Traditional medicinal plants have long been used to treat various ailments in Keiyo district. How... more Traditional medicinal plants have long been used to treat various ailments in Keiyo district. However to date there are no records on medicinal plants used by the Keiyo despite threats of rapid disappearance of indigenous knowledge from deforestation, overexploitation among other factors. The purpose of the study was to document medicinal plants used by the Keiyo community in order to preserve traditional medical knowledge for future research and potential development of new drugs.The research team comprised of professionals from the fields of medicine and botany. Local leaders, community elders, church leaders and other stakeholders were used to identify herbalists and convince them to provide information. Semi structured interviews, group discussions and observations were used to collect information on traditional knowledge from herbalists. Details of the medical conditions treated, herbal preparations used, treatment methods, local plant names and methods of collection of herbs w...
A signed informed consent (IC) form proves voluntary participation in a study. Yet the developmen... more A signed informed consent (IC) form proves voluntary participation in a study. Yet the development of accessible and understandable IC forms comes with its own set of challenges, particularly when conducting international research. This study explores understanding by participants in an Eldoret-based clinical trial of IC and its implications as well as whether they will volunteer for future trials. In mid-2010, in-depth interviews with trial participants were recorded in audio format. Content analysis provides a description of trial participants' experiences and thoughts. All participants were informed about the trial and its voluntariness and they consented. However, some were too ill to scrutinize trial details. Thus, they relied on their health care provider's advice, or on their guardians. In general, participants understood their role and were happy to volunteer or invite others to participate in future trials. They also emphasised the importance of an open on-going dialogue in order for participants to be able to ask questions. Clinical trial participants in Eldoret seem to understand their role, but rely on providers and guardians when consenting. They are very willing to participate in future trials. Evaluation of research participants' opinions may improve trial protocols, increase comprehension and guard against manipulation of study participants. In addition, this research focus should guide development of consent forms and process that facilitates a truly IC.
Traditional medicinal plants have long been used to treat various ailments in Keiyo district. How... more Traditional medicinal plants have long been used to treat various ailments in Keiyo district. However to date there are no records on medicinal plants used by the Keiyo despite threats of rapid disappearance of indigenous knowledge from deforestation, overexploitation among other factors. The purpose of the study was to document medicinal plants used by the Keiyo community in order to preserve traditional medical knowledge for future research and potential development of new drugs.The research team comprised of professionals from the fields of medicine and botany. Local leaders, community elders, church leaders and other stakeholders were used to identify herbalists and convince them to provide information. Semi structured interviews, group discussions and observations were used to collect information on traditional knowledge from herbalists. Details of the medical conditions treated, herbal preparations used, treatment methods, local plant names and methods of collection of herbs w...
A signed informed consent (IC) form proves voluntary participation in a study. Yet the developmen... more A signed informed consent (IC) form proves voluntary participation in a study. Yet the development of accessible and understandable IC forms comes with its own set of challenges, particularly when conducting international research. This study explores understanding by participants in an Eldoret-based clinical trial of IC and its implications as well as whether they will volunteer for future trials. In mid-2010, in-depth interviews with trial participants were recorded in audio format. Content analysis provides a description of trial participants' experiences and thoughts. All participants were informed about the trial and its voluntariness and they consented. However, some were too ill to scrutinize trial details. Thus, they relied on their health care provider's advice, or on their guardians. In general, participants understood their role and were happy to volunteer or invite others to participate in future trials. They also emphasised the importance of an open on-going dialogue in order for participants to be able to ask questions. Clinical trial participants in Eldoret seem to understand their role, but rely on providers and guardians when consenting. They are very willing to participate in future trials. Evaluation of research participants' opinions may improve trial protocols, increase comprehension and guard against manipulation of study participants. In addition, this research focus should guide development of consent forms and process that facilitates a truly IC.
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