Are racial and ethnic minorities less willing to participate in health research?

David Wendler, Raynard Kington, Jennifer Madans, Gretchen Van Wye, Heidi Christ-Schmidt, Laura A Pratt, Otis W Brawley, Cary P Gross, Ezekiel Emanuel, David Wendler, Raynard Kington, Jennifer Madans, Gretchen Van Wye, Heidi Christ-Schmidt, Laura A Pratt, Otis W Brawley, Cary P Gross, Ezekiel Emanuel

Abstract

Background: It is widely claimed that racial and ethnic minorities, especially in the US, are less willing than non-minority individuals to participate in health research. Yet, there is a paucity of empirical data to substantiate this claim.

Methods and findings: We performed a comprehensive literature search to identify all published health research studies that report consent rates by race or ethnicity. We found 20 health research studies that reported consent rates by race or ethnicity. These 20 studies reported the enrollment decisions of over 70,000 individuals for a broad range of research, from interviews to drug treatment to surgical trials. Eighteen of the twenty studies were single-site studies conducted exclusively in the US or multi-site studies where the majority of sites (i.e., at least 2/3) were in the US. Of the remaining two studies, the Concorde study was conducted at 74 sites in the United Kingdom, Ireland, and France, while the Delta study was conducted at 152 sites in Europe and 23 sites in Australia and New Zealand. For the three interview or non-intervention studies, African-Americans had a nonsignificantly lower overall consent rate than non-Hispanic whites (82.2% versus 83.5%; odds ratio [OR] = 0.92; 95% confidence interval [CI] 0.84-1.02). For these same three studies, Hispanics had a nonsignificantly higher overall consent rate than non-Hispanic whites (86.1% versus 83.5%; OR = 1.37; 95% CI 0.94-1.98). For the ten clinical intervention studies, African-Americans' overall consent rate was nonsignificantly higher than that of non-Hispanic whites (45.3% versus 41.8%; OR = 1.06; 95% CI 0.78-1.45). For these same ten studies, Hispanics had a statistically significant higher overall consent rate than non-Hispanic whites (55.9% versus 41.8%; OR = 1.33; 95% CI 1.08-1.65). For the seven surgery trials, which report all minority groups together, minorities as a group had a nonsignificantly higher overall consent rate than non-Hispanic whites (65.8% versus 47.8%; OR = 1.26; 95% CI 0.89-1.77). Given the preponderance of US sites, the vast majority of these individuals from minority groups were African-Americans or Hispanics from the US.

Conclusions: We found very small differences in the willingness of minorities, most of whom were African-Americans and Hispanics in the US, to participate in health research compared to non-Hispanic whites. These findings, based on the research enrollment decisions of over 70,000 individuals, the vast majority from the US, suggest that racial and ethnic minorities in the US are as willing as non-Hispanic whites to participate in health research. Hence, efforts to increase minority participation in health research should focus on ensuring access to health research for all groups, rather than changing minority attitudes.

Conflict of interest statement

Competing Interests: The authors have declared that no competing interests exist.

Figures

Figure 1. Ethnic and Racial Composition of…
Figure 1. Ethnic and Racial Composition of the United States
Data from year 2003.
Figure 2. Comparison of African-American versus non-Hispanic…
Figure 2. Comparison of African-American versus non-Hispanic White Consent Rates
Circle diameter is proportional to the sample size of the individual studies. The diamond represents the overall OR. The vertical line indicates the 95% confidence interval on the OR. Blue indicates interview and non-intervention studies; red indicates clinical intervention studies.
Figure 3. Comparison of Hispanic versus non-Hispanic…
Figure 3. Comparison of Hispanic versus non-Hispanic White Consent Rates
Circle diameter is proportional to the sample size of the individual studies. The diamond represents the overall OR. The vertical line indicates the 95% confidence interval on the OR. Blue indicates interview and non-intervention studies; red indicates clinical intervention studies.
Figure 4. Comparison of Minority versus non-Hispanic…
Figure 4. Comparison of Minority versus non-Hispanic White Consent Rates in Surgical Intervention Trials
Circle diameter is proportional to the sample size of the individual studies. The diamond represents the overall OR. The vertical line indicates the 95% confidence interval on the OR.

