of the presentation, Marcus

shares his own story:
For a long time, I was hallucinating and was caught up in my own be-
liefs, and no one really helped me. I was homeless for a while and wan-
dering the streets. I was arrested and put in jail. But once I found a team
of people who were kind and understood what I was going through, I
was able to recover. The turning point for me was meeting a peer sup-
port specialist at the hospital. I thought I was all alone and that there
was no hope for me or my future. I was grieving over being broken and
everything I had lost. The peer support specialist shared that he had had
similar experiences and feelings, that someone else had told him that
sometimes others must hold on to your hope for you. He said that step
by step, he had found his way from there to a very good place, a place
where he felt stronger and wiser for his struggles. He expressed confi-
dence that I would get there too. I had been told that I would never work
and that I had a lifelong condition, but his words allowed me to begin
to trust and to try, step by step, to get my life back. And I did. Three
years ago, I got married. I graduated from college. I realized that I could
help people as much from my own lived experience as from any theory,
so I became a peer support specialist myself. The people I meet every
day are remarkable—they are scientists, artists, musicians, researchers,
teachers, writers. They’re sensitive, honest, humorous, creative. They
teach me so much. If you have ever been told that psychosis is a condi-
tion you can never get over, you have been told wrong. With the right
support and people who believe in you, the experience of psychosis can
create greater awareness, compassion, and understanding. But when
you experience it, you feel like the only one. It’s our job to make sure no
one is left feeling alone.
History of Peer Support in Early

Psychosis
Marcus’s story is reflective of the broad history of peer support. Peer
support is an emerging field with increasing evidence of its effective-
ness (Chinman et al. 2014) and has a long history with a growing body
of research, spanning cultures and health care conditions (Tang 2013).
One study (Davidson et al. 2012) compared individuals in hospital set-
tings who received care as usual with those who received care as usual
and support from a peer recovery mentor. This study demonstrated
“statistically significant main findings for the number of hospitaliza-
tions and the number of days spent in the hospital, with participants as-
signed recovery mentors doing significantly better than those without
a recovery mentor” (Davidson et al. 2012, p. 125). Other findings from
this study concluded that participants assigned a peer recovery mentor
experienced a “significant decrease in substance use,” as well as a “de-
Implementing Peer Support in Early Psychosis Programs 297
crease in depression and increases in hope, self-care, and a sense of

well-being” (Davidson et al. 2012, p. 125).
The peer support movement in the United States arose alongside
other civil rights movements in the 1960s and 1970s, including the Inde-
pendent Living movement, which brought civil rights to individuals
with a range of disabilities (Deegan 1992). Many leaders in the mental
health peer support movement have stories of profound indignities and
injustices: being ignored until they were held against their will and
forced into demeaning and harmful care or being told that they were
unemployable, that their hopes and ambitions were not realistic, that
their actual truths were delusional, or that they should expect to be dis-
abled for life.
Historically, despite negative attitudes and beliefs in the larger soci-
ety, individuals with psychosis found their way to recovery because of
their own resilience, the caring of people who believed in them, and
mental health clinicians who had positive attitudes despite the system
barriers they faced. As individuals with lived experience found each
other, they began to recognize the importance of working through their
trauma regarding the injustices they experienced as consumers. They
also recognized and advocated for the idea that recovery exists, is
achievable, and does not necessarily require an absence of all symp-
toms. By creating local informal support networks and alternatives de-
veloped and delivered by peers, leaders in the consumer movement
(also known as the psychiatric survivor movement) provided informal
support systems and began to challenge pathology-driven practices.
They focused on supporting the person in a holistic healing and growth
process in the community (Mead 2003). Individuals with lived experi-
ence have played central roles in advocating for change and have won
formal systemic recognition that recovery exists and is achievable, as
well as highlighting the importance of peer support as a core element of
care (Frese and Davis 1997).
Family peer support emerged in the United States in the 1970s as a
result of many of the same injustices, although family members’ per-
spectives were different as they struggled to find help for their loved
ones. During that time, families were commonly told, “There’s nothing
we can do until he’s an imminent threat to himself or others.” Much of
the early family peer support movement focused on basic concerns for
survival, safety, and access to services for loved ones and was a reaction
to predominant theoretical models that held that families caused
schizophrenia. Family members of loved ones with mental health diag-
noses largely embraced the medical model and the treatment system,
whereas advocacy by the individual consumer movement focused on
the system’s coercive injustices and dehumanizing approach to care.
Ultimately, both the individual and family peer support movements
were fueled by recognition of and belief in each person’s importance
and capabilities. According to the College for Behavioral Health Lead-

ership Peer Services Toolkit, the peer support movement has “contin-
ued to evolve to connect people to their communities, and offer
information on rights, advocacy, services and supports, recovery, and
whole health” (Hendry et al. 2014, p. 11).
Since the 1990s, peer support has become mainstream both for its in-
formal community role and as a professional discipline that is widely
viewed as a central element of effective community-based treatment.
Peer support specialist services are currently considered best practice
by the Substance Abuse and Mental Health Services Administration,
are available in all 50 states, and are reimbursable by Medicaid in 35
states (www.mentalhealthamerica.net/peer-services). Peer support
certification programs have been developed in most states and nation-
wide to allow for billing, with careful attention to ethical consider-
ations, supervision, and training needs. Earlier models of early
psychosis intervention did not include professional peer support as an
identified element. However, with an emphasis on feedback and partic-
ipatory decision making, along with advocacy, many early psychosis
programs now include individual and, to a lesser degree, family peer
support within their coordinated specialty care teams (Jones 2015;
Thurley et al. 2014).
Core Roles and Attributes of

Peer Support
Peer support is based on nonhierarchical sharing of common experi-
ence not defined by clinical language or concepts. Individual peer sup-
port specialists are receptive to the individual’s viewpoint without
predetermined clinical assumptions. They support the individual in
making meaning from his or her own reality and supporting construc-
tive assertion of power. They refrain from participation in diagnostic
decision making and decision making related to involuntary care, ex-
cept as an advocate for the individual and family (Mead 2003; Mead et
al. 2001). Peer support can occur in any setting (e.g., outpatient, crisis,
hospital, employment, housing) and may incorporate a broad range of
foci, including mental health recovery, medical wellness, and commu-
nity integration.
Peer support specialists have the unique role of being able to relate to
individuals on a personal level and address fears, confusion, uncertainty,
and/or anxiety about receiving mental health services. They are non-
judgmental, try not to overreact, and remain attuned to the perspective of
the person with whom they are working. In the words of one peer sup-
port specialist, the role is to be “endlessly curious about their client’s
thoughts, activities, values and worldview. They remain ‘unimpressed’
when meeting a highly symptomatic client, thereby providing accep-

tance, understanding, encouragement and normalization. They are
equally unimpressed when a previously symptomatic client ‘clears.’”
(T.Casebeer, personal communication, March 2018). In other words, the
individual is fully accepted as an important and interesting person
whose point of view matters regardless of his or her mental state.
Peer support specialists on early psychosis teams contribute to all
aspects of care and treatment and emphasize that individuals are not
defined by their diagnosis or symptoms. They offer a point of view that
is holistic and focuses on the individual’s beliefs, culture, and values.
As a current early psychosis peer support specialist stated, “They know
from life experience that no one can be reduced to a particular set of
symptoms or a diagnosis” (T. Casebeer, personal communication,
March 2018).
In contrast to individual peer support specialists, family peer sup-
port specialists partner with family members and their support systems
throughout the assessment process to provide education and informa-
tion specific to their needs. Both individual and family peer support
specialists focus on helping individuals discover and build on their per-
sonal resources and strengths and feel empowered to make the changes
they desire. As noted by a current peer support specialist, “Many peo-
ple will respond well to an interaction with a peer that is driven by in-
tention to create a human connection, give the person space to be heard
in a nonjudgmental manner, and to lessen power imbalances as much
as possible. A person told me they liked working with peers because we
never told her what to do; we just listened” (N.Caruso, personal com-
munication, March 2018).
Peer support specialists play a vital role in shared decision making.
They encourage individuals to learn about the multiple treatment op-
tions available to them within the program, understand the pros and
cons, and collaborate with their team and support system to decide
what option is best for them individually. They rely on their own lived
experience and practical knowledge to support the individual in mak-
ing informed decisions about the most appropriate and helpful treat-
ment for them. Peer support specialists and other members of the team
work with individuals to understand their preferences and what is im-
portant to them on the basis of their goals. As noted by a current peer
support specialist, they “act as a subtle stimulus for their clients’ self-
actualization” (T.Casebeer, personal communication, March 2018). Peer
support specialists assist individuals in weighing benefits and risks
with regard to decisions about changing jobs, starting medication or
switching to a different medication, or moving out of their parents’
home to live on their own.
Peer support specialists safeguard the importance of individuals be-
ing heard by others and of making their own decisions and choices on the
basis of the information that they have regarding risks and benefits, while
remaining actively concerned for the person’s safety and well-being.
Family peer support specialists help family members understand and
express their own values and concerns, as well as navigate differences
in perspective and decisions by their loved ones. Individual peer support
specialists can also be helpful in encouraging parents to allow their young
person a certain amount of space for risk taking, and family peer support
specialists can provide a different point of view for young people as well
as help them navigate developmental changes within family roles.
Individual and family peer support specialists also play a critical
role in engaging individuals and families in psychoeducation and in de-
livering these interventions with a focus on empowerment. Peer sup-
port specialists engage with the individual, listen, and “allow their
clients a place to unroll and explore their story/experience and share
aspects of their own life history where relevant” (T.Casebeer, personal
communication, March 2018). They use their own lived experience to
share information on multiple topics, including but not limited to cop-
ing skills, relationships, communication, normalization of grief related
to experiencing symptoms, medications, self-advocacy, treatment op-
tions, typical adolescent and young adult development, substance use,
legal rights, benefits, relapse prevention, and early and late stages of re-
covery. Individual psychoeducation is tailored to the person’s values,
needs, and goals. Peer support specialists share their own lived experi-
ences within these topic areas from a strengths-based perspective that
focuses on recovery. Their perspective allows individuals to hear mes-
sages of hope and to understand that the recovery process can vary and
is not linear.
Marcus Meets William

Denise, who attended the early psychosis community education event
at the public library where Marcus was a presenter, calls the program
because of her concerns about her boyfriend, William. William is a 23-
year-old African American young man who has become fearful that oth-
ers are trying to hurt him, is disorganized, and is unable to go to his job.
As a result, William was fired. He has been sleeping throughout the day
and staying up all night. He told Denise he thinks she can read his
thoughts, and he has started talking to himself. Denise is fearful to leave
him alone at home but must get to her full-time job to pay the bills. Wil-
liam and Denise have been living together for 2 years and have a small
dog named Mac.
Denise arranges for Marcus and Sadie, the early psychosis interven-
tion screener, to visit their home and meet William. An initial conversa-
tion with Denise and William identifies William’s many strengths.
William is a high school graduate who has been studying to enter med-
icine. He loves animals and has continued taking Mac out for walks on
days when he feels safe in the neighborhood. William reports that listen-
ing to music sometimes helps him feel better. William’s grandparents

live in the area and have some intermittent contact with him. William is
willing to talk but does not want to sign any paperwork to receive ser-
vices through the early intervention program. He does not understand
why no one else can see that he is being followed when he leaves the
home and does not see a reason for mental health treatment. He ex-
presses concern that he is being watched by the police and worries
about his safety. He and Denise argue frequently, and William expresses
frustration that no one believes that what he is experiencing is real. Wil-
liam’s sleep has been worsening. He spends most of his time isolated in
the basement, listening to music or playing video games.
During the home visit, Marcus listens nonjudgmentally and empa-
thetically, and he and William connect over a similar taste in music. Wil-
liam sets up another appointment with Marcus to listen to music together
the following day. In the meantime, Marcus, Sadie, and other early inter-
vention team members provide education and information about symp-
toms of psychosis to Denise. Shameka, the early intervention family peer
support specialist, sets up an appointment to meet with Denise later that
week, in which she shares her own experiences as the mother of a young
woman who developed symptoms of psychosis. Shameka speaks to the
unique challenges in supporting a loved one who is struggling while at
the same time addressing one’s own self-care and personal needs.
Shameka assists Denise in coming up with ideas about how to reduce her
own stress levels and how she can get her own support.
William and Marcus meet a couple more times at William’s home,
and Marcus discusses his own past struggles with paranoia and diffi-
culty sleeping and talks about what has been helpful to him. Marcus is
open about his own path to finding understanding and recovery.
Through multiple conversations, William begins to feel less anxious
about leaving the house and agrees to sign paperwork to engage in on-
going services with the early intervention team. William and Denise
work with Marcus, Shameka, and William’s primary clinician, Miranda,
to come up with strengths-based, recovery-oriented treatment goals.
Denise notes that the support of the team has helped to reduce conflict
between her and William and increase their positive communication.
William’s most pressing goal is that he wants a job but is unsure if
he will be able to keep the job because he was fired previously for not
showing up to work. Marcus empathizes with William around this con-
cern and says that he and his team members will support William in get-
ting a job as well as keeping a job once he is hired. He and William meet
with the supported employment specialist, Jorge, to talk about what
type of job William may be interested in and to discuss the pros and cons
of different work environments and schedules.
William is frightened of taking medications and fearful of being put
in the hospital against his will. He is reluctant to talk to the psychiatrist,
Louise, but is more comfortable being open with Marcus. Marcus empa-
thizes, reminds William about the shared decision-making process, and
helps William think through his goals and fears. Marcus and William
meet with Louise together. William is surprised that Louise shares an in-
terest in some of his favorite musical artists and is easier to talk to and a
more receptive listener than he had expected. He decides to try a low
dose of antipsychotic medicine.
As time goes on, William participates in treatment and periodically
confides in Marcus about decisions he is making and things that are
bothering him. He continues to express concern that the police are
watching him and fears being harmed by police when he leaves home.
Marcus helps William express this concern to the team. This leads to a
broader discussion about times in the past when William felt he was tar-
geted by police on the basis of his race, and the whole team engages
with Denise, William, and William’s grandparents about this topic. Wil-
liam feels it would be helpful to check out his feelings of being targeted
with Denise, Marcus, his grandparents, or other team members when he
feels this way. Marcus and the rest of the early intervention team view a
person’s symptoms through a social and cultural lens, paying attention
to their individual experiences and how they make sense of these expe-
riences. As a result, the team and William’s loved ones agree that Wil-
liam’s feelings of being targeted by police might not be related to his
symptoms of psychosis and might be based in reality.
With Marcus’s help, William feels more and more comfortable ex-
pressing his perspectives and needs to the team and advocating for him-
self. Marcus encourages William to participate in opportunities to share
his perspective, such as a focus group about how to improve the program.
Marcus invites William to attend a meet-up group in the community and
offers to attend the group with him. He also offers to connect William to
an advocacy group that meets monthly, which William says he will think
about. He likes the idea of working with others to improve services for
young people and has gained confidence in his ability to speak with oth-
ers about his own experiences through his work with Marcus.
Defining “Peer” in Early Psychosis

Programs
Just as with all roles in early psychosis intervention teams, peer support
services must be modified to address the unique developmental and
cultural needs of adolescents and young adults. One active debate is
whether peer is defined by experience of psychosis or other mental
health condition, age, or some other criterion such as prior participation
in community mental health services. The experience of psychosis is
different from other mental health conditions, and an individual whose
lived experience does not include psychosis may not be as able to relate
to individuals who are experiencing this condition as would an individ-
ual who has experienced psychosis. However, even when individuals
have experienced psychosis, in their training and practice they must
recognize that experiences are widely variable and that there is no sin-
gle “right” answer.
The optimal combination for peer support specialists working in

early psychosis intervention programs likely includes mentoring and en-
gagement by individuals with some psychosis experience, as well as the
ability to relate to individuals developmentally. Many of the challenges
faced by individuals in early psychosis programs relate to normal devel-
opmental changes associated with changing roles and relationships,
emergence of an adult identity, and increased pressure to learn new skills
and take on adult responsibilities. Thus, peer support may also focus on
the developmental challenges and tasks of being a young adult.
Peer support specialists also play a significant role in the transition
process as individuals prepare for discharge from early psychosis inter-
vention services. Through their participation in mental health services,
individuals often become interested in continuing in advocacy work af-
ter they complete the program. Peer support specialists help individu-
als identify their strengths and build on them to tell their stories and
practice receiving feedback in a safe and supportive environment. Peer
support specialists are key in assisting individuals in creating and revis-
ing personal wellness or relapse prevention plans and building their
support networks. They connect individuals and families with oppor-
tunities for continued engagement as graduates of the early psychosis
program, as well as opportunities to explore other informal and formal
prospects outside the program. In addition, they act as role models for
those who want to become peer support specialists themselves.
Creating an Environment Conducive

to Peer Support
The peer support core values and practices of nonjudgment, empathetic
listening, reciprocal learning, consciousness of the dynamics of power,
advocacy for voice and rights, and fundamental belief in each person
challenge and infuse clinical cultures with a more humanistic, positive
way of thinking and operating. It is important for clinicians, adminis-
trators, and policy makers to understand the unique history, values,
and approach of peer support to facilitate rather than diminish its im-
pact. In addition, authentic inclusion of peer support often involves
profound and personal rethinking of explicit and implicit biases, nega-
tive assumptions, reactivity to symptomatology, and overly medical-
ized and pathologizing approaches to care. When peer support on early
psychosis intervention teams is done well, it can transform a team’s un-
derstanding and capacity to engage with and support the individuals
and family members it serves.
Peer support certification curricula and job descriptions sometimes
leave out the values and principles of peer-developed peer support
(Kaufman et al. 2016; Penney 2018). Negative attitudes and clinical cul-
tures within existing care systems that do not align with the principles
of peer support jeopardize the discipline (Stastny and Brown 2013).
Thus, it is important to focus on maintaining the integrity of peer support
at all levels of conceptualization, implementation, decision making, and
practice and to proactively educate policy makers, administrators, clini-
cians, and other staff about the core principles and practices of peer sup-
port. Supervision should support a careful thought process around
intentional self-disclosure. Other team members should be conscious
of, and challenge, statements and assumptions that might suggest that
individuals and/or families experiencing psychosis are somehow “less
than” others.
It is also very important for early psychosis intervention teams to
understand and value the peer support role and not assign tasks that
minimize or are inconsistent with their role. An example of this would
be looking to the peer support specialist on a team as a transportation
provider outside his or her typical peer support role. As a current peer
support specialist notes, it is important for peer support specialists “not
to be assigned case management tasks that involve doing anything for
the person rather than with them. For example, I would not set up an
intake for an individual on my own accord like a service coordinator
might. But as a peer I would sit with the person while they call on
speakerphone and give as much support in making that intake as they
request” (N.Caruso, personal communication, March 2018).
Agencies must create a structured way to involve individuals in re-
covery to participate meaningfully in agency operations, such as clinical
decision making, staff hiring and training, community education, quality
improvement, and oversight. Peer support specialists work together with
individuals and families receiving early psychosis services and in a mu-
tually beneficial relationship to give voice to individuals’ lived experi-
ences in order to create change within the mental health system. Peer
support specialists assist individuals in their recovery by identifying pos-
sible barriers to participation and using problem-solving strategies with
the individuals and team to address those barriers. Peer support spe-
cialists act as a connection for individuals to participate in educational,
vocational, or community activities. As noted by a current peer support
specialist, “sharing experiences and insights are a fantastic way to learn
from one another, and ultimately, progress to advocating together for
better mental health services in the future” (N.Cohrs, personal commu-
nication, March 2018).
Conclusion
Full integration of peer support specialists into early psychosis inter-
vention treatment teams is based on a clearly defined peer support
model. Peer support is a transformative and highly effective strategy

for improving engagement, relevance, and outcomes. Peer support is
highly aligned with core concepts of first-episode psychosis care, such
as resilience, partnership, recovery, and shared decision making. The
peer support field continues to grow in available knowledge, training,
and effectiveness, and it holds an important key to the future of the
early psychosis field.
KEY CONCEPTS
• Peer support is a distinct role with its own history grounded in
social justice, intentional community, and belief in recovery.
• Peer support follows the principles of nonhierarchical reci-
procity; listening; learning and exploring together; and advo-
cating for the individual’s rights, voice, and self-determination.
Individual and family peer support emerged through sepa-
rate but interrelated histories and brings different perspec-
tives to recovery. Professional peer support is increasingly
understood as a core element of early psychosis treatment.
• Peer support provides a bridge between the individual and
clinical team in all aspects of treatment. Peer support is
transformative in nature and, when embraced, may lead to
a deep shift in understanding, language, and practice
within early psychosis teams as well as the larger organiza-
tion providing treatment.
• To fully embrace the peer support role, it is important for
all members of early psychosis teams to value lived experi-
ence as an important source of knowledge and become
comfortable with strategic self-disclosure. Teams must
intentionally cultivate positive cultural norms that chal-
lenge language, assumptions, and practices that are dis-
criminatory and/or negative.
• As with other members of the treatment team, training,
supervision, and mentoring, along with pay equity and
opportunities for career advancement, are of critical
importance to individuals in professional peer support
positions.
1. How does the concept of peer support services change the

conversation around mental health treatment in a broad
sense?
2. How does integrating peer support services change the role of

clinicians, medical staff, and other treatment team members?
3. How would you collaborate with individual and family peer

support specialists in your role as part of a treatment team?
4. What are your ideas about how early psychosis teams can
foster nonhierarchical collaborative learning?
5. What do you see as the role of story and self-disclosure in

your own practice? How might the context, philosophy, and
practices of peer support influence your practice?
Suggested Readings
Caughey M: Creating deep democracy through peer wellness services.
Global Journal of Community Psychology Practice 5(1):1–17, 2014
Center for Practice Innovations at Columbia Psychiatry: OnTrackNY
Peer Specialist Manual. New York, OnTrackNY, February 2017.
www.ontrackny.org/portals/1/Files/Resources/Peer%20Specialist
%20Manual%20Final%202_17.17.pdf?ver=2017-04-04-063602-080.
International Association for Peer Supporters: National Practice Guide-
lines for Peer Supporters. Norton, MA, International Association
for Peer Supporters, 2012. Available at: https://na4ps.files.word-
press.com/2012/09/nationalguidelines1.pdf. Accessed February
22, 2019.
Mead S, Hilton D, Curtis L: Peer support: a theoretical perspective. Psy-
chiatric Rehabilitation Journal, 25(2):134–141, 2001 11769979
References
Chinman M, George P, Dougherty RH, et al: Peer support services for individ-
uals with serious mental illnesses: assessing the evidence. Psychiatr Serv
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Davidson L, Bellamy C, Guy K, Miller R: Peer support among persons with se-
vere mental illnesses: a review of evidence and experience. World Psychia-
try 11(2):123–128, 2012 22654945
Deegan PE: The independent living movement and people with psychiatric dis-
abilities: taking back control over our own lives. Psychiatr Rehabil J 15(3):3–
19, 1992
Frese FJ, Davis WW: The consumer-survivor movement, recovery, and consumer
professionals. Prof Psychol Res Pr 28(3):243–245, 1997
Hendry P, Hill T, Rosenthal H: Peer Services Toolkit: A Guide to Advancing and
Implementing Peer-Run Behavioral Health Services. Albuquerque, NM,
College for Behavioral Health Leadership, 2014
Jones N: Peer Involvement and Leadership in Early Intervention in Psychosis
Services: From Planning to Peer Support and Evaluation. Alexandria, VA,
National Association of State Mental Health Program Directors, 2015.
Available at: www.nasmhpd.org/sites/default/files/Peer-Involvement-
Guidance_Manual_Final.pdf. Accessed February 1, 2018.
Kaufman L, Kuhn W, Stevens Manser S: Peer Specialist Training and Certifica-
tion: A National Overview. Austin, TX, Texas Institute for Excellence in
Mental Health, 2016
Mead S: Defining Peer Support. West Chesterfield, NH, Intentional Peer Sup-
port, 2003. Available at: https://docs.google.com/document/d/1WG3ul
nF6vthAwFZpJxE9rkx6lJzYSX7VX4HprV5EkfY/edit. Accessed February
8, 2018.
Mead S, Hilton D, Curtis L: Peer support: a theoretical perspective. Psychiatr
Rehabil J 25(2):134–141, 2001 11769979
Penney D: Defining “Peer Support”: Implications for Policy, Practice, and Re-
search. Sudbury, MA, Advocates for Human Potential, 2018. http://
ahpnet.com/AHPNet/media/AHPNetMediaLibrary/White%20Papers/
DPenney_Defining_peer_support_2018_Final.pdf. Accessed February 22,
2019.
Stastny P, Brown C: Peer specialist: origins, pitfalls and worldwide dissemina-
tion [in Spanish]. Vertex 24(112):455–459, 2013 24511563
Tang P: A Brief History of Peer Support: Origins. Chapel Hill, NC, Peers for
Progress, 2013. Available at: http://peersforprogress.org/pfp_blog/a-
brief-history-of-peer-support-origins. Accessed February 8, 2018.
Thurley M, Monson K, Simpson R: Youth Participation in an Early Psychosis
Service. Melbourne, Australia, Orygen Youth Health, 2014
CHAPTER
18
Family Intervention and

Support in Early Psychosis
A robust body of research suggests that specialized treatment pro-

grams for first-episode psychosis (FEP) can improve clinical and func-
tional outcomes (Bird et al. 2010; Kane et al. 2016). These treatment
programs typically comprise both pharmacological and psychosocial
components, including a family support intervention. Bolstering sup-
port for families may be an especially valuable aspect of care in non-
affective FEP because the distress, worry, and confusion experienced
by the loved ones of an individual with FEP are well documented (Jansen
et al. 2015). Furthermore, caregiver burnout may be a particular risk in
early psychosis (Onwumere et al. 2018) and can undermine participant
support. Unfortunately, lack of family support (Jones et al. 2017) and/or
relatives’ expression of their distress, concern, and dissatisfaction (high
expressed emotion) (Alvarez-Jimenez et al. 2012) are associated with
negative early treatment outcomes. In light of these findings, it is perhaps
not surprising that there have now been several published reviews and
meta-analyses confirming the benefits on the participant and relative FEP
outcomes of offering family support and education (Bird et al. 2010).
Because schizophrenia and bipolar illness usually develop during ad-
olescence or young adulthood, many individuals diagnosed with the dis-
order still rely on their families of origin for their primary social support
as they become ill. Young people diagnosed with these disorders often fail
to achieve developmental milestones (e.g., graduating from high school or
college, getting a first job, moving out of the parental home) in a timely
309
manner. This “offtimedness” often extends the period of the individual’s

dependence on his or her relatives and places an additional burden and
stress on the family. Relatives are often worried and confused by illness-
related behavior changes and developmental lags. They may not immedi-
ately recognize the presence of a mental illness or may refuse to believe
that the illness is present even when it is brought to their attention. Family
interventions can play a key role in helping these relatives cope success-
fully with the illness and support the recovery of their loved one.
It is important to think broadly about family member inclusion in re-
covery from FEP. Although most FEP materials highlight the involve-
ment of parents or guardians, other kin are also important. Some
individuals with psychosis marry or enter conjugal-like relationships,
and thus their partners may be the key relatives to engage in the FEP
program. Not surprisingly, the stresses of living with a serious psychi-
atric illness can have a profound impact on a couple, and rates of sepa-
ration and divorce are higher in couples in which one person has been
diagnosed with schizophrenia (Thara and Srinivasan 1997).
The needs and value of including siblings in care should also be con-
sidered. The development of a psychosis in a brother or sister can be
very troubling. Furthermore, in many families, when the psychosis de-
velops, much (if not all) of the parental nurturance goes into supporting
the ill child, and there is less focus on the other children. Sports events
are missed; there is less time to help with homework; vacations get can-
celed. Siblings often experience the loss of the brother or sister as they
have known him or her and the loss of their parents’ attention and guid-
ance. Sibling involvement in an FEP family education program pro-
vides a forum for answering siblings’ questions, validating their sense
of loss, and encouraging their continued development. It can also be a
useful tool to engage siblings in supporting the person’s recovery.
In this chapter, we present the overall principles and strategies for
involving families in FEP treatment. We discuss consent and confiden-
tiality issues first, then review the optimal credentials and characteris-
tics of an effective FEP family clinician. We then discuss the components
of a comprehensive FEP family intervention, incorporating a stepped-
care approach, and follow with a brief case description. We conclude
with a review of key points, relevant questions to consider when devel-
oping a local family FEP program, and helpful resources.
Principles and Strategies for Involving

Relatives in Treatment of First-Episode
Psychosis
There is a robust literature confirming the benefits of involving family
members in the care of individuals diagnosed with long-standing psy-
Family Intervention and Support in Early Psychosis 311
chotic disorders (Lyman et al. 2014), so it is not surprising that many

clinical research groups have designed and implemented family inter-
vention programs as part of their FEP programs. Unfortunately, signif-
icant design differences across studies render identification of the
optimal FEP family program among these variants difficult. For one
thing, the centrality of the family intervention to the overall FEP pro-
gram often determines who actually is enrolled in the program. Partic-
ipants who do not have consenting family members may not be eligible
for an FEP program with a strong family emphasis. In addition, family
interventions themselves also often differ substantially in structure. For
example, both multifamily and single-family interventions have been of-
fered. In light of these variations, it is currently impossible to conclude
that one particular family intervention is preferable to another—the char-
acteristics of the FEP program, as well as the participating individuals’
and relatives’ needs and preferences, will all likely dictate parameters of
the specific family intervention offered at a particular site. The critical
point is that some type of a high-quality family intervention should be available
in every FEP program.
Addressing Consent and

Confidentiality Issues
Individuals with FEP are typically young; most programs serve popu-
lations ranging from midteenage years to mid to late thirties. These
transitional-age individuals may legally be minors or adults, but even
those who are adults are often still dependent on their relatives for
meeting their instrumental and affiliative needs. A small percentage
will be married or in conjugal-like relationships.
Negotiating consent for family involvement in care and establishing
guidelines around sharing information among family members is often
accomplished easily with individuals with FEP, although it can sometimes
become complicated. Some individuals will be minors, and their parents
or another responsible adult will be able to consent to their treatment and
have access to their medical information. In addition, as will be discussed
more fully below, many participants, even those of legal age, are brought
to these programs by a family member, often a parent, and the participant
will often readily consent to involving his or her family in care.
A small subset of individuals with FEP will be reluctant to have their
relatives involved in their care, and some will outright refuse consent to
do so. There are many possible reasons for this: the young person may
be estranged from his or her relatives or may be suspicious of them, or
he or she may want to assert his or her independence. In considering
how to proceed, the FEP staff should carefully consider the unique cir-
cumstances of the individual and his or her family. There are certainly
understandable and reasonable circumstances that would make some-

one reluctant to have a family member involved in his or her treatment,
including a history of abuse or neglect. However, barring such negative
factors, particularly if the individual and relative reside together, in-
volving the relative in mental health care can be an invaluable resource
for recovery. If the individual-relative relationship is strong, a good FEP
family education program can render it stronger; if the relationship is
fractious or barely exists, a good FEP family education program can be
a mechanism for healing and bonding. It can be easy for a busy clinician
to immediately accede to a person’s reluctance to involve a family
member in care rather than view this as the beginning of a dialogue
about the issue; however, it is important to remember that most often,
the young person will have a relationship (good or bad as it may be)
with that family member long after ending participation in the FEP pro-
gram. Shoring up the relationship during FEP program participation
can be a critical aspect of recovery.
If the young person expresses reluctance to involve his or her family
in care on entry into an FEP program or if a minor withdraws consent
for family involvement when he or she turns 18 and the treatment team
sees value in encouraging reconsideration of the decision, the following
strategies may prove helpful.
1. Keep the topic open. After an initial refusal, the possibility of family
involvement can be raised again during treatment team meetings or
times of transition. An exacerbation of symptoms or a new opportu-
nity such as a job or return to school sometimes galvanizes people,
and they become open to trying new strategies; this can be a time of
family reengagement.
2. Use shared decision making to assure that the person with FEP thor-
oughly weighs the benefits and risks of family involvement in care.
Some young people will give an immediate negative response to a
request for family involvement in care because they want autonomy
and wish to assert their independence. They may not fully consider
the benefits of having the treatment team help them enlist their fam-
ily members in their recovery. Exploring with a trusted clinician the
potential benefits of family involvement in care can be useful in
making the decision of whether or not to involve family members.
3. Acquaint the young person with the benefits of family involvement
in care for the relatives. Some individuals are concerned about bur-
dening their relatives and thus are hesitant to ask them to come to
sessions. However, if the clinician describes the benefits for relatives
(e.g., having the opportunity to have their questions or concerns ad-
dressed, learning stress management), this sometimes helps the in-
dividual acquire some perspective on the relative’s concerns and
engenders interest in family involvement.
4. Consider a limited consent for release of medical information.

