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Exemplar 1:: Cardiff Metropolitan University Application For Ethics Approval

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The document outlines the process and requirements for obtaining ethics approval for research projects at Cardiff Metropolitan University. Key information to include in an application is a description of the research project, participants, methodology, and consent procedures.

To complete the ethics approval application, researchers need to provide their name and supervisor, project details like title and duration, information on any funding, whether the research involves NHS patients/staff or human samples, and a non-technical summary of the research.

Once the form is completed, researchers must obtain the required signatures and then submit the application to their School Research Ethics Committee. Data collection cannot begin until ethics approval is received.

EXEMPLAR 1:

CARDIFF METROPOLITAN UNIVERSITY


APPLICATION FOR ETHICS APPROVAL

When undertaking a research or enterprise project, Cardiff Met staff and students are obliged
to complete this form in order that the ethics implications of that project may be considered.
If the project requires ethics approval from an external agency such as the NHS or MoD, you
will not need to seek additional ethics approval from Cardiff Met. You should however
complete Part One of this form and attach a copy of your NHS application in order that your
School is aware of the project.
The document Guidelines for obtaining ethics approval will help you complete this form. It is
available from the Cardiff Met website.
Once you have completed the form, sign the declaration and forward to your School Research
Ethics Committee.
PLEASE NOTE:
Participant recruitment or data collection must not commence until ethics approval has been
obtained.
PART ONE
Name of applicant: Bhadrani Banerjee
Supervisor (if student project): Raul Villamarin Rodriguez
School: Universal Business School
Student number (if applicable): 1904
Programme enrolled on (if applicable): CMBA13
Project Title: Application of Chatbot in Health Care
Sector
Expected Start Date: 10/09/2019
Approximate Duration: 2 weeks
Funding Body (if applicable): Click here to enter text.
Other researcher(s) working on the project: NO

Will the study involve NHS patients or staff? No

Will the study involve taking samples of No


human origin from participants?

In no more than 150 words, give a non technical summary of the project
To be completed for all projects. If only secondary research is to be undertaken it is
recommended that this is overtly stated in this section
Exemplar 2

Does your project fall entirely within one of the following categories:
Paper based, involving only documents in No
the public domain
Laboratory based, not involving human No
participants or human tissue samples
Practice based not involving human No
participants (eg curatorial, practice audit)
Compulsory projects in professional practice No
(eg Initial Teacher Education)
If you have answered YES to any of these questions, no further information regarding your
project is required.
If you have answered NO to all of these questions, you must complete Part 2 of this form

DECLARATION:
I confirm that this project conforms with the Cardiff Met Research Governance
Framework
Signature of the applicant: Date: 10/09/2019

FOR STUDENT PROJECTS ONLY


Name of supervisor: Date: 10/09/2019

Signature of supervisor:
Research Ethics Committee use only
Decision reached: Project approved
Project approved in principle
Decision deferred
Project not approved
Project rejected
Project reference number: Click here to enter text.
Name: Click here to enter text. Date: Click here to enter a
date.
Signature:

Details of any conditions upon which approval is dependant:


Provided a summary sheet is submitted with the application you can state ‘see summary
sheet’. If no summary sheet is used all conditions must be described here

PART TWO Only to be completed if primary research is to be undertaken


A RESEARCH DESIGN
A1 Will you be using an approved protocol in your Choose an item.
project?
A2 If yes, please state the name and code of the approved protocol to be used 1
Most CSM projects will not use a protocol so this section will be n/a

A3 Describe the research design to be used in your project


At post graduate level it is quite common for researchers to make more than one
application per thesis i.e. for the PI to apply for ethical approval for each stage of the data
collection as the results of the data collected in the first round may significantly impact
upon the data collection method and or information required in subsequent stages. In this
case a statement should be included to specify which stage of the research the application
is being sought for at the start of this section.

Describe your project’s overall design and the method of data collection which will be
used. This should include why you need to do the type of data collection you have
chosen. If more than one type of research method is used you must describe both/ all.

You should include


- research method(s) such as interviews or focus groups and why
- sample and sampling, who you will ask to participate, convenience, random etc
and why
- the anticipated size of the sample
- a justification of the number of participants
- how you will recruit them and how long their will participation take
- how you will protect participants confidentiality and anonymity
- a description of what method of analysis you will use, e.g. thematic analysis,
including tools such as SPSS, excel, NVIVO etc, and why it is/ they are appropriate

If your data collection will involve the use of a questionnaire, you should provide a copy of
the questionnaire with your application. In cases where the questionnaire has not yet been
finalised you should give examples of the kinds of questions which participants will be
answering. Similarly, if your data collection will involve the use of interviews or focus
groups, you should provide details of the topics which will be discussed and a Participant
information Sheet and Participant Consent Form.

If you intend to undertake the data collection within an organisation (i.e. employees) or at an
event (i.e. participants) you must also provide a (draft) letter to the organisation or event
managers asking for permission to do the research on their premises. Where access may be
contentious or difficult enclosing confirmation that you have approval can help support the
application

1
An Approved Protocol is one which has been approved by Cardiff Met to be used under supervision of designated
members of staff; a list of approved protocols can be found on the Cardiff Met website here

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