Attitudes of African Americans toward participation in medical research

Journal of Applied Social Psychology

Volumn 29, Issue 3, 1999, Pages 552-574

  Armstrong, Tonya D ^a   Crum, Larry D ^a,b   Rieger, Randall H ^a   Bennett, Trude A ^a   Edwards, Lloyd J ^a  

^a UNIVERSITY OF NORTH CAROLINA   (United States)

^b University of North Carolina at Chapel Hill   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 0033084251     PISSN: 00219029     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1559-1816.1999.tb01401.x     Document Type: Article

References (34)

1. Ballard, E. L., Nash, F., Raiford, K., & Harrell, L. E. (1993). Recruitment of African American elderly for clinical research studies of dementia: The CERAD experience. Gerontologist, 33, 561-565.
2. Brawley, O. W., & Tejeda, H. (1995). Minority inclusion in clinical trials: Issues and potential strategies. Journal of the National Cancer Institute Monographs, 17, 55-57.
3. Broad, W., & Wade, N. (1982). Betrayers of the truth: Fraud and deceit in the halls of science. New York, NY: Simon & Schuster.
4. Caplan, A. L. (1992). When evil intrudes. Hastings Center Report, 22, 29-32.
5. Des Jarlais, D. C., & Stepherson, B. (1991). History, ethics, and politics in AIDS prevention research. American Journal of Public Health, 81, 1393-1394.
6. Edgar, H. (1992). Outside the community. Hastings Center Report, 22, 32-35.
7. Gamble, V. N. (1993). A legacy of distrust: African Americans and medical research. American Journal of Preventive Medicine, 9(Suppl. 6), 35-38.
8. Giachello, A. L. (1992). Reconciling the multiple scientific and community needs. In D. M. Becker, D. R. Hill, J. Jackson, D. M. Levine, F. A. Stillman, & S. M. Weiss (Eds.), Health behavior research in minority populations: Access, design, and implementation (NIH Publication Number 92-2965, pp. 237-241). Washington, DC: Department of Health and Human Services.
9. Goertzel, T. (1994). Belief in conspiracy theories. Political Psychology, 15, 731-742.
10. Hatch, J., Moss, N., Saran, A., Presley-Cantrell, L., & Mallory, C. (1993). Community research: Partnership in African American communities. American Journal of Preventive Medicine, 9(Suppl. 6), 27-31.
11. Jeanquart-Barone, S. (1993). Trust difference between supervisors and subordinates: Examining the role of race and gender. Sex Roles, 29, 1-11.
12. Jones, J. H. (1981). Bad blood: The Tuskegee Syphilis Experiment. New York, NY: Free Press.
13. Jones, J. H. (1992). The Tuskegee legacy: AIDS and the African American community. Hastings Center Report, 22, 38-40.
14. Josephson, E. (1970). Resistance to community surveys. Social Problems, 18, 117-129.
15. King, P. A. (1992). The dangers of difference. Hastings Center Report, 22, 35-38.
16. Lin, K. M. (1992). Ethical aspects of psychopharmacological studies in different ethnic groups. Clinical Neuropharmacology, 15 (Suppl. 1), 483A-484A.
17. Mays, V. M., & Jackson, J. S. (1991). AIDS survey methodology with Black Americans. Social Science and Medicine, 33, 47-54.
18. McGraw, S. A., McKinlay, J. B., Crawford, S. A., Costa, L. A., & Cohen, D. L. (1992). Health survey methods with minority populations: Some lessons from recent experience. Ethnicity and Disease, 2, 273-287.
19. Merkatz, R. B., & Junod, S. W. (1994). Historical background of changes in FDA policy on the study and evaluation of drugs in women. Academic Medicine, 69, 703-707.
20. Millon-Underwood, S., Sanders, E., & Davis, M. (1993). Determinants of participation in state-of-the-art cancer prevention, early detection/screening, and treatment trials among African Americans. Cancer Nursing, 1, 25-33.
21. Montera, D. (1977). Research among racial and cultural minorities: An overview. Journal of Social Issues, 33, 1-10.
22. Moore, J. W. (1977). A case study of collaboration: The Chicano Pinto Research Project. Journal of Social Issues, 33, 144-158.
23. National Center for Health Statistics. (1993). Healthy People 2000 Review 1992 (DHHS Publication No. PHS 93-1232-1). Hyattsville, MD: U.S. Public Health Service.
24. National Institutes of Health. (1994). NIH guidelines on the inclusion of women and minorities as subjects in clinical research. Washington, DC: Author (59 FR 11146-11151).
25. National Institutes of Health Revitalization Amendment, Pub. L. No. 103-143, §492B (1993).
26. Roberson, N. L. (1994). Clinical trial participation: Viewpoints from racial/ethnic groups. Cancer, 74(Suppl. 9), 2687-2691.
27. Savitt, T. (1978). Medicine and slavery: The diseases and health care of African Americans in antebellum Virginia. Urbana, IL: University of Illinois Press.
28. Svensson, C. K. (1989). Representation of American Blacks in clinical trials of new drugs. Journal of the American Medical Association, 261, 263-265.
29. Thomas, S. B., & Quinn, S. C. (1991). Public health then and now: The Tuskegee Syphilis Study, 1932-1972: Implications for HIV education and AIDS risk education programs in the African American community. American Journal of Public Health, 81, 1498-1505.
30. Tsukashima, R. T. (1977). Merging fieldwork and survey research in the study of a minority community. Journal of Social Issues, 33, 133-143.
31. Vernon, S. W., Roberts, R. E., & Lee, E. S. (1984). Ethnic status and participation in longitudinal health surveys. American Journal of Epidemiology, 119, 99-113.
32. Weiss, C. H. (1977). Survey researchers and minority communities. Journal of Social Issues, 33, 20-35.
33. Welsh, K. A., Ballard, E., Nash, F., Raiford, K., & Harrell, L. (1994). Issues affecting minority participation in research studies of Alzheimer disease. Alzheimer Disease and Associated Disorders, 8, 38-48.
34. Zinn, M. B. (1979). Field research in minority communities: Ethical, methodological, and political observations by an insider. Social Problems, 27, 209-219.