Young people with FEP are often willing to share some information
with their relatives (e.g., their treatment plan) but are less willing to
have information shared about other topics (e.g., sexual relation-
ships, drug use). As an opening strategy to involve families in care,
the FEP team can agree to these restrictions and then work with the
individual to modify the rules over time if they seem too constrict-
ing. Much of the assessment and initial family illness education can
be successfully accomplished without the clinician revealing inti-
mate details of the young person’s life.
Who Should Provide First-Episode

Psychosis Family Services?
Several members of the team are likely to interact with the relatives of
the young person with FEP. For example, relatives may have questions
about the young person’s medications that warrant a meeting with the
prescriber, or they may want to discuss substance abuse issues with
whoever on the team is addressing these issues. However, many FEP
programs find it most efficient to have the program director also as-
sume the designated role of family clinician. There are several reasons
for this delegation of duties. FEP program directors are typically re-
sponsible for program recruitment and often have the first contact with
the individual’s relatives. This early contact can serve as a foundation
for later family work. In addition, family work involves integrating as-
pects of all components of the FEP program, and the program director
is uniquely situated to accomplish this task. Finally, the director is often
the team member with a more advanced clinical degree—typically at
least a master’s degree—and is often a licensed clinician. Advanced
clinical training is essential because family work can be very compli-
cated. Just having several related individuals in a session makes it more
complex. With families, this can be even more thorny because the rela-
tionship history preceding the development of the psychosis as well as
current stress and symptom levels often color interactions in a negative
way; this can require clinical skill to navigate.
Components of a First-Episode
Psychosis Family Program
Some families make an accommodation to the development of psychosis
in a loved one with grace and acceptance; others struggle and may need
more support. A stepped-care approach has been suggested for family
work in FEP (Onwumere et al. 2011), and in fact this model was re-
flected in the design of the family component in the Recovery After an
Initial Schizophrenia Episode Early Treatment Program (RAISE-ETP;
Kane et al. 2016). The components of an FEP stepped-care model are
presented in Table 18–1.
TABLE 18–1. Stepped-care model of family intervention for recent-

onset psychosis
Interventions offered to all individuals with FEP and relatives (with the
individual’s consent)
Active engagement
Individual assessment of relatives
Brief illness education (group or individual)
Brief consultation
Access to the treatment team
Invitations to relatives to join treatment planning meetings
More intensive optional interventions tailored to specific family need
Multifamily support groups
Formal communication and problem-solving skills training
Referral for individual supportive psychotherapy for relatives
Abbreviation. FEP=first-episode psychosis.
Interventions Offered to Individuals and Relatives

ACTIVE ENGAGEMENT
As described in Chapter 6, “Engaging Families and Individuals in
Care,” case finding and engagement is often the most challenging task
in establishing an FEP program. Some individuals experiencing an FEP
may be reluctant or too distressed to seek treatment on their own, and
a first contact with a relative, rather than with the person with FEP, is
common during engagement in an FEP program. This contact often in-
volves an initial phone call or meeting with family members alone be-
cause the individual may still be in the hospital, may feel too ill or
distressed to join, or may see little need for help. Accommodating this
initial contact with relatives alone often stretches agencies that are used
to instituting the informal but frequently used rule “the individual has
to want help and must contact the agency himself or herself” as a re-
quirement for service entry. Nevertheless, given the high probability of
initial relative-only contact, it is incumbent on the FEP program director
or recruiter to become comfortable with discussing services and “pitch-

ing” the program to family members first.
In considering strategies for engagement in an FEP program, it is
important for the FEP program director or recruiter to consider likely
pathways to care. Because some individuals have had mental health
challenges long before they developed a psychosis, their family mem-
bers will already be familiar (at least in broad strokes) with how the
mental health system works, may already be clients of the agency, and
often comprehend the need for continuity and maintenance of care.
Other families will be new to the system and will need an overall orien-
tation on how services are organized and paid for, as well as the impor-
tance of sustained care. These families are typically facing an
unanticipated psychiatric crisis in their loved one, so they may be un-
derstandably distressed themselves and may require repeated exposure
to information. Finally, it is important to note that many FEP programs
are established in public or nonprofit mental health agencies but will of-
ten be recruiting individuals who are younger than age 26 and thus are
still covered under their parents’ private health insurance. These indi-
viduals may have been seeking care in the private sector prior to FEP
program entry; they may have little understanding of how the public
and/or nonprofit agency works and may have expectations that differ
from how the agency conducts business. This transition to a new, often
larger, and sometimes seemingly impersonal system needs to be han-
dled with tact and understanding.
Engaging the individual in care involves providing factual informa-
tion about the program as well as using motivational enhancement tech-
niques to counter what may be initial reluctance to enter an intensive
FEP program. Many potential program participants and their loved
ones may be eager to receive FEP services tailored to their unique
needs. Others may be less enthusiastic. Young people may demonstrate
reluctance to enter the program, and it is important to recognize that
family members may also be hesitant to support their loved one’s en-
rollment; use of motivational enhancement techniques may be import-
ant with them as well.
Families may be reluctant to support engagement in an FEP pro-
gram for many reasons. They may not believe the individual is ill or be-
lieve it is a transitory problem that will clear on its own. They may have
little concept of how mental health services work and may not immedi-
ately see the value of a specialized FEP program. They may have many
other burdens in their lives that they judge (often correctly) will inter-
fere with participation in the FEP program, or they may have their own
mental health challenges that interfere with help seeking. These are all
formidable obstacles to accessing care, and each one will require pa-
tience and empathy on the part of the FEP program director or recruiter
in these initial conversations.
In every meeting with the family, it is essential that the FEP staff con-
vey an attitude of hope and belief in the possibility of recovery. In initial
contacts with family members, the FEP program director or recruiter
must be prepared for either an enthusiastic or a more reserved family
reaction to the program. He or she must inquire about and listen carefully
to any concerns raised by either relatives or the person with FEP and be
equipped with an array of both practical suggestions and motivational
interviewing skills to address the issues raised by the individual and
relatives.
Cultural and ethnic considerations also play a role in family engage-
ment. There is a robust literature indicating that stressful life experi-
ences heighten risk for psychosis. Immigration can be a risk factor for
some (but by no means all) cultural groups, and institutional racism has
also been hypothesized to be a contributing factor. Thus, members of
minority groups are often overrepresented in samples of individuals
experiencing psychosis, especially nonaffective psychosis (Dealberto
2010). FEP program directors and recruiters must learn to interact effec-
tively with individuals from diverse backgrounds if they are to be suc-
cessful. This effort can raise many challenges. Language barriers
require the use of translators, which can be clinically complicated be-
cause of boundary issues if the translator is another member of the fam-
ily or an unpaid volunteer community member.
Furthermore, psychosis in a child in an immigrant family can be
uniquely disruptive. In many immigrant communities, the older chil-
dren in the family may become the conduits to the new country because
they often become more familiarized with the cultural norms through
school and social media. These children are often especially valued by
the family and are the target of high expectations. Understandably, if
one of these children develops a psychotic illness, it can be especially
destabilizing for the family. The relatives not only are dealing with un-
expected illness but also may have lost their in-house language transla-
tor as well as the person who navigates much of the family’s
interactions with the new society. The situation may be further compli-
cated by the family’s cultural beliefs about the causes or treatment of
the psychosis, which may conflict with the teaching and practices of the
majority culture. Engaging such an individual and his or her relatives
in an FEP program can be challenging; it requires the sensitivity and
empathy of the FEP program manager or recruiter and perhaps consul-
tation with cultural experts (often a member of a local religious group
or another medical professional) to learn enough about the concerns
and pressures impinging on the family to interact effectively with them.
Finally, it must be noted that in spite of the best efforts of the care
team and the consent of the individual, some families will not become
involved in the FEP program, even when the individual consents to
their involvement. Often, this absence reflects other pressures in the
family, such as complicated work schedules, caretaking for other family

members, or mental illness in the relative. Sometimes, the best the team
can do is keep the door open, extend an open invitation to the family to
engage with the team at a later time, and reach out assertively to the
family if circumstances change.
INDIVIDUAL ASSESSMENT OF RELATIVES

Most FEP programs have a standard assessment tool that is used with
participants, and responses provide a wealth of information to inform
clinicians about how to be helpful to families in their efforts to support
the recovery of their loved ones. However, as was discussed in the pre-
vious subsection, “Active Engagement,” relatives may have their own
concerns about their loved one, so it is essential that the family clinician
conduct a separate assessment with at least one relative (and more if
possible if they intend to participate in the family sessions). This meet-
ing can be vital for alliance building.
Further, integrating the information obtained in the individual and
relative assessments is critical to developing an effective treatment team
for the individual. Knowing that a family member sees nothing wrong
with the individual smoking marijuana and, in fact, smokes it with him
or her or that the family member discourages medication adherence can
be invaluable in designing a family education program tailored to the
unique needs of the participant. Similarly, the family response to the de-
velopment of psychosis in a loved one may be colored by the fact that
either this is a new experience for them or, alternatively, this individual
is another in a long line of family members who have serious mental
health challenges. This information can be essential to establishing the
appropriate affective tone for the sessions. Trying to provide good fam-
ily education about psychosis without an assessment is like trying to
box with one hand tied behind your back.
It is preferable that the family assessment is conducted individually,
with just the clinician and the family member present. Although many
agencies have a “no secrets” policy and are reluctant to see family mem-
bers in the absence of the individual with FEP, relatives may be hesitant
to share important information in the individual’s presence, especially
early during FEP treatment, because they fear that sharing information
(such as the fact that the individual is aggressive or is not taking his or
her medication as prescribed) in front of the individual will create prob-
lems at home.
A private meeting can also be invaluable in learning about issues the
psychosis has raised for other family members. For example, in a
blended family, the behavior and increased dependence resulting from
the psychosis often can become a source of friction between the parent
and stepparent, causing the parent to have the added burden of trying
to protect the young person from the criticism of the stepparent. Al-
though the parent may be unlikely to disclose this situation in a conjoint

interview with the individual, he or she may be very willing to discuss
it privately with the family clinician. Similarly, parents who have expe-
rienced serious mental illness in themselves or in other family members
may be especially distressed by the development of psychosis in their
child and may need a place to discharge their anxiety or guilt; doing so
in front of the child may be counterindicated, but this is still very useful
information for the family clinician to have. Although it is optimal to
cultivate open sharing of information among all participants in the FEP
program, this may take time and should be a goal of the family inter-
vention rather than a prerequisite for entry to the program.
When considering potential topics that may be important to assess
when beginning to work with a new family in an FEP program, the
items in Table 18–2 can serve as a guideline and can be augmented as
needed. The clinician should also be alert to any other needs or con-
cerns the relative raises that might benefit from being addressed in case
management. By linking the family with agencies that can assist in
meeting these needs, the stress level on the individual can be reduced
and a stronger alliance built, to the benefit of all. For example, indigent
family members may disclose pressing needs that are not necessarily re-
lated to the individual in treatment (e.g.,visa concerns, employment
challenges, financial concerns).
BRIEF ILLNESS EDUCATION

The provision of family illness education has several goals: 1) engage and
motivate the family in support of the recovery treatment plan; 2) help the
family develop hopeful, realistic short-term and long-term expectations
for the individual’s functioning; 3) assist the family in learning how to
be helpful to the individual; and 4) assure that participants have an ac-
curate understanding of factors that improve and hinder good out-
comes. Typical topics covered in a brief educational program for
psychosis are presented in Table 18–3.
Illness education can often seem like a deceptively easy enterprise—
simply providing factual information to individuals to whom it might
be important. However, given the complexity of the educational goals,
the variation in participants and families, and the uncertainties of early
psychosis, the task of providing good illness education to individuals
and their loved ones can be more nuanced than it first appears. There
are many resources available to facilitate this education (see Suggested
Readings at the end of the chapter). Strategies for optimizing brief ill-
ness education are presented in the appendix at the end of the chapter.
Brief illness education can be offered in an extended group work-
shop format or in a series of 5–10 individual sessions. Typically, both the
individual and his or her relatives are invited, although if the individual
elects not to attend, the relatives can still do so. The benefits of a group
TABLE 18–2. Assessment probes for relatives supporting an

individual in an FEP program
What are the circumstances of the relative’s life (e.g., age, marital status,
employment, health concerns, kin relation to individual)?
What does the family member understand about the individual’s disorder
(label, symptoms, treatment, causes)?
Has the family member had prior experience with mental illness in himself or
herself or in a loved one?
What factors does the family member think make the symptoms and the
individual’s situation better?
What factors does the family member think make the symptoms and the
individual worse?
What are the individual’s strengths?
What does the relative think about the individual’s treatment plan? What does
he or she like about it? What are his or her concerns? How does he or she feel
about the prescribed medication?
What are the main difficulties the relative is having as a result of the psychotic
illness? How does he or she cope with them?
Is the individual’s illness causing any stress or strain in other family
relationships?
Is there an issue about the individual’s substance use? How does the relative
feel about that?
Is there any concern about safety or aggression in the home? How is the
relative managing that?
What are the other significant concerns in the relative’s life (e.g., health, job,
finances, other family members)?
What strengths does the relative bring to this challenge?
Does the relative have a social network (people on whom he or she can rely)?
Are there any important impending changes coming up for the family?
What additional items (if any) are pertinent to this family?
Abbreviation. FEP=first-episode psychosis.
educational setting include provision of opportunities for families to

learn from each other, the potential for participants to develop a larger
social support network, and cost-effectiveness if the group is large
enough. The advantages of individual sessions are the ability to hold
meetings at the specific time and location most convenient for the par-
ticipants and the capacity to tailor the information provided to the
unique needs of the family. Many agencies do not have sufficient FEP
TABLE 18–3. Topics covered in brief illness education for families of

individuals with psychosis
Facts about psychosis (e.g., symptoms prevalence, causes, prognosis,
treatment)
Medication
Coping with stress
Developing resilience
Relapse prevention planning
Developing a collaboration with mental health professionals
Effective communication
Supporting recovery from psychosis
enrollment to cultivate multifamily groups, but these groups can pro-

vide some real advantages to participants if they are an option.
BRIEF CONSULTATION
Subsequent to illness education, families often need assistance solving
real-world problems, developing plans to meet treatment goals, or ac-
cessing resources to support their loved one’s recovery. Sometimes
there are decisions to be made—such as the individual deciding about
applying for disability benefits or returning to school or moving to his
or her own place—that may have an impact on relatives. Families can
often benefit from expert consultation in these situations, either with
the family clinician or with an FEP case manager if the program has one.
Typically, a few conjoint sessions to address a specific issue can be use-
ful; often, these sessions can incorporate formal problem solving or use
of a pro-and-con decisional balance exercise.
ACCESS TO THE TREATMENT TEAM

Although the family clinician is likely to have the most contact with the
participant’s relatives, FEP programs rely on interdisciplinary teams to
be successful, and family involvement may be important for bolstering
medication adherence, practicing skills, and supporting work or school
engagement. It is essential that the family clinician have a strong grasp
on the individual’s treatment program and liaise with other treatment
team members when family engagement in other components of the
FEP program may be beneficial. Conjoint meetings with the individual,
relative(s), family clinician, and other FEP team members can be invalu-
able in supporting the treatment plan.
INVITATIONS TO RELATIVES TO JOIN TREATMENT

PLANNING MEETINGS
Three key aspects of an effective FEP program are instituting an inter-
disciplinary team, systematically monitoring the individual’s progress,
and adjusting the treatment plan as needed (White et al. 2015). Typi-
cally, treatment planning team meetings are held at least 2–3 times per
year for each participant, and encouraging relatives to attend these
meetings is an important aspect of an effective family program. Rela-
tives can be an essential source of information about an individual, such
as when the person is not taking medication, is aggressive, or is now
willingly attending family functions that he or she previously refused
to attend. Relatives can also make or break a treatment plan. For exam-
ple, an individual can articulate a treatment goal of looking for a job and
have support from the treatment team, but if a relative discourages the
activity because he or she believes that employment may precipitate a
relapse or burden the family, there is a high likelihood the goal will not
be met. The treatment team meeting also provides a forum for the fam-
ily to have their concerns addressed. Individuals often spend 2–3 years
in an FEP program, but much of the contact with the family is front-
loaded. Relatives’ ongoing attendance at team meetings can be extremely
useful in continuing the alliance with the family as the individual enters
the later phases of treatment.
More Intensive Optional Interventions Tailored to

Specific Family Need
Indicators of a need for a more intensive level of family services in an FEP
program include 1) lack of progress on the individual’s goals, 2) high levels
of conflict in the family, and/or 3) relatives initiating frequent contact with
the clinic with many concerns about treatment and/or the individual. In
considering whether to recommend a more intensive family intervention,
the treatment team should also take into account 1) family attendance and
motivation during early program participation and 2) whether the indica-
tors of a need for intensive services reflect an illness management problem
or another concern (e.g., finances, parental marital strife) that might best be
handled through accessing another resource. If the problem seems illness
related and the family has been attending sessions, then a recommendation
for a course of more intensive intervention can be made.
MULTIFAMILY SUPPORT GROUPS

McFarlane et al. (2015) have developed a comprehensive multifamily
group intervention for individuals experiencing a very early psychosis
(duration less than 30 days) or those at clinical high risk of developing
psychosis. The 2-year program is composed of a multiple-family group
intervention, assertive case management, medication, and supported

employment or education, and it is directed at individuals between
ages 15 and 25 years who enroll with their families. The family interven-
tion involves active engagement (“joining”), an educational workshop,
and then twice-monthly multifamily problem-solving and support ses-
sions. This intervention has been evaluated in a six-site quasi-experi-
mental trial with very good results (McFarlane et al. 2015).
In some FEP programs that incorporate individual family educa-
tion, multifamily support groups are offered as a maintenance treat-
ment once individual family work is completed. Group meetings can
reduce stigma, encourage positive role-modeling, and increase families’
social networks. However, there are obstacles as well. Some individuals
do not want their families involved in their care, some individuals’ fam-
ilies refuse to be involved or cannot attend regularly, and some FEP pro-
grams are too small to recruit enough family members.
FORMAL COMMUNICATION AND PROBLEM-SOLVING

SKILLS TRAINING
Evidence-based family programs used with individuals diagnosed
with longer-term schizophrenia and bipolar illness typically include
formal problem-solving training, and some also offer communication
skills instruction (McFarlane 2016) to help families compensate for ill-
ness deficits and manage stress more effectively. However, this kind of
skills training requires intensive effort across multiple sessions as well
as home practice to promote generalization; it follows the core tenets of
behavioral interventions, including demonstrations, practice, model-
ing, coaching, prompting, and rehearsals (see Mueser and Glynn 1999).
Although this intensive training will likely be of value to families with
clear deficits in these domains, many families entering FEP programs
have an adequate level of communication and problem-solving skills
and/or benefit sufficiently from the standard family program that ad-
ditional skills training is not warranted.
REFERRAL FOR INDIVIDUAL SUPPORTIVE

PSYCHOTHERAPY FOR RELATIVES
Although many relatives are able to function well and support the indi-
vidual’s recovery with the help of the FEP program, a small subset have
a difficult time regaining their equilibrium after the diagnosis of psy-
chosis. These family members often may be struggling with their own
mental health challenges, have multiple other stressors in their lives
(e.g., health challenges in themselves or another loved one, financial
pressures, isolation, family conflict), or find the idea of mental illness in
a loved one objectionable. The family clinician may notice that the rela-
tive is very agitated or distressed during sessions or makes rejecting
statements to the individual; the situation may be so extreme as to in-
terfere with the session agenda. Confronted with such a circumstance,

the family clinician can, as an initial intervention, meet separately with
the relative for a session or two and provide him or her the opportunity
to discharge some of his or her concerns in a reassuring, supportive en-
vironment while not exposing the individual to added stress. However,
if the relative continues to interact in such a way that the family clini-
cian deems it may be harmful for the individual to continue or it be-
comes impossible to provide the FEP content, the family clinician may
find it useful to refer the family member for separate counseling to pro-
vide a forum to explore his or her feelings and attitudes about the indi-
vidual’s psychiatric illness while not derailing the treatment of the
individual with FEP.
A Case Description of First-Episode

Psychosis Family Intervention
Tanisha, a 39-year-old African American single mother, was referred to

the FEP program by the social worker at the hospital where her 17-year-
old son, Denzel, was hospitalized for a psychotic episode. Formerly a B
student and very active on the basketball team, Denzel started talking
about being “punished” by the voices in his head one night and threat-
ened suicide if the voices did not quiet. Tanisha’s aunt had struggled
with mental illness, and Tanisha recognized that something was very
wrong with Denzel. She called 911, and Denzel was admitted to the local
county hospital.
Interventions Offered to All Individuals With FEP

and Their Relatives
ACTIVE ENGAGEMENT
Denzel was hospitalized for 5 days, and Tanisha was referred to the lo-
cal FEP program manager and family therapist, Chris. Chris was warm
and attentive when Tanisha called to explain her situation and concerns
about Denzel. Chris set up an initial appointment for a morning the fol-
lowing week, a few days after Denzel’s planned discharge. On the day
of the appointment, Denzel said he was “too tired from the medication”
and refused to go to the appointment.
Tanisha was not sure what to expect and felt bad that Denzel had not
come to the clinic with her, but she was very worried and went to the
appointment anyway. Chris agreed to see her and told her that “this
happens a lot—family members often come alone at first.” He explained
about the program, and Tanisha liked what she heard. She was espe-
cially interested in helping Denzel graduate from high school—he had
only 4 more months. Chris also told Tanisha that there was a family pro-
gram to help her help Denzel. She was glad of that because she knew she
was stressed about Denzel and she thought her older son, Brandon, was,
too—he had been angry and was saying that Denzel was just trying to
get attention. Chris told Tanisha that Brandon would be welcome to be
part of the family sessions, as would Denzel.
Chris spent some time trying to help Tanisha figure out the next step
with Denzel—he offered to come to her house or to set up another ap-
pointment at the clinic later in the day when Denzel might be more
awake. Tanisha decided to set up a late afternoon appointment at the
clinic 2 days later and bring only Denzel initially. Denzel was nervous
about going back to school and thought he needed some help to figure
out what to do, so he reluctantly agreed to go to the appointment with
his mother.
Denzel liked Chris when they met—he thought he paid attention
and was encouraging, telling Denzel that he still had a chance at going
to college if he wanted to down the road. Denzel and Tanisha were in-
troduced to the other FEP team members: the prescriber, supported em-
ployment and education (SEE) specialist, therapist, and peer counselor.
Denzel agreed to be evaluated for the FEP program, and Tanisha was
glad when he was accepted. Although Denzel was a legal minor, Chris
made a point of informing him that he needed to consent to having his
mother and brother come to family sessions, and that he did not have to
attend these sessions if he did not want to do so. Chris asked Denzel
what he thought might be the benefits for himself and his family if they
learned more about how to help him get back on track and what might
be the problems. Denzel did not like the idea of his family meeting with
the staff without him, but he knew his mother really wanted to be part
of the family program, so he agreed to attend the family meetings with
Tanisha and Brandon.
INDIVIDUAL ASSESSMENT OF RELATIVES
Tanisha then began the family part of the program. She completed an in-
terview with Chris, in which they talked about Denzel, but Chris was also
interested in her life and what bothered her. She talked about how hard it
was to be a working single mom, how she always felt bad about the fact
that Denzel and Brandon’s father left when Denzel was a baby, and how
she was worried about both of the boys—Denzel because of his illness and
Brandon because he seemed so angry about it. Tanisha had seen her aunt
struggle with homelessness and being in and out of hospitals, and she got
tearful when she thought about the same thing happening to Denzel.
Chris also spent time helping Tanisha identify her strengths and
support system; afterward, she thought it had been a very long inter-
view, but she felt more hopeful about Denzel. She also encouraged Bran-
don to meet with Chris; he did not want to go to the individual
assessment but agreed to go to the family education session Tanisha had
scheduled the next week.
BRIEF ILLNESS EDUCATION
Denzel, Tanisha, and Brandon attended eight family education sessions.

The sessions were supposed to be weekly, but because of Tanisha’s work
schedule as a nurse, sessions were scheduled closer to every 2 weeks.
The family covered the topics listed in Table 18–2. Chris made the ses-
sions very conversational and nonstressful and gave everyone useful in-
formation sheets to take home. Tanisha liked three things best about the
sessions: 1) Chris encouraged Denzel to describe what the voices he
heard were like and how he coped with them. She had been afraid to ask
Denzel about the voices, but she was curious and was glad he was
talking about them. 2) Brandon attended the sessions and seemed to
grow calmer and more supportive of Denzel as he learned more about
the illness and how Denzel was struggling. He also shared how frighten-
ing it was when Denzel got ill and talked about suicide. 3) Tanisha was
afraid that Denzel was going to have to go to the hospital again at some
point, but she was reluctant to bring up the topic because she thought
Denzel would think she did not have confidence in him. She was very re-
lieved Chris had them do planning about relapse prevention.
BRIEF CONSULTATION
By the time the family finished the education sessions, Denzel had been
in the FEP program for 4 months. He had worked closely with the SEE
specialist, who had been able to help him finish high school by getting
tutoring and credit for some FEP activities. Things were going well until
Tanisha noticed that Denzel was staying up later and seemed more agi-
tated and irritable. Denzel denied he was hearing voices or felt stressed,
but after graduation, he started getting up later and later and staying up
until 4 or 5 in the morning. Sleeping problems were one of the relapse
warning signs that Chris had identified in the family sessions, so Tani-
sha called Chris, who suggested a family consultation to address two is-
sues: 1) Was Denzel having a relapse? 2) What was Denzel going to be
doing after graduation? Denzel did not want to attend the sessions, but
Tanisha was able to convince him to go to at least one meeting with her;
Brandon had to work and was unable to attend.
During the session, Denzel had a hard time following the discussion
and seemed agitated, although he denied experiencing an increase in
symptoms. Chris reviewed the stress management techniques they had
covered in the family education and individual therapy sessions and
also checked in with Denzel about whether he had missed any medica-
tion. Denzel said he hated the medication and was stopping it. Tanisha
got very upset. Chris reminded Tanisha that many young people stop
taking their medication when they feel better and asked Denzel to come
to his next appointment with the prescriber so he could tell him more
about his problems with the medication. Tanisha and Chris also encour-
aged Denzel to meet with the SEE specialist to make a plan to keep busy
over the summer.
Chris scheduled a follow-up consultation meeting a week later; only

Tanisha attended. She reported that Denzel was doing about the same;
he had decided not to take the medication, even after the appointment
with the prescriber, and was sill mostly hanging around the house.
Chris reviewed the relapse plan so that Tanisha would know how to get
help if the situation deteriorated and encouraged her to make sure she
continued to take good care of herself, use her coping skills and social
supports, and keep in contact with the team. They set up a time for a
phone call the following week.
Over the next year, the family had three more rounds of brief con-
sultation to address the following: 1) managing after a relapse (Denzel
had been hospitalized again briefly 6 months into the program), 2) help-
ing Brandon and Denzel get along better together (10 months into the
program), and 3) helping Denzel figure out if he was ready to move out
to live with his girlfriend (13 months into the program).
ACCESS TO THE TREATMENT TEAM
As can be seen, Tanisha had ample opportunity to interact with Chris,

the FEP project director and family clinician. She also sat in on several
meetings with the SEE specialist and Denzel to discuss how to handle
negotiations with the school regarding Denzel’s graduation and future
plans. She met Denzel’s individual therapist and prescriber during the
FEP orientation.
INVITATIONS TO RELATIVES TO JOIN TREATMENT

PLANNING MEETINGS
Tanisha was invited to Denzel’s treatment team meetings quarterly with

all the members of the team. This was helpful to Tanisha when Denzel
was rehospitalized about 3 months after he stopped taking his medica-
tion, and she appreciated the team’s guidance and support. By Denzel’s
second year in the FEP program, he was doing much better. He had a
girlfriend and a part-time job as an assistant basketball coach at a local
Boys Club and was considering enrolling in community college. He
took his medication most days, although he hated the side effects and
said he was “not going to take it forever.” The primary contact Tanisha
had with the treatment team was at these meetings and during occa-
sional phone calls with Chris.
More Intensive Optional Interventions