References

    1. Hussain-Gambles M. Ethnic minority under-representation in clinical trials: Whose responsibility is it anyway? J Health Organ Manag. 2003;17:138–143.
    1. Britton A, McKee M, Black N, McPherson K, Sanderson C, et al. Threats to applicability of randomized trials: Exclusion and selective participation. J Health Serv Res Policy. 1999;4:112–121.
    1. Allmark P. Should research samples reflect the diversity of the population? J Med Ethics. 2004;30:185–189.
    1. Freedman LS, Simon R, Foulkes MA, Friedman L, Geller NL, et al. Inclusion of women and minorities in clinical trials and the NIH Revitalization Act of 1993—The perspective of NIH clinical trialists. Control Clin Trials. 1995;16:277–285.
    1. Shavers VL, Lynch CF, Burmeister LF. Factors that influence African-Americans' willingness to participate in medical research studies. Cancer. 2001;91(Suppl):233–236.
    1. Green BL, Partridge EE, Fouad MN, Kohler C, Crayton EF, et al. African-American attitudes regarding cancer clinical trials and research studies: Results from focus group methodology. Ethn Dis. 2000;10:76–86.
    1. Thompson EE, Neighbors HW, Munday C, Jackson JS. Recruitment and retention of African American patients for clinical research: An exploration of response rates in an urban psychiatric hospital. J Consult Clin Psychol. 1996;64:861–867.
    1. Dennis BP, Neese JB. Recruitment and retention of African American elders into community-based research: Lessons learned. Arch Psychiatr Nurs. 2000;14:3–11.
    1. Shavers-Hornaday VL, Lynch CF, Burmeister LF, Torner JC. Why are African Americans under-represented in medical research studies? Impediments to participation. Ethn Health. 1997;2:31–45.
    1. Gauthier MA, Clarke WP. Gaining and sustaining minority participation in longitudinal research projects. Alzheimer Dis Assoc Disord. 1999;13:S29–S33.
    1. Svensson C. Representation of American blacks in clinical trials of new drugs. JAMA. 1989;261:263–265.
    1. Williams CL, Tappen R, Buscemi C, Rivera R, Lezcano J. Obtaining family consent for participation in Alzheimer's research in a Cuban-American population: Strategies to overcome barriers. Am J Alzheimers Dise Other Demen. 2001;16:183–187.
    1. Shavers VL, Lynch CF, Burmeister LF. Racial differences in factors that influence the willingness to participate in medical research studies. Ann Epidemiol. 2002;12:248–256.
    1. El-Sadr W, Capps L. The challenge of minority recruitment in clinical trials for AIDS. JAMA. 1992;267:955.
    1. Reverby SM. More than fact and fiction: Cultural memory and the Tuskegee syphilis study. Hastings Cent Rep. 2001;31:22–28.
    1. Thomas CR, Pinto HA, Roach M. Participation in clinical trials: Is it state-of-the-art for African Americans and other people of color? J Natl Med Assoc. 1994;86:177–182.
    1. Bonner GJ, Miles TP. Participation of African Americans in clinical research. Neuroepidemiology. 1997;16:281–284.
    1. Kirp DL, Bayer R. Needles and race. Atlantic Monthly. 1993 July:38–42.
    1. Gamble VN. Under the shadow of Tuskegee: African Americans and health care. Am J Public Health. 1997;87:1773.
    1. Heiat A, Gross CP, Krumholz HM. Representation of the elderly, women and minorities in heart failure clinical trials. Arch Intern Med. 2002;162:1682–1688.
    1. Mason S, Hussain-Gambles M, Leese B, Atkin K, Brown J. Representation of South Asian people in randomized clinical trials: Analysis of trials' data. BMJ. 2003;326:1244–1245.
    1. Svensson CK. Representation of American blacks in clinical trials of new drugs. JAMA. 1989;13:263–265.
    1. Hall WD. Representation of blacks, women and the very elderly (aged > or = 80) in 28 major randomized clinical trials. Ethn Dis. 1999;9:333–340.
    1. Killien M, Bigby JA, Champion V, Fernandez-Repollet E, Jackson RD, et al. Involving minority and underrepresented women in clinical trials: The National Centers of Excellence in Women's Health. J Womens Health Gend Based Med. 2000;9:1061–1070.
