Earning the Trust of African American Communities to Increase Representation in Dementia Research
Author(s) -
Elena Portacolone,
Nynikka R. Palmer,
Peter A. Lichtenberg,
Catherine Waters,
Carl V. Hill,
Sahru Keiser,
Leah Vest,
Marsha Maloof,
Thi Tran,
Paula Fernández Martínez,
Javier Guerrero,
Julene K. Johnson
Publication year - 2020
Publication title -
ethnicity and disease
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.767
H-Index - 67
eISSN - 1945-0826
pISSN - 1049-510X
DOI - 10.18865/ed.30.s2.719
Subject(s) - distrust , dementia , african american , focus group , representation (politics) , gender studies , public relations , sociology , political science , gerontology , psychology , medicine , disease , politics , law , ethnology , pathology , anthropology
Black/African American populations are underrepresented as participants in dementia research. A major barrier to participation of African American older adults in dementia research is a tendency to distrust research institutions owing to both historical and contemporary racism. Building on the Ford framework, the objective of our study was to examine factors that influence participation in dementia research among African American older adults and caregivers, with an emphasis on understanding factors related to trust. Data were collected during January 2019 and March 2020 from 10 focus groups with African American older adults (n=91), 5 focus groups with caregivers (n=44), and interviews with administrators of community-based organizations (n=11), and meetings with our Community Advisory Board. Inductive/deductive content analysis was used to identify themes. The results identified an overall tension between distrust of researchers and a compelling desire to engage in dementia research. This overarching theme was supported by six themes that provided insights about the multiple layers of distrust, as well as expectations about the appropriate conduct of researchers and academic institutions. Strong commitment to the community was identified as a priority. The findings suggest that a paradigm shift is needed to increase the representation of African Americans in dementia research. In this new paradigm, earning the trust of African American communities becomes a systemic endeavor, with academic, state, and national institutions deeply committed to earning the trust of African American communities and guiding researchers in this endeavor. The findings also generated actionable recommendations to help improve representation of African American older adults in dementia research.
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