Chris referred the family to the monthly relative support group after
they finished the brief education component of the program, but Tani-
sha often had to work evenings and was not able to attend. Chris had
limited time with the family and knew that mother and son seemed to
communicate well, so he incorporated brief communication skills train-
ing in the brief consultations for Denzel and Brandon rather than offer-
ing more formal sessions. Chris had considered that Tanisha might
benefit from her own therapy when she appeared so distraught at the
beginning of the program, but she calmed over time and was able to re-
turn to more involvement with her church, which seemd to give her
support and comfort. Therefore, Chris did not raise the issue of a referral
for individual counseling with her.
KEY CONCEPTS
• Family support can play a key role in recovery from psy-
chosis, especially for younger individuals experiencing a
first episode.
• Relatives often experience high levels of distress when
their loved one develops a psychosis or relapses.
• There is a robust body of literature to suggest that embed-
ding family support within a comprehensive first episode
of psychosis (FEP) program offers optimal outcomes.
• There have been many family programs proposed as part
of FEP programs, and there is no way to discern at this
point if one yields more benefits than another.
• A stepped-care model of increasing family intervention,
tailored to individual and family needs, is recommended in
order to provide services efficiently.
1. What family services does your agency currently offer to all

individuals? Should these services be upgraded?
2. Are agency staff skillful in eliciting consent for family in-

volvement in care? Are they competent in shared decision
making? Do they know how to discuss limited consent for re-
lease of information?
3. Do staff have sufficient information about psychosis to edu-

cate families well? Do they need a primer or access to better
materials? Who can help them stay current?
Suggested Readings
Bennett M, Drapalski A, Dixon L, et al: Family Treatment and Resources
Manual. New York, OnTrackNY, 2018. Available at: www.ontrack
ny.org/Portals/1/Files/Resources/Family%20Treatment%20
and%20Resources%20Manual%204.18%20Final.pdf?ver=2018-05-01-
120346-543. Accessed December 11, 2018. OnTrackNY also has
some great videos of individuals and families presenting issues in
FEP recovery that can be accessed at http://practiceinnova-
tions.org/Consumers/family and-community-support.
Glynn SM, Cather C, Gingerich S, et al: NAVIGATE Family Education
Program (FEP). Bethesda, MD, National Institute of Mental Health,
2014. Available at: http://navigateconsultants.org/manuals. Ac-
cessed December 11, 2018. This is the family education manual used
in the RAISE-ETP study.
Greenstein, L: Experiencing a Psychotic Break Doesn’t Mean You’re Bro-
ken. Arlington, VA, National Alliance on Mental Illness, March 12,
2018. Available at www.nami.org/Blogs/NAMI-Blog/March-2018/
Experiencing-a-Psychotic-Break-Doesn-t-Mean-You-re. Accessed De-
cember 11, 2018.
National Alliance on Mental Illness: What Is Early and First-Episode Psy-
chosis? Arlington, VA, National Alliance on Mental Illness, 2016.
Available at: www.nami.org/NAMI/media/NAMI-Media/Images/
FactSheets/What-is-Early-and-First-Episode-Psychosis.pdf.
Accessed January 30, 2019.
National Institute of Mental Health: Fact Sheet: First Episode Psychosis.
Bethesda, MD, National Institute of Mental Health, 2015. Available
at: www.nimh.nih.gov/health/topics/schizophrenia/raise/fact-
sheet-first-episode-psychosis.shtml. Accessed December 11, 2018.
Substance Abuse and Mental Health Services Administration: Under-
standing a First Episode of Psychosis: Caregiver: Get the Facts.
Rockville, MD, Substance Abuse and Mental Health Services Ad-
ministration, 2018. Available at https://store.samhsa.gov/system/
files/sma16-5005.pdf. Accessed January 30, 2019.
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APPENDIX
Clinical Strategies for Optimizing Brief
Family Education
Help Participants Recognize

the Psychiatric Disorder
The symptoms of most nonpsychiatric disorders (e.g., coughing, an-
gina, fever) are easily recognized as being due to physiological prob-
lems that are beyond the client’s control. In contrast, psychiatric
symptoms (e.g., depression, anxiety, social withdrawal) are less readily
viewed as reflecting a “disorder” and are more likely assumed to be un-
der the client’s voluntary control. One reason why relatives often be-
lieve clients have control over their psychiatric symptoms is that many
symptoms are defined by the absence of particular behaviors or emo-
tions (e.g., negative symptoms in schizophrenia, avoidance in anxiety
disorders) rather than the conspicuous presence of other behaviors (e.g.,
bizarre behavior, responding to internal stimuli). A second reason why
some psychiatric symptoms may be thought to be under voluntary con-
trol is that almost everyone has experienced at least mild levels of de-
pression or anxiety with which they have successfully coped and that
they did not allow to interfere much with day-to-day functioning.
These experiences can lead to a false impression that psychiatric pa-
tients could recover from their problems if only they tried hard enough.
The goal of helping the family recognize and accommodate the individ-
ual’s psychiatric disorder is achieved chiefly through providing infor-
mation about the causes of the illness and factors that improve or
hinder recovery. At the same time, the individual is encouraged to pur-
sue his or her dreams, take responsibility in areas where this seems pos-
sible, and avoid assuming the “sick role” and diminishing expectations
for a full life. Thus, improving coping, avoiding substance use, and us-
ing skills are all important concepts to convey.
Abstracted from Glynn SM, Cather C, Gingerich S, et al: Navigate Family Education Pro-
gram (FEP). Unpublished manual, 2014.
Manage Initial Diagnostic Uncertainty

First-episode psychosis (FEP) can presage a number of subsequent psy-
chiatric diagnoses (e.g., schizophrenia, schizoaffective disorder, bipolar
illness, delusional disorder, psychotic depression) but it can also remit
completely. Because the diagnosis is likely to evolve while the individ-
ual is in the FEP program, the family clinician must be comfortable with
diagnostic and prognostic uncertainty. Some individuals will go on to
develop longer-term disorders with poorer functioning, but many will
either remit or be able to function well. Thus, the treatment team needs
to model (and have) hope, while being honest about issues on which
there is uncertainty. Individuals and families may have been given
firmer diagnoses by prior treatment teams; the family clinician will
need to be adept at discussing the diagnostic uncertainty inherent in
early psychosis.
Present Information in an Honest,

Direct Manner
Family clinicians sometimes feel uncomfortable when talking with a in-
dividual and his or her relatives about the psychosis. All too often, pro-
fessionals are keenly aware of their own limits in treating serious
mental illness, and they recognize the difficult and long struggle many
individuals and relatives will face. Nobody likes to be the bearer of bad
news. An understandable response of some professionals is to “protect”
these participants from what they perceive to be potentially upsetting
information about the client’s condition. This occurs particularly in FEP,
when there may still be some doubt about the accuracy of the client’s di-
agnosis and the client and relatives may seem overwhelmed and/or
fragile.
The common, but often erroneous, assumption is that individuals
and relatives will be shocked and dismayed to learn that the client has
a specific psychiatric disorder. The opposite is often true. Participants
frequently express gratitude to professionals who are direct in educat-
ing them about their disorder, even when it is a serious one. A vital
principle of illness education is that the family clinician always strives
to provide participants directly and honestly with the most accurate
facts available about the disorder, while never deliberately withholding
information. Through direct communication about the individual’s dis-
order, the family clinician creates a supportive and collaborative work-
ing relationship with the whole family that will endure throughout the
course of therapy.
Avoid Making Assumptions About

Participants’ Beliefs
Individuals and relatives come to the experience of a psychosis with a
whole life history learning about psychiatric illness through the media,
their social networks, and (possibly) personal experiences. The family
clinician can have no way of knowing in advance what beliefs partici-
pants are bringing to the work. Religious beliefs may color how individ-
uals conceptualize the illness, and even medical and mental health
professionals may have ideas that are inconsistent with optimal recov-
ery strategies as supported by research. Thus, the family clinician
should not make any assumptions about a shared knowledge and atti-
tude base among participants. Rather, he or she should always ask
questions to discern how the participants understand topics prior to
presenting educational materials and tailor discussions to accommo-
date unusual beliefs.
Make Sessions Lively and Interactive

The family clinician cannot rely solely on didactic teaching methods but
must strive to make the educational sessions as interactive as possible.
Successful educational sessions require that the family clinician contin-
ually elicit the individual’s and relatives’ experiences with the disorder.
The family clinician must probe the participants regarding their knowl-
edge about educational topics to be covered, including what they have
heard about the disorder (e.g., myths, readings they have done). There
are check-ins with participants throughout the sessions regarding the
information presented and the pace of the presentation. Clinician sto-
ries and experiences can be invaluable in making critical educational
points. The family clinician should ask frequent questions to elicit the
participants’ understanding of the material presented. By adopting an
interactive approach to education, the family clinician is able to evalu-
ate the participants’ acquisition of basic information about the disorder,
identify any misinformation they hold about the disorder, and pace the
presentation of new material accordingly. Furthermore, by continually
seeking feedback and input, the family clinician avoids the pitfalls of
overloading participants with information, resulting in boredom and
disengagement.
The information is summarized using visual aids, such as black-
boards and handouts. Videos (often from YouTube or trusted resources)
can be very helpful but should be screened by the clinician for accuracy.
The teaching format resembles a cross between a classroom, with the
family clinician assuming the role of the teacher, and a discussion, with
the family clinician acting as a facilitator. The conversation is guided by

the family clinician so as to cover the curriculum as planned while so-
liciting the experiences and understanding of participants and their
comments and questions throughout the session.
One useful strategy for keeping the sessions lively to elicit the indi-
vidual’s personal experiences when discussing symptoms and making
these the focus of conversation. The individual can be connoted as “the
expert” and given an opportunity to expand on his or her experiences.
Many families may have discussed psychosis in general or may have
read it about it on the Internet but have not actually discussed what the
individual is living and how it impacts him or her. This conversation
can help engender empathy and understanding in relatives.
CHAPTER
19
Suicide Risk, Assessment,

and Intervention in Early
Psychosis
APPROXIMATELY 15% of people who die by suicide are psy-

chotic at the time of their death. In the United States in 2017, 47,173 peo-
ple died by suicide (Centers for Disease Control and Prevention 2018),
and so it can be estimated that 7,076 people with psychosis died by sui-
cide that year. Many of those who died by suicide may have been in
their first psychotic episode because the risk is 1.6–2.0 times higher in
the first few years than in later years, although the suicide risk remains
increased throughout the lifespan when psychosis is present. The good
news is that most people with psychosis do not die by suicide, and early
identification (Melle et al. 2006) and treatment can help reduce the risk
of suicide attempts (Fedyszyn et al. 2014).
Suicidal Ideation and Behavior

When suicide is being discussed, it is important to be specific about
whether suicidal ideation, suicide attempts, or death by suicide is the focus.
Suicidal ideation is relatively frequent, particularly among people with
psychosis, and has been found to be present among 20%–40% of individu-
als early in the course of psychotic disorders. Most people with suicidal
ideation do not engage in suicidal behavior. Studies have shown that the
335
rate of suicide attempts during the first few years of psychosis is around
10%, with the first attempt often occurring before any treatment contact.
Death by suicide in the first 3 years ranges from 1.9% to 3% (Nordentoft
et al. 2015). Compared with the general population, in which the age-
adjusted rate is 14 per 100,000 (Centers for Disease Control and Preven-
tion 2018), the rate for those with early psychosis is significantly high. One
can see that suicidal ideation is a warning sign for suicide; however, suicide
risk can be understood only by considering a host of biological, psycholog-
ical, social, and environmental factors that contribute to risk. It is also im-
portant to remember that many people who die by suicide die on their first
attempt, so assessing for risk and having conversations about distress and
suicidal ideation are important components of clinical care.
Although there has been little research regarding risk factors for sui-
cide among individuals with early psychosis, several factors emerge
consistently (Nordentoft et al. 2015). These factors include previous sui-
cide attempt, prior or comorbid major depression, alcohol and other
substance use, and poor premorbid problem solving. Longer duration
of untreated psychosis and more severe psychotic symptoms have also
been associated with suicide attempts. A study by Melle et al. (2006)
demonstrated that a public information campaign about early signs of
psychosis decreased the time between first symptoms and first mental
health contact and resulted in fewer people experiencing suicidal ide-
ation as assessed at clinical intake.
Long-term factors that have been found to be associated with suicide
risk across mental health conditions include early abuse, neglect or
trauma, family history of mental health conditions or suicide, chronic
physical health conditions or pain, head trauma, and genetics associated
with sensitivity to stress and resilience. Shorter-term environmental and
social factors that can precipitate suicidal behavior include prolonged
stress such as that caused by ongoing harassment, bullying, or relation-
ship problems; stressful life events such as divorce or financial problems;
exposure to suicide; and access to lethal means (Figure 19–1). Many con-
tributors must be present before any individual is at risk for suicide, and
there is no single cause. Like people without psychosis, individuals with
psychosis report that suicide attempts may be precipitated by loss of a
love relationship or another significant social stressor. Among people with
psychosis, it is often reported that being bothered by psychotic symptoms
and depression each served as a precipitant.
Case Example 1: “Not Right in My Head”

Sue was 15 years old when she made her first of four suicide attempts.
The year prior to her first attempt, she had dropped out of high school
because of poor grades and difficulty functioning. For a year, she would
not come out of her room in her mother’s house and suffered from se-
vere self-neglect, unable to engage in activities of daily living. She had
Suicide Risk, Assessment, and Intervention in Early Psychosis 337
Psychological Social and

Biological
factors environmental
factors factors
Current life events
Lethal means
SUICIDE
FIGURE 19–1. A conceptual model for understanding suicide: interac-

tion of risk and protective factors.
Source. American Foundation for Suicide Prevention.
referential delusions, engaged in limited communication, and had

avolition and affective blunting. Prior to her psychosis, she experienced
two major depressive episodes lasting 2–3 months each. In the past, she
had been physically abused by her mother, who had an alcohol use dis-
order. Her father had two brief psychotic episodes during cannabis use.
Sue made her first attempt because “My mind was not working right
and I was not right in my head—probably because I didn’t get enough
sleep.” After an overdose, she was admitted to a medical unit at a local
hospital, where she stayed for a few days before being transferred to a
psychiatric inpatient unit.
The case of Sue demonstrates the multiple factors that contribute to

suicidal behavior. She had experienced previous depressions, was
likely psychotic when hiding in her room for a year, functioned poorly
premorbidly, had a history of being abused, and had a family history of
mental illness and substance use. Early intervention could have been
helpful in preventing her suicidal behavior.
Warning Signs for Suicidal Behavior

Suicidal ideation is not static; it often comes and goes, such that a person
is not always acutely suicidal or even thinking about suicide. Although
this makes it difficult to detect more immediate risk, it does mean that in-
terventions can be implemented to help individuals learn to manage sui-

cidal ideation and prevent suicidal behavior. The key is to identify
warning signs, which may be long-standing or may be brief or fleeting
(Figure 19–2). Warning signs do not always include suicidal ideation,
however. Sometimes in the months and weeks before an attempt, indi-
viduals may speak about killing themselves and express feelings of
hopelessness, entrapment, and being a burden to others. They may talk
about having no reason to live or note that family and friends will not
miss them after they are gone. These individuals may often feel de-
pressed or anxious, or they may appear to lack interest. They may be eas-
ily agitated or irritable, or recently may have experienced something that
led him to feel humiliated. Behaviorally, they may increase use of alcohol
or drugs, withdraw from activities, and isolate themselves from family
and friends. They may sleep too much or too little or have insomnia.
Sometimes, people visit or call friends and family to “say good-bye” or
give away possessions. Not all warning signs will be present, but some
will, and it is easy to write them off as unimportant, as part of a phase or
as a form of attention seeking. It is important to keep in mind that sui-
cidal individuals, at least in their suicidal crisis, lose access to their usual
problem-solving and coping abilities. They experience cognitive inflexi-
bility and believe that nothing will end their pain (American Foundation
for Suicide Prevention 2019). If they are able to get through the crisis, it
is possible that they may never engage in suicidal behavior.
For people with psychosis, command auditory hallucinations may
or may not result in suicidal behavior. Some people resist acting on
voices telling them to kill themselves, whereas others respond to their
voice(s) and engage in suicidal behavior. There are no data providing
information about who will or will not act in response to command au-
ditory hallucinations. In fact, a person may not engage in suicidal be-
havior related to command auditory hallucinations at one point in his
or her illness but may respond at another time. Therefore, command au-
ditory hallucinations always need to be taken seriously, and a person
experiencing such voices can develop tools for coping and managing
rather than reacting in response.
Case Example 2: Thought to Action

Ted was 28 years old and had a history of alcohol use disorder that was
in remission when his psychotic symptoms began. He did not receive
treatment even though he had been experiencing delusions and halluci-
nations for a couple of years and his functioning was declining. He
heard voices berating him and had paranoid and referential delusions
that people were talking about him and accusing him of malevolent be-
havior. He had periods of depressed mood, but his symptoms never met
the criteria for major depression. One day, in a matter of minutes, Ted
quickly picked up a razor and made cuts on his arm, saying that he
thought someone in Spain wanted to kill him. He had considerable
FIGURE 19–2. Warning signs of suicidal ideation and behavior.

Source. American Foundation for Suicide Prevention.
bleeding and was brought by a family member to the local emergency

department, where he received wound care and antibiotics but no
stitches. He was admitted to the inpatient psychiatric unit.
In Ted’s case, there were many notable risk factors for suicide, and
he was hearing berating voices that made him uncomfortable and also
had frightening paranoid delusions. He was experiencing significant
distress because he had never received treatment. Members of his sup-
port system were not aware of the process that was unfolding, and his
suicide risk was not detected. This highlights the need for public edu-
cation about psychosis and suicide.
Assessment of Suicide Risk

The goal of a suicide risk assessment is to gather information to gain
knowledge about the individual’s potential suicide contributors and
protective factors. The assessment provides the foundation for ongoing
assessment and understanding of the person’s suicide risk over time. A

suicide risk assessment includes obtaining a full description of past and
present suicidal ideation and behavior as well as an evaluation of the
previously noted risk factors, including mental health conditions,
health history, premorbid adjustment, family history of mental health
conditions and suicidal behaviors, history of trauma or abuse, impul-
siveness and aggressive behavior, current levels of pain, and general
sense of health and well-being. Substance use, including its impact on
mood and behavior, is often a factor in suicidal behavior. It is important
to note any changes in patterns and consequences of use and other po-
tentially risky behavior. It is also important to gain a sense of the per-
son’s usual level of optimism and pessimism and his or her hopes and
aspirations for the future.
All of this information is relevant for foreseeing both longer-term
and short-term risk. Such an evaluation serves as a barometer for ongo-
ing assessment of risk and provides a context for risk considerations
throughout treatment. Even with the best assessment, however, sui-
cidal behavior may be sustained over months and years, or the time be-
tween thought and action can be minutes to hours, and intervention is
not always possible. This highlights the need for ongoing assessment
and inclusion of how to address suicide risk as part of an intervention
plan.
Clinicians should ask directly about suicidal ideation and behavior.
This will not make the person suicidal, and it may bring relief. When as-
sessing an individual for past and current suicidal ideation and behav-
ior, it is important to ask about ideation and behavior separately. With
regard to ideation, it is critical to ask the individual to describe his or her
thoughts and their frequency and persistence, as well as planfulness
and intent to die. Suicide is often an ambivalent act, so any intent is of
concern. The clinician should gather a thorough history of the method
used or being considered, what occurred or might occur as a result of
applying the method, and any medical damage and intervention from
previous attempts. In addition, the clinician should explore the individ-
ual’s understanding of lethality. People are not necessarily knowledge-
able about lethality, so the individual’s perception of lethality provides
insight into his or her thinking.
It is important to understand the circumstances, including thoughts
and feelings, that surrounded previous attempts because such under-
standing is a window into future risk and intervention. A clinician can-
not make assumptions about what the person is thinking and feeling. If
risk factors and warning signs emerge, it is important ask about them.
However, just because a person does not have a past attempt or past sui-
cidal behavior does not mean that he or she is not at risk; 60% of suicide
deaths occur on the first attempt (Bostwick et al. 2016). Ongoing consid-
eration of risk factors over the course of treatment can save a life.
Assessment of acute risk also involves identifying current psychiatric

and medical conditions and the effectiveness and side effects associated
with current treatment. Because life stress can serve as a precipitant of
suicidal behavior, the clinician should become knowledgeable about any
stressors or changes that may be current or pending in the near future. If
the individual is taking medications, a review of medications, including
effectiveness, adherence, and side effects, is essential. The person’s re-
port, as well as information from previous clinicians and the availability
of social support for adherence, should be considered.
Case Example 3: “You Don’t Look Psychotic”

Ramon was entering college when he began hearing voices, and months
later he experienced his first episode of major depression. He had never
experienced any suicidal ideation and had no history of suicide attempt.
He was hospitalized to treat his psychotic symptoms and depression.
Once stabilized, he was discharged to outpatient treatment, continuing to
take risperidone and venlafaxine. He looked good physically and was
functioning well. He returned to school and felt well for the next 8 months.
The clinician felt that given Ramon’s return to full functioning, he prob-
ably had never been psychotic and suffered only from depression.
Shortly thereafter, Ramon began hearing voices again, and his thoughts
became more paranoid. Distressed at the return of his symptoms, he
killed himself.
This case highlights the importance of keeping in mind individuals’

self-reported symptom history, their medical records, their feelings
about their psychotic illness, their adherence to and benefit from medi-
cation, and their sense of well-being, especially when a medication
change is being considered. It also serves as a reminder that effective
treatment is possible and that people with psychosis can have full and
enriching lives. With appropriate medication, Ramon was able to return
to his premorbid level of functioning. His family was aware of the re-
surgence of his psychotic symptoms during the medication change and
believed that the treating clinician was monitoring him closely.
Brief Interventions to Prevent

Suicidal Behavior
The months and weeks before and after the first treatment contact are
critical when working with someone in the early phase of psychosis
(Ayesa-Arriola et al. 2015). The individual is facing a major life change.
Supports may be weakened because of recent isolation or behavior. The
individual is likely to be having difficulty processing current informa-
tion and may generally be quite uncomfortable. New medications may
be on the horizon, and they may take time to become effective and may
induce unwanted side effects. Most often, the clinician has never seen
the person at his or her best and most functional level, and it may be dif-
ficult to imagine that the individual has ever been different from his or
her current clinical presentation. For these reasons, it is useful to include
family and other social supports in the process of early intervention.
The first and most immediate interventions depend on the level of
suicide risk, stability of thought and behavior, and available resources.
Concern about immediate risk, based on the person’s presentation, may
warrant constant observation and extended stay in an emergency de-
partment, crisis center, or inpatient hospital. Just because someone is
thinking about suicide does not mean that he or she is at imminent risk
and needs to be hospitalized. Partial hospitalization, rapid referral,
brief intervention in the emergency department, and/or safety plan-
ning with follow-up may be effective interventions.
Regardless of the clinical intervention, from the outset, it is essential
to limit access to lethal means and provide lethal means counseling to
available supports about how to safely store or remove potential means.
Suicide can occur only when there is access to lethal means, and re-
moval of access is one of the most effective interventions in the suicidal
crisis. Suicidal individuals who are in crisis are lacking cognitive flexi-
bility, and their rigid and limited thinking makes it difficult for them to
generate alternative methods if their primary plan is thwarted. By lim-
iting access to lethal means, there is time for the situation and person to
de-escalate and increases the likelihood of intervention.
Developing a crisis or safety plan has been found to be effective for sui-
cidal individuals with psychosis (Fedyszyn et al. 2014; Nordentoft et al.
2002). The value of such plans is that they provide a set of tools for the in-
dividual to use when heading toward a suicidal crisis. These plans include
specifying distracting activities that can be engaged in alone or with others
and identifying family and friends or community members who can be
contacted when the person is experiencing distress. The individual should
also be provided with names of professionals who can be reached out to
during emergencies and numbers for crisis hotlines, textlines, or other ser-
vices that are available 24/7. Personal warning signs and reasons for living
are also identified, as are steps to be taken to eliminate access to lethal
means. Throughout treatment, the plan can be updated and revised. The
safety plan needs to be developed collaboratively on the basis of what the
person can and will do. It should be written down, and it needs to be feasi-
ble and accessible. It is also helpful to include family members or other
close contacts in the development of the plan. Smartphone apps for safety
planning, such as SafetyNet and MY3, are available so that the plan can be
easily accessible and revised as needed.
During the crisis, evaluation of physical health is often not under-
taken, yet we know that delirium or other mental status changes can be
accompanied by psychosis, agitation, and/or mood alterations, some-

times initially in the absence of altered sensorium. Further, some psy-
chotic and mood disorders can be precipitated by brain trauma,
infection, or metabolite imbalance. The individual should undergo a
medical workup, including neuroimaging to rule out brain injury,
stroke, or tumor, and the clinician should consider a range of possible
factors, including infection; hypoxia; hyperthyroidism or hypothyroid-
ism; substance intoxication or withdrawal; heavy metal poisoning; vita-
min B12, thiamine, or folate deficiencies; seizures; encephalopathy; and
renal, hepatic, or cardiac failure. Much suffering can be avoided by
identifying physical health conditions that can lead to disruption of
mental status and brain functioning, both abruptly and gradually. At
the outset of treatment, it is essential to have a thorough workup that
includes blood tests, possible neuroimaging, lumbar puncture, and/or
electroencephalography, and in some circumstances consideration of
metabolomics and genetic anomalies can prove fruitful.
Case Example 4: “Where’s My Cortisol?”

Meredith is a 20-year-old college student who was doing well in school
her first semester. In the middle of her second semester, she became ex-
tremely depressed and unable to leave her room. She became paranoid
about her peers and was grandiose about her importance and abilities.
She stopped going to class and avoided other people. As she began fail-
ing classes, she became more distressed. One day Meredith decided it
was time to end it all, and she made a very serious suicide attempt, caus-
ing multiple knife wounds. She was hospitalized psychiatrically and
sent home with a medical leave of absence. Her anxiety often made it
impossible for her to leave her house, and her family did not understand
and viewed her as lazy. She began psychotherapy, and the therapist re-
quested that she have a complete physical. Ultimately, after Meredith
spent months in this condition, a cousin agreed to accompany her to a
primary care physician. A simple blood test revealed that she had liter-
ally no cortisol, and her physician conducted follow-up tests, determin-
ing that the cause was Addison’s disease. Cortisol replacement therapy
was started. Meredith’s mood immediately improved and her anxiety
decreased, although it remained to some degree. She spoke about her
suicide attempt, saying, “That wasn’t me, and I see that now that I feel
back to myself.” In retrospect, Meredith realized that her decline was
more gradual and occurred over an extended time. Given how terrible
she felt before being diagnosed, she is motivated to manage her Addi-
son’s disease to avoid the mental health and physical symptoms.
Meredith’s case emphasizes the importance of treating the whole

person, mind and body. Without the physical evaluation, she would
have suffered much longer and might have died by suicide.
Clinical Treatment to Reduce

Suicide Risk
Evaluation for medication or adherence to an already prescribed medi-
cation regimen is a vital component for early intervention. Researchers
have demonstrated that as psychotic symptoms improve, risk is de-
creased, although risk remains because of the multidetermined nature
of suicide (Riesselman et al. 2015). Clozapine and lithium have been
found to decrease suicide risk. Treatment with the goal of eliminating
psychotic and affective symptoms while minimizing side effects is a
process that takes time. Collaboration between the clinician, the person
experiencing psychotic symptoms, and his or her family is critical. Psy-
chotic symptoms can be very distressing, so careful attention to maxi-
mizing benefits obtained from medication through ongoing discussions
about symptoms is critical. Recall how the lack of communication and
close monitoring of Ramon contributed to his death by suicide.
Medication alone, however, is not enough, and the combination of
medication and psychotherapy has been found to be more effective than
medication alone. Psychotherapies such as cognitive-behavioral therapy
(CBT) or interpersonal therapy can be helpful to the person with respect
to managing his or her thoughts and feelings and improving social con-
nections. When it comes to reducing suicide risk, developing tools the in-
dividual can use to manage his or her suicidal behavior directly have
been shown to be effective (Kasckow et al. 2011). Therapies such as CBT–
suicide prevention (CBT-SP), dialectical behavior therapy, attachment-
based family therapy, and collaborative assessment and management of
suicidality have all been found to reduce suicidal behavior, although not
all have been evaluated specifically for people with early psychosis. Each
of these therapies provides a theoretical framework for understanding
how to approach the management of suicidal ideation so that the suicidal
thought does not translate into action. In general, these approaches aim
to identify proximal risk factors and stressors, consider negative thoughts
and feelings, improve emotion regulation and behavioral control, and de-
velop effective problem-solving skills.
Enlisting the support of family and friends is an essential compo-
nent of living with mental health conditions and suicide risk. Obtaining
consent in the first session to be able to contact at least one person in the
individual’s life is important. It can be explained that this contact is for
emergencies if the person is a danger to self or others and to locate the
individual if he or she is not responding. In addition, the clinician can
suggest that this emergency contact and other friends and family mem-
bers can be helpful in treatment because they can observe changes in
thought and behavior that could be essential for assessing risk. Many
suicide loss survivors report that they were excluded from therapy, and
we have learned that their input is critical and potentially life-saving. In

addition to addressing suicide risk, engaging supports in treatment
with people with early psychosis has been found to be beneficial for
treatment implementation and effectiveness (Nordentoft et al. 2002).
Conclusion
Suicide risk in early psychosis is a concern. Suicide is complex, with
many health, historical, social, and environmental factors converging in
the context of life stress and accessibility of lethal means. Early identifi-
cation of psychosis can reduce suicide risk. A comprehensive evalua-
tion of suicidal ideation and behavior and contributors to suicide risk is
the first component of an effective treatment plan. Interventions that re-
duce psychotic and mood symptoms are essential but not sufficient for
managing suicide risk, and suicidal ideation and suicidal behavior
must be addressed directly. Enlisting supports and developing a well-
rounded treatment plan can provide the opportunity for people with
early psychosis to develop a life worth living.
KEY CONCEPTS
• Suicide is complex, and there is no single cause but rather a
confluence of risk factors, including life stress and access to
lethal means.
• A full assessment of suicidal ideation and behavior and
potential contributors and protective factors at the begin-
ning of treatment, and continued assessment and monitor-
ing throughout treatment, are critical.
• In addition to reducing symptoms and improving func-
tioning, tools to manage suicidal ideation and behavior
reduce the transition from suicidal thought to suicidal
behavior.
• Inclusion of supports and continuity of care are key factors
for suicide reduction.
1. Do you spend time with your clients discussing current and

past suicidal ideation and factors that contribute to suicide
risk and prevention? How can you facilitate such conversa-

tions so that clients do not act on these thoughts?
2. Have you developed a suicide prevention plan for your clin-

ical practice?
3. Would you think that your thoughts and feelings about sui-
cide and suicidal clients might contribute to their comfort
discussing suicidal ideas and concerns about their life?
4. How would you ask a client if he or she has lethal means at

home, and how would you ask him or her to remove them
from the home or limit access?
Suggested Readings
American Foundation for Suicide Prevention: www.afsp.org
Galynker I: The Suicidal Crisis. New York, Oxford University Press,
2017
Jamison KR: An Unquiet Mind: A Memoir of Moods and Madness.
New York, Knopf, 1995
Nordentoft M, Madsen T, Fedyszyn I: Suicidal behavior and mortality
in first-episode psychosis. J Nerv Ment Dis 203(5):387–392, 2015
25919385
References
American Foundation for Suicide Prevention: Suicide statistics. 2019. Available
at: https://afsp.org/about-suicide/suicide-statistics. Accessed January 30,
2019.
Ayesa-Arriola R, Garcia Alcaraz E, Hernández BV, et al: Suicidal behaviour in
first-episode non-affective psychosis: specific risk periods and stage-related
factors. Eur Neuropsychopharmacol 25(12):2278–2288, 2015 26475577
Bostwick JM, Pabbati C, Geske JR, McKean AJ: Suicide attempt as a risk factor
for completed suicide: even more lethal than we knew. Am J Psychiatry
173(11):1094–1100, 2016 27523496
Centers for Disease Control and Prevention: Fatal Injury Reports, National, Re-
gioal and State, 1981ﬂ2017. Atlanta, GA, Centers for Disease Control and
Prevention, 2018. Available at https://webappa.cdc.gov/sasweb/ncipc/
mortrate.html. Accessed January 30, 2019.
Fedyszyn IE, Robinson J, Harris MG, et al: Suicidal behaviours during treatment
for first-episode psychosis: towards a comprehensive approach to service-
based prevention. Early Interv Psychiatry 8(4):387–395, 2014 23964750
Kasckow J, Felmet K, Zisook S: Managing suicide risk in patients with schizo-
phrenia. CNS Drugs 25(2):129–143, 2011 21254789
Melle I, Johannesen JO, Friis S, et al: Early detection of the first episode of schizo-
phrenia and suicidal behavior. Am J Psychiatry 163(5):800–804, 2006 16648319
Nordentoft M, Jeppesen P, Abel M, et al: OPUS study: suicidal behaviour, sui-
cidal ideation and hopelessness among patients with first-episode psycho-
sis: one-year follow-up of a randomised controlled trial. Br J Psychiatry
181(suppl 43):s98–s106, 2002 12271808
Nordentoft M, Madsen T, Fedyszyn I: Suicidal behavior and mortality in first-
episode psychosis. J Nerv Ment Dis 203(5):387–392, 2015 25919385
Riesselman A, Johnson E, Palmer E: Lithium and clozapine in suicidality: shed-
ding some light to get out of the dark. Mental Health Clinician 5(5):237–
243, 2015
CHAPTER
20
Using Technology to
Advance Early Psychosis
Intervention
Benjamin Buck, Ph.D.
Dror Ben-Zeev, Ph.D.
YOUNG people experiencing first-episode psychosis (FEP) are

members of a so-called digital native generation and express strong in-
terest in the delivery of mental health services via the Internet, social
media, and mobile devices (Lal et al. 2015). Interventions and service-
delivery strategies that leverage technology may also be particularly
well suited to addressing already identified service gaps in FEP care. As
noted by Lal and colleagues (2015), technology-enhanced interventions
have the potential to be convenient, accessible, and consistent. They
also allow individuals with FEP to remain anonymous and thus circum-
vent barriers posed by stigma. Finally, the reduced burden on individ-
uals, their families, and clinics to meet staffing needs is reduced when
people can reach evidence-based services without having to go to a
brick-and-mortar clinic.
When an individual with FEP initiates contact with a provider, there
are myriad moments in which the use of innovative technologies could
enhance the quality of detection, intervention, and maintenance of
gains from treatment. First, early-phase psychosis intervention requires
assessment to appropriately identify individuals who might be at risk
for future chronic mental illness; existing tools are limited in their abil-
349
ity to accurately predict who will convert to chronic and persistent psy-
chotic illness.
Second, interventions best suited for FEP (i.e., coordinated specialty
care; Kane et al. 2016) are still widely underused, even after individuals
experience a first episode. Approximately half of individuals who experi-
ence FEP do not receive either psychosocial or pharmaceutical treatment in
the first year, and following that episode, 12-month mortality is 24 times
higher than in an age-matched comparison sample (Schoenbaum et al.
2017). Technology-enhanced interventions may provide lower-cost
standardized options for delivery of care that are flexible, consistently
available, and convenient.
Third, a persisting challenge in FEP intervention pertains to mainte-
nance of treatment gains. Although FEP programs have demonstrated
short-term efficacy, some chart review studies demonstrate reduced
sustained impact over time (Gafoor et al. 2010). Online or mobile ap-
proaches provide ample options for stepped-down services that might
maintain gains generated by intensive first-episode interventions in a
less restrictive setting.
A growing body of evidence suggests that individuals with severe
mental illnesses seek support online—from support groups, chat rooms,
message boards, and online gaming communities (Highton-Williamson
et al. 2015). Previous research has demonstrated that this is a common
practice in efforts to connect with others with similar experiences and to
receive support for progress toward one’s recovery goals (Naslund et al.
2014). It remains to be seen whether these novel technologies can effec-
tively address the needs of individuals in the midst of a first episode.
Their ubiquity, however, underscores the need for researchers and pro-
viders to develop their understanding of these resources and how they
can be adapted to address service gaps. In this chapter we provide several
prototypes of innovations in the application of technology to first-episode
intervention that show potential to improve care in three areas: (1) detec-
tion (i.e., assessment of risk and selection of treatment course), (2) inter-
vention (i.e., delivery of treatments themselves), and (3) maintenance of
treatment gains (i.e., stepped-down services). Finally, we use a brief clini-
cal vignette to highlight opportunities for technology to address limita-
tions and gaps in care in the treatment of individuals with FEP.
Detection: Clinical Decision Support

and Risk Prediction
Early intervention can reduce the long-term impact of a psychotic epi-
sode; its effectiveness, however, is dependent on valid early detection.
An array of instruments have been used to identify individuals at risk
for conversion to an episode of psychosis (Rotondi et al. 2005), includ-
Using Technology to Advance Early Psychosis Intervention 351
ing the Structured Interview for Psychosis-Risk Syndromes (SIPS;