    1. Murthy VH, Krumholz HM, Gross CP. Participation in cancer clinical trials: Race-, sex-, and age-based disparities. JAMA. 2004;291:2720–2726.
    1. Hussain-Gambles M, Atkin K, Leese B. Why ethnic minority groups are under-represented in clinical trials: A review of the literature. Health Soc Care Community. 2004;12:382–388.
    1. Bartlett C, Davey P, Dieppe P, Doyal L, Ebrahim S, et al. Women, older persons, and ethnic minorities: Factors associated with their inclusion in randomized trials of statins 1990 to 2001. Heart. 2003;89:327–328.
    1. Kressin NI, Meterko M, Wilson NJ. Racial disparities in participation in biomedical research. J Natl Med Assoc. 2000;92:62–69.
    1. Centers for Disease Control and Prevention. National Health Interview Survey (NHIS) 2005 Available: . Accessed 26 October 2005.
    1. Centers for Disease Control and Prevention. The National Immunization Survey. 2005 Available: . Accessed 26 October 2005.
    1. Centers for Disease Control and Prevention. National Health and Nutrition Examination Survey. 2005 Available: . Accessed 26 October 2005.
    1. DerSimonian R, Laird N. Meta-analysis in clinical trials. Control Clin Trials. 1986;7:177–188.
    1. Giselle CS, Thomas SB, St. George DM. Distrust, race, and research. Arch Intern Med. 2002;162:2458–2463.
    1. Sugarman J, Kass NE, Goodman SN, Perentesis P, Fernandes P, et al. What patients say about medical research. IRB. 1998;20:1–7.
    1. Brown DR, Topcu M. Willingness to participate in clinical treatment research among older African Americans and whites. Gerontologist. 2003;43:62–72.
    1. American Stroke Association, American Heart Association. Heart disease and stroke statistics—2003 update. Dallas: American Heart Association; 2002. Available: . Accessed 26 October 2005.
    1. Hobbs F, Stoops N. US Census Bureau (2002 November) Demographic trends in the 20th century. Census 2000 special reports, series CENSR-4. Washington (D. C.): US Government Printing Office; Available: . Accessed 26 October 2005.
    1. Gifford AL, Cunningham WE, Heslin KC, Andersen RM, Nakazono T, et al. Participation in research and access to experimental treatments by HIV-Infected patients. N Engl J Med. 2002;346:1373–1382.
    1. King TE. Racial disparities in clinical trials. N Engl J Med. 2002;346:1400–1402.
    1. Sateren WB, Trimble EL, Abrams J, Brawley O, Breen N, et al. How sociodemographics, presence of oncology specialists, and hospital cancer programs affect accrual to cancer treatment trials. J Clin Oncol. 2002;20:2109–2117.
    1. Haynes MA, Smedley BD, editors. The unequal burden of cancer: An assessment of NIH research and programs for ethnic minorities and the medically underserved. Washington (D. C.): National Academy Press; 1999. 352 pp.
    1. Underwood SM, Alexander GG. Participation of minorities and women in clinical cancer research. Ann Epidemiol. 2000;10:S1.
    1. Simon MS, Du W, Flaherty L, Philip PA, Lorusso P, et al. Factors associated with breast cancer clinical trials participation and enrollment at a large academic medical center. J Clin Oncol. 2004;22:2046–2052.
    1. Lee JY, Marks JE, Simpson JR. Recruitment of patients to cooperative group clinical trials. Cancer Clin Trials. 1980;3:381–384.
    1. Hunter CP, Frelick RW, Feldman AR, Bavier AR, Dunlap WH, et al. Selection factors in clinical trials: results from the Community Clinical Oncology Program Physicians' Patient Log. Cancer Treat Rep. 1997;71:559–565.
    1. Appel LJ, Vollmer WM, Obarzanek E, Aicher KM, Conlin PR, et al. Recruitment and baseline characteristics of participants in the Dietary Approaches to Stop Hypertension trial. J Am Diet Assoc. 1999;99:S69–S75.
