Clinical trial participation among underserved communities: Insights from the Louisiana Community Engagement Alliance

Diverse, equitable and inclusive participation in clinical research is needed to ensure evidence-based clinical practice and lessen disparities in health outcomes. Yet, clinical trial participation remains critically low in minoritized communities, particularly among Blacks. The Louisiana Community...

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Veröffentlicht in:The American journal of the medical sciences 2023-10, Vol.366 (4), p.254-262
Hauptverfasser: Craig, Leslie S., Sarpong, Daniel F., Peacock, Erin M., Theall, Katherine P., Williams, LaKeisha, Al-Dahir, Sara, Davis, Terry C., Arnold, Connie L., Williams, Allie, Fields, Tynesia, Wilson, Michelle, Krousel-Wood, Marie
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container_end_page 262
container_issue 4
container_start_page 254
container_title The American journal of the medical sciences
container_volume 366
creator Craig, Leslie S.
Sarpong, Daniel F.
Peacock, Erin M.
Theall, Katherine P.
Williams, LaKeisha
Al-Dahir, Sara
Davis, Terry C.
Arnold, Connie L.
Williams, Allie
Fields, Tynesia
Wilson, Michelle
Krousel-Wood, Marie
description Diverse, equitable and inclusive participation in clinical research is needed to ensure evidence-based clinical practice and lessen disparities in health outcomes. Yet, clinical trial participation remains critically low in minoritized communities, particularly among Blacks. The Louisiana Community Engagement Alliance against COVID-19 Disparities (LA-CEAL) was launched in response to the disproportionate impact of COVID-19 on Black Louisianans to understand community barriers and preferences and increase inclusive participation in research. This study aims to understand perceptions regarding COVID-19 trial participation among underrepresented Louisianans. A rapid assessment integrating cross-sectional, surveys among federally qualified health center (FQHC) patients and community residents, and focus group discussions (FGDs) from community representatives was conducted in 2020-2021. Factors and perceptions underlying trial participation were identified using logistic regression models and thematic analyses, respectively. Quantitative findings (FQHC: N=908, mean age=46.6 years, 66.4% Black; community: N=504, mean age=54.2 years, 93.7% Black) indicated that 0.9% and 3.6%, respectively, ever participated in a COVID-19 trial. Doctors/Healthcare providers were most trusted (FQHC=55.1%; community=59.3%) sources of information about trials. Advancing age was associated with increased odds of being very willing to participate (ORFQHC=1.03, 95% CI 1.02-1.05; ORCommunity=1.02, 95% CI 1.00-1.04). Qualitative data (6 FGDs, 29 attendees) revealed limited awareness, experimentation/exploitation-based fears, and minimal racial/ethnic representation among trialists as barriers to participation. COVID-19 trial participation rates were low in our sample. Altruism was a key facilitator to participation; fear, mistrust, and low awareness were predominant barriers. Community-centered approaches, engaging informed providers and trusted community members, may facilitate inclusive trial participation.
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Yet, clinical trial participation remains critically low in minoritized communities, particularly among Blacks. The Louisiana Community Engagement Alliance against COVID-19 Disparities (LA-CEAL) was launched in response to the disproportionate impact of COVID-19 on Black Louisianans to understand community barriers and preferences and increase inclusive participation in research. This study aims to understand perceptions regarding COVID-19 trial participation among underrepresented Louisianans. A rapid assessment integrating cross-sectional, surveys among federally qualified health center (FQHC) patients and community residents, and focus group discussions (FGDs) from community representatives was conducted in 2020-2021. Factors and perceptions underlying trial participation were identified using logistic regression models and thematic analyses, respectively. Quantitative findings (FQHC: N=908, mean age=46.6 years, 66.4% Black; community: N=504, mean age=54.2 years, 93.7% Black) indicated that 0.9% and 3.6%, respectively, ever participated in a COVID-19 trial. Doctors/Healthcare providers were most trusted (FQHC=55.1%; community=59.3%) sources of information about trials. Advancing age was associated with increased odds of being very willing to participate (ORFQHC=1.03, 95% CI 1.02-1.05; ORCommunity=1.02, 95% CI 1.00-1.04). Qualitative data (6 FGDs, 29 attendees) revealed limited awareness, experimentation/exploitation-based fears, and minimal racial/ethnic representation among trialists as barriers to participation. COVID-19 trial participation rates were low in our sample. Altruism was a key facilitator to participation; fear, mistrust, and low awareness were predominant barriers. 