Miller et al. 2003) and the Comprehensive Assessment of At-Risk Men-
tal States (CAARMS; Yung et al. 2005), as well as traditional symptom
severity interviews such as the Brief Psychiatric Rating Scale (BPRS;
Overall and Gorham 1988) and the Positive and Negative Syndrome
Scale (PANSS; Kay et al. 1987). These instruments typically contain
some combined examination of family history of psychotic disorder
and the severity of positive, negative, and general psychopathology
symptoms. Meta-analytic estimates (Fusar-Poli et al. 2012) suggest that
once young people are identified with one of these instruments as being
at high risk, they have an 18% risk of transition after 6 months, 22% after
1 year, 29% after 2 years, and 36% after 3 years.
Determining risk involves a complex Bayesian calculation that com-
bines multiple factors concurrently. Technologies that automate this
process could facilitate such calculations, thus making them more com-
mon in regular practice. Cannon and colleagues (2016) piloted the use
of a psychosis risk calculator built on clinical, cognitive, and demographic
characteristics, including select SIPS items, cognitive skill in symbol
coding, a brief general cognitive assessment, a recent decline in func-
tioning, the experience of trauma, male gender, and a history of psycho-
sis. This calculator was later validated by a second research group
(Carrión et al. 2016), providing strong predictions of conversion that
improved on existing instruments (area under the curve 0.790: 95% con-
fidence interval 0.644–0.937). Predictions are represented in two plots
that symbolize the 1- and 2-year risk of conversion to psychosis based
on a sample of 596 clinical high-risk participants from the North Amer-
ican Prodrome Longitudinal Study (Figure 20–1).
Cannon and colleagues’ risk calculator is comparable to extant risk
calculators for other chronic medical conditions, including heart dis-
ease and cancer. However, given the paucity of published studies
demonstrating effective use of the risk calculator in treatment settings,
the impact on long-term outcomes of having access to such a calculator
is unknown. It is also unclear whether such tools are best suited for pri-
mary care or general mental health clinics rather than those dedicated
to specialized care for FEP. Regardless, providers who use calculators
that easily and concisely summarize risk estimates may be empowered
to better identify and triage individuals with greater needs, share these
estimates with clients and their families to engage them in care, and use
such estimates to inform treatment selection.
One limitation of automated risk calculation is its dependence on
factors that are already identified or assessed by clinicians. Other tech-
nologies go a step further by attempting to identify risk factors that are
undetectable to typical clinical interviews. One prototype of such a tool
is in the automated analysis of free speech. Bedi and colleagues (2015)
assessed 34 clinical high-risk individuals on a quarterly basis after com-
FIGURE 20–1. Screenshot of the North American Prodrome Longitudi-

nal Study individualized risk calculator.
Source. Cannon et al. 2016; http://riskcalc.org/napls. The photos of computing devices
were downloaded from the PEXELS database (www.pexels.com). Used with permission
of the developers.
pleting open-ended, 1-hour qualitative interviews at a baseline visit. Of

this initial sample of 34 participants, 5 individuals converted to schizo-
phrenia. The speech patterns of these 5 were compared with the non-
converters according to their internal coherence using latent semantic
analysis (LSA). LSA estimates the coherence of a speech sample by as-
sessing the extent to which each utterance relates to the content of
speech that preceded that utterance. The strongest predictors that dis-
tinguished converters from nonconverters was the minimum coherence
(or maximum discontinuity) during the interview, as well as use of de-
terminers (e.g., that, what, whatever) and maximum phrase length. With
these characteristics, a machine-trained algorithm was able to use base-
line speech data to successfully predict conversion with 100% accuracy
relative to SIPS predictions at the same points, which were significantly
less accurate.
This methodology was later validated with multiple forms of speech

elicitation in a second sample of 59 individuals at clinical high risk
(Corcoran et al. 2018). This study demonstrated consistent accuracy
(72%) in the ability of the LSA algorithm to distinguish the speech of in-
dividuals with recent-onset psychosis from that of nonclinical controls.
Although all of these technologies are in their infancy, they show re-
markable promise in improving quality and dissemination of tools aim-
ing to predict an individual’s future conversion to psychosis. Between
computerized risk calculators and automated analysis of speech, a 2- to
3-hour assessment could considerably improve the quality of such pre-
dictions, whether specifically in FEP clinics or in settings where staff are
likely to encounter individuals at potential risk (i.e., schools, commu-
nity mental health centers, or primary care clinics).
Mobile Interventions: A Therapist

in Your Pocket
Although assessment and risk calculators provide useful tools for identi-
fying individuals broadly at risk (or in need of treatment), there is addi-
tional utility for individuals in identifying their high-risk moments. There
is increasing evidence that psychotic symptoms are not static but, rather,
that episodes emerge when an individual is faced with environmental
stressors. Individuals in the midst of a first episode demonstrate increased
sensitivity to stressful events, ascribe aberrant salience to otherwise neu-
tral stimuli (Reininghaus et al. 2016a), and tend to anticipate threat at
greater levels than do control subjects (Reininghaus et al. 2016b).
These findings have bolstered extant theories of psychosis, such as
the cognitive model of positive symptoms (Garety et al. 2001), which ar-
gues that psychotic symptoms emerge from aberrant cognitive pro-
cesses in response to stress (i.e., the stress-vulnerability model) (Zubin
and Spring 1977). Advances in mobile health (mHealth) technologies al-
low assessment at these critical moments and opportunities to disrupt
the means through which symptoms impact functioning. Ecological
momentary assessment (EMA) involves a device (usually a smart-
phone) that prompts an individual to complete brief assessments in
day-to-day life. Sudden changes in presentation or symptom exacerba-
tion might identify a relapse; when these changes occur, brief interven-
tions could help prevent psychosis.
The FOCUS smartphone intervention system (Figure 20–2) prompts
users to complete brief (i.e., two-item) assessments of changes in a num-
ber of domains, including sleep quality, auditory hallucinations, mood,
and social engagement (Ben-Zeev et al. 2013). FOCUS was developed
by researchers, clinicians, and individuals with schizophrenia and is
designed to assess current symptoms and deliver brief interventions

that are well suited to address those changes. In pilot studies of persons
with chronic schizophrenia (Ben-Zeev et al. 2014), individuals were
prompted five times per day (in addition to having ongoing access to
the app as desired). On the basis of responses to brief assessments of
changes in the clinical areas of interest, the app provides brief interven-
tions with illustrative images (in text, audio, or video) derived from var-
ious evidence-based approaches in the treatment of psychosis: cognitive
restructuring, behavioral activation, illness management and recovery,
social skills training, and sleep hygiene. Pilot research has demonstrated
FOCUS to be acceptable to patients, and over a study period of 1 month,
a sample of 33 individuals with schizophrenia or schizoaffective disorder
experienced significant reductions in positive symptoms of psychosis,
general psychopathology, and depression, mood, and anxiety symptoms
that were significantly correlated with the number of contacts recorded
by the FOCUS system (Ben-Zeev et al. 2014).
Beyond delivering illness management tools in real time, mHealth
systems can also be used to facilitate ongoing assessment and coordina-
tion with the clinic. Providers can view securely delivered FOCUS data
shortly after they are collected and, in response, contact individuals di-
rectly to conduct additional assessment or provide support. These as-
sessments can also be used in in-person sessions to generate insight or
facilitate changes in treatment plan. A provider and client can reflect to-
gether on changes throughout the week; examine relationships be-
tween cognitive, emotional, and behavioral factors; and build a coping
strategy accordingly.
Measurement-based care (MBC), which incorporates frequent as-
sessment into the course of individual psychiatric treatment to facilitate
clinical decision making, is demonstrated to consistently improve out-
comes across a range of conditions (Fortney et al. 2017), but few studies
have examined the impact of implementation of MBC in FEP treatment
settings. Case studies have been reported that outline the roles of
mHealth support specialists as providers who check, interpret, and fol-
low up on EMA data. With improved access to day-to-day functioning,
the mHealth support specialist is empowered to provide personalized
interventions (e.g., sleep hygiene support, cognitive restructuring) by
phone or video conferencing, depending on need in a time-sensitive
manner (Jonathan et al. 2017).
Niendam and colleagues (2018) provided an example of mobile
MBC in their description of Ginger.io, an app that prompts individuals
to respond to daily and weekly surveys of medication adherence,
mood, and social activities and weekly surveys of symptoms. The re-
sults of these surveys are provided to clinicians via a simple dashboard.
Additionally, clinicians are provided with alerts and warnings if pa-
tients report significant changes via the app. Clinicians are then in-
FIGURE 20–2. Example screenshots of FOCUS (Ben-Zeev et al. 2013)

video (left) and text-only interventions (right).
Source. iStockPhoto. Posed by model.
structed to review survey responses with clients during their regularly

scheduled sessions. Participant retention in the Ginger.io study was
high (66% of enrolled individuals remained for at least 6 months), and
people consistently completed the weekly (77%) and daily (69%) sur-
veys. Almost half (40%) of individuals reported that the app helped
them remember to take medication. The daily and weekly assessments
of mood and positive symptoms were highly correlated to clinician-
rated symptoms, suggesting that these tools provide valid estimates of
symptom levels.
A similar system, LifeData, conducts daily and weekly surveys re-
lated to similar key recovery outcomes and shares them with providers
(Kumar et al. 2018). More than half (56%) of all eligible clients across
four community outpatient early psychosis clinics enrolled, and, of this
sample, a majority reported that sharing daily and weekly surveys with
their treatment team improved the quality of their treatment services,

their relationship to the treatment team, and their motivation to main-
tain medication and symptom management routines.
Although EMA might improve assessment by providing access to
clients in the moment and in their daily lives, other limitations remain.
EMA is still susceptible to social desirability or minimization and can be
perceived as burdensome or disruptive to clients. To address these lim-
itations, systems have been developed to collect data to generate esti-
mates of risk using existing sensors in smartphones. Passive sensing
using existing mobile phone sensors—including cameras, micro-
phones, accelerometers, and GPS—has been piloted in general under-
graduate samples to predict relevant psychological domains. In these
pilot studies, sensor-generated estimates of physical activity, sleep du-
ration, and geospatial locations were associated with daily stress (Ben-
Zeev et al. 2015). More recently, these methods have been piloted in
samples of individuals with schizophrenia. Although full study results
are forthcoming, five individuals’ data streams over the course of 1 year
have been published to demonstrate the wide range of relapse signatures
that precede a psychiatric hospitalization in both sensing and EMA
data. For example, individuals from this sample produced data sug-
gesting different indicators, including a significant physical activity
drop-off, sleep disruptions, atypical device activities, and exacerbation
of symptoms recorded via EMA (Ben-Zeev et al. 2017).
Combined with a clinician review mechanism (i.e., a dashboard), if
signs of relapse can be identified and relayed to treatment teams, inter-
ventions can be provided much more efficiently and effectively to pre-
vent significant functional disruption. Although these are exciting
developments, empirical work examining these technologies is scant,
and future study and validation will define the specific uses of these
tools. Nonetheless, at present, a number of potentially useful technolo-
gies have demonstrated feasibility and acceptability in the population
with severe mental illness.
Online Interventions and Telehealth:

A Clinic on Your Desktop
Mental health systems that leverage mobile devices often provide so-
called “just-in-time” interventions, or brief strategies that are designed
to provide support in the moment as a supplement to usual care. Addi-
tional advancements using technology go beyond such brief services to
provide prolonged access to services, including evidence-based ther-
apy modules, online social communities, and contact with clinical pro-
viders. The delivery of integrated services online circumvents a number
of ongoing barriers in the treatment of FEP. These systems are proposed
to require fewer individual providers per client and therefore could be

more affordable to clinics. They are also designed to increase availabil-
ity because they can be accessed at any time and do not require the in-
dividual to leave home. This ease of access and anonymity could reduce
barriers instituted by the perceived stigma of regularly attending a psy-
chiatric clinic in person. Further, if online interventions are able to en-
gage clients who have completed a course of treatment in a first-episode
clinic, they could reduce the drop-off in treatment benefits that tends to
occur after individuals terminate these services (Gafoor et al. 2010). On-
line intervention services could be a proper strategy for delivering
anonymous “booster” sessions after the completion of more intensive
services. In this manner, online and mobile interventions provide a po-
tential critical answer to the extant gap in stepped-down care for indi-
viduals with FEP.
One example is HORYZONS (Alvarez-Jimenez et al. 2013), an on-
line system that integrates peer-to-peer social networking, individual-
ized psychosocial interventions, and contact with providers as online
facilitators (Figure 20–3). HORYZONS was based on positive psychol-
ogy principles and self-determination theory, with a particular focus on
generating autonomy, mastery, and a sense of social connection. Given
the particular disruption to one’s social network that often occurs be-
cause of a psychotic episode, HORYZONS is centered on the social
community. It is designed to provide a Facebook news feed–style up-
date stream, where users can share their experiences and perspectives
with one another. Further, participants can propose and complete spe-
cific behavioral challenges and solicit suggestions and feedback
through a “talk it out” forum. In addition to the social community,
HORYZONS provides psychoeducation and interactive therapy mod-
ules in line with mindfulness-based intervention, positive psychology
techniques, and facilitated social connections. The system is designed for
a provider to function in the role of facilitator; the facilitator can suggest
content to individual clients, monitor site content for safety, and contact
individuals to provide additional support should the need arise.
Pilot data for HORYZONS (Alvarez-Jimenez et al. 2013) included 20
individuals who had experienced a recent FEP, and results demonstrated
that individuals used the system frequently (log-ins M=13.50, standard
deviation=11.95) and on a consistent basis (70% for at least 3 of 4 weeks).
Participants found it to be useful, and 90% said they would recommend
it to others. In particular, social networking features were popular (95%
of participants used these features), and usability statistics compared
favorably with existing short-term open-access Internet-based mental
health programs. Over the 1-month study period, users also demon-
strated a significant drop (d=0.60) in depressive symptoms.
Web-based interventions have also been applied to address barriers
that emerge in the application of family-based therapies and psychoed-
FIGURE 20–3. Screenshot of HORYZONS, a platform designed for in-

dividualized positive psychology interventions and peer support for indi-
viduals with first episode of psychosis.
Source. Alvarez-Jimenez et al. 2013; rawpixel.com via PEXELS. The photo of the com-
puting device was downloaded from the PEXELS database (www.pexels.com).
ucation for the loved ones of an individual with FEP. Rotondi and col-
leagues (2005, 2010) designed an online psychoeducation intervention for
both individuals with schizophrenia (not exclusively FEP) and a support
person involving a website that provides psychoeducation, online ther-
apy group bulletin boards, an opportunity to ask experts questions, and
relevant community news. Studies examining this intervention randomly
assigned people with schizophrenia and family supports (preserving dy-
ads) to treatment as usual or an enhanced treatment condition that in-
volved access to the online intervention. Across studies, this approach
appeared to be feasible and acceptable to participants. Three-month out-
comes revealed that individuals with schizophrenia with access to the in-
tervention reported lower perceived stress and higher social support
relative to the treatment-as-usual condition (Rotondi et al. 2005). Follow-
up studies examining one-year outcomes (Rotondi et al. 2010) revealed
a significant decrease in positive symptoms and an increase in knowl-
edge of illness among individuals with schizophrenia. Support persons
similarly experienced an increase in knowledge about the illness rela-
tive to usual care.
Conclusion
There are ample opportunities for digital health technologies to en-
hance the delivery services for individuals with FEP. We provide a de-
monstrative example of how these approaches may be integrated in a
technology-enhanced coordinated care clinic (TECCC) for FEP.
Case Example
Eric is an 18-year-old high school senior. At the behest of his parents and
friends, Eric presented to his primary care provider, reporting to her that
he has felt “down, tired, and worn down” for several months. What Eric
did not report was that he has also experienced consistent auditory hal-
lucinations that comment on his daily activities. He has also stopped at-
tending extracurricular activities, and his grades have dropped from a
3.0 GPA to a semester GPA of 1.0. Noting that Eric reported that his
mother has bipolar disorder and a paternal uncle had schizophrenia,
Eric’s primary care physician referred him to a TECCC for FEP. On ar-
rival at the TECCC, Eric completed a 2-hour baseline assessment, in-
cluding cognitive assessments, a prodromal symptom interview, and an
open-ended speech sample, which was automatically transcribed and
run through machine-learning algorithms. Eric’s risk of conversion
probability was calculated by the prodromal risk calculator, and he was
scheduled for a series of appointments with individual and family pro-
viders, as well as medication management with the clinic psychiatrist.
Partially as a result of these services, Eric’s functioning stabilizes. He
began scheduling get-togethers with old friends and engaging with his
parents and siblings. Eric’s interpersonal style in treatment, however, is
somewhat guarded. He is quiet, shy, and sometimes reluctant to share
his difficulties and stressors with his individual providers. Eric does not
tell his treatment team that he has been experiencing increased distress
during evenings in the last several weeks as he anticipates final exams,
the end of high school, and the departure of close friends for college. As
he ruminates, particularly after dark, he notices that he starts to feel as
though his neighbors are watching his computer monitor, a suspicion
that is fostered by his continued auditory hallucinations.
Thankfully, Eric has access to an mHealth app after hours. On this app
Eric reports that he has been experiencing increased auditory hallucina-
tions in the evenings. When his ratings of depressive or positive symp-
toms spike, Eric’s mobile app provides brief suggestions of interventions
to try, including cognitive restructuring exercises that challenge his beliefs
about the power and uncontrollability of his voices. The app also pro-
vides him with reminders to continue taking his medication. Together
with passive sensing of changes in behavior (i.e., Eric’s late hours and in-
creased phone activity into the late hours), these EMA ratings are trans-
mitted to Eric’s individual provider at TECCC. This leads to an open
conversation at the clinic about recent changes in Eric’s presentation. Eric
is relieved to able to discuss these stressors with his provider.
After several months of active treatment, Eric demonstrates signifi-

cant changes since he first engaged with his primary care provider. He
is open with friends and family members about his psychotic symp-
toms, and he has a well-crafted relapse prevention plan. He plans to at-
tend a local college and is working part time at a nearby coffee shop. He
also is interested in providing peer support to other individuals receiv-
ing care at TECCC. Because of his improved functioning and busy
schedule, he realizes he is unlikely to be able to attend twice-weekly ses-
sions at the TECCC. As his providers prepare for the end of their regu-
larly scheduled visits, they introduce him to the online recovery
community through TECCC. In this online recovery community, Eric
has ongoing access to continuously updated evidence-based therapy
modules. He is particularly interested in those centered on a new inter-
est of his, meditation. He also appreciates that the online community
has a base of users who are open about their own experiences with psy-
chosis. Eric has time to come back to the clinic only once every month or
two, but he logs on to the online community frequently, particularly
when he is more distressed.
Eric’s parents are also involved in the stepped-down relapse pre-
vention plan. They are given access to a companion online community
for the loved ones of individuals with psychosis. This is particularly
useful as Eric’s parents prepare for his move to his own apartment. They
seek support not only from clinic facilitators but also from fellow family
members of young people with FEP who have dealt with the stress of
watching their loved one recover. Eric and his family members learn
new skills to support him as he recovers, moves away from home, and
eventually graduates from college with a degree in computer science.
Eric’s story demonstrates that technology-enhanced interventions do

not have to revolutionize existing treatment practices; rather, they can
have a significant impact on the effectiveness and accessibility of treat-
ment through addressing existing gaps in care. None of these technolo-
gies are proposed at present to replace existing in-person mental health
services; rather, they are proposed to supplement and improve existing
care to amplify its potential impact. Although available tools provide ex-
citing developments in ideal conditions, this area is a nascent one.
Many health technologies reviewed in this chapter demonstrate im-
pressive findings in pilot trials and feasibility studies; however, fewer
have been well validated in large-scale randomized trials. Further, a
number of the interventions described in this chapter have promising
results with samples of individuals with chronic schizophrenia but not
persons in the midst of FEP. Although large-scale demonstrations of ef-
fectiveness of the newest technologies in FEP are few, their feasibility is
clear and their potential is notable. As these tools and systems evolve,
the number of clinical uses that could be addressed by them will only
grow. If the development of FEP services mirrors development of nu-
merous areas in health services, or even the development of business or
transportation, technology will play a significant role in expansion and

sustainability of effective interventions for this population.
KEY CONCEPTS
• Several technology-enhanced assessments and interventions
show promise in the treatment of first-episode psychosis
(FEP); these tools apply across detection, intervention, and
maintenance of treatment gains.
• Technology-enhanced interventions may be particularly
well suited to address challenges that are specific to FEP
care, including individual engagement, cost, and step-
down care services.
• Prototype digital health resources have limitations. They
lack large-scale empirical validation, and many have been
examined only in a chronic psychosis population.
1. What existing service gaps or weaknesses in your particular

clinic are best addressed with technology?
2. What is the degree of comfort of your clinical staff with using

technology in FEP treatment? How does this comfort level
compare with that of the typical individual?
3. What is the current role of the Internet and mobile devices in

the lives of individuals at your clinic? How might any existing
enthusiasm in this area be leveraged in the service of recovery?
Suggested Readings
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Am J Psychiatr Rehabil 15(4):357–376, 2012
O’Hanlon P, Aref-Adib G, Fonseca A, et al: Tomorrow’s world: current

developments in the therapeutic use of technology for psychosis.
BJPsych Advances 22:301–310, 2016)
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CHAPTER
21
Inpatient Care for Early

Psychosis
A RECOVERY-ORIENTED PERSPECTIVE
Zheala Qayyum, M.D.
Kristen Sayles, M.S., R.N.
Hyun Jung Kim, M.D.
Gerrit Van Schalkwyk, M.B., Ch.B.
INDIVIDUALS in the early stages of psychosis may require hospi-

talization for a variety of reasons. Symptoms may be severe to the point
of impairing functioning. Individuals’ thoughts, speech, and behavior
may be a source of concern to themselves or others, leading to contact
with mental health providers and, potentially, inpatient treatment. In
some cases, individuals may come into contact with law enforcement
owing to behaviors that are a consequence of their mental illness. Un-
fortunately, hospitalization is frequently the result of a concern that is
held by family, legal, or medical systems, and patients may not always
understand the process as a therapeutic intervention (Van Schalkwyk et
al. 2015a). Inpatient hospitalization may involve direct or observed ex-
posure to emergency medication administration, restraint, or seclusion,
and patients who do not have an explicit understanding of the purpose
365
of the inpatient setting may form negative impressions of it being a re-

strictive environment in which they find themselves contained against
their will.
Despite this potential disconnect, hospitalization is also an opportu-
nity to develop shared treatment goals, clarify diagnosis, and engage
the patient’s family in a critical process of ongoing psychoeducation. In
this chapter, we present a recovery-oriented approach to inpatient treat-
ment for people in early psychosis in which we aim to shift the focus
from rapid symptom reduction and medication toward a consideration
of how evidence-based treatment can be best provided in a way that is
responsive to the patient’s own agenda. It is our view that although
such an approach expands the task of the initial hospital stay, it has the
potential to promote better overall engagement with services and lead
to improved treatment outcomes in terms of both symptom relief and
psychosocial aspects of recovery.
Developing Shared Treatment Goals

The goals of hospitalization may appear obvious when considered from
a purely biomedical framework—from this perspective, the goal is to
make an accurate diagnosis and initiate treatment that will reduce
symptoms. Although this is an important goal, it is seldom the only
goal and may at times be in conflict with the patient’s perspective on the
key issues he or she is facing. In a qualitative study of 11 individuals
who spoke about their experience of initial treatment for psychotic
symptoms, participants described a disconnect between their major
concerns—everyday challenges such as getting along with family and
doing well at work and school—and the issues that appeared to be the
focus of their treatment, such as safety, medication adherence, and
symptom reduction (Van Schalkwyk et al. 2015a). Ironically, in some
cases it appeared that a treatment approach that overemphasized these
aspects ultimately undermined treatment engagement and thus wors-
ened, rather than improved, adherence to recommended treatment.
The experience of individuals in the first episode of psychosis has
been the subject of a number of qualitative studies (Boydell et al. 2010),
and a key finding is the importance of developing shared priorities for
treatment. In an optimal setting, this should not lead to the develop-
ment of conflict. If patients receive detailed education about their diag-
nosis, the likely clinical course, and the potential utility of a range of
treatments, it is likely that they, too, will prioritize treatment that seeks
to minimize their symptoms. Challenges arise when these treatment
goals are imposed in a noncollaborative manner.
Even in instances where clinical teams are motivated to develop
shared treatment goals, there may be challenges when patients do not
Inpatient Care for Early Psychosis 367
experience their current situation as indicative of a treatable illness. In

these cases, a number of strategies are possible. First, it is critical to ex-
plore whether there are any issues in the patient’s life around which he
or she would like to receive support. In our clinical experience, individ-
uals in the early stages of psychosis often have prominent concerns
around issues such as identity formation, mood symptoms, and social
functioning. Empirical research exploring treatment priorities has also
identified the importance of general and physical wellness for many pa-
tients (Ramsay et al. 2011). By identifying and including these goals in
the overall treatment approach, it is more likely that a collaborative
treatment relationship will emerge from which ongoing discussions can
be had around aspects of treatment that patients may consider to be of
lesser importance.
It is important to recognize that patients may decide not to take
medication and that having a diagnosis of a psychotic disorder does not
imply that a patient is unable to exercise choices as a health care con-
sumer. Patients may believe that the side effects of medication will out-
weigh the benefit or that they are not experiencing sufficient
impairment from their symptoms to warrant medication in the first
place. In inpatient settings, our experience is that power struggles and
paternalistic approaches are for the most part ineffective and may in
some instances lead to only short-term treatment adherence that falls
apart after the patient returns home. Rather, an ongoing dialogue is in-
dicated, in which trust is built over time and an effort is made to under-
stand in better detail the patient’s own vision for his or her life. This
may include frank feedback from the provider on how the patient’s
symptoms could obstruct these goals but should also include support
and suggestions for other practical strategies for how such challenges
can be overcome. In a recent clinical example, a patient who was refus-
ing medication frequently became paranoid during group therapy and
would shout at other patients and then run to her room. In the course
of a therapeutic encounter, it was suggested to the patient that the way
she was responding to these situations put her at risk of being targeted
in her community and that she might benefit from learning some new
coping skills for managing these uncomfortable feelings.
There may be instances when patients continue to avoid medication
despite efforts at collaborative treatment engagement, and clinical
teams become concerned as to the patients’ safety and ability to achieve
a meaningful recovery. A range of approaches to this problem exists.
Some jurisdictions will support the involuntary administration of med-
ication, but in our view, this approach has significant limitations, and
when it is used, it should not replace ongoing efforts at developing a
shared treatment plan. At times, it may be appropriate to allow a pa-
tient to reenter his or her community even if he or she is experiencing a
high degree of symptoms, while ensuring the ongoing availability of
treatment and engaging family to the maximum extent possible to en-

