Challenging assumptions about minority participation in US clinical research
- PMID: 22021285
- PMCID: PMC3222419
- DOI: 10.2105/AJPH.2011.300279
Challenging assumptions about minority participation in US clinical research
Abstract
Although extensive research addresses minorities' low participation in clinical research, most focuses almost exclusively on therapeutic trials. The existing literature might mask important issues concerning minorities' participation in clinical trials, and minorities might actually be overrepresented in phase I safety studies that require the participation of healthy volunteers. It is critical to consider the entire spectrum of clinical research when discussing the participation of disenfranchised groups; the literature on minorities' distrust, poor access, and other barriers to trial participation needs reexamination. Minority participation in clinical trials is an important topic in public health discussions because this representation touches on issues of equality and the elimination of disparities, which are core values of the field.
References
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- Epstein S. Inclusion: The Politics of Difference in Medical Research. Chicago: University of Chicago Press; 2007.
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- US Census Bureau. National Population Estimates, July 1 and April 1, 2000 to July 1, 2008. Available at: http://www.census.gov/popest/overview.html. Accessed July 4, 2011.
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- Pinn VW, Roth C, Bates AC, Wagner R, Jarema K. Monitoring Adherence to the NIH Policy on the Inclusion of Women and Minorities as Subjects in Clinical Research (Comprehensive Report: Fiscal Year 2007 and 2008 Tracking Data). Bethesda, MD: National Institutes of Health, Department of Health and Human Services; 2009.
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- Lamberti MJ, State of the Clinical Trials Industry: A Sourcebook of Charts and Statistics. Boston: CenterWatch; 2009.
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