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Sarpong, Daniel F. ; Peacock, Erin M. ; Theall, Katherine P. ; Williams, LaKeisha ; Al-Dahir, Sara ; Davis, Terry C. ; Arnold, Connie L. ; Williams, Allie ; Fields, Tynesia ; Wilson, Michelle ; Krousel-Wood, Marie</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c345t-9852d22f2059591c8e3a16724ac954a4136c15c1a4012dbc4eb7496045f4a76f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Clinical trial participation</topic><topic>Community</topic><topic>COVID-19</topic><topic>COVID-19 - epidemiology</topic><topic>Cross-Sectional Studies</topic><topic>Diversity, Equity</topic><topic>Focus Groups</topic><topic>FQHCs</topic><topic>Humans</topic><topic>Inclusion</topic><topic>Louisiana</topic><topic>Middle Aged</topic><topic>Mixed methods</topic><topic>Qualitative Research</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Craig, Leslie S.</creatorcontrib><creatorcontrib>Sarpong, Daniel F.</creatorcontrib><creatorcontrib>Peacock, Erin M.</creatorcontrib><creatorcontrib>Theall, Katherine P.</creatorcontrib><creatorcontrib>Williams, LaKeisha</creatorcontrib><creatorcontrib>Al-Dahir, Sara</creatorcontrib><creatorcontrib>Davis, Terry C.</creatorcontrib><creatorcontrib>Arnold, Connie L.</creatorcontrib><creatorcontrib>Williams, Allie</creatorcontrib><creatorcontrib>Fields, Tynesia</creatorcontrib><creatorcontrib>Wilson, Michelle</creatorcontrib><creatorcontrib>Krousel-Wood, Marie</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>The American journal of the medical sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Craig, Leslie S.</au><au>Sarpong, Daniel F.</au><au>Peacock, Erin M.</au><au>Theall, Katherine P.</au><au>Williams, LaKeisha</au><au>Al-Dahir, Sara</au><au>Davis, Terry C.</au><au>Arnold, Connie L.</au><au>Williams, Allie</au><au>Fields, Tynesia</au><au>Wilson, Michelle</au><au>Krousel-Wood, Marie</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Clinical trial participation among underserved communities: Insights from the Louisiana Community Engagement Alliance</atitle><jtitle>The American journal of the medical sciences</jtitle><addtitle>Am J Med Sci</addtitle><date>2023-10-01</date><risdate>2023</risdate><volume>366</volume><issue>4</issue><spage>254</spage><epage>262</epage><pages>254-262</pages><issn>0002-9629</issn><issn>1538-2990</issn><eissn>1538-2990</eissn><abstract>Diverse, equitable and inclusive participation in clinical research is needed to ensure evidence-based clinical practice and lessen disparities in health outcomes. Yet, clinical trial participation remains critically low in minoritized communities, particularly among Blacks. The Louisiana Community Engagement Alliance against COVID-19 Disparities (LA-CEAL) was launched in response to the disproportionate impact of COVID-19 on Black Louisianans to understand community barriers and preferences and increase inclusive participation in research. This study aims to understand perceptions regarding COVID-19 trial participation among underrepresented Louisianans. A rapid assessment integrating cross-sectional, surveys among federally qualified health center (FQHC) patients and community residents, and focus group discussions (FGDs) from community representatives was conducted in 2020-2021. Factors and perceptions underlying trial participation were identified using logistic regression models and thematic analyses, respectively. Quantitative findings (FQHC: N=908, mean age=46.6 years, 66.4% Black; community: N=504, mean age=54.2 years, 93.7% Black) indicated that 0.9% and 3.6%, respectively, ever participated in a COVID-19 trial. Doctors/Healthcare providers were most trusted (FQHC=55.1%; community=59.3%) sources of information about trials. Advancing age was associated with increased odds of being very willing to participate (ORFQHC=1.03, 95% CI 1.02-1.05; ORCommunity=1.02, 95% CI 1.00-1.04). Qualitative data (6 FGDs, 29 attendees) revealed limited awareness, experimentation/exploitation-based fears, and minimal racial/ethnic representation among trialists as barriers to participation. COVID-19 trial participation rates were low in our sample. Altruism was a key facilitator to participation; fear, mistrust, and low awareness were predominant barriers. Community-centered approaches, engaging informed providers and trusted community members, may facilitate inclusive trial participation.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>37517691</pmid><doi>10.1016/j.amjms.2023.07.011</doi><tpages>9</tpages></addata></record>
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subjects Clinical trial participation
Community
COVID-19
COVID-19 - epidemiology
Cross-Sectional Studies
Diversity, Equity
Focus Groups
FQHCs
Humans
Inclusion
Louisiana
Middle Aged
Mixed methods
Qualitative Research
title Clinical trial participation among underserved communities: Insights from the Louisiana Community Engagement Alliance
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