sure the patient’s safety. This experience of allowing the patient to have
a chance to succeed may serve to greatly advance a treatment alliance,
provided necessary safety planning is in place—this includes ensuring
that a clinical team will be available to check in on the patient and that
family feels empowered to bring the patient back to the hospital if
safety concerns arise. Patients may end up doing well despite the con-
cerns of the clinical team. And when patients do return to the hospital,
they may immediately have a greater degree of trust in a clinical team
that did not coerce them into treatment but remains available to provide
support in helping them return to their communities more successfully.
Milieu Considerations
A well-managed therapeutic inpatient environment can set the stage for
effective treatment engagement, but considerable effort is required to
achieve this aim. Teenagers and young adults experiencing early psy-
chosis require several milieu considerations in order to decrease their
distress, facilitate optimal functioning, and provide an environment
that supports recovery. Critical to this aim is an environment that pro-
vides evidence-based care that is free of coercion, provides appropriate
interventions to decrease anxiety, and instills hope and a sense of em-
powerment for both the patient and his or her family.
The inpatient environment has the potential to generate anxiety, be-
ing an unfamiliar space where individuals do not have access to com-
forts and supports that may have been available at home. Further,
anxiety symptoms have been clearly linked with psychosis (Achim et
al. 2011; Addington et al. 2011; Yun et al. 2011). A study of at-risk ado-
lescents described the profile of an individual at high risk for psychosis
as being characterized by high levels of anxiety symptoms, particularly
cognitive anxiety (Granö et al. 2014). As such, it is of primary impor-
tance that efforts are taken to reduce sources of anxiety and provide
necessary structure that can reduce risks for thought and behavioral
disorganization. Cognitive-behavioral therapy and psychoeducational
groups designed to decrease anxiety and increase problem-solving
skills for both the patient and the family are linked to decreased emer-
gency department visits and decreased negative symptoms (Calvo et al.
2014). Other non-medication-based interventions to aid in this en-
deavor include yoga, sensory interventions, art therapy, music therapy,
and problem-solving groups. Such interventions may both directly help
symptoms and increase resilience by imbuing a sense of self-efficacy
and capacity for positive, prosocial engagement.
The use of sensory rooms is a proactive prevention tool that helps to
maintain a noncoercive therapeutic environment while providing a
calm and quiet space where a person with psychotic symptoms can feel
safe. Sensory rooms are generally a well-soundproofed space that con-
tains a range of items that can either increase sensory stimulation (e.g.,
music players, deep and soft chairs, scented oils) or decrease stimulation
by providing an escape from the regular milieu environment. Sensory
rooms allow staff to build rapport and remain present with the patient
during times of distress but also remain open to continued expression of
emotions in a safe space (Seckman et al. 2017). In addition, the use of
sensory room tools ensures optimal sensory modulation tailored to in-
dividual preferences and needs, which allows the patient to practice
self-regulation during times of distress (Sutton et al. 2013). This in turn
increases resiliency and autonomy and decreases risk for relapse.
Studies suggest that yoga is effective in decreasing anxiety and in-
creasing self-efficacy (Kwasky and Serowoky 2018). In addition, yoga
has the potential to help young people learn to self-soothe, regulate emo-
tional responses, and decrease distress from anxiety-producing situations
such as hospitalization and family conflict (Re et al. 2014). Use of art, in
particular mandala art therapy, can increase a sense of hope and poten-
tially increase subjective well-being and resilience (Kim et al. 2018).
It is important that staff supporting the milieu are involved with
regular discussions regarding the patient’s diagnosis and clinical needs.
A daily “huddle” may be helpful in order to review each case in detail,
from initial presentation to the last 24 hours of each patient’s response
to interventions. At our program at Butler Hospital, we use a range of
additional mechanisms for improving dissemination of the clinical for-
mulation and treatment plan. Key techniques include the following:
• Biweekly walking rounds with the patient and entire treatment team
to increase knowledge and communication from a patient-inclusive
perspective, which serves to get everyone on the same page, includ-
ing the adolescent or young adult patient
• Weekly case studies to learn from and increase future skillful inter-
ventions
• Monthly educational meetings designed to teach staff new skills,
such as mindfulness, cognitive-behavioral therapy, and general
group leadership
• Biannual team building exercises to increase trust, communication,
and active listening skills
• Leading by example and providing in-the-moment feedback for
staff during their care of a patient with psychosis, which leads to in-
creased competency and tolerance when intervening with an agi-
tated or paranoid patient
• Leadership that validates staff and encourages them to use interven-
tion tools that empower the patient during times of stress or impul-
sive behaviors rather than coercive interventions to maintain safety
Youth in their first episode may experience both short- and long-
term fear if exposed to other patients who have significant issues
around aggression or appear disengaged from treatment or whose be-
havior otherwise suggests that mental illness is a chronic and debilitat-
ing condition. In this context, we find it optimal to place patients
experiencing their first episode of psychosis on our adolescent unit,
where they can experience support and hope by observing similar-age
peers who may have less chronic or serious mental health concerns.
Supporting youth in the first episode of psychosis during hospital-
ization is not without challenges. There are financial challenges, with
limited resources available to support education and training of staff
and to purchase necessary equipment for therapeutic interventions.
The short length of stay that is typical in modern hospitals may make it
difficult to achieve adequate stabilization and illness education. A short
length of stay may also contribute to an ever-changing milieu dynamic
(given rapid patient turnover), which can cause an increase in psychotic
symptoms and anxiety despite the therapeutic environment.
Family Engagement
The involvement and engagement of the family in the treatment of pa-
tients with early psychosis cannot be emphasized enough, particularly
in the inpatient setting. Family engagement has consistently been asso-
ciated with better outcomes and can influence both treatment adher-
ence and the course of the illness (Del Vecchio et al. 2015; Doyle et al.
2014; Knock et al. 2011). It is important to bear in mind that because the
onset of psychotic symptoms can begin in adolescence, the patient may
still be embedded within the family and thus may be subject to the atti-
tudes, beliefs, and help-seeking behaviors of the family. The family’s
concerns can include worry about isolative behaviors or social and
emotional withdrawal, fear of stigma, fear of loss, and parental guilt
(Connor et al. 2016). Understanding that family systems can be complex
can be helpful in identifying the key members who provide support
and are trusted by the patient. In the case of minors, clarification of legal
custody status and authority for medical decision making is important
to obtain, as well as supporting documents when necessary.
During an inpatient hospitalization, it can be distressing for family
members to relinquish the care of a loved one to the inpatient treatment
team while facing unanswered questions and uncertainty. Some fami-
lies may have uncertainty about how to discuss their concerns with the
mental health team and can benefit from clear and repeated information
and an invitation to engage (Lucksted et al. 2016). Establishing contact
with the family at the onset of the hospitalization and involving them
in treatment planning by arranging formal family meetings can help
mitigate some of this expected anxiety.
Family meetings provide an opportunity to synthesize input from

family members, outpatient providers, school systems, pediatricians or
primary care physicians, and social services when involved. It is often
helpful to gather the key players, especially those who have established
a trusted relationship with the patient and family prior to the hospitaliza-
tion. Our experience from collaborating with the Specialized Treatment
Early in Psychosis (STEP) program at Yale University has illustrated that
such collaboration allows for a smoother transition from outpatient care
to a shorter, better-coordinated inpatient hospital stay when needed and
vice versa. This also allows both inpatient and outpatient teams to ad-
dress the family’s uncertainty about the course of treatment following the
acute hospitalization and to establish direct engagement.
One of the most important goals of having a family meeting is to fos-
ter engagement and provide thorough psychoeducation. The diagnosis,
including genetic and environmental risks such as substance abuse and
trauma, should be discussed while providing a scaffolding to facilitate
appropriate interpretation of the information provided. It is also im-
portant to address diagnostic uncertainty when present. The uncer-
tainty may be due in part to ambiguity in clinical presentation,
prominent confounding factors, or lack of data to ascertain with clarity
the onset of an early psychotic episode. Education about symptoms
such as hallucinations and paranoia should be presented in a way that
minimizes stigma about psychiatric illness and medical jargon. This
makes symptoms—such as an exaggeration of the normal fear re-
sponse—more relatable and understandable. Although it is necessary
to explain the roles of stress and individual coping responses in the ill-
ness, it is also important to highlight the role of family support and re-
silience. which may instill hope and promote a sense of agency in the
family. At times, family members may be overwhelmed with all the in-
formation and details of the discussion, so it is appropriate to provide
informational materials to support the data reviewed that family can re-
fer to at a later time.
Families may benefit from therapeutic support of their own in order
to find guidance in dealing with stressful situations, gain a better under-
standing of the illness, and improve familial communication. This can
help reduce such emotions as criticism, hostility, enmeshment, and con-
flict. Families also have their own beliefs about psychopharmacological
interventions that are important to explore because they will influence
patient and family engagement. This may be especially pertinent to treat-
ment adherence once the patient transitions out of the inpatient setting
and even more so depending on the severity of the illness. Family mem-
bers are often ideally suited to provide medication monitoring and to en-
sure the patient’s adherence to treatment recommendations.
Often, family members will ask for guidance about how to navigate
the youth’s independence while needing to provide supervision, espe-
cially in the critical period following discharge. It is helpful to identify

shared goals with the patient that can be worked toward with family
support. Emphasis should be placed on focusing on health and well-
ness as the path to enable attainment of social and academic engage-
ment or employment while recruiting the family’s support in fostering
a sense of agency in the youth. At times, it can be difficult to foretell the
pace of these next steps; often, they require a slow and deliberate reas-
sessment of the patient’s progress and stress tolerance. Here again, if
possible, introduction and involvement of the outpatient treatment
team while the patient is hospitalized can be extremely helpful.
Family engagement is also essential in safety planning for dis-
charge. Although the risk of violence due to psychiatric illness is low,
there is a relatively elevated risk of violence toward self and others as-
sociated with early psychosis, compounded by impulsivity and sub-
stance use, particularly in those who are not taking antipsychotic
medications (Moulin et al. 2018; Nielssen et al. 2012). Ensuring that the
medications are securely stored and appropriately administered and
that the patient does not have access to weapons is crucial.
If there are significant deficits in independent functioning, necessi-
tating greater supervision, support, and monitoring, an assessment of
the patient’s decisional capacity for the short term may be required. The
inpatient hospitalization may be the time to introduce the family to pur-
suing conservatorship of the patient for medical decision making if nec-
essary. This should be considered only when attempts at fostering
patient autonomy and decision making have failed, when ongoing non-
adherence to treatment recommendations have evidently placed and
continue to place the patient at higher than acceptable risk of unsafe be-
haviors, or when the patient is no longer capable of taking care of him-
self or herself even with the supports provided. It is important to
approach this as a last resort and on a temporary basis, with the plan to
reevaluate the conservatorship while working to enhance the patient’s
ability to regain independent functioning.
Making and Communicating

a Diagnosis
A thorough biopsychosocial formulation can be a valuable tool in mak-
ing a developmentally informed assessment of early psychosis. Often,
the inpatient hospitalization is the first contact the patient and the fam-
ily has with the mental health system. It is therefore critical that they ex-
perience the diagnostic process as thorough and trustworthy and that
the diagnosis is communicated in a thoughtful and convincing manner.
A comprehensive diagnostic approach should involve the exclusion
of drugs of abuse or medical illness as contributing to the presenting
symptoms (Gray et al. 2016). When presentations are atypical, addi-

tional workup may include electroencephalography and magnetic res-
onance imaging to exclude less common neurological disorders
(Dalmau et al. 2008). A developmentally informed perspective is also
valuable in placing the symptoms in context—early trauma or signs of
developmental delay may speak to the potential for a distinct underly-
ing diagnosis. Autism spectrum disorders are a particularly important
consideration to explore because there can be significant overlap in clin-
ical presentation (Van Schalkwyk et al. 2015b).
Hearing the diagnosis of a psychotic disorder can be difficult for a
family, especially because in early psychosis many patients are navigat-
ing school and beginning to separate and individuate from their par-
ents, which the illness can disrupt. There may also have been symptoms
preceding the onset of frank psychotic symptoms that were more con-
sistent with anxiety, depression, or obsessive-compulsive disorder,
leading to diagnostic confusion. It is often helpful to emphasize that
mental illness is something the patient has and does not define the pa-
tient. Supporting the identity of the patient is paramount, and this is of-
ten lost in the context of the patient and family members feeling
helpless in the confines of an inpatient unit.
For some patients and families, the biological model of explaining
the illness may provide a framework for understanding what to expect.
For many other patients, however, the explanation of psychiatric symp-
toms as understandable psychological and emotional responses to life
events can help reduce fear and stigma (Read et al. 2006). The continued
support of the inpatient and outpatient teams should be emphasized,
and the diagnosis should be communicated in an optimistic, nonlabel-
ing manner. The treatment team must model and convey hope in a man-
ner that is believable to the patient.
If there is inadequate evidence to support that what the patient is ex-
periencing is truly a first psychotic episode, then it is prudent to high-
light the diagnostic uncertainty and hold off until there is further
information. Often, the diagnosis becomes clearer over the course of
time, sometimes over a few inpatient encounters. The initial presenta-
tion may resemble or be confounded by other variables such as concur-
rent substance use, anxiety, or affective disorders. A thorough
discussion of the possible trajectories of the current presentation can
function as a starting point for ongoing evaluation and conversation,
acting as a bridge until diagnostic certainty is attained.
Approaching Medication
Patients presenting for inpatient hospitalization for early psychosis
range from those who are medication naïve to those who have been
started on antipsychotic medications as outpatients prior to their hospi-
talization and those who have been treated for depressive or anxiety
disorders previously. It is important to consider that the biological
model encapsulates the assumption that medications are the primary
means through which the absence of symptoms can be achieved. With
a recovery-oriented approach, however, we hope to facilitate patient en-
gagement, integration, and meaningful functioning even if complete re-
mission is not achieved. Therefore, medications are only part of the
comprehensive biopsychosocial treatment plan that is to be developed
for the patient.
Evidence-based practices should guide the selection of a suitable an-
tipsychotic agent. Findings from the Treatment of Early Onset Schizo-
phrenia Spectrum Disorders (TEOSS) study indicated treatment response
in the first 2 weeks of treatment for both first- and second-generation
antipsychotics (Sikich et al. 2008). This is closely reflected in what we
have found to be the average length of stay for patients with early psy-
chosis, although some patients may need a longer inpatient stay, espe-
cially if the first trial of medication does not result in an adequate
clinical response and medications need to be switched. The TEOSS
study also showed no signifsicant differences in efficacy between first-
and second-generation antipsychotic agents, although the side effects
were different. Risperidone was associated with greater weight gain,
and olanzapine was associated with significantly higher weight and in-
creases in fasting cholesterol, low-density lipoprotein, insulin, and liver
transaminase levels when compared with molindone. Akathisia was
more prominent in patients who received molindone, whereas prolac-
tin elevation was greatest in the risperidone group.
Research has identified no significant differences in discontinuation
rates or symptom control between first- and second-generation antipsy-
chotic medications (Crossley et al. 2010). There is also no clear evidence
to suggest the superiority of one particular second-generation antipsy-
chotic over another. Aripiprazole tends not be associated with dyslipid-
emia or hyperprolactinemia, although it is still associated with weight
gain in youth. Younger patients and adolescents may also respond to
standard doses of risperidone, whereas ziprasidone and aripiprazole
may be effective at lower doses (Datta et al. 2012). Therefore, the selec-
tion of antipsychotic medications requires a thoughtful discussion with
the patient, led in part by the side effect profiles of these agents and pa-
tient preference.
The inpatient setting presents the unique challenge of ensuring that
treatment response is observed with appropriate symptom reduction in
a short period of time. This often requires starting at a low dose fol-
lowed by aggressive medication titration. The antipsychotic agent
should be titrated to the usual effective dose and observed for response
for at least a few days unless limited by side effects, in which case the
medication should be switched to a different agent that has lower prob-
ability of the adverse effects experienced. For more treatment-refractory

illness or in severe cases with profound negative symptoms, medica-
tions such as clozapine may also need to be considered (Veerman et al.
2017). In psychotic patients who present with malignant catatonia or
catatonia that is nonresponsive to benzodiazepine treatment, electro-
convulsive therapy should be used (Benarous et al. 2018). Electrocon-
vulsive therapy may also be a treatment consideration if the patient’s
medical status or medical history precludes treatment with antipsy-
chotic medications (Flamarique et al. 2017).
Starting any antipsychotic medication requires obtaining informed
consent from the patient. In the case of minors, their guardians can pro-
vide permission to start psychopharmacological treatment, but an ado-
lescent patient’s own engagement and assent are very important
because involuntary treatment has been shown to negatively impact
medication adherence (Timlin et al. 2015). Patients older than 18 years
are required to provide autonomous informed consent. This can pose a
challenge if the patient is reluctant to initiate a medication trial, which
often may be because of his or her psychotic state or paranoid ideation
regarding medications rather than being an indicator of autonomous
functioning or beliefs about medications (Schwartz et al. 1988). In such
cases, involuntary medications may need to be pursued to minimize the
untreated duration of psychotic illness.
Rarely, the patient may be agitated or combative, in which case
emergent use of antipsychotic medications may be warranted because
not using involuntary medications at this time in particular can result
in increased risk of seclusion and restraint or violent episodes (Flammer
and Steinert 2016). However, it is important to retain the therapeutic al-
liance and reestablish the patient’s role in leading decisions about his or
her own treatment as soon as is safely possible. In such instances, dis-
cussing the temporary nature of the intervention, emphasizing the pos-
itive effects of the medications to alleviate the symptoms that the
patient finds particularly bothersome, and, most importantly, recruiting
family support are often helpful.
Even in cases where the patient is older than 18 years, it is important
to have the family involved, engaged, and on board with the need for
psychopharmacological intervention because improved familial rela-
tional functioning closely correlates with medication adherence for the
youth (Timlin et al. 2015). There may be hesitancy to initiate an antipsy-
chotic medication, particularly if negative symptoms are predominant
or psychotic symptoms are not overt or because of familial concerns
about the stigma surrounding mental illness. Previous experience with
side effects may also fuel reluctance, especially around sensitivity to
weight gain, extrapyramidal symptoms, or dystonic reactions, which
can be acutely distressing for the patient. In this situation, any history
of a positive antipsychotic response for a family member might be help-
ful, although this course must be taken with caution so as not to perpet-
uate any negative identification with a family member who has chronic
psychotic illness. Additional caution is warranted in the use of antipsy-
chotic medications in patients with neurodevelopmental disorders be-
cause they may demonstrate greater sensitivity to adverse effects.
It is helpful to have the patient’s recovery goals be as closely aligned
to treatment goals as possible, with pharmacological treatment being a
vehicle to facilitate this onward journey. Youth taking antipsychotic
medications have reported benefits such as better concentration and ac-
ademic performance, improved relationships with others, and im-
proved self-control. Reasons for disliking medications include feeling
different, fear of social stigma, and concerns about long-term effects. In
adolescent patients, it was also found that good familial support and
lack of perceived coercion to take medication result in improved medi-
cation adherence (Moses 2011).
During the hospitalization, close assessment of antipsychotic re-
sponse and careful monitoring for side effects are required. Obtaining
laboratory tests to establish the baseline metabolic and hepatic function
is important, along with electrolytes and complete blood counts. There
may be underlying baseline risk factors for metabolic syndrome in
medication-naïve patients that should be identified (Fleischhacker et al.
2013). Laboratory tests ideally should be repeated periodically during
the inpatient admission because transient transaminitis and neutrope-
nia can occur. Electrocardiographic monitoring is also important be-
cause patients with early psychosis are at an elevated risk for QTc
prolongation during even a relatively short period (2–4 weeks) of treat-
ment with antipsychotic medications (Zhai et al. 2017). Additionally, as-
sessment for extrapyramidal symptoms and involuntary movements
should be incorporated into the daily examination of the patient. Clini-
cians also should hold a high suspicion for catatonia in patients with
significant social withdrawal and slowing or unusual excitation. Using
scales such as the Abnormal Involuntary Movement Scale (AIMS; Guy
1976) or the Catatonia Rating Scale (CRS; Bräunig et al. 2000) is often
helpful in tracking the severity of symptoms.
Successful Transitioning
A successful hospitalization should include a positive transition back to
the community along with outpatient care. Building a collaborative
therapeutic alliance with patients and families is critical for this goal
(Bonnie et al. 2015). Although some youth develop insight into their
mental health difficulties, others do not and may deny that they have
treatment needs at all. Engaging the family is a key strategy in support-
ing such youth—even for the patients who have reached the age of ma-
jority. It is important to respect patients’ autonomy while reassuring

them that family involvement can be extremely helpful to increase the
chance of successful transition back to the community.
If the patient is still in school, coordination of transition planning
with the school is necessary. The capacity of individual schools to ad-
dress student mental health concerns is vastly varied, especially as it re-
lates to severe mental health concerns such as psychotic disorders.
Many schools and colleges do not have relevant protocols or resources
in place and may need guidance from the treatment team on how to
support the student’s successful transition back to the learning environ-
ment. Educators and support staff are typically eager to receive recom-
mendations provided by the inpatient team, although available
resources may limit their capacity to implement all the recommenda-
tions provided.
Providing a comprehensive sign-out to the outpatient treatment
team when the patient is discharged from the inpatient service should
be considered the standard of care. In addition to basic information
about the patient’s diagnosis, hospital course, discharge medications,
and plans, further in-depth discussion regarding recommendations for
future treatment and foreseeable challenges can be extremely valuable
information to the outpatient team for a successful transition of care. If
available, referrals to specialized outpatient programs (such as CSC
model clinics) should be considered. These programs may deliver com-
prehensive care involving pharmacological treatment, individual ther-
apy, family interventions, and case management. Some of these
programs are even able to provide inpatient outreach services to engage
with patients and begin the process of developing a treatment alliance
while the patients are still in the hospital.
In the year following a new psychosis diagnosis, the death rate for
young people is 24 times higher than for young people without psycho-
sis (Schoenbaum et al. 2017). Thorough safety plans, including storage of
medications, supervision, and removal of potential weapons, should be
explicitly discussed with patients and, if possible, with family. If relevant,
psychoeducation regarding substance use and its impact on psychotic
disorders should be provided along with motivational interventions pro-
moting abstinence.
Conclusion
Inpatient hospitalizations may often be the first time a patient with
early psychosis makes contact with the mental health system or health
care in general. At other times, this may be a recurrent experience over
a prolonged clinical course. Regardless, it is important to create a ther-
apeutic alliance in the inpatient setting that moves away from solely
emphasizing psychopharmacological treatment and instead steps to-

ward integrating what is important to the patient and his or her family.
The inpatient setting is ideally suited to providing a safe physical
space that allows for close monitoring and observation, but it is also
confining and can make the patient feel more helpless. This is important
to consider because patients may respond to these feelings with anger
or increasing isolation. The clinical team is responsible for creating an
environment where the patient can safely explore these issues and find
greater understanding of how the treatment recommendations pre-
sented will align with his or her own goals.
The team should also conduct thorough diagnostic evaluations, for-
mulate a comprehensive treatment plan, and facilitate coordination of
care. It is paramount to engage the patient’s family and other social sup-
port systems involved to facilitate a smooth transition from the hospi-
tal. The hospitalization should not only focus on reduction of
symptoms so as to successfully and safely transition patients back to
care in the community but also support patients in finding hope and
what gives meaning to their life, help reestablish their identity, and al-
low them to take responsibility for their own recovery.
KEY CONCEPTS
• There are multiple specific considerations that may help
support individuals in the early stages of psychosis during
their hospitalization.
• The impulse to prioritize starting antipsychotic medication
may prove counterproductive if a treatment alliance is not
fostered.
• Family engagement and collaboration with outpatient ser-
vices is critical in ensuring that gains made during hospi-
talization are sustained and built on.
1. How might an inpatient unit strive to create a positive envi-

ronment for a patient in the early stage of psychosis?
2. What steps can be taken to foster a treatment alliance?
3. What are some options when patients are not interested in

taking medications?
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CHAPTER
22
Care for Adolescents on the

First-Episode Psychosis
Continuum
Rhoshel K. Lenroot, M.D.
Tresha A. Gibbs, M.D.
ALTHOUGH the peak age of onset of psychotic disorders is in late

adolescence and early adulthood, a substantial number of individuals
first experience psychotic symptoms during adolescence (here defined
as ages 13–17 years). Adolescence is also a particularly important time
for identifying individuals who may be at clinical high risk for psycho-
sis because this is the developmental stage when the majority of indi-
viduals who ultimately transition to a psychotic disorder will
experience their first prodromal symptoms. In samples of help-seeking
adolescents at clinical high risk, approximately 25% transition to a full
psychotic disorder over 2 years. Even in those who do not transition,
the presence of attenuated psychotic experiences is associated with gen-
eral psychopathology and impairment in social functioning (Fusar-Poli
et al. 2017).
Recognition of the importance of adolescence in early intervention
efforts has resulted in most clinical services for early psychosis span-
ning an age range that begins at around 13–15 years and extends into
the mid-twenties. Structuring services to cross the transition from ado-
lescence into adulthood has many benefits, including the ability to
maintain continuity of care during the period of greatest vulnerability
383
for onset of psychotic disorders. However, it also requires that the ser-
vices staff be able to work effectively with young people who are in dif-
ferent developmental stages.
Adolescence, by definition, is the period of transition between child-
hood and adulthood. Sexual maturation is one of the defining factors,
which may occur relatively early during adolescence, whereas neuro-
development continues well into early adulthood. The social environ-
ment and accompanying expectations also change during this period,
typically shifting from being largely oriented to and determined by the
family environment and structured educational settings to having more
emphasis on developing and sustaining social relationships in the
larger community. These changes occur within the context of the in-
creasing latitude and responsibility in decision making that are associ-
ated with adult status.
The onset of psychosis during this critical period can adversely af-
fect an adolescent’s ability to navigate these developmental tasks, with
potentially long-term adverse effects beyond the functional impact of
the symptoms themselves. Participating with same-age peers in the
tasks of establishing social networks and sexual relationships can be
particularly challenging if adolescents’ ability to interpret social cues is
limited or if they are socially withdrawn because of anxiety or paranoia.
Cognitive difficulties such as poor concentration and working memory
not only impact scholastic performance but can also specifically impact
the ability to manage competing demands and complex decisions
needed to develop independence. Establishing a sense of identity can
be particularly difficult for young people if they or those around them
have become unsure whether they can trust their beliefs and percep-
tions about the world.
Developmental characteristics thus need to be taken into account
when caring for adolescents and their families. Although data are
sparse, there is some evidence that a younger age of onset of psychotic
symptoms may be associated with particular clinical and biological
characteristics and risk factors. Psychosocial interventions that are effec-
tive in adults may not be suitable for the level of cognitive development
of an adolescent, and although the indications for psychopharmaco-
logical treatments are similar in adolescents and adults, the small
amount of research available suggests some additional specific consid-
erations to take into account when working with adolescents. How-
ever, despite the challenges of working with adolescents, there may
also be an increased potential for positive outcomes. One of the few
outcome studies of intervention programs for first-episode psychosis
that examined age effects found more robust functional improvements
in individuals who presented before the age of 18, suggesting that
these younger individuals may also be more able to respond to appro-
priate intervention (Amminger et al. 2011).
Adolescents on the First-Episode Psychosis Continuum 385
Extensive reviews of diagnosis and treatment of individuals with

first-episode psychosis or who are considered to be at clinical high risk
for psychosis are provided in Chapter 8, “Assessment and Targeted In-
tervention in Individuals at Clinical High Risk for Psychosis,” and
Chapter 9, “Medical Workup for First-Episode Psychosis.” In this chap-
ter, we focus on aspects of these conditions specifically relevant to ado-
lescents presenting before age 18.
Developmental Considerations
in the Presentation of Early Psychosis
There is extensive evidence that young people who go on to develop a
psychotic disorder often have early evidence of social, motor, and lan-
guage problems. In the Avon Longitudinal Study of Parents and Chil-
dren, individuals in England were evaluated at multiple time points
from infancy to young adulthood, and these evaluations identified pro-
gressive deficits in functional IQ over the lifespan for those who devel-
oped psychosis by late adolescence (Mollon et al. 2018). In addition to
functional IQ, lags in working memory, attention, visuospatial func-
tioning, and language were noted throughout development. These dra-
matic signs were not seen in the young people who developed affective
disorders. Adolescents who have transitioned to primary psychotic dis-
orders are consistently found to have impairments in cognitive func-
tions such as social cognition, verbal fluency, and memory, which likely
contribute to the functional deterioration characteristic of these disor-
ders. Although adolescents at clinical high risk are also more likely on
average to have difficulty with cognition, particularly in domains of at-
tention, memory, visuospatial ability, and processing speed, recent find-
ings have suggested that these deficits are more severe in the subset of
individuals who eventually develop psychosis and remain relatively
mild in those who do not (Seidman et al. 2016).
Generally and historically, the data have supported the finding that
onset of schizophrenia before age 18 is associated with worse cognitive
function. In a meta-analysis that compared cognitive assessment find-
ings in persons with schizophrenia before age 19, onset after 19, and on-
set after age 40, younger individuals had significant deficits compared
with older ones (Rajji et al. 2009). These included deficits in full-scale
IQ, processing speed, verbal and working memory, and executive func-
tion. A study of the 20-year course of schizophrenia found social func-
tioning to be relatively preserved from the beginning of the disorder,
suggesting that the highest level of functioning prior to the disorder
tends to be retained (Velthorst et al. 2017). This is consistent with a re-
cent meta-analysis of longitudinal changes in cognition in early psycho-
sis, which did not find evidence of further cognitive decline in either
clinical at-risk subjects or those with a first episode of psychosis (Bora

and Murray 2014). However, despite the substantial evidence of earlier
onset being associated with worse cognitive function at presentation,
an early psychosis intervention program that looked at relative out-
comes of individuals who presented before age 18 found that they had
greater functional improvements, raising the question of whether the
greater plasticity of the adolescent brain could be an advantage when
provided with appropriate intervention (Amminger et al. 2011).
Longitudinal brain imaging studies suggest that the progressive
brain changes observed in adolescent-onset psychosis converge on sim-
ilar findings as seen in imaging studies of adults with chronic psycho-
sis, specifically decrease in frontal and temporal gray matter volumes,
increase in lateral ventricular volume, and decrease in cerebellar vol-
ume. What appears unique to those who develop psychotic disorders at
a younger age is more rapid loss of frontal cortical regions, particularly
over the first few years of their illness (Fraguas et al. 2016).
A number of risk factors have been associated with the development
of psychosis, including biological factors (e.g., male gender, family his-
tory of psychosis, obstetric complications) and environmental factors
(e.g., urbanicity), coming from a minority population, exposure to early
life stressors, and cannabis use (van Os et al. 2010). The risk factors that
appear to be most strongly associated with an earlier age of onset include
male gender, obstetric complications, family history of psychosis, and
cannabis use, although there is some evidence that the accumulation of
several factors, including migration status and social class at birth, that
are not individually predictive may together increase the likelihood of
developing psychosis earlier in life (O’Donoghue et al. 2015).
A history of childhood trauma is relatively common in adolescents
at clinical high risk, appears to predict risk of transition to psychotic dis-
order, and has been associated with severity of psychotic symptoms
(Mayo et al. 2017). Whether the vulnerable individual is more likely to be
traumatized or whether trauma is causally related to psychosis is cur-
rently unclear. In addition to exposure to potentially traumatic events
such as domestic or community violence or sexual abuse, an often under-
recognized source of traumatic interpersonal experiences that may have
an adverse effect on development and is relatively common in adoles-
cents is bullying in schools and on social media. Screening for traumatic
experiences and for symptoms of posttraumatic stress in children re-
quires a developmental approach, and the use of adolescent-specific
screening tools for posttraumatic stress disorder (PTSD) is encouraged.
Treatment of PTSD, if present, is essential (Mayo et al. 2017).
For some people, adolescence includes experimentation with a vari-
ety of substances, including tobacco, alcohol, and cannabis, and there is
strong evidence that cannabis is a dose-dependent risk factor for
chronic psychotic disorder. Data suggest that adolescence is a period in
which the developing brain is particularly sensitive to effects of canna-

