TY - JOUR
T1 - Drug Development
AU - Bosire, Edna N.
AU - Kamau, Lucy Wambui
AU - Udeh-Momoh, Chinedu T.
AU - Shah, Jasmit
AU - Blackmon, Karen
AU - Kiio, Caroline Kalondu
AU - Meier, Irene B.
AU - Narayan, Vaibhav
AU - Nesic-Taylor, Olivera
AU - Merali, Zul
N1 - Publisher Copyright:
© 2025 The Alzheimer's Association. Alzheimer's & Dementia published by Wiley Periodicals LLC on behalf of Alzheimer's Association.
PY - 2025/12/1
Y1 - 2025/12/1
N2 - BACKGROUND: Advancements in dementia research are in part contingent on participation in clinical research. Clinical trials can help researchers determine if new drugs, devices, or diagnostic procedures for dementia are safe and effective. However, little is known about clinical trials for dementia in resource constrained settings such as Kenya. The aim of our research was to explore people's understanding of dementia clinical trials, their attitudes and perceptions towards dementia clinical trials and what can be done to enhance enrollments on such clinical trials. METHOD: This was an ethnographic study involving 8 focused group discussions (FGDs; age and gender stratified; n=81) in Nairobi to understand people's perceptions about dementia clinical trials. All FGDs were conducted in both English and Kiswahili each lasting about 90 minutes and took place in Kibera and Mathare informal settlements in Nairobi, Kenya. Data were transcribed verbatim and thematically analyzed by Nvivo version 14 software. RESULT: Younger participants had a basic understanding of clinical trials compared to older participants. Participant's willingness to engage in clinical trials for dementia research varied across age and gender groups, and this was influenced by both individual and collective perceptions. Many participants expressed their willingness to participate if they believed the research would contribute to a greater good, such as helping others, improving healthcare or contributing to medical advancement. However, there was hesitation, driven by fear of side effects, concerns about the integrity of the research process, and religious or cultural beliefs. For future motivation to participate in dementia clinical trials, participants recommended a need to ensure their families were involved in such studies, provide financial incentives and sensitizing community members on potential benefits of being participants in clinical trials. CONCLUSION: Findings reported from our study may be useful in developing strategies that can enhance participation in dementia clinical research and advance efforts dedicated to finding effective treatments for dementia in Kenya and other similar contexts.
AB - BACKGROUND: Advancements in dementia research are in part contingent on participation in clinical research. Clinical trials can help researchers determine if new drugs, devices, or diagnostic procedures for dementia are safe and effective. However, little is known about clinical trials for dementia in resource constrained settings such as Kenya. The aim of our research was to explore people's understanding of dementia clinical trials, their attitudes and perceptions towards dementia clinical trials and what can be done to enhance enrollments on such clinical trials. METHOD: This was an ethnographic study involving 8 focused group discussions (FGDs; age and gender stratified; n=81) in Nairobi to understand people's perceptions about dementia clinical trials. All FGDs were conducted in both English and Kiswahili each lasting about 90 minutes and took place in Kibera and Mathare informal settlements in Nairobi, Kenya. Data were transcribed verbatim and thematically analyzed by Nvivo version 14 software. RESULT: Younger participants had a basic understanding of clinical trials compared to older participants. Participant's willingness to engage in clinical trials for dementia research varied across age and gender groups, and this was influenced by both individual and collective perceptions. Many participants expressed their willingness to participate if they believed the research would contribute to a greater good, such as helping others, improving healthcare or contributing to medical advancement. However, there was hesitation, driven by fear of side effects, concerns about the integrity of the research process, and religious or cultural beliefs. For future motivation to participate in dementia clinical trials, participants recommended a need to ensure their families were involved in such studies, provide financial incentives and sensitizing community members on potential benefits of being participants in clinical trials. CONCLUSION: Findings reported from our study may be useful in developing strategies that can enhance participation in dementia clinical research and advance efforts dedicated to finding effective treatments for dementia in Kenya and other similar contexts.
UR - https://www.scopus.com/pages/publications/105025834667
U2 - 10.1002/alz70859_099671
DO - 10.1002/alz70859_099671
M3 - Article
C2 - 41447581
AN - SCOPUS:105025834667
SN - 1552-5260
VL - 21
SP - e099671
JO - Alzheimer's and Dementia
JF - Alzheimer's and Dementia
ER -