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Factors Influencing Successful Recruitment of Racial and Ethnic Minority Patients for an Observational HIV Cohort Study in Washington, DC

Bibliographic Data

ID18928176
AuthorsMaria Jaurretche (0000-0003-4604-3287, Milken Institute), Mark Levy (0000-0002-2164-1726, Milken Institute), Amanda D Castel (0000-0002-9095-2413, Milken Institute), Lindsey Powers Happ (0000-0002-6782-1618, Milken Institute), Anne K Monroe (0000-0003-3201-3845, Milken Institute), Karen F Wyche (0000-0003-2299-319X, George Washington University, corresponding author), On Behalf Of The Dc Cohort Executive Committee
Year2022
Volume9
Issue3
Pages767-778
Publication date2022-06-01
Open AccessYes
TypeARTICLE
VenueJournal of Racial and Ethnic Health Disparities (JOURNAL)
Journal identifiersISSN: 2196-8837 • E-ISSN: 2197-3792
PublisherSpringer Science and Business Media LLC (PUBLISHER)
DOI10.1007/s40615-021-01015-6
OpenAlexW4229057345
LanguageEN
Citations received2
References cited34

Alternative medicine · Demographics · Ethnic group · Family medicine · Health care · Informed consent · Observational study · Demography · Ethics in Clinical Research · HIV/AIDS Research and Interventions · Medicine · Patient-Provider Communication in Healthcare · Gerontology

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    Open Access•Shaheerah N Eruotor, Shaheerah Nur Id-Din Eruotor et al.•Analyses of Social Issues and…•2022

  • Investigating people’s attitudes towards participating in longitudinal health research

    Open Access•Sibille Merz, Philipp Jaehn et al.•International Journal for Equity…•2023

  • Research electronic data capture (Redcap)—A metadata-driven methodology and workflow process for providing translational research informatics support

    Open Access•Paul A Harris, Robert Taylor et al.•Journal of Biomedical Informatics•2009

  • The Redcap consortium

    Open Access•Paul A Harris, Robert Taylor et al.•Journal of Biomedical Informatics•2019

  • Structure and quality of outpatient care for people living with an HIV infection

    Open Access•Esther A N Engelhard, Colette Smit et al.•AIDS Care•2016

  • Research participation, trust, and fair compensation among people living with and without HIV in Florida

    Christa Cook, Jasmine A Mack et al.•AIDS Care•2018

  • HIV-related stigma, depression, and social support are associated with health-related quality of life among patients newly entering HIV care

    Crystal Chapman Lambert, Andrew O Westfall et al.•AIDS Care•2020

  • Black–White Differences in Willingness to Participate and Perceptions About Health Research

    Open Access•Fern J Webb, Jagdish Khubchandani et al.•Journal of Immigrant and Minority…•2018

  • Perspectives on the Role of Patient-Centered Medical Homes in HIV Care

    Gregory Pappas, Yujiang Jia et al.•American Journal of Public Health•2014

  • Whose Responsibility Is It to Dismantle Medical Mistrust? Future Directions for Researchers and Health Care Providers

    Jessica Jaiswal•Behavioral Medicine•2019

  • Conducting in-depth interviews with and without voice recorders

    Open Access•Rwamahe Rutakumwa, Joseph Mugisha et al.•Qualitative Research•2020

  • Conspiracy Beliefs Are Not Necessarily a Barrier to Engagement in HIV Care Among Urban, Low-Income People of Color Living with HIV

    Open Access•Jessica Jaiswal, N Singer et al.•Journal of Racial and Ethnic…•2018

Citations per year0.5
Citation span2022 - 2023 (2)
Highly citedNo

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