bis, such that heavy cannabis exposure is associated with earlier onset
of emotional, behavioral, and/or cognitive symptoms and greater risk
of developing psychosis (Ongür et al. 2009). Exposure to highly potent
tetrahydrocannabinol (THC) in particular is associated with behavioral
disturbances. The growing legalization of marijuana means increased
access; according to the Youth Risk Behavior Surveillance Data from
2017, 20% of high school students had used cannabis in the preceding
month (Kann et al. 2018). The proportion of adolescents who view mar-
ijuana use as potentially harmful has been dropping steadily, with a 2017
U.S. national survey finding that only 34% of eighth graders and 14% of
twelfth graders felt that occasional use was risky (Johnston et al. 2018).
In addition to effects of age, studies suggest that genetic risk factors
may interact with cannabis exposure. Several studies have found that indi-
viduals with a family history of psychosis are more sensitive to becoming
psychotic after cannabis use. Potential specific genetic risk factors have also
been identified. One is the gene encoding catechol-O-methyltransferase
(COMT), an enzyme that plays a key role in the breakdown of dopa-
mine in the prefrontal cortex. Several studies reported that individuals
with the genetic variant of COMT that breaks down dopamine more
quickly have an increased risk of developing psychosis following expo-
sure to cannabis (Arendt et al. 2008; Kahn et al. 2011), although other
studies did not find such an association (Boydell et al. 2007). A second
gene, AKT1, encodes an enzyme that interacts with glycogen synthase
kinase during cell processes such as transcription, apoptosis, and pro-
liferation. AKT1 is stimulated by cannabinoids, and cannabis users with
a specific polymorphism in AKT1 have been found to have a signifi-
cantly higher (twofold to sevenfold) risk of developing psychosis.
Other genetic factors that have been linked to risk for psychosis in can-
nabis users with less evidence thus far include DAT1, neuregulin 1, and
brain-derived neurotrophic factor (Radhakrishnan et al. 2014).
Differential Diagnosis
The clinical differential diagnosis of an adolescent presenting with pos-
itive symptoms of hallucinations, paranoia, or other delusions or disor-
ganized thought is broad and may include affective disorders, anxiety
disorders, obsessive-compulsive disorder, trauma- or stressor-related
conditions, substance use disorders, personality disorders, and neuro-
developmental disorders. Clinicians should maintain a developmental
perspective when interviewing, assessing, and diagnosing adolescents.
Adolescents are likely to present for evaluation after referral by a school
official, pediatrician, primary care provider, or family member. Adoles-
cents are more likely than adults to present with negative symptoms
and flat affect (Ballageer et al. 2005).
The clinician may face a diagnostic challenge because suspicion of a

psychotic disorder may not be the anticipated focus of the initial pre-
sentation. Often, the presenting complaints described by the adolescent
or referrer may be mood, social, and cognitive functioning problems, in-
cluding irritability, depression, social withdrawal, or difficulties with
attention. The adolescent may be experiencing failure to progress as ex-
pected in coursework because of inattention or lack of motivation. He
or she may avoid social contact and be notably paranoid in the school
social setting. The adolescent may not reveal the presence of hallucina-
tions or delusions unless directly questioned. Questionnaires such as
the 21-item Prodromal Questionnaire (PQ-B) developed by Cannon and
Loewy (Loewy et al. 2011); the Early Psychosis Screener (EPS; Brodey et
al. 2017); and the Yale University Prevention through Risk Identifica-
tion, Management, and Education (PRIME) Screen (Miller et al. 2004)
may help elucidate symptoms.
An additional consideration is that it is not uncommon for children
and adolescents to have psychotic experiences, although most of them do
not progress to a psychotic disorder as they age. The prevalence of hallu-
cinations among adolescents ages 13–18 is approximately 7.5% (Sikich
2013). Symptoms that are termed psychotic experiences versus a disorder
are usually transient hallucinations, mostly stress induced, and are not
associated with functional impairment or abnormal social cognition
and insight. Signs of apparent paranoid ideation may overlap with ad-
olescent self-consciousness, and signs perceived as thought process and
thought content abnormalities on mental status examination may be
due to learning or neurodevelopmental disorders, some of which may
affect expressive language skills in affected adolescents. Psychotic
symptoms are more common in adolescents with trauma-related disor-
ders, and a unique aspect of assessing the trauma experience in adoles-
cents is that they may not yet have a narrative or labels for their
experience. A trauma-informed approach to assessment is essential.
Whereas adults may commonly obtain mental health care through
acute care settings because of active and impairing positive symptoms,
adolescents can present earlier because of their immersion in the family,
school, and community systems. This provides an opportunity for close
assessment earlier in the course of the illness and the opportunity to in-
tervene before the potentially steep decline in social functioning that
has been observed in both affective psychosis and schizophrenia-re-
lated disorders. The positive effects of early intervention on symptom,
cognitive, and functional outcomes have now been well demonstrated,
supporting the value of early recognition and diagnosis (Amminger et
al. 2011).
Considering relevant genetic, acute, or chronic medical or neurolog-
ical disorders is essential in the initial assessment. This process includes
assessing for symptoms to suggest a genetic syndrome, epilepsy, tumor,
metabolic disorders, autoimmune illness, substance use, or traumatic

brain injury. For adolescents with a history of childhood deviations in
physical, neurological, psychological, or social development or marked
difficulties in academic achievement, a more detailed developmental
history and assessment are needed to contextualize any current signs
and symptoms.
Neuropsychological testing can identify the degree and domains of
cognitive impairment, and projective testing can elaborate on psychotic
thoughts or identify more subtle levels of thought disorder, which may
be helpful for understanding the client and obtaining rehabilitative
supports. Neuropsychological testing is less likely to be helpful in diag-
nosing individuals at high risk or in predicting long-term course.
For adolescents, it is important to assess the family structure and
functioning as a routine part of the evaluation. It is not uncommon for
family relationships to undergo a period of strain during the period of
individuation and related changes in expectations that are part of nor-
mal maturation. When there are worries that a young person is devel-
oping a mental illness, these strains can become more severe.
The prodromal stage of schizophrenia has been associated with neg-
ative experiences in the parent-caregiver relationship (Tomlinson et al.
2014). Family members may struggle during the prodromal phase with
uncertainty about their adolescent and with how to obtain help. The ex-
perience of feeling “criticized” by parents and caregivers is a common
experience in adolescents who are developing their unique identity. In
the context of a new onset mental illness, high expressed emotion can
worsen anxiety and social functioning (Onwumere et al. 2009). For ad-
olescents who have transitioned to schizophrenia, a family with high ex-
pressed emotion puts them at increased risk of relapse. On the other
hand, healthy parent-child relationships in adolescents can decrease ad-
olescent risk behaviors such as drinking and substance use. The struggles
with external and internal conflicts that adolescents may be having in ne-
gotiating changing relationships with authority figures within their fam-
ily system may also affect their relationships with clinicians, and this can
become particularly challenging when the experience of family relation-
ships has been problematic because of loss, abuse, or neglect.
Cultural factors are important to consider in interacting with adoles-
cents and their families. The meaning of specific symptoms commonly
associated with psychosis may be different across cultures. For exam-
ple, in some cultures, seeing or hearing loved ones who have died is ac-
cepted as part of the grieving process. Auditory hallucinations of
helpful voices or other unusual perceptions may be considered by ado-
lescents or their family as a special ability, sometimes inherited, rather
than a sign of pathology. However, international studies have found
that most cultures do identify a pathological state associated with the
disordered thoughts and behavior of chronic psychosis. Being attentive
to the meanings of the symptoms for an individual adolescent and fam-

ily while remaining alert to evidence of functional impairment or dis-
tress can help to guide assessment. Focusing on the presence of distress
associated with unusual perceptions, rather than on how they should
be interpreted, can help to support the therapeutic alliance by identify-
ing common treatment goals around improving function.
Suicide risk among adolescents with psychosis is a serious concern,
and there is strong evidence that these adolescents are more likely to die
by suicide, particularly in the first 3 years after diagnosis, compared
with the general population (Simon et al. 2018). Clinicians should
screen for depressed mood and a significant decline in role functioning,
both of which may lead to hopelessness and self-harm. Suicidal ide-
ation is common among young people at clinical high risk for psycho-
sis. A study by Gill et al. (2015) suggested that suicidal ideation in
adolescents may not come to light unless there is active screening for
passive suicidal ideation and intensity of suicidal thoughts. They sug-
gested using the Columbia Suicide Severity Rating Scale to accurately
characterize the presence of suicidality in these adolescents on a spec-
trum of thoughts and behaviors. Negative symptoms may obscure the
evaluation, but screening for passive suicidal ideation in particular in
this population is encouraged (Gill et al. 2015; Taylor et al. 2015).
Identification and Engagement

Despite the accumulating evidence that early intervention in psychosis
is associated with better long-term outcomes, duration of untreated
psychosis is often still prolonged. Some studies have found that dura-
tion of untreated psychosis is longer in adolescents than adults. As dis-
cussed in the section on developmental considerations above, a variety
of factors may make it more difficult to identify at-risk adolescents and
engage them in treatment, and these will differ for each child and fam-
ily system. Predominant negative symptoms can delay initial diagnosis
until onset of either frank psychosis or bizarre behavior. The level of
family engagement may impact time to treatment referral because the
meaning of the behavioral change is often seen from the lens of the fam-
ily’s cultural, medical, and social history or circumstances. Stigma, par-
ticularly the idea that people with mental illness are “crazy,” is still
common and may add to reluctance to seek help. Parents’ fears that
they may potentially be blamed can also impede engagement with ser-
vices. Schools with many high-risk youth may struggle to identify and
meet the needs of adolescents with prodromal symptoms. In some
school systems, the adolescent experiencing prodromal symptoms is
more likely to drop out of school than receive a clinical referral for be-
havioral change. The frequent ambiguity of clinical presentations in ad-
olescents may also delay accurate diagnosis.
As discussed in more detail in Chapter 4, “Early Intervention and Pol-

icy,” and Chapter 11, “Intervening Early,” over the past 20 years there has
been increasing support for specialized multidisciplinary early psychosis
services. These services aim to decrease duration of untreated psychosis
through early identification and rapid access to appropriate interventions
for young people with first-episode psychosis and those who are at clinical
high risk (Lloyd-Evans et al. 2011; Tiffin and Welsh 2013). Case identifi-
cation is facilitated through intensive outreach to families and community
organizations, paired with rapid access to assessment and treatment.
Schools are a particularly important partner for services working
with adolescents because teachers, advisors, coaches, or other school
personnel may be the first to notice that an adolescent is struggling.
Building partnerships with schools can also facilitate obtaining educa-
tional support for adolescents in order to minimize academic disrup-
tion. Schizophrenia is one of the conditions covered under the
Individuals with Disabilities Education Act (IDEA) under the category
of serious emotional disturbance. Adolescents with psychosis may also
be eligible for 504 plans, which provide support based on Section 504 of
the federal Rehabilitation Act of 1973. Opportunities to explore sup-
ported employment should also be considered with youth.
The coordinated specialty care approach for individuals identified
in the earliest phases of their illness has been shown to lead to better
long-term outcomes, including less cognitive deterioration and im-
proved social and vocational functioning (Albert et al. 2017; Amminger
et al. 2011). For adolescents, willingness to engage with services may be
enhanced by creating a youth-friendly space that is more congruent
with young people’s developmental needs than is commonly found in
either pediatric or adult settings and that explicitly involves families
while also recognizing that the young person is on the path to adult-
hood. Maintaining a recovery-based orientation that can support ado-
lescents in identifying strengths and learning to manage symptoms in
the context of navigating toward developmentally appropriate social,
educational, and vocational goals is critical. Involving trained youth
peer specialists may be a particularly effective intervention for helping to
establish engagement because it meshes with adolescents’ developmen-
tally normal tendency to seek out peers rather than adults. Peer special-
ists can be an important source of social connection in the presence of a
psychiatric disorder typically associated with increasing isolation.
Psychosocial Interventions
Current clinical guidelines concur that psychosocial interventions are
an essential component of treatment for adolescents with first-episode
psychosis and are the recommended first-line intervention for those at
clinical high risk (Addington et al. 2017; Crockford and Addington

2017; Early Psychosis Guidelines Writing Group and EPPIC National
Support Program 2016; UK National Institute for Health and Care Ex-
cellence 2013). There is as yet relatively little research regarding specific
effects of psychosocial treatments in adolescents or of interventions de-
veloped specifically for this population, highlighting a critical gap in
the evidence base. The discussion that follows therefore relies primarily
on data available from adult populations.
Family interventions have been associated with stabilization of
symptoms, improved general function, and decreased risk of relapse
and are included within current clinical guidelines as an essential part
of effective treatment. Family interventions may be particularly import-
ant for adolescents because they are more likely to be living within a
family system. Although different models for family intervention have
been studied, most combine psychoeducation with therapeutic inter-
ventions to facilitate problem solving, stress management, and commu-
nication skills within the family (Tiffin and Welsh 2013).
Family interventions can be carried out either with a single family
or in a group of several families, who meet regularly for up to 2 years.
Although multifamily group models include the same components as
other family interventions, they have the potential for the added benefit
of the creation of a support network among the participating families,
which can enhance each family’s sense of agency and decrease the
stigma and social isolation experienced by many families. However, it
is important to determine with each family whether they prefer a single
or group format because cultural or other considerations may affect
their level of comfort in participating in either model.
Individual therapies for adolescents with first-episode psychosis typi-
cally include psychoeducation, relapse prevention, and stress manage-
ment, in addition to other components as indicated such as social skills
and life skills training. At present, cognitive-behavioral therapy for psy-
chosis (CBTp) has been recommended by the National Institute for Health
and Care Excellence in the United Kingdom for use in adolescents on the
basis of the relatively robust evidence base for its positive effects in adults.
However, it is not clear whether adolescents have the same level of benefit
from this specialist intervention. One study comparing CBTp with sup-
portive counseling in both adolescents and young adults found that the
younger group benefited more from the supportive therapy, whereas the
older group benefited from CBTp (Haddock et al. 2006). This result may
speak to the need to modify CBTp for the different level of cognitive ma-
turity in adolescents, or it may support the positive effects of a less specific
supportive intervention in younger individuals.
The increasing recognition of the potential impact of exposure to
stressful life events during development on the risk for psychosis, clin-
ical course, and response to treatment is also raising questions about
how best to modify psychotherapeutic interventions to address

trauma-related symptoms in individuals with early psychosis. Al-
though there is not yet sufficient evidence to support a specific model,
the integration of components from therapies such as trauma-focused
cognitive-behavioral therapy (TF-CBT) are currently being considered.
TF-CBT is a model that has been well validated in adolescents and may
hold promise in this population as well (Mayo et al. 2017).
Recognition of the central role of cognitive deficits in determining
functional capacity of individuals with psychosis has stimulated efforts to
develop interventions for cognitive remediation. Cognitive remediation
therapy consists of behavioral training techniques targeting cognitive pro-
cesses such as memory, attention, executive function, and social cognition
or meta-cognition. The goal of cognitive remedial therapy is for gains in
these areas to generalize to daily living and to persist over time (Wykes et
al. 2011). There has been sufficient evidence for the positive effects of cog-
nitive remediation therapy for adults with schizophrenia that it has now
been incorporated into several guidelines for treatment (Wykes et al.
2011). There is as yet much less known about effectiveness in adolescents,
although preliminary reports have shown beneficial effects of cognitive
remediation therapy for adolescents with first-episode psychosis (Puig et
al. 2014) and for young people who are at clinical high risk (Loewy et al.
2016). Much work remains to be done to determine what the optimal cog-
nitive remediation strategy may be for this age group, but the potential
benefits of addressing cognitive deficits during adolescence and decreas-
ing adverse effects on educational and vocational trajectories suggest that
developments in this area should be watched closely.
Pharmacological Interventions for

Adolescents With First-Episode
Psychosis
Antipsychotics effectively decrease positive psychotic symptoms for most
individuals with first-episode psychosis, resulting in relief of distress and
improvement in social functioning. Several of these medications have been
approved by the U.S. Food and Drug Administration for this indication
and are considered safe with known side effects. Studies among adoles-
cents have shown modest response rates, such as 34%–50% in the Treat-
ment of Early Onset Schizophrenia Study (TEOSS; Sikich et al. 2008). In
this study, 119 adolescents with schizophrenia were randomly assigned to
treatment with atypical antipsychotics risperidone or olanzapine or the
typical antipsychotic molindone. Over the 8 weeks of the study, symptoms
declined 21%–47% for participants in all groups, with peak response rate in
2 weeks and no significant difference between typical versus atypical anti-
psychotics (Sikich et al. 2008). In another study based on a network meta-

analysis of data of adolescents with psychosis, Pagsberg et al. (2017) found
that there was equivalence in Positive and Negative Syndrome Scale score
reduction with aripiprazole, asenapine, paliperidone, risperidone, queti-
apine, and molindone. The response for ziprasidone was not as strong,
suggesting it may not be the ideal first-line agent.
The role of long-acting injectables is particularly pertinent to adoles-
cents with first-break psychosis. In this population, adherence and in-
sight may be influenced both by the disorder and by the adolescent’s
developmental stage. The clinician may thus need to consider long-acting
injectables very early on. Although research on long-acting injectables
in adolescents is sparse, an observational study comparing effects of
three available long-acting formulations (risperidone, aripiprazole, and
paliperidone palmitate) in 30 adolescents found that all three medica-
tions were largely well tolerated and resulted in similar levels of im-
provement as measured by the Children’s Global Assessment Scale
(Fortea et al. 2018). These adolescents had a combination of a psychotic
disorder with high levels of comorbid disruptive behavior and sub-
stance use and were prescribed an injectable drug because of a history
of low adherence and poor insight.
Clozapine has been found to be effective in adolescents with early-
onset schizophrenia (Schneider et al. 2014). Benefits include its efficacy
in treatment-resistant cases and its low risk of movement-related extra-
pyramidal symptoms. However, the side-effect profile includes symp-
toms that may be particularly difficult for adolescents to tolerate, such
as weight gain, metabolic changes, drowsiness, salivation, and possible
increased seizure risk. The required clozapine protocol of repeat blood
draws to monitor for agranulocytosis may be inconvenient and possi-
bly aversive to some adolescents. Nonetheless, it serves an important
role in the clinical toolbox for select populations.
Adverse effects are an aspect of treatment with all medications. In-
formed consent procedures with adequate information on risks and
benefits and guideline-based monitoring and intervention for adverse
long-term impacts facilitate safe prescribing. Consideration of the meta-
bolic risk profile when selecting an antipsychotic medication is an essential
aspect of harm mitigation for adolescents for whom long-term, possibly
lifetime, treatment is the expectation. Although efficacy of antipsychotic
medications is similar to what is seen in adults, younger people are more
likely than adults to respond to lower doses. They may also be more sensi-
tive to weight gain and movement side effects. For these reasons, a “start
low, go slow” approach is highly recommended. Detailed comparative
data can be found in the 2017 Association for Healthcare Research and
Quality comparative effectiveness publication (Pillay et al. 2017).
Treating affective symptoms in this population can improve the
treatment course and minimize risk of harm to self or others. In adoles-
cents with first-episode psychosis, onset of depressive symptoms may

be an indication for initiation of a first-line agent, typically a selective
serotonin reuptake inhibitor, with close monitoring for onset of any
change in behavior. New-onset impulsivity, psychomotor activity, or
aggressive or hostile behavior may require diagnostic reassessment and
consideration of mood-stabilizing treatment for what may be a devel-
oping bipolar spectrum illness.
Often, adolescents and their families will inquire about the long-
term plan for treatment after the stabilization or even remission of pos-
itive psychotic symptoms. Unfortunately, at present there are limited
empirical data on the best course. The plan should be individualized for
each individual, and it may be necessary to observe an adolescent over
time to confirm a definitive diagnosis. Providers should consider using
a shared decision-making approach with the adolescent and family in
order to maintain engagement and allow for ongoing candid discus-
sions about treatment priorities as the course of the disorder unfolds.
A diagnosis of first-episode schizophrenia tends to remain stable,
whereas individuals with schizophreniform disorder, major depressive
disorder with psychotic features, or substance-induced psychosis are
more likely to receive an alternative diagnosis at follow-up points. For
individuals with schizophrenia experiencing their first episode of psy-
chosis, the most conservative recommendation to date is to avoid dis-
continuation because it leads to relapse. A recent systematic review of
studies reporting recurrence rates following medication discontinua-
tion estimated that symptoms recurred in 77% of patients after 1 year
and in more than 90% of patients by 2 years (Zipursky et al. 2014). Ad-
vising families of this data can assist in decision making. Clinical signs
that a psychotic experience is not a chronic psychotic disorder and thus
that the adolescent may be a good candidate for discontinuation of
treatment after remission of positive symptoms include a sudden onset
of symptoms, rapid resolution of symptoms with treatment, and no sig-
nificant loss in function. For an adolescent with schizophrenia who
wishes to discontinue treatment, provider and family should have an
open discussion about risks and benefits of this decision. Particularly
among adolescents, it is important to validate individuals’ attempts at
understanding their illness and its treatment, to engage them respect-
fully in a developmentally appropriate way, and to aim for an overall
positive treatment experience.
Pharmacological Interventions for

Adolescents at Clinical High Risk
It would be ideal to have an intervention that could prevent transition
to psychosis in at-risk adolescents, and efforts to identify such treat-
ments are under way. Studies to date have not supported the use of an-
tipsychotics for prevention of psychosis because they have not shown
evidence of sustained differences in transition rates, and side effects
such as weight gain are considerable (Stafford et al. 2015). Existing
guidelines generally also do not recommend use of antipsychotics for
attenuated psychosis symptoms unless there is significant clinical dis-
tress that cannot be adequately addressed by first-line psychosocial
treatments such as CBTp (Addington et al. 2017; Early Psychosis Guide-
lines Writing Group and EPPIC National Support Program 2016; UK
National Institute for Health and Care Excellence 2013). There has been
some evidence that antidepressants may have an impact on the rate of
transition to psychosis (Cornblatt et al. 2007). Fatty acids such as eicos-
apentaenoic acid demonstrate some promise as well (McGorry et al.
2017). Psychotropic medications do play a clear role in treating the co-
occurring conditions that are common in clinical high-risk adolescents,
such as depression and anxiety, when individuals with these conditions
have not responded to psychosocial interventions.
Conclusion
Working with adolescents who are learning to manage symptoms of
psychosis requires that the clinician be willing to adapt to meet devel-
opmental needs of young people who may be at very different places
along the road to adulthood. One of the hardest tasks for both the clini-
cian and the young person and his or her family can be the willingness
to tolerate uncertainty. Although the body of knowledge about diagno-
sis and intervention for adolescents who are experiencing first-episode
psychosis or who are at clinical high risk for psychosis has been grow-
ing rapidly, we still lack the means to predict accurately what the clini-
cal course is likely to be for an adolescent who has just started having
symptoms. Therefore, a critical aspect of treatment is maintaining a re-
covery-oriented framework that includes attention to preserving en-
gagement through potentially changing clinical states and the
flexibility to adjust approaches as needed. Although adolescence can
add challenges for clinicians, it also is a time when effective interven-
tion can make an enormous difference in the course of a life.
KEY CONCEPTS
• Thirty percent of individuals with a psychotic disorder have
their first episode during adolescence.
• Developmental differences should be kept in mind during

assessment and diagnosis of adolescents with psychosis.
• Assessment of family function and inclusion of the family
in the treatment process is particularly important in ado-
lescents, who are likely to be living with their family.
1. What might the differences be in processes around informed
consent and confidentiality when working with youth
younger than age 18?
2. How might a clinician approach or partner with schools in

communicating with youth and families about mental health
concerns?
3. Given that hallucinations are more common in younger teens

but often resolve, how might clinicians determine when hallu-
cinations indicate clinical high risk or first-episode psychosis?
4. What are some strategies for supporting secondary school

youth in interacting with their peers and discussing what is
happening to them?
Suggested Readings
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of children and adolescents with schizophrenia-spectrum disor-
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ic symptoms in children and adolescents. Child Adolesc Psychiatr
Clin N Am 22(4):655–673, 2013 24012079
Tiffin PA, Welsh P: Practitioner review: schizophrenia spectrum disorders
and the at-risk mental state for psychosis in children and adoles-
cents—evidence-based management approaches. J Child Psychol
Psychiatry 54(11):1155–1175, 2013 24102356
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CHAPTER
23
Special Populations: College

and University Students
Mehak Chopra, D.O.
THE college or university setting presents many challenges for young

people—particularly those with an emerging illness. Psychotic symp-
toms are generally still developing in college students, resulting in di-
agnostic uncertainty at the initial point of identification and treatment.
Students presenting with first-onset of psychotic symptoms may go on
to develop a schizophrenia spectrum disorder, but their symptoms
could also be due to substance use, mood disorders, trauma, or certain
medical conditions. Because the etiology of psychosis can vary, a com-
prehensive assessment is essential.
This chapter is presented as an update to Hardy KV, Gonzalez-Flores B, Ballon JS: “Inter-
vening Early in First-Episode Psychosis in a College Setting,” in University Student Mental
Health: A Guide for Psychiatrists, Psychologists, and Leaders Serving in Higher Education. Ed-
ited by Roberts LW. Washington, DC, American Psychiatric Association Publishing, 2018,
pp. 285–298. Copyright © 2018 American Psychiatric Association Publishing. Used with
permission.
403
Universities often struggle with how to respond ethically and le-

gally to students presenting in crisis with psychosis (Hardy et al.
2018a). Although college is an exciting time for students, it is a major life
transition with numerous demands and challenges. Academic stress,
social pressures, continuous sleep disruptions, separation from family,
and an increase in responsibilities can leave students more vulnerable
to substance use and other mental health problems. Given these de-
mands, college students may experience their first onset or exacerba-
tion of mental health problems. Consider the following example.
Case Example 1
Sam is an 18-year-old student athlete on the tennis team who spends
many hours practicing his sport. After a successful high school career,
he enrolled in an elite university as a pre-med student. Over the course
of his freshman year, Sam started to feel sad and more irritable, frus-
trated, and anxious. He was having difficulty sleeping and noticed it
was challenging to pay attention in class and during practice. His coach
and teammates also noticed that he wasn’t playing tennis as well as in
the past. Sam confided in a friend that he was hearing the voices of an
angel and a demon in his head. He felt that his mind was torn between
the good and evil of these spirits, and this interrupted his concentration
in other tasks. Sam presented to his student health center reluctantly. He
did not say he was hearing voices, but he did mention that he felt as if
things were not going well for him in his mind. Sam was referred for
supportive psychotherapy, and he told his counselor that his parents
would not approve of him being on medication. After building rapport
with his therapist, he revealed that he felt that taking medication was a
sign of weakness. Despite a robust coordinated specialty care (CSC) ser-
vice located in his county, Sam was not referred for specialized early
psychosis treatment. He began to speak more openly with his counselor
about auditory hallucinations and referential ideas. At the end of the
quarter, Sam expressed to his brother that he was having thoughts of
suicide. He was taken to a local hospital and admitted to an inpatient
unit. He was put on medical leave from school, and he stopped playing
competitive tennis. After his hospitalization, Sam was sent home, and it
is unclear if he will ever be able to reenroll at his university.
Unfortunately, this case presents a common description of how the

onset of psychosis, and access to treatment, occurs for thousands of
young adults in the United States each year. Symptoms of psychosis
typically emerge in late adolescence and early adulthood, mapping
onto the period when young people are starting college or university.
Nearly 70% of U.S. high school students enrolled in college in 2017 (U.S.
Bureau of Labor Statistics 2018). With 100,000 new cases of psychosis
occurring each year in the United States, it can be expected that a signif-
icant number of students will experience their first episode of psychosis
while on a college campus.
Special Populations: College and University Students 405
Specialized early psychosis services are now more broadly available

in the United States. However, to provide early intervention, there must
first be effective early identification. Research has demonstrated that
the duration of untreated psychosis (DUP) is an important factor in the
long-term prognosis of individuals experiencing a first episode of psy-
chosis. Although college-age individuals who engage in higher educa-
tion may have a shorter mean DUP, the DUP still exceeds optimal for
most (Hardy et al. 2018b). Early psychosis studies consistently find that
shorter DUP is associated with better symptom and functional out-
comes, but no research has addressed an optimal DUP for return to full
academic and occupational functioning. Clinical experience and extrap-
olation from existing evidence suggest that a DUP less than 12 weeks
may be most likely to achieve this high bar.
Challenges in the identification of psychosis exist in all settings but
may be particularly acute in a college setting, where students present
with a range of mental health problems. Young people experience in-
creased autonomy and decreased oversight as they transition to a col-
lege campus and spend less time with family members while engaging
in education and work activities. Increased anonymity can result in
mental health difficulties going unrecognized and untreated. Broadly
speaking, symptoms are considered to cross the threshold to full psy-
chosis when they are experienced with 100% conviction and have an
impact on the behavior or functioning of the individual. However, psy-
chotic disorders often have a prodromal period, or a time preceding the
onset of full psychosis when attenuated symptoms may occur. During
this stage, symptoms are often nonspecific and may be ascribed to other
diagnoses, including depression, anxiety, or attention-deficit/hyperac-
tivity disorder, or simply may be considered a normative reaction to the
stressors of college life. However, a deeper look will often reveal accom-
panying attenuated (or subthreshold) symptoms or even brief, full psy-
chotic symptoms that may indicate high risk for developing full
psychosis. Early symptoms often include distressing and impairing
perceptual disturbances such as hearing or seeing things that other peo-
ple do not experience, unusual thoughts, or suspiciousness. It is import-
ant to assess for signs of psychosis because early identification will
shorten DUP and help to identify the most appropriate treatment plan
for the young person. The Prodromal Questionnaire-Brief (PQ-B) is a
simple self-report screening tool that can assist with identification of
early psychosis (Loewy et al. 2011).
One of the first signs that a student is struggling with a mental
health problem is a change in academic performance. Faced with possi-
ble hallucinations or preoccupying thoughts in the form of delusions, as
well as possible cognitive symptoms, a student struggling with psycho-
sis may have decreased grades, turn in incomplete assignments, or miss
classes. Additionally, there are often observable changes in behavior
atypical for the young person. However, when examining behavior, it is

important to consider the cultural and environmental context. Case Ex-
ample 1 describes a spiritual battle that Sam was experiencing between
an angel and a demon, but this would not be clearly indicative of a po-
tential problem if this type of language is normative for a person’s reli-
gious background.
Studies have demonstrated the impact of psychosis on cognitive
functioning, which may consequently have an effect on academic func-
tioning. In the North American Prodromal Longitudinal Study
(NAPLS), people at clinical high risk for schizophrenia were compared
with healthy control subjects and people diagnosed with schizophre-
nia. Cognitive changes were seen in the high-risk group and are a key
component of the composite risk score that has been developed from
this work (Cannon et al. 2016). Cognitive changes in early psychosis
typically relate to processing speed, verbal learning, and working mem-
ory. Deficits in these areas put students at a great disadvantage com-
pared with their peers. Further, many students look to psychoactive
substances, including psychostimulants—prescribed or not—to help
improve these deficits. These medications unfortunately can worsen
nascent psychotic symptoms.
Beyond cognitive changes, social changes are also typically seen at
the onset of psychosis. Many students will become withdrawn and be-
gin to isolate themselves socially. Withdrawing into their own thoughts
often further separates students from peers, making detection more dif-
ficult. However, this also presents an opportunity for early detection be-
cause behavior that is atypical for the student may be a red flag for
further investigation. Residential college settings surround students
with a range of roommates, resident advisors, and deans who may no-
tice changes in behavior and encourage evaluation. When the student
presents for evaluation, screening tools for early signs of psychosis may
aid in the detection of symptoms indicative of a risk of developing psy-
chosis (Loewy et al. 2005).
The college setting provides some advantages for early identifica-
tion. Students expose their thinking in assignments and classroom dis-
cussion. They have committed to a course schedule, and deviations
from that schedule may highlight onset of behavioral change. Similarly,
they are engaged in social networks with peers and resident advisors
who may also notice changes in thought or behavior. Compared with
same-age peers who are not employed or in school, opportunities for
identification of changes in cognition and behavior are extensive.
In addition to the college years being a vital time period for early de-
tection of psychosis, it is also important to keep in mind that high school
students may present with prodromal symptoms. Data from a study in
Australia showed that nearly one-third of people diagnosed with a psy-
chotic illness are diagnosed between ages 15 and 19 (Amminger et al.
2006). High school is an important time in a youth’s life when he or she

is experiencing many transitions. It is a time of both social stressors and
academic challenges. In this setting, it is important for school staff to be
vigilant for persistent changes in the mood or demeanor of a student.
Barriers to Treatment Among College

