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Recruiting Older Black Americans for Genomic Research

Bibliographic Data

ID15315276
AuthorsJodi Winship (0000-0003-1125-0913, Virginia Commonwealth University, corresponding author), Jodi M Winship (Virginia Commonwealth University), Marissa Mackiewicz (0000-0003-3354-3178, Virginia Commonwealth University), Muhammad Babar (0000-0002-1795-114X, 2 Virginia Commonwealth University iCubed Commonwealth Scholars Program, Virginia Commonwealth University, Richmond, VA), Dave L Dixon (0000-0001-7560-9521, Virginia Commonwealth University), Elvin T Price (0000-0001-6046-7540, 3 Virginia Commonwealth University iCubed Health and Wellness in Aging Across the Lifespan Core, Virginia Commonwealth University, Richmond, VA), Lana Sargent (0000-0001-5555-9985, Virginia Commonwealth University), Lana J Sargent (3 Virginia Commonwealth University iCubed Health and Wellness in Aging Across the Lifespan Core, Virginia Commonwealth University, Richmond, VA)
Year2024
Volume34
Issue4
Pages185-191
Publication date2024-10-01
Open AccessNo
TypeARTICLE
VenueEthnicity & Disease (JOURNAL)
Journal identifiersISSN: 1049-510X • E-ISSN: 1945-0826
PublisherEthnicity & Disease, Inc (PUBLISHER)
DOI10.18865/ethndis-2023-75
PMID39463816
OpenAlexW4403590919
LanguageEN
References cited28

The lack of diversity in genomic studies is a disparity that influences our understanding of human genomic variation and threatens equity in the benefits of precision medicine. Given our current genomic research with Black older adults, we conducted a qualitative study to elucidate participants' knowledge, attitudes, and beliefs about genomic research and research participation and what factors contribute to their willingness to participate and to gain insights into barriers that researchers may have in recruiting Black Americans. We conducted semistructured interviews (N=16) with previous genomic research participants, and an inductive thematic approach was used to code and interpret the data. The mean age was 70, 82% reported <$15,000 annual income, and 100% participated in genomic research. The results note that genomic research is poorly understood despite participation in prior genomic studies, and cultural beliefs about health and managing health impact an individual's research participation. Although not all participants identified with historical distrust, those who did report health system distrust also contributed distrust in research. Relationship building facilitates research participation, especially when perceived as personally relevant and meaningful. Participant incentives and convenience to engage in the study are less important if the personal benefits or relevance of the research are clear. Our results provide new context into the importance of relationship building and research literacy and highlight new considerations for engaging racially diverse populations in research

Family medicine · MEDLINE · Political science · Biomedical Ethics and Regulation · Ethics in Clinical Research · Medicine · Psychology · Race, Genetics, and Society · Gerontology

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Highly citedNo

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