Engagement with a diverse Stakeholder Advisory Council for research in dementia care
Autor: | Sara S. Masoud, Carole L. White, Deborah James, Ashlie Glassner, Neela K. Patel, Mayra Mendoza, Sheran Rivette |
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Rok vydání: | 2021 |
Předmět: |
Medicine (General)
Health (social science) media_common.quotation_subject Stakeholder engagement 03 medical and health sciences 0302 clinical medicine Resource (project management) R5-920 Stakeholders mental disorders medicine Dementia Quality (business) 030212 general & internal medicine media_common Medical education Engagement 030503 health policy & services Research Stakeholder Capacity building medicine.disease Caregivers General Health Professions Medicine Council 0305 other medical science Psychology Inclusion (education) Qualitative research Research Article |
Zdroj: | Research Involvement and Engagement Research Involvement and Engagement, Vol 7, Iss 1, Pp 1-12 (2021) |
ISSN: | 2056-7529 |
Popis: | Background The inclusion of stakeholders throughout the research process has been gaining recognition as an approach that can improve the quality and impact of research. Stakeholder engagement for dementia care research has been identified as a national priority, though evaluation of engagement strategies and their impact has been limited. In dementia care research, stakeholders can include individuals living with dementia, family care partners, and health and social care professionals in dementia care. A Stakeholder Advisory Council (SAC) was established to identify priorities for dementia care research that are most important to stakeholders. Strategies to build capacity for research and facilitate engagement among the SAC were used to identify the research priorities. This study describes the experiences of SAC members engaged in the research process. Methods To evaluate stakeholder engagement, semi-structured interviews were conducted with members of the SAC to understand their experiences and perspectives on the strategies used to facilitate engagement and build capacity for research. Interviews were recorded, transcribed, and thematically analyzed using a mixed inductive and deductive approach. Findings were presented to members of the SAC to determine whether they felt their perspectives and experiences were accurately represented. Final domains and themes presented here were approved by the SAC. Results Interviews (N = 11) were conducted with members of the SAC representing each stakeholder group; persons living with dementia (n = 2); family care partners (n = 4), and health and social care professionals in dementia care (n = 5). Ten themes were categorized into four overarching domains: accessibility, council infrastructure, values and environment, and benefits of involvement. Conclusions Findings from this qualitative study are a resource for researchers seeking to collaborate with diverse stakeholder groups to represent their perspectives in research, including individuals living with dementia. The domains and themes identified here support the inclusion of diverse stakeholders in the research process, centering engagement and capacity building strategies around individuals living with dementia. Supplementary Information The online version contains supplementary material available at 10.1186/s40900-021-00297-8. Plain English summary Involving stakeholders in research about dementia care is recognized as an important approach to develop findings that are relevant to individuals living with dementia, family care partners, and health and social professionals in dementia care. Still, this approach is not often used and there is a need for more information about how researchers can engage stakeholders in the research process and the impact of engagement from the perspectives of stakeholders. In this paper, we describe how a mixed group of stakeholders was engaged for a project to identify priorities for dementia care research and their perspectives of the experience. A Stakeholder Advisory Council (SAC) worked together to develop their skills in research and connected with their communities to determine what is most important to be studied in the field of dementia care research. To understand the perspectives of the stakeholders involved in this project, we conducted individual interviews with members of the SAC. This study will help researchers understand how they can collaborate with stakeholders in dementia care and the benefits of including individuals living with dementia, family care partners, and professional stakeholders in the research process. Supplementary Information The online version contains supplementary material available at 10.1186/s40900-021-00297-8. |
Databáze: | OpenAIRE |
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