Students With Serious Mental Illness
Individuals with serious mental illness are often challenged by stereo-
types, prejudice, and discrimination from the general public and even
from health care professionals. They are often depicted as dangerous, vi-
olent, and unreliable in media reports and popular culture. These stigma-
tizing attitudes delay help seeking and are a significant barrier to
initiating treatment. There are three distinct forms of stigma: 1) public
stigma, 2) perceived stigma, and 3) personal stigma. Public stigma is de-
fined as the collective negative views about mental illness held by a com-
munity; perceived stigma refers to one’s beliefs regarding how society
views individuals with mental illness; and personal stigma includes
one’s self-directed negative thoughts and beliefs about mental illness and
how they impact one’s ability to succeed (Kosyluk et al. 2016).
Stigma impacts a person at multiple levels, including academic per-
formance and retention, self-esteem, job occupation, housing retention,
and overall quality of life. Feelings of guilt and shame are often associ-
ated with stigma. Because of the fears of being labeled as “mentally ill,”
many people with serious mental illness withdraw from their inner so-
cial circles, especially during the early stages of psychosis when unchal-
lenged delusions begin to become concrete. Furthermore, students who
isolate themselves have lower levels of community engagement and so-
cial relationships. Withdrawal from social networks may make identifi-
cation even more challenging.
Research has found that unfamiliarity with serious mental illness is
a strong predictor of stigmatizing attitudes. A major obstacle in con-
necting students with mental health services is the lack of familiarity of
the symptoms and early warning signs of psychosis (Feeg et al. 2014).
A survey conducted by the University of South Carolina asked 87 faculty
members about their familiarity with mental disorders (Brockelman and
Scheyett 2015). The researchers found that the least familiar mental dis-
orders were personality disorders (43.5%), schizophrenia (42.3%), and
paranoia (41.7%). Faculty often struggle with how to respond to stu-
dents in distress. Brockelman and Scheyett (2015) found that the most
common approach was to extend the deadline for assignments and dis-
cuss mental health concerns with the student. Nearly 80% consulted
with the college’s office of disability support or counseling center to
gather more information about the resources available on campus. Al-
though that number is encouraging, it is not known how many of those

consultations resulted in referral to CSC or other specific early psycho-
sis services for further management.
Another barrier to initiating psychiatric treatment is lack of empa-
thy. For front-line student health professionals who are not experienced
in caring for people with psychosis, it is often difficult to empathize
with the student’s experience, especially during active symptoms. Too
often, individuals with serious mental illness feel blamed for their dis-
order or worry that their psychotic symptoms will be viewed as a sign
of weakness or that they will be viewed as being “crazy.” To address
this issue, Bunn and Terpstra (2009) had medical students simulate the
experience of auditory hallucinations by listening to headphones. The
medical students had to continue with their daily activities while listen-
ing to the voices. The study found that this experience led to higher lev-
els of empathy toward individuals with severe mental illness. A similar
approach could be adapted to training for on-campus health profes-
sionals and faculty.
Given its distinct environment, college presents a unique opportu-
nity to identify and treat serious psychopathology. Early intervention
leads to better academic, social, health, and occupational outcomes. Re-
ducing stigma and other treatment barriers is essential to improving the
trajectory for students with serious mental illness.
Treatment Accommodations to Help

Students With Psychosis Stay in School
College administrators and health officials often run into a significant di-
lemma when considering how best to help students once an episode of
psychosis has been identified. There are often concerns about student pri-
vacy. Privacy laws can be difficult to understand and can present limita-
tions because college students are generally over the age of majority and
can make decisions for themselves yet often are still dependent on par-
ents financially and emotionally. The two privacy laws at the center of the
discrepancy are the Family Educational Rights and Privacy Act (FERPA),
which protects student privacy, and the Health Insurance Portability and
Accountability Act (HIPAA), which concerns privacy of medical infor-
mation. In 2008, the U.S. Department of Health and Human Services and
the U.S. Department of Education issued joint guidelines on the intersec-
tion of FERPA and HIPAA (U.S. Department of Education 2011; U.S. De-
partment of Health and Human Services and U.S. Department of
Education 2008). Student health records are specifically covered under
FERPA; however, a mechanism exists for alerting parents to potential
mental health crises. The exceptions for privacy are outlined in the Code
of Federal Regulations, 34 CFR § 99.31(a); one exception is that information

may be shared with parents in an emergency situation.
Once onset of psychosis has been identified in a student, administra-
tors face a difficult decision regarding the suitability for continuing en-
rollment in school. At the heart of the dilemma is the need to balance
risks for the student and the university if the student continues to be in-
volved in a potentially high-pressure academic environment while also
trying to find the best long-term solution for the student. Many schools
have de facto policies mandating (or strongly recommending) medical
leave after an initial episode. These policies are based in dated beliefs
regarding the need for convalescence, often to the detriment of the stu-
dent. Sending a student home is not without risk to the student because
there may not be adequate mental health resources (such as a CSC
clinic) in his or her hometown. Further, many college students who re-
turn home find themselves socially isolated while their peers remain at
their respective universities. Students sent home then fall off their edu-
cational trajectory and are not given an opportunity to maintain their
academic level. Lack of intellectual stimulation and structure can also
undermine coping strategies for managing psychosis.
The Bazelon Center for Mental Health Law (2007) has proposed a set
of guidelines for campus mental health treatment. The nearly 50 guide-
lines suggest that schools create a policy to support students to main-
tain their academic progress, providing counseling and voluntary
leaves of absence when needed. In addition, schools should provide ed-
ucation to students and student health leaders on campus about mental
health issues. College counseling centers should be available to stu-
dents 24/7, including during school holidays. There should be access to
emergency services when needed, and student health centers should
make provisions for ongoing care to prevent crises from developing.
When students need to take time away from school, they should be al-
lowed to maintain contact with peers and professors, including con-
tinuing coursework remotely if possible. When involuntary leave is
necessary, the head of the counseling center should be included in any
committee making these case-by-case decisions. Ultimately, schools
should provide the resources needed to help maintain students as close
to the university as possible.
When students are able to stay enrolled, the college or university
further has obligations under federal disability rights law—the same as
for students with physical disabilities. These accommodations may take
the form of increased time for exams or taking tests in a private area.
Students should be allowed to retroactively withdraw from classes if
their performance was significantly impacted by their psychiatric
symptoms and they were unable to complete the necessary coursework
to pass the class. Students should be allowed to select a reduced course
load if full-time status is overwhelming. Housing accommodations
should also be taken into consideration, including whether or not stu-

dents should have roommates, depending on their specific psychiatric
needs. These accommodations should be arranged in consultation with
the treatment provider for the student because the university may re-
quire documentation of the illness and need for accommodation from a
mental health professional (U.S. Department of Education 2011).
Recommendations
Because the college years are a time of transition when young people
may experience a first episode of psychosis, it is critical for colleges and
universities to provide training to staff in early identification of psycho-
sis and make efforts to encourage students to use on-campus mental
health services when they are in distress. Shared decision making, an
individualized approach, and provision of reasonable accommodations
are important aspects of treatment planning. A summary of recommen-
dations is provided in Table 23–1.
Consider the following case in contrast to Sam’s experience pre-
sented earlier. Perhaps we might have seen a different trajectory for
Sam if there had been supports in place to identify psychosis earlier as
in the case of Ronaldo.
Case Example 2
Ronaldo, an 18-year-old young man, enrolled in a university after a suc-
cessful high school career. After several months of school, Ronaldo no-
ticed decreased motivation and difficulty concentrating, which affected
his athletic performance. He received his first C ever. Given the difficulty,
he began to put in extra hours in the library and found himself working
through the night on several occasions. Todd, the resident advisor in Ron-
aldo’s dorm, received training during orientation on recognizing signs of
early psychosis and was given information on how best to respond. He
noticed a change in Ronaldo’s behavior and talked to him about it. Al-
though Ronaldo reassured Todd that everything was fine, they agreed to
check in again in a couple of weeks. Todd informed the resident dean of
the concerns and they agreed to monitor the situation.
When Todd and Ronaldo reconnect 2 weeks later, Ronaldo confides
that he has been hearing things and worries that his roommate may be
able to read his mind. Todd provides Ronaldo with information about
auditory hallucinations, including information on how common these
phenomena are and different reasons why they might occur (stress,
sleep deprivation, psychosis, drugs). They agree to set up an appoint-
ment with a psychiatrist at the Wellness Center, and Todd accompanies
Ronaldo to this appointment. The Wellness Center counselor conducts
an assessment, in which Ronaldo reports that he has been hearing voices
and thinks he is hearing the voice of his angel talking to him. The coun-
TABLE 23–1. Summary of general guidelines

Basic principles
• Universities should make extra efforts to ensure that faculty and college
counseling staff are trained in early identification of the signs of psychosis
and use of early psychosis screening measures such as the Prodromal
Questionnaire (PQ), PRIME Screen-Revised (PS-R), and Structured
Interview for Psychosis-Risk Syndromes (SIPS).
• College faculty and staff members should encourage students to use on-
campus mental health services if they exhibit academic, behavioral, and/or
emotional difficulties that could be related to an underlying mental health
condition.
• College counseling centers should make direct efforts to engage and
encourage students to access mental health services.
• College counseling centers and emergency psychiatric services should be
available 24/7.
Treatment planning
• Appropriate treatment and management should follow the coordinated
specialty care model, which emphasizes having a shared decision-making
and individualized treatment plan.
• Treatment care should involve a comprehensive approach that includes
evidence-based psychotherapy, medication management for first-episode
psychosis, family psychoeducation and support, case management, and
housing and academic accommodations.
• If the student has been hospitalized, college counseling centers should obtain
consent from the student to work closely with the hospital treatment team to
ensure aftercare planning.
Accommodations and leaves of absence
• College and universities should provide reasonable housing and academic
accommodations to allow students to maintain their academic progress and
social relationships.
• If a medical leave of absence is necessary, students should be allowed to
remain in contact with peers and professors to maintain a strong social
support network.
• Absences for treatment and hospitalization should count as excused
absences. Students should not be sanctioned or punished for missing classes
because of a mental health condition.
Source. Adapted from Bazelon Center for Mental Health Law 2007.
selor recommends that Ronaldo receive further evaluation at the local

CSC program. He also suggests that Ronaldo reach out to his family for
additional support. Ronaldo does this, and his family come to his next
appointment at the CSC clinic. Ronaldo is accepted into the service and
immediately meets with an educational support specialist. Together,
Ronaldo and his family work with the college to establish a plan to sup-
port Ronaldo in his studies, including an amended schedule for the re-
mainder of the semester, thus allowing him to continue to stay
matriculated.
Students presenting with a recent onset of psychosis are heteroge-

neous and present with many different needs. Although many will
have cognitive and social deficits at the onset of illness, this is not the
case for all students. The overall panoply of symptoms that one can
have, from hallucinations and delusions to primarily negative symp-
toms including cognitive difficulties and social isolation, means that
careful attention must be paid to the specific needs of each individual
student. Successful treatment of students in this age group requires an
appreciation of the common symptoms and a unique and personalized
approach to treatment. There is no “one size fits all” approach to treat-
ment of psychotic illnesses.
KEY CONCEPTS
• College presents a unique opportunity for identifying stu-
dents with early psychosis and shortening their duration
of psychosis.
• With early intervention and appropriate educational sup-
ports, young people experiencing onset of psychosis while
enrolled in college can access treatment and continue
progress toward their educational goals.
• Providing strong institutional support that is easily accessi-
ble and free of stigma gives students with severe mental ill-
ness the best chance of continued academic success.
• Forced medical leaves should be used minimally after all
other options have been exhausted. When students need
to take time away from school, they should be allowed to
maintain contact with peers and professors and continue
coursework remotely.
1. What supports can best help students seek evaluation in a

college setting? How can the process be simplified for stu-
dents seeking psychiatric care? How do students ordinarily
find their way to psychiatric treatment? What can be done to
help lower the barriers for students seeking treatment for a
potential psychotic disorder?
2. How can a university or college help support and treat stu-

dents with new-onset psychosis? What is the process for the
family to be involved, and when and how are they contacted?
How are the treatment options discussed with students and
families? How does your university typically handle a new-
onset psychotic disorder? What are the treatment options for
students?
3. How does your coordinated specialty program interface with

colleges and universities in your area to support early identi-
fication and referral for students with emerging psychosis?
Suggested Readings
Books and Reports

Bazelon Center for Mental Health Law: Supporting Students: A Model
Policy for Colleges and Universities. Washington, DC, Judge David
L. Bazelon Center for Mental Health Law, May 15, 2007. Available
at: www.bazelon.org/wp-content/uploads/2017/04/Supporting
StudentsCampusMHPolicy.pdf. Accessed October 15, 2018.
National Collaborating Centre for Mental Health: Psychosis and schizo-
phrenia in children and young people, in Psychosis and Schizophre-
nia in Children and Young People: Recognition and Management
(NICE Clinical Guidelines No 155). Bethesda, MD, National Center
for Biotechnology Information, 2013. Available at: www.bazelon.org/
wp-content/uploads/2017/04/SupportingStudentsCampusMH
Policy.pdf. Accessed January 26, 2019.
Roberts LW: Student Mental Health: A Guide for Psychiatrists, Psychol-
ogists, and Leaders Serving in Higher Education. Washington, DC,
American Psychiatric Association Publishing, 2018
Websites and Social Media Resources

Students With Schizophrenia Facebook page: www.facebook.com/
studentswithschizophrenia
Students With Schizophrenia website, www.sws.ngo
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preliminary validation of a self-report screening measure for prodromal
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Prodromal Questionnaire—Brief version (PQ-B). Schizophr Res 129(1):42–
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U.S. Bureau of Labor Statistics: College enrollment and work activity of recent
high school and college graduates summary. April 26, 2018. Available at:
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U.S. Department of Education: Students with Disabilities Preparing for Postsec-
ondary Education. Washington, DC, U.S. Department of Education, 2011.
Available at: https://ed.gov/about/offices/list/ocr/transition.html. Ac-
cessed January 26, 2019.
U.S. Department of Health and Human Services; U.S Department of Education:
Joint guidance on the application of the Family Educational Rights and Pri-
vacy Act (FERPA) and the Health Insurance Portability and Accountability
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partment of Health and Human Services, November 2008. Available at:
www2.ed.gov/policy/gen/guid/fpco/doc/ferpa-hipaa-guidance.pdf.
Index
Page numbers printed in boldface type refer to tables and figures.
ACA. See Affordable Care Act pharmacological interventions,

Acamprosate, for management of 395–396
substance use and early psychosocial interventions,
psychosis, 257 391–393
N-acetylcysteine, for management of psychotic experiences versus
substance use and early disorder, 388
psychosis, 257 schools as partner for services,
Addison’s disease, 343 391
Adolescents. See also College and suicide risk, 390
university students; Family first-person account of psychosis,
age of people in early stages of 60–68
psychosis, 96–97 high-risk, 6
case examples of interviews with, longitudinal brain imaging studies,
98, 99 386
cognition in, 393 mental health and, 8
cultural factors in interaction with, participation and peer support, 5
389–390 PTSD in, 386–387
developmental characteristics of, referrals for diagnosis, 387–388
384, 397 TF-CBT for, 393
emergence of psychosis-risk transition to adult service systems,
syndrome, 111 55–56
engagement in work and school, Adults
282–283 adult-onset schizophrenia, 64
first-episode psychosis continuum first-person account of psychosis,
and, 16, 383–401 61–64
age of onset, 383, 396 Advocacy, and schizophrenia, 67–68,
CBT for, 392 75
developmental considerations, Aerobic exercise
385–387 affective symptoms and, 275–276
differential diagnosis, 387– effects on cognition, 266–273
390 effects on functional outcome,
family function and inclusion, 276–277
397 effects on positive and negative
identification and engagement, symptoms, 273–275
390–391 studies assessing effects of,
overview, 383–385 267, 268–271, 272
417
Aerobic exercise (continued) second-generation, 187

overview, 265 selection of, 188–190, 191–199
role in treatment of early psychosis, shared decision making in
265–280 treatment, 203–205
Affordable Care Act (ACA), 45, 48 side effects of, 200
Alcohol, acute intoxication and APA. See American Psychiatric
withdrawal symptoms of, 247 Association
Alcohol, Smoking and Substance APSS. See Attenuated positive
Involvement Screening Test symptom syndrome
(ASSIST), 253 Aripiprazole
Alcohol use disorder in first-episode psychosis clinical
case example of, 338–339 trials, 197, 198–199
management of substance use for management of first-episode
and early psychosis, 257 psychosis in adolescents, 393
American Psychiatric Association for management of substance use
(APA) and early psychosis, 256
guidelines for initial medical response rate and drug dosing,
workup of first-episode 190, 200
psychosis, 134, 135 Asenapine, for treatment of first-
treatment guidelines for schizo- episode psychosis, 190
phrenia, 202 Assessment
Amisulpride, in first-episode assessing and treating trauma in
psychosis clinical trials, 195 team-based early psychosis
Amitriptyline, for management of care, 151–167
comorbid psychosis and brief consultation with family, 320
trauma, 165 individual assessment of relatives,
Anti-N-methyl-D-aspartate (anti- 317–318, 319
NMDA), 141 in individuals at clinical high risk
Antiphospholipid antibody for psychosis, 107–132
syndrome, 141 of people in early stages of
Antipsychotic medications psychosis, 95–105
consequences of long-term use, age and, 96–97
202 case examples of, 98, 99
first-generation, 187 diagnosis, 104
long-acting injectable formulations, family collaboration, 97
256 framework for, 100
for management of substance use initial interview, 96
and early psychosis, 256 interviewer’s role, 97
for medication management of reason for referral, 98
comorbid trauma and termination of, 103
psychosis, 165 ASSIST. See Alcohol, Smoking and
observation of hospitalized Substance Involvement
patient and, 374–375 Screening Test
response rate and drug dosing, Attenuated positive symptom
190, 200 syndrome (APSS), 113, 129
Index 419
Attenuated psychosis syndrome CAFE. See Comparison of Atypicals

Conditions for Further Study in in First Episode of Psychosis
DSM-5, 109, 129 California, CSC in, 53–55
Autoimmune disorders, in first- Cannabidiol (CBD), 244
episode psychosis medical Cannabis-induced psychosis, 244, 248
workup, 141–142 Cannabis use disorder, for manage-
Autoimmune encephalitis, 141 ment of substance use and early
Avon Longitudinal Study of Parents psychosis, 257
and Children, 385 CAPS-5. See Clinician-Administered
PTSD Scale
B3 deficiency, 142 Careers. See Employment, supported,
B12 deficiency, 142 for people in early psychosis
BACS-SC. See Brief Assessment of Cariprazine, for treatment of first-
Cognition in Schizophrenia– episode psychosis, 190
Symbol Coding Case examples
Bazelon Center for Mental Health of access to treatment team, 326
Law, 409 of active engagement, 323–324
BDNF. See Brain-derived neurotrophic of alcohol use disorder, 338–339
factor of brief consultation, 325–326
Benzodiazepines, contraindications of brief illness education, 325
for PTSD, 165 of brief intervention for prevention
Bipolar illness, 309–310 of suicidal behavior, 343
BIPS. See Brief intermittent psychotic of career profile and employment
syndrome and education plan, 286
BPRS. See Brief Psychiatric Rating of CBTp, 217–219, 220
Scale of clinical high risk for psychosis,
Brain-derived neurotrophic factor 107–109, 128
(BDNF), 273, 275 of early detection of schizophrenia,
Brief Assessment of Cognition in 23–30, 40–41
Schizophrenia–Symbol Coding of employment, 292
(BACS-SC), 109, 123 of family engagement, 86–87
Brief intermittent psychotic syndrome of first-episode medical workup,
(BIPS), 114, 129 133–134, 144–146
Brief Psychiatric Rating Scale (BPRS), of first-episode psychosis family
190, 351 intervention, 323–327
Bullying, 153, 167 first-person accounts of psychosis,
Bupropion (Zyban), for 59–75
management of tobacco use of individual assessment of
disorder and early psychosis, relatives, 324
257 of interview with youth, 98, 99
CAARMS. See Comprehensive Assess- of relatives and treatment
ment of At-Risk Mental States planning meetings, 326
CAARMS-B. See Comprehensive of NAVIGATE team, 224–225
Assessment of At-Risk Mental of peer support, 89–90, 300–302
States-Brief of peer support specialist, 296
Case examples (continued) CFDA. See Community Programs for

of psychopharmacology for early Outreach and Intervention With
psychosis, 204–205 Youth and Young Adults at
of substance use, 241–242, 258–259 Clinical High Risk for Psychosis
of suicidal ideation and behavior, Grant Program
338–339 Chantix (varenicline), for management
of suicide assessment, 341 of tobacco use disorder and early
of suicide attempts, 336–337 psychosis, 257
of supported education, 289, 292 Child and Adolescent Trauma Screen
of team-based CSC, 172–177, 180 (CATS), 157
of TECCC for FEP, 359–361 Childhood trauma, 153, 167, 386
of technology to advance early Children’s Health Insurance Program
psychosis intervention, 359– (CHIP), 47
361 CHIP. See Children’s Health Insurance
of trauma and team-based early Program
psychosis care, 152, 156, 159– CHIPRA. See CHIP Re-authorization
160, 163–164 Act of 2009
of university students, 404, 410 CHIP Re-authorization Act of 2009
Case management (CHIPRA), 50
of early psychosis service, 5 Chlorpromazine
teams and, 178 in first-episode psychosis clinical
Catechol-O-methyltransferase trials, 191
(COMT), 387 for treatment of psychosis, 11–12
CATS. See Child and Adolescent CIDAR. See Center for Intervention
Trauma Screen Development and Advanced
CBD. See Cannabidiol Research
CBSST. See Cognitive-behavioral Clinical Global Impressions scale, 190
social skills training Clinician-Administered PTSD Scale
CBTp. See Cognitive-behavioral (CAPS-5), 157
therapy for psychosis Clinician burnout, 309
CBT-SP. See CBT-suicide prevention; Clozapine, 134
Cognitive-behavioral therapy in first-episode psychosis clinical
CBT-suicide prevention (CBT-SP), trials, 191, 192–196, 198
344 for management of comorbid
CCBHCs. See Certified community psychosis and trauma, 165
behavioral health clinics for management of first-episode
Center for Intervention Development psychosis in adolescents, 393,
and Advanced Research 394
(CIDAR), 188, 199 response rate and drug dosing,
Centers for Disease Control and 190, 200
Prevention, 135 for treatment of first-episode
Centers for Medicare and Medicaid psychosis, 190
Services, 50–51 Code of Federal Regulations, 408–409
Certified community behavioral Cognition
health clinics (CCBHCs), 49 in adolescents, 393
Index 421
changes in college and university lack of empathy with, 408

students, 406 overview, 403
impact of physical exercise in recommendations, 410, 411, 412
treatment of early psychosis social changes in, 406
and, 266–273, 277–278 stigma of mental illness in, 407
neuropsychological testing for College for Behavioral Health
impairment, 389 Leadership Peer Services
Cognitive-behavioral social skills Toolkit, 298
training (CBSST), 127–128 Columbia Suicide Severity Rating
Cognitive-behavioral therapy (CBT) Scale, 390
to decrease anxiety during Columbo style, 215. See also Cognitive-
hospitalization, 368 behavioral therapy for psychosis
for intervention of substance use Communication. See also Teams
and early psychosis, 255 in assessment and diagnosis, 126–
to reduce suicide risk, 344 127
Cognitive-behavioral therapy for listening skills, 316
psychosis (CBTp), 85–86, 88, making and communicating a
173–175, 214–219 diagnosis, 372–373
for adolescents, 392 problem-solving skills training
assessment and formulation, 215– and, 322
216 rapport and CBPp, 173–174
case example of, 217–219, 220 Community
choice of, 235–236 awareness of mental health issues, 5
Columbo style, 215 inclusion of peer experiences, 82
comparison with IRT, 225–226, outreach education in, 80, 82, 90
227–234 raising awareness of psychosis, 14
engagement and, 215 recovery from schizophrenia, 64–67
goals, 215 role in support of recovery, 60–68
interventions, 216–217 teams and, 178
key elements of, 215 trauma and, 153, 155
relapse prevention, 217 Community Programs for Outreach
trauma and, 160, 163 and Intervention With Youth
College and university students, and Young Adults at Clinical
403–415. See also Adolescents High Risk for Psychosis Grant
accommodations for school, 408– Program (CFDA), 49
410, 411 Comparison of Atypicals in First
barriers to treatment of students Episode of Psychosis (CAFE),
with serious mental illness, 188, 194
407–408 Comprehensive Assessment of At-Risk
case examples of, 404, 410, 412 Mental States (CAARMS), 351
change in academic performance, Comprehensive Assessment of At-
405–406 Risk Mental States-Brief
cognitive changes in, 406 (CAARMS-B), 109–110, 119, 121
forced medical leave, 412 constructs, 119, 121
institutional support for, 412 diagnostic features, 112–114
Comprehensive Assessment of At- symptoms of, 115

Risk Mental States-Brief CSC. See Coordinated specialty care
(continued) Cultural Formulation Interview, 179
diagnostic subtypes, 112–114 Culture
model of psychosis risk onset, 120 in assessment and diagnosis, 124–
scoring summary, 122 127
COMT. See Catechol-O- assessment and treatment of
methyltransferase trauma in team-based early
Confidentiality, 311–313 psychosis care and, 158
Connecticut, population health of family, 316
system specifications for early family and, 97–98
intervention services in, 38–39 in interaction with adolescents,
Consent, 311–313 389–390
for pharmacological management sensitivity to, 84
of first-episode psychosis in teams and, 179, 185
adolescents, 394
withdrawal of, 312 Determiners, 352
Contingency management, for Diagnostic and Statistical Manual of
intervention of substance use Mental Disorders (DSM)
and early psychosis, 255 DSM-III, 12
Coordinated specialty care (CSC), DSM-5
18–20, 24, 41, 46–49, 84 Conditions for Further Study,
in California, 53–55 129
clinical concepts for treatment, Cultural Formulation Interview,
177–181 179
description, 46–47 diagnostic criteria for PTSD,
FEP and, 47 156
financing early psychosis treat- proposed diagnostic criteria
ment, 46–49, 55 for attenuated psychosis
for first-episode psychosis, 161–162 syndrome, 110–111
NIMH definition of, 172 first edition in 1952, 11–12
programs, 172 Digital native generation, 349
as providers of early intervention, Dissociation, 108
85 Disulfiram, for management of
recovery, 184 substance use and early
shared decision making, 184 psychosis, 257
Coping skills, 61–62, 163 DSM. See Diagnostic and Statistical
COPS. See Criteria of Prodromal Manual of Mental Disorders
Syndromes DUP. See Duration of untreated
Cortisol, 343 psychosis
Criteria of Prodromal Syndromes Duration of untreated psychosis
(COPS), 115 (DUP), 12, 41, 80, 405
psychosis-risk syndromes, 118–119 early intervention and, 128
scoring summary, 116–117 heuristic model in STEP’s
severity scales, 115, 118–119 catchment, 32
Index 423
long-term outcomes of, 13 schools as partner for services

time period of, 129 working with adolescents,
391
Early and Periodic Screening, supported, 289–292
Diagnostic, and Treatment case example of, 289
(EPSDT) program, 47 IPS for students in high school,
Early Assessment and Support 290
Alliance (EASA) model, 4, 18, key elements of, 293
172, 176 postsecondary education, 290–
Early Detection, Intervention, and 291
Prevention of Psychosis providing education supports,
Program (EDIPPP), 19 291–292
Early Intervention in Psychiatry EIP. See Early intervention for
(journal), 3–4 psychosis programs
Early intervention for psychosis (EIP) EIS. See Early intervention services
programs, 80 Empathy, 408
Early intervention services (EIS), 24 Employment, supported, for people
Early Psychosis Global Working in early psychosis, 281–294
Group, 192 case example of, 292
Early Psychosis Guidelines Writing conducting an individualized job
Group, 396 search, 287–288
Early Psychosis Screener (EPS), engaging people, 282–283
388 family support for, 283
Early Treatment and Intervention in IPS services, 283–289
Psychosis (TIPS), 80 key elements of, 293
EASA. See Early Assessment and overview, 281–282
Support Alliance model Emsley and Risperidone Working
Ecological momentary assessment, Group 1999, 191
353, 356 Endocrine disorders, in first-episode
EDMR. See Eye movement desensiti- psychosis medical workup, 142–
zation therapy 143
Education, 61–63. See also Psychoed- Engagement
ucation case example of family engage-
brief illness education for families ment, 87
of individuals with psychosis, definition, 79–80, 81
320 family engagement in inpatient
goals, 318 care for early psychosis, 370–
strategies for optimizing, 330– 372
333 interventions for individuals and
community awareness of mental relatives, 314–317
health issues, 5, 14 case example of, 323–324
family support for, 283 maintaining active engagement
IPS core principles of, 284 through recovery, 87–90
outreach education in the safety planning, 372
community, 80, 82, 90 stages of, 79–90
Engagement (continued) culture and, 97–98, 316

in stagewise substance use in early psychosis therapy, 5
treatment, 254 family intervention and
technology and, 283 support, 309–333
timing of, 83 intensive interventions, 321
in treatment for individuals and encouraging engagement and
families, 83–87 support of, 15
creating accessible, flexible engagement in inpatient care for
programs for, 83–84 early psychosis, 370–372
person-centered and goal- engaging in care, 79–93
driven services, 84–85 exposure to STEP specifications,
using multiple-family groups to 38
strengthen engagement, 86–87 first-episode psychosis family
of youth in work and school, 282– services, 313
283 family function and inclusion,
Environment 397
creating environment conducive interventions offered to
to peer support, 303–304 individuals and relatives,
toxic-metabolic disorders and, 142 314–321
EPPIC National Support Program, 396 first-person account of psychosis
EPS. See Early Psychosis Screener and, 61
EPSDT. See Early and Periodic formal communication and
Screening, Diagnostic, and problem-solving skills
Treatment program training, 322
EUFEST. See European Union First inclusion in individual’s recovery,
Episode Schizophrenia Trial 310
European Union First Episode individual assessment of relatives,
Schizophrenia Trial (EUFEST), 317–318, 319
188, 194 case example of, 324
Evans-Stoddart model, 28 invitations to relatives to join
Exercise, 266. See also Aerobic exercise, treatment planning meetings,
role in treatment of early 321
psychosis case example of, 326
Eye movement desensitization involvement in assessment and
therapy (EDMR), 160 treatment of trauma in early
psychosis care, 164
Family. See also Adolescents maintaining active engagement
brief consultation with, 320 through recovery, 87–90
brief illness education, 318–320, 320 multifamily support groups, 321–
case example of, 325 322
goals, 318 patient’s medical workup and, 146
case example of brief consultation, peer support and, 297–298
325–326 principles and strategies for
case example of FEP family involving relatives in
intervention, 323–327 treatment, 310–311
Index 425
referral for individual supportive case examples of, 133–134,

psychotherapy for relatives, 144–146
322–323 conditions for consideration in
support initial workup, 140–144
for employment and medical causes of psychosis,
education, 283, 293 138–139
in recovery from psychosis, 327 overview, 133
teams for case management suggested workup for medical
services, 178 causes of psychosis, 136
therapeutic support for, 371–372 multi-element early intervention
using family psychoeducation to services, 171–186
engage families, 85–86 pre-FES, 25
using multiple-family groups to presentation of information, 331
strengthen engagement, 86–87 principles and strategies for
Family Educational Rights and involving relatives in
Privacy Act (FERPA), 408 treatment of, 310–333
Federation of Families for Children’s sessions, 332–333
Mental Health, 53 First-Episode Psychosis Services
FEP. See First-episode psychosis Fidelity Scale (FEPS-FS), 51
FEPS-FS. See First-Episode Psychosis First-episode services (FES), 24–25, 41
Services Fidelity Scale First-generation antipsychotics, 187
FERPA. See Family Educational Fluoxetine, for management of
Rights and Privacy Act comorbid psychosis and
FES. See First-episode services trauma, 165
FIRST Coordinated Specialty Care, FOCUS smartphone intervention
172 system, 353–354, 355
First-episode psychosis (FEP). See also Folate deficiency, 142
Psychosis
APA guidelines for initial medical GAF. See Global Assessment of
workup of, 135 Functioning
assessing and treating trauma in GED. See General educational
team-based early psychosis development tests
care, 151–169 General educational development
avoiding assumptions about (GED) tests, 290
participants’ beliefs, 332 Genetic disorders, in first-episode
components of psychosis family psychosis medical workup, 144
program for, 313–323 Genetic risk and deterioration
stepped-care model of family syndrome (GRDS), 112, 129
interventions, 314 German Research Network, 196
CSC and, 47 Global Assessment of Functioning
managing initial diagnostic (GAF), 112–114
uncertainty, 331 Government Performance and
medical causes of, 138 Results Modernization Act, 51
medical workup for, 133–149 Graduated Recovery From Initial
baseline medical evaluation, 135 Psychosis (GRIP), 223
GRDS. See Genetic risk and inpatient care for early psychosis,
deterioration syndrome 365–381
GRIP. See Graduated Recovery From CBT to decrease anxiety during
Initial Psychosis hospitalization, 368
Group therapy developing shared treatment
in early psychosis service, 5 goals, 366–368
multiple-family group format, 86, family engagement, 370–372
321–322 goals, 366
using multiple-family groups to key techniques for intervention,
strengthen engagement, 86– 369–370
87 making and communicating a
diagnosis, 372–373
Hallucinations, 69–70, 296 medication and, 373–376
Hallucinogens, 251 milieu considerations, 368–370
Haloperidol overview, 365–366
in first-episode psychosis clinical recovery goals, 376
trials, 191–194, 196 staff daily “huddle,” 369
for management of substance use transitioning, 376–377
and early psychosis, 256 use of sensory rooms, 368–369
response rate and drug dosing, HVLT-R. See Hopkins Verbal Learning
190, 200 Test–Revised
Health care. See also Medicaid; Hyperthyroidism, 143
Medicare Hypothyroidism, 143
teams and, 178
in the United States, 34 IDEA. See Individuals with Disabilities
Health Information Technology for Education Act
Economic and Clinical Health Identity-based trauma, 153, 155
Act of 2009 (HITECH), 50 IEP. See Individualized Education
Health Insurance Portability and Program
Accountability Act (HIPAA), IEPA. See International Early Psychosis
408 Association
HIPAA. See Health Insurance Illness Management and Recovery
Portability and Accountability program, 223
Act Imipramine, for management of
HITECH. See Health Information comorbid psychosis and
Technology for Economic and trauma, 165
Clinical Health Act of 2009 Immigrants, 316
HIV, 140 Individualized Education Program
Home-based care in early psychosis (IEP), 290
service, 5 Individual placement and support
Hopkins Verbal Learning Test– (IPS) services, 283–289
Revised (HVLT-R), 109, 123 advancing careers, 289
HORYZONS, 357–358, 358 career profile and employment
Hospitalization and education plan, 286–287
case example of, 70–74 case example of, 286
Index 427
conducting an individualized job observation skills, 100

search, 287–288 structured, 101–104
core principles of supported IPAQ. See International Physical
employment and education, Activity Questionnaire
284 IPS. See Individual placement and
intake assessment, 284–285 support services
IPS specialist, 282 IQ, 142, 385
providing job supports, 288–289 IRT. See Individual resiliency training
strength-based approach to, 282
for students in high school, 290 Jail Diversion Program (JDP), 65–66
team-based approach to, 283, 286 JDP. See Jail Diversion Program
Individual resiliency training (IRT),
219–225 Kraepelinian paradigm, 2
case example of, 224–225
choice of, 235–236 LAI. See Long-acting injectable
clinical and technical influences formulations
on, 222–223 Langston’s pathways to FES, 31, 32
comparison with CBTp, 225–226, Language, in assessment and
227–234 diagnosis, 126–127
description, 221 Latent semantic analysis, 352, 353
development of, 221–222 LEC. See Life Events Checklist
goals, 219 Legislation
psychiatric rehabilitation Affordable Care Act, 45, 48
approaches to, 222 CHIP Re-authorization Act of
structure and organization of, 223 2009, 50
theories of well-being, 221 Family Educational Rights and
theory of reasoned action, 222 Privacy Act, 408
Individuals with Disabilities Government Performance and
Education Act (IDEA), 47–48, 391 Results Modernization Act, 51
Infectious diseases, in first-episode Health Information Technology
psychosis medical workup, 140– for Economic and Clinical
141 Health Act of 2009, 50
Insight, 115, 128 Health Insurance Portability and
International Early Psychosis Accountability Act, 408
Association (IEPA), 3–4 Individuals with Disabilities
International Physical Activity Education Act, 47–48, 391
Questionnaire (IPAQ), 268 Mental Health Services Act, 54
Internet, 349. See also Technology Rehabilitation Act of 1973, 391
Interviews. See also Motivational Social Security Act, 47
interviewing LifeData, 355–356
Cultural Formulation Interview, Life Events Checklist (LEC), 157
179 Long-acting injectable (LAI) formu-
framework for, 100 lations, for management of sub-
initial, 96 stance use and early psychosis,
interviewer’s role in, 97, 101 257
Lurasidone, for treatment of first- Model of Recovery Supports, 254

episode psychosis, 190 Models
biological model, 373–374
Marijuana, 241–242, 244, 387 cognitive-behavioral therapy for
MBC. See Measurement-based care psychosis model, 86, 88
Measurement-based care (MBC), 354 conceptual model for under-
Medicaid, 47, 48, 49–50 standing suicide, 336, 337
Medicare, 48 CSC, 18–20, 24, 41, 46–49, 84–85,
Medication. See Antipsychotic medi- 161–162, 172, 184
cations; Psychopharmacology; Early Assessment and Support
individual drug names Alliance model, 4
Melatonin, for management of sleep Evans-Stoddart model, 28
disorder, 241–242 evidence-based practices for
Mental disorders psychosis, 18
access to service, 5 heuristic model for DUP in STEP’s
barriers to treatment of college catchment, 32
students with serious mental Model of Recovery Supports, 254
illness, 407–408 multimodal care models, 19
clinical epidemiology of onset of, 7 multiple-family group format
community awareness of mental model, 86
health issues, 5, 14 of psychosis risk onset, 120
helping participants recognize of shared decision making, 204
psychiatric disorder, 331 staging model for framework of
public perception of, 2 early intervention, 17
recovery from, 2, 84 stepped-care model of family
reform of, 4, 8 intervention for recent-onset
stigma of mental illness in, 407 psychosis, 314
Mental Health Services Act (MHSA), stress-diathesis model, 211
54 stress-vulnerability model, 216–
Mental Health Services Block Grants 217, 222
(MHBGs), 19, 48–49, 54 Molindone, in first-episode psychosis
Mental Health Services Oversight and clinical trials, 195
Accountability Commission, 54 Motivational interviewing, 255
Metacompetencies, 213 Multiple-family group format (MFG-
Methylprednisolone, 134 FPE) model, 86, 88
MFG-FPE. See Multiple-family group MY3 (phone app), 342
format model
MHBGs. See Mental Health Services Naltrexone
Block Grants for management of opioid use
MHSA. See Mental Health Services Act disorder and early psychosis,
MindMap campaign, 34 258
Mirtazapine, for management of for management of substance use
comorbid psychosis and and early psychosis, 257
trauma, 165 NAMI. See National Alliance on
Mobile outreach, 6 Mental Illness
Index 429
NAPLS. See North American Obesity, 39

Prodromal Longitudinal Study OnTrackNY, 172, 176
NASMHPD. See National Opioids, acute intoxication and
Association of State Mental withdrawal symptoms of, 249
Health Program Directors Opioid use disorder, 257–258
National Alliance for the Mentally Orygen Youth Health, 102
Ill, 53 Outreach education, 80, 82, 90
National Alliance on Mental Illness Outreach services in rural settings,
(NAMI), 65, 67, 79 181–183
National Association of State Mental
Health Program Directors PACE. See Personal Assessment and
(NASMHPD), 82 Crisis Evaluation Clinic
National Behavioral Health Quality PAFIP. See Programa Atención Fases
Framework, 51 Iniciales de Psicosis
National Center for PTSD, 157 Paliperidone
National Institute of Mental Health in first-episode psychosis clinical
(NIMH), 18, 49, 172 trials, 197
National Institute on Drug Abuse for management of substance use
(NIDA) “quick screen,” 252 and early psychosis, 256
National Quality Forum, 51 PANS, 141
National Survey on Drug Use and PANSS. See Positive and Negative
Health (NSDUH), 50 Syndrome Scale
NAVIGATE program, 172, 176, 219, Paraneoplastic syndromes, in first-
221, 223 episode psychosis medical
case example of, 224–225 workup, 141–142
Nefazodone, for management of Paroxetine, for management of
comorbid psychosis and trauma, comorbid psychosis and
165 trauma, 165
Neurological disorders, in first- Partnerships
episode psychosis medical community-academic, 18
workup, 143–144 in early psychosis service, 6
Nicotine replacement therapy, 257 PCL-5. See Posttraumatic Stress
NIDA. See National Institute on Disorder Checklist for DSM-5;
Drug Abuse PTSD Checklist for DSM-5
NIDA-Modified ASSIST, 252–253 PCT. See Phencyclidine
NIMH. See National Institute of Peers. See also Teams
Mental Health case example of, 89–90
North American Prodromal in early psychosis programs,
Longitudinal Study (NAPLS), 160
18, 123, 351, 406, 352 implementing peer support in
Norwegian Early Treatment and early psychosis programs,
Intervention in Psychosis (TIPS), 295–307
32, 34 case example of, 300–302
NSDUH. See National Survey on core roles and attributes of
Drug Use and Health peer support, 298–300
Peers (continued) shared decision making in,

implementing peer support in 203–205
early psychosis programs in first-episode psychosis clinical
(continued) trials, 191–199
creating an environment intervention in early psychosis
conducive to peer service, 5
support, 303–304 long-acting injectables for
defining “peer” in, 302–303 adolescents, 394
history of, 296–298, 305 medication management of
principles of, 305 comorbid trauma and
role of specialists in, 298–300, psychosis, 165
303–304 patient’s refusal of, 367
specialist’s story, 295–296 treatment adherence, 367
inclusion of peer experiences, Phencyclidine (PCT), acute
82 intoxication and withdrawal
influences on substance use users symptoms of, 250
in psychosis, 253 Phenelzine, for management of
maintaining active engagement comorbid psychosis and
through recovery, 87–90 trauma, 165
narrative about, 87–90 PIER. See Portland Identification and
participating in social networks, Early Referral
384 Polymyositis, 141
support in early psychosis Population health
therapy, 5, 88–89 for early detection, 26–28, 27, 41
case example of, 89 outcomes, 26, 28
as support specialists, 66 pathways, networks, and systems
Pellagra, 142 for, 29–35
Personal Assessment and Crisis concepts of, 30–35
Evaluation (PACE) Clinic, 99–100 heuristic model for DUP in
Person-centered care, 178 STEP’s catchment, 32
Persuasion, 254 intervention services, 33
Pharmacotherapy. See also individual Langston’s pathways to FES,
drug names 31, 32
for adolescents with first-episode population health-based early
psychosis, 393–395 intervention services in
discontinuation of, 395 Connecticut, 38–39
in first-episode psychosis, 187–188, Portland Identification and Early
187–209, 200 Referral (PIER), 18, 80, 82
case example of, 204–205 peer narrative about, 87–90
response rate and drug dosing, Positive and Negative Syndrome
190, 191–199, 200, Scale (PANSS), 37, 190, 274, 351,
selection of an antipsychotic 394
drug, 188–190, 191–199 Posttraumatic stress disorder (PTSD),
treatment 107, 153
duration of, 200–202 in adolescents, 386–387
Index 431
diagnosis of, 157 Comprehensive Assessment of

DSM-5 diagnostic criteria for, 156 At-Risk Mental States-Brief,
Posttraumatic Stress Disorder 119
Checklist for DSM-5 (PCL-5), determining presence of insight
155 in psychosis, 115
PQ-B. See Prodromal Questionnaire- Prodromal Questionnaire-Brief,
Brief 124
PREP. See Prevention and Recovery risk calculator, 123–124, 125,
in Early Psychosis 126
Prevention and Recovery in Early structured interview, 111, 115,
Psychosis (PREP), 18 118–119
Prevention through Risk Identifica- cannabis-induced, 244
tion, Management, and Educa- in college and university students,
tion (PRIME) Screen, 388 403–415
PRIME. See Prevention through definition of, 109–111
Risk Identification, diagnosis of, 64, 109–111
Management, and Education diagnostic features, 110
Screen duration of untreated, 12
Prodromal Questionnaire-Brief (PQ-B), early intervention
124, 388, 405 access and quality of care, 50–51,
Prodrome, 12, 109–110 56
Programa Atención Fases Iniciales assessment in, 95–105
de Psicosis (PAFIP), 193, 198 challenges of, 1–3
Prolonged exposure, 160 CSC in the United States, 19–20
Psychoeducation, 85–86. See also core components of, 5–6
Education developmental framework of,
Psychopharmacology 16
case example of, 204–205 family intervention and
clinical trials for people in early support, 309–333
psychosis, 191–199, 201 financing treatment, 46–50
evaluation for adherence to CSC, 46–49
medication regimen, 344 patchwork, 49–50
improvement in psychosis with, growth in the United States,
201 11–22
medication refusal, 203 history of, xv, 11–12, 17–19
model of shared decision making, implementing peer support in
204 early psychosis programs,
Psychosis. See also Case examples; 295–307
First-episode psychosis literature on, 3–4
acute phase care, 5 policy and, 45–58
aerobic exercise in treatment of principles of, 13–16
early psychosis, 265–280 improving access and
assessment in individuals at engagement, 15
clinical high risk for, 107–132 raising community
case example of, 107–109, 128 awareness, 14
Psychosis (continued) psychosocial rehabilitation

early intervention (continued) interventions, 13
psychotherapeutic interven- recovery from, 5, 15
tions, 211–239 substance use and early psychosis,
reform of, 7–8 241–263, 244, 245–246
research and, 3–4 transitioning from chronic care to
resistance to, 4, 6–7 early intervention, 12–13
staging model, 17 treatment of, 64
suicide and, 335–3479 untreated psychosis versus
supported employment and duration of untreated illness,
education for, 281–294 25–26
team-based approach to, 171– workup for medical causes of,
186 136
training, workforce, and Psychosis risk calculator, 351, 352
service delivery systems, Psychosis-risk syndrome, 111
51–53, 56 Criteria of Prodromal Syndromes
using technology to advance, and, 118–119
349–363 diagnostic subtypes, 110, 112–114
engaging families and individuals familiarity with criteria for, 109
in care, 79–93 model of psychosis risk onset,
evidence-based models for, 18 120
first-episode, 2–3 stigma associated with diagnostic
care for adolescents, 383–401 label, 127
medication used in clinical treatment, 127–128
trials, 191–199 Psychosocial interventions, 254–255
psychopharmacology, 187–209 Psychotherapy. See also Cognitive-
triggered by substances, 245– behavioral therapy for
246 psychosis (CBTp); Individual
without substances, 245–246 resiliency training
first-person accounts of, 59–75 early intervention principles and
funding for, xv psychotherapy interventions,
global neglect of, 1 212–213, 212
in individuals at clinical high risk interventions for early psychosis,
for psychosis 211–239
cultural considerations in overview, 211
assessment and diagnosis, referral for individual supportive
124, 126–127 psychotherapy for relatives,
presence of insight in, 115 322–323
treatment, 127–128 in a team setting, 213, 214
inpatient care for early psychosis, PTSD. See Posttraumatic stress
70–74, 365–381 disorder
medical causes of, 138–139 PTSD Checklist for DSM-5 (PCL-5),
onset and entry into care, 41 157
prevention of second psychotic
episode, 202 Quality of care, 50–51
Index 433
Quetiapine Rituals, 133–134

in first-episode psychosis clinical Role-modeling, 322
trials, 194, 195, 197–199
for management of comorbid Sac-EDAPT. See Sacramento Early
psychosis and trauma, 165 Diagnosis and Preventative
response rate and drug dosing, Treatment clinic
190, 200 Sacramento Early Diagnosis and Pre-
for treatment of first-episode ventative Treatment (Sac-EDAPT)
psychosis, 190 clinic, 54
SafetyNet (phone app), 342
RAISE. See Recovery After an SAMHSA. See Substance Abuse and
Initial Schizophrenia Episode Mental Health Services
Project Administration
RAISE-ETP. See Recovery After an Scale of Prodromal Symptoms (SOPS),
Initial Schizophrenia Episode 109, 112–114
Early Treatment Program severity scales, 115, 119
Recovery After an Initial Schizophre- negative scales, 118
nia Episode Early Treatment Pro- positive symptom domain,
gram (RAISE-ETP), 50, 172, 314 116–117, 118
Recovery After an Initial Schizophre- symptom constructs, 115
nia Episode (RAISE) Project, 4, Schizophrenia. See also Specialized
18, 19 Treatment Early in Psychosis
Rehabilitation Act of 1973, 391 adult-onset, 64
Relapse signatures, 356 advocacy and, 67–68, 75
Religion, in assessment and diagnosis, building systems for early
126 intervention services, 35–37,
Research Domain Criteria, 7 36, 38–39
Research Interview Life Events Scale, case example of, 23–30, 40–41
123 diagnosis of, 68–69, 309–310
Risperidone DSM-III diagnostic criteria for, 12
in first-episode psychosis clinical early detection of, 23–44
trials, 191, 193–199, early intervention services
for management of comorbid paradigm, 24
psychosis and sleep disorder, engaging families and individuals
241–242 in care, 79–93
for management of comorbid first-episode psychosis, 24–25
psychosis and trauma, 165 identity and, 59
for management of first-episode impact of physical exercise, 273–
psychosis in adolescents, 393 274
for management of schizophrenia, living with, 71–72
66–67 onset of symptoms of, 24
for management of substance use population health for early
and early psychosis, 256 intervention of, 26–28, 27
response rate and drug dosing, presentation of acute crisis, 76
190, 200 prodrome to, 12, 389
Schizophrenia (continued) Specialized Treatment Early in

psychosocial rehabilitation Psychosis (STEP), 18, 172, 371.
interventions, 13 See also Schizophrenia
randomized controlled trials, 188 heuristic model for DUP in
recovery, 39, 68 STEP’s catchment, 32
beginning phases of, 65–66 population health-based early
in the community, 64–67 intervention services in
remission, 39 Connecticut, 38–39
stagewise treatment for, 254 SSRIs. See Selective serotonin reuptake
stress-vulnerability model, 216– inhibitors
217, 222 STEP. See Specialized Treatment Early
symptoms of, 70 in Psychosis
SCID-5-CV. See Structured Clinical Stepped-care model of family
Interview for DSM-5 Disorders— interventions, 314
Clinician Version Stimulants, acute intoxication and
SCID-CV. See Structured Clinical withdrawal symptoms of, 248
Interview for DSM-IV Axis I Stress-diathesis model, 211
Disorders, Clinician Version Stress-vulnerability model, 216–217,
Second-generation antipsychotics, 187 222
Sedatives, acute intoxication and Structured Clinical Interview for
withdrawal symptoms of, 247 DSM-5 Disorders—Clinician
Seizures, 143 Version (SCID-5-CV), 157
Selective serotonin reuptake Structured Clinical Interview for
inhibitors (SSRIs), for DSM-IV Axis I Disorders,
management of comorbid Clinician Version (SCID-CV),
psychosis and trauma, 165 108
Sertraline Structured Interview for Psychosis-
for management of comorbid Risk Syndromes (SIPS), 103, 108,
psychosis and trauma, 165 109–110, 351
for treatment of PTSD, 107 description of, 111, 115
Service delivery systems diagnostic features, 112–114
policy for early intervention, 51–53 diagnostic subtypes, 112–114
in team-based approach to early Students. See Adolescents; College
intervention, 182–183 and university students;
Sjögren’s syndrome, 141 Education; Youth
SMART goals, 230 Substance Abuse and Mental Health
Smoking, 39, 102, 243 Services Administration
Social and Occupational Functioning (SAMHSA), 48–49, 156, 177–178,
Assessment Scale (SOFAS), 112– 298
114 Substance-induced psychosis, 244
Social Security Act, 47 Substance use, 102
SOFAS. See Social and Occupational acute intoxication and withdrawal
Functioning Assessment Scale symptoms, 247–251
SOPS. See Scale of Prodromal case examples of, 241–242, 258–259
Symptoms early psychosis and, 241–263
Index 435
case example of, 258–259 clinical treatment to reduce

consequences of, 242–243 suicide risk, 344–345
interventions, 254–258 developing a crisis/safety
medication management, plan, 342
256–258 overview, 335
psychosocial interventions, warning signs for suicide
254–255 behavior, 337–339, 339
maintenance, treatment, relapse Supported employment and
prevention, and recovery, education specialist, 324
258–259 Systemic lupus erythematosus, 141–
management of, 252 142
peer influences and, 253
recommendations, 259 Teams. See also Communication;
relapse prevention, 254 Coordinated specialty care
screening and evaluation, 252– (CSC); Peers
253 access to treatment team, 320
substance-induced psychosis case example of, 326
versus first-episode approach to IPS services, 283,
psychosis, 243–252, 245– 286
246 assessing and treating trauma in
longitudinal observation, team-based early psychosis
260 care, 151–169
treatment client-centered interventions for
assessing motivation for substance use and early
recovery, 253–254 psychosis, 259
stagewise treatment for collaboration, 176, 213, 214
schizophrenia, 254 for first-episode psychosis family
triggers for, 258 services, 313
overview, 242 in medical workup for first-episode
Suicide psychosis, 146
attempt, 88, 336, 337 multidisciplinary treatment team,
case examples, 336–337, 338–339, 176–177
341, 343 overview, 171
ideation and behavior, 335–337 psychotherapies in a team setting,
assessment, 345 213–214, 214
conceptual model of, 336, 337 shared decision making, 179–180,
prevention, 38 203–205
risk, assessment, and team-based approach to early
intervention in early intervention, 171–186
psychosis, 335–347 case example of, 172–177, 180
among adolescents, 390 clinical concepts for CSC
assessment, 339–341 treatment, 177–181
brief interventions for CSC, 171–174,
prevention of suicidal services in rural settings, 181–
behavior, 341–345 183
Technology (continued) Tobacco use disorder, 243, 257

team-based approach to early Toxic-metabolic disorders, in first-
intervention (continued) episode psychosis medical
services in rural settings workup, 142
(continued) Training
outreach activities, 182 for assessment and treatment of
service delivery, 182–183 trauma in team-based early
team training and function- psychosis care, 165–166
ing, 181–182 cognitive-behavioral social skills
TECCC. See Technology-enhanced training, 73
coordinated care clinic policy for early intervention, 51–53
Technology for team-based approach to early
to advance early psychosis intervention, 181–182
intervention, 349–363 Transitional-age youth, 16
assessments and interventions, Trauma
361 assessing and treating trauma in
case example of, 359–361 team-based early psychosis
clinical decision support and care, 151–169
risk prediction, 350–353, case example of, 152, 155–156,
352 158–159, 160, 163–164
mobile interventions, 353–356, cultural factors, 158
355 differential diagnosis, 157–158
online interventions and family involvement, 164–165
telehealth, 356–358, 357 future directions, 166
overview, 349–350 measures for assessment, 156–
engagement of youth and, 283 157
Technology-enhanced coordinated medication management, 165
care clinic (TECCC), 359–361 overview, 151–152
case example of, 359–361 relapse, 163
Telehealth, 356–358, 357 training and consultation, 165–
Temporal lobe epilepsy, 143 166
TEOSS. See Treatment of Early-Onset treatment approaches, 158–160
Schizophrenia Spectrum in childhood, 153, 167, 386
Disorders study cognitive-behavioral therapy for
TESI-C. See Traumatic Events treating psychosis and, 160,
Screening Inventory for 163
Children cycle of, 154
Tetrahydrocannabinol (THC), 244, 387 exposure to, 167
TF-CBT. See Trauma-focused medication management of
cognitive-behavioral therapy comorbid psychosis and, 165
THC. See Tetrahydrocannabinol screening, 156
Theory of reasoned action, 222 temporal characteristics of, 155
Thyroid storm, 143 trauma-informed care, 159–160,
TIPS. See Norwegian Early Treatment 161–162
and Intervention in Psychosis treatment, 167
Index 437
types and prevalence of, 152–155 Velocardiofacial syndrome, 14

bullying and interpersonal Venlaxine, for management of
victimization, 153 comorbid psychosis and
childhood trauma, 153 trauma, 165
community, intergeneration, Victimization, 167
and identity-based bullying, 153, 167
trauma, 153, 155 case example of, 217–219
trauma in early psychosis, interpersonal, 153
152–153
Trauma-focused cognitive-behavioral Well-being, 71, 221. See also
therapy (TF-CBT), 160 Individual resiliency training
for adolescents, 393 Workforce development
Trauma-informed care, 159–160, 161– to create clinically expert mental
162 health professionals, 6
Traumatic Events Screening Inventory policy for early intervention, 51–
for Children (TESI-C), 157 53, 56
Treatment of Early-Onset providing training, 16
Schizophrenia Spectrum World Health Organization, 252–253
Disorders (TEOSS) study, 374, consensus statement on early
393, 195 intervention of psychosis, 14
22q11 deletion syndrome, 144
Yoga, 268, 369. See also Aerobic
United States. See also California; exercise, role in treatment of
Connecticut early psychosis
CSC in, 19–20 Youth. See Adolescents
growth of early intervention in Youth MOVE National, 53
psychosis in, 11–22 Youth Risk Behavior Surveillance
health care in, 34 Data, 387
historical context of early
intervention support and Ziprasidone
funding, 17–19 in first-episode psychosis clinical
peer support movement in, 297– trials, 195, 197–198
298 for treatment of first-episode
psychosis, 190
Varenicline (Chantix), for management Zyban (bupropion), for management
of tobacco use disorder and early of tobacco use disorder and
psychosis, 257 early psychosis, 257
Vasculitis syndrome, 141
“Grounded in research but illustrated with clinical experience and the
voice of the consumer, this book brings to life the treatment of first-episode psycho-
sis. The book takes a broad and detailed approach, from policy and public health
to individual and family engagement and treatment. The theme of the book is re-
covery, and the focus on improving outcomes permeates the various chapters. This
book makes a significant contribution to the field of early intervention.”
Intervening Early in PSYCHOSIS

Donald Addington, Professor, Department of Psychiatry, University of Calgary;
Member, Mathison Centre for Mental Health Research and Education
“This book, which is based on a wealth of clinical and research experience, is
A TEAM APPROACH
an invaluable resource for clinicians and agencies who are all working toward early
intervention in psychosis with transitional-age youth. The authors offer a compre-
hensive understanding of all aspects of early intervention, including both young
people who may be at serious risk of developing psychosis and those who are expe-
riencing a first episode. This highly user-friendly text offers case descriptions, step-
by-step instructions for assessments and interventions, and excellent guidelines for
a team-based approach to early intervention for psychosis.”
Jean Addington, Ph.D., Professor of Psychiatry, Cumming School of Medicine,
University of Calgary
With expert guidance on developing specialty care services for young peo-
ple experiencing first-episode psychosis, Intervening Early in Psychosis: A Team
Intervening
Approach offers a multimodal approach that aims for recovery and remission. The
first book of its kind to focus on the U.S. health care environment, it provides a
detailed examination of a range of evidence-based treatments, from the psycho-
Early in
PSYCHOSIS
logical and psychosocial to peer, family, lifestyle, and technological interventions,
all punctuated by clinical case examples.
Special emphasis is placed on the interplay between these individual interventions,
as well as the collaboration between multidisciplinary partners, including licensed
therapists, medical providers, peers, and vocational specialists. An individual and
family perspective on the experience of living with psychosis complements this
interdisciplinary care model, underscoring the importance of engaging clients and
A Team Approach
their support network within a philosophy of shared decision making.
With additional chapters that discuss advocacy issues and policy considerations
when establishing coordinated specialty care services, Intervening Early in Psycho-
sis is the most comprehensive resource available for those interested in expanding
their knowledge of the early identification and treatment of adolescents and young
adults with psychotic disorders. Hardy
Ballon
Noordsy
ISBN 978-1- 61537-175- 4 Adelsheim Edited by
9 0 0 00
9 7 8 1 6 1 5 3 71 7 5 4 WWW.APPI.ORG Douglas L. Noordsy, M.D.
Cover design: Rick A. Prather
Cover image: © iStock.com Steven Adelsheim, M.D.

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The Book of the Month is supplied as PDF; no other formats will

Intervening Early in PSYCHOSIS

“This book, which is based on a wealth of clinical and research experience, is

1 Introduction: EARLY INTERVENTION IN PSYCHOSIS—

2 Growth of Early Intervention in Psychosis in the

3 Early Detection of Schizophrenia: A POPULATION

4 Early Intervention and Policy . . . . . . . . . . . . . . . . . . . . . . . 45

5 First-Person Accounts of Psychosis and

7 Assessment of People in the Early Stages of

8 Assessment and Targeted Intervention in

9 Medical Workup for First-Episode Psychosis . . . . . . . . .133

10 Assessing and Treating Trauma in Team-Based

11 Intervening Early: A TEAM-BASED APPROACH . . . . . . . . . . . . 171

12 Psychopharmacology for People in Early Psychosis . . .187

13 Psychotherapeutic Interventions for

14 Substance Use and Early Psychosis . . . . . . . . . . . . . . . . .241

15 Role of Aerobic Exercise in the Treatment of

17 Implementing Peer Support in Early Psychosis

18 Family Intervention and Support in Early Psychosis . . 309

19 Suicide Risk, Assessment, and Intervention in

20 Using Technology to Advance Early Psychosis

21 Inpatient Care for Early Psychosis:

22 Care for Adolescents on the First-Episode Psychosis

23 Special Populations: College and

Steven Adelsheim, M.D.

Jacob S. Ballon, M.D., M.P.H.

Deborah R. Becker, M.Ed., CRC

Iruma Bello, Ph.D.

Dror Ben-Zeev, Ph.D.

Mary F. Brunette, M.D.

Benjamin Buck, Ph.D.

Kristin Cadenhead, M.D.

John D. Cahill, M.D., Ph.D.

Nybelle Caruso, B.S., PSS

Mehak Chopra, D.O.

Lisa Dixon, M.D., M.P.H.

Robert E. Drake, M.D., Ph.D.

Maria Ferrara, M.D.

Chantel Garrett, B.S.

Tresha A. Gibbs, M.D.

Shirley M. Glynn, Ph.D.

Howard H. Goldman, M.D., Ph.D.

Michael Haines, QMHA, PSS

Kate V. Hardy, Clin.Psych.D.

Jill Harkavy-Friedman, Ph.D.

Debra R. Hrouda, Ph.D.

Rebecca Jaynes, LCPC

Agnieszka Kalinowski, M.D., Ph.D.

Skylar Kelsven, M.S.

Hyun Jung Kim, M.D.

David Kimhy, Ph.D.

Yulia Landa, Psy.D., M.S.

Carlos Larrauri, M.S.N., APRN, PMHNP-BC, FNP-BC

Rhoshel K. Lenroot, M.D.

Ally Linfoot, PSS

Rachel L. Loewy, Ph.D.

Sarah Lynch, LCSW

Nyamuon Nguany Machar