    1. Brawley O, Tejeda H. Minority inclusion in clinical trials issues and potential strategies. J Natl Cancer Inst Monogr. 1995;17:55–57.
    1. Swanson GM, Ward AJ. Recruiting minorities into clinical trials: Toward a participant-friendly system. J Natl Cancer Inst. 1995;87:1747–1759.
    1. Hunt S, Bhopal R. Self reports in research with non-English speakers. BMJ. 2003;327:352–353.
    1. Robinson D, Woerner MG, Pollack S, Lerner G. Subject selection biases in clinical trials: Data from a multicenter schizophrenia treatment study. J Clin Psychopharmacol. 1996;16:170–176.
    1. McKay JR, Alterman AI, Snider EC, O'Brian CP. Effect of random versus nonrandom assignment in a comparison of inpatient and day hospital rehabilitation for male alcoholics. J Consult Clin Psychol. 1995;63:70–78.
    1. Gorkin L, Schron EB, Handshaw K, Shea S, Kinney MR, et al. Clinical trial enrollers vs. nonenrollers: The CAST and REACT project. Control Clin Trials. 1996;17:46–59.
    1. Rimer BK, Schildkraut JM, Lerman C, Lin TH, Audrain J. Participation in a women's breast cancer risk counseling trial. Who participates? Who declines? High Risk Breast Cancer Consortium. Cancer. 1996;77:2348–2355.
    1. Corbie-Smith G, Viscoli CM, Kernan WN, Brass LM, Sarrel P, et al. Influence of race, clinical, and other socio-demographic features on trial participation. J Clin Epidemiol. 2003;56:304–309.
    1. Kaluzny A, Brawley O, Garson-Angert D, Shaw J, Godley P, et al. Assuring access to state-of-the-art care for U.S. minority populations: The first 2 years of the Minority-Based Community Clinical Oncology Program. J Natl Cancer Inst. 1993;1:1945–1950.
    1. Moore DA, Goodall RL, Ives NJ, Hooker M, Gazzard BG, et al. How generalizable are the results of large randomized controlled trials of antiretroviral therapy? HIV Med. 2000;1:149–154.
    1. Westerberg VS, Miller WR, Tonigan JS. Comparison of outcomes for clients in randomized versus open trials of treatment for alcohol use disorders. J Stud Alcohol. 2000;61:720–727.
    1. Diener-West M, Earle JD, Fine SL, Hawkins BS, Moy CS, et al. The COMS randomized trial of iodine 125 brachytherapy for choroidal melanoma, II: Characteristics of patient enrolled and not enrolled. Arch Ophthalmol. 2001;119:951–965.
    1. CASS Investigators. Coronary artery surgery study (CASS): A randomized trial of coronary artery bypass surgery. Comparability of entry characteristics and survival in randomized patients and nonrandomized patients meeting randomization criteria. J Am Coll Cardiol. 1984;3:114–128.
    1. Paradise JL, Bluestone CD, Bachman RZ, Colborn DK, Bernard BS, et al. Efficacy of tonsillectomy for recurrent throat infection in severely affected children. Results of parallel randomized and nonrandomized clinical trials. N Engl J Med. 1984;310:674–683.
    1. Williford J, Krol WF, Buzby GP. Comparison of eligible randomized patients with two groups of ineligible patients: Can the results of the VA Total Parenteral Nutrition clinical trail be generalized? J Clin Epidemiol. 1993;46:1025–1034.
    1. Marcus SM. Assessing non-consent bias with parallel randomized and nonrandomized clinical trials. J Clin Epidemiol. 1997;50:823–828.
    1. King SB, Barnhart HX, Kosinski AS, Weintraub WS, Lembo NJ, et al. Angioplasty or surgery for multivessel coronary artery disease: Comparison of eligible registry and randomized patients in the EAST trial and influence of treatment selection on outcomes. Am J Cardiol. 1997;79:1453–1459.
    1. Hochman JS, Sleeper LA, Webb JG, Sanborn TA, White HD, et al. Early revascularization in acute myocardial infarction complicated by cardiogenic shock. N Engl J Med. 1999;341:625–631.
    1. Feit F, Brooks MM, Sopko G, Keller NM, Rosen A, et al. Long-term clinical outcome in the Bypass Angioplasty Revascularization Investigation Registry: Comparison with the randomized trial. Circulation. 2000;101:2795–2802.

Source: PubMed

3
Tilaa