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Understanding Research Participation Experiences Among Persons Identifying as African, Caribbean, and Black in
Background:
Health research in Canada has insufficiently engaged African, Caribbean, and Black (ACB) people, yielding under-representation of their priorities and unmet health needs.
Objective:
To understand research experiences and priorities among ACB people in British Columbia.
Methods:
Cross-sectional data from an online survey was summarized using descriptive statistics. Content analysis was used for open-ended text responses. Data collection and analysis was conducted with ACB community partners.
Results:
Of 56 respondents, 50.0% were aged 16 to 25 years; 78.6% identified as women. Although only 42.9% had previous research experience, 91.1% were willing to participate. Participation barriers included time constraints (53.1%) and mistrust (30.6%). Facilitators included perceived benefits to ACB individuals/communities (83.9%) and opportunities to share perspective(s) (60.7%). Research priorities included mental health, substance use, and sexual and reproductive health.
Conclusion:
Findings highlight ACB individuals' willingness to participate in health research, while identifying participation barriers and facilitators. Researchers must build trust through anti-racist community engagement efforts.
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