SCOPUS 정보 검색 플랫폼

American Journal of the Medical Sciences

Volumn 322, Issue 5, 2001, Pages 241-245

Ethical challenges in community-based research

(2) Marshall, Patricia A a Rotimi, Charles b

a CASE WESTERN RESERVE UNIVERSITY SCHOOL OF MEDICINE (United States)

b HOWARD UNIVERSITY COLLEGE OF MEDICINE (United States)

Author keywords

Community research; Informed consent; Multicultural; Population based research; Stereotyping

Indexed keywords

COMMUNITY; CONFERENCE PAPER; CONFIDENTIALITY; EPIDEMIOLOGICAL DATA; INFORMED CONSENT; MEDICAL ETHICS; MEDICAL RESEARCH; POPULATION RESEARCH; PRIVACY; SOCIAL ASPECT; STEREOTYPY; BIOETHICS; BIOMEDICAL AND BEHAVIORAL RESEARCH; EPIDEMIOLOGY; ETHNIC GROUP; HEALTH CARE PLANNING; HUMAN; RESEARCH; REVIEW;

BIOMEDICAL AND BEHAVIORAL RESEARCH;

BIOETHICAL ISSUES; COMMUNITY HEALTH PLANNING; EPIDEMIOLOGY; ETHICS, PROFESSIONAL; ETHNIC GROUPS; HUMANS; INFORMED CONSENT; RESEARCH;

EID: 0035167444 PISSN: 00029629 EISSN: None Source Type: Journal
DOI: 10.1097/00000441-200111000-00001 Document Type: Conference Paper

Times cited : (63)

References (40)

1
- 0003392970
- DHEW Publication No. (OS) 78-0012. Washington DC: US Government Printing Office
- (1978) The Belmont Report: Ethical principles and guidelines for the protection of human subjects of research

2
- 0003433351
- Geneva, Switzerland: World Health Organization
- (1993) International ethical guidelines for biomedical research involving human subjects

3
- 85031485907
- Geneva, Switzerland: International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use
- (1996) Guidelines for good clinical practice

4
- 0003424636
- Baltimore: Urban and Schwarzenberg
- (1986) Ethics and regulation of clinical research, 2nd ed.
- Levine, R.J.¹

5
- 0003408414
- New York: Oxford University Press
- (1986) A history and theory of informed consent
- Faden, R.R.¹ Beauchamp, T.L.²

6
- 0003861671
- Bloomington: Indiana University Press
- (1987) The patient as partner: A theory of human experimentation ethics
- Veatch, R.M.¹

7
- 0004043376
- New York: Oxford University Press
- (1998) The ethics of biomedical research: An international perspective
- Brody, B.A.¹

8
- 0003666563
- Oxford: Elsevier Science Ltd.
- (1998) Research on human subjects: Ethics, law and social policy
- Weisstub, D.N.¹

9
- 0026264744
- Obligations and responsibilities of epidemiologists to research subjects
- (1991) J Clin Epidemiol , vol.44 , Issue.SUPPL. 1
- Last, J.M.¹

10
- 84985257193
- Issues in preparing ethical guidelines for epidemiological studies
- (1991) Law Med Health Care , vol.19 , pp. 175-183
- Dickens, B.M.¹

11
- 0030852258
- Ethical issues of genetic testing and their implications in epidemiologic studies
- (1997) Ann Epidemiol , vol.7 , pp. 363-366
- Bondy, M.¹ Mastromarino, C.²

12
- 0002521711
- Anthropology and bioethics: Perspectives on culture, medicine and morality
- Sargent C, Johnson T, editors. Westport (CT): Praeger Publishing Co.
- (1996) Medical anthropology: contemporary theory and method, 2nd ed. , pp. 349-373
- Marshall, P.A.¹ Koenig, B.A.²

13
- 0000176531
- Ethical issues in immigrant health care and clinical research
- Loue S, editor. New York: Plenum Press
- (1998) Handbook of immigrant health , pp. 203-226
- Marshall, P.A.¹ Koenig, B.A.² Grifhorst, P.³

14
- 0030227764
- Trust the fragile foundation of contemporary biomedical research
- (1996) Hastings Cent Rep , vol.26 , pp. 25-29
- Kass, N.E.¹ Sugarman, J.² Faden, R.³

15
- 0003580455
- Westport (CT): Praeger Publishers
- (1994) It just ain't fair: The ethics of health care for African Americans
- Dula, A.¹

16
- 0026517589
- The challenge of minority recruitment for clinical trials
- (1992) JAMA , vol.267 , pp. 954-957
- El-Sadre, W.¹ Capps, L.²

17
- 0026381402
- Are research participants truly informed? Readability of informed consent forms used in research
- (1991) Ethics Behav , vol.1 , pp. 239-252
- Ogloff, J.R.¹ Otto, R.K.²

18
- 0026948334
- Consent forms: How to determine and improve their readability
- (1992) Oncol Nurs Forum , vol.19 , pp. 1523-1528
- Meade, C.D.¹ Howser, D.M.²

19
- 0032490122
- Informed consent for clinical trials: A comparative study of standard versus simplified forms
- (1998) J Natl Cancer Inst , vol.90 , pp. 668-674
- Davis, T.C.¹ Holcombe, R.F.² Berkel, H.J.³

20
- 0029890456
- Consent form readability in university-sponsored research
- (1996) J Fam Pract , vol.42 , pp. 606-611
- Goldstein, A.O.¹ Frasier, P.² Curtis, P.³

21
- 0032085786
- Cultural diversity and informed consent
- (1998) J Clin Ethics , vol.9 , pp. 173-176
- Agard, E.¹ Finkelstein, D.² Wallach, E.³

22
- 0032159989
- Informed consent in a multi-cultural cancer patient population: Implications for nursing practice
- (1998) Nurs Ethics , vol.5 , pp. 412-423
- Barnes, D.M.¹ Davis, A.J.² Moran, T.³

23
- 0028512330
- Making research consent forms informative and understandable: The experience of the Indian Health Service
- (1994) Cambridge Q Healthcare Ethics , vol.3 , pp. 510-521
- Freeman, W.L.¹

24
- 0002623420
- Biomedical rituals and informed consent: Native Canadians and the negotiation of clinical trust
- Weisz G, editor. Philadelphia: University of Pennsylvania Press
- (1990) Social science perspectives on medical ethics , pp. 41-64
- Kaufert, J.M.¹ O'Neil, J.D.²

25
- 0031087894
- Communication through interpreters in healthcare: Ethical dilemmas arising from differences in class, culture, language, and power
- (1997) J Clin Ethics , vol.8 , pp. 71-87
- Kaufert, J.M.¹ Putsch, R.W.²

26
- 0037849664
- Crystal City (VA): National Bioethics Advisory Commission
- (2000) The relevance of culture for informed consent in U.S.-funded international research
- Marshall, P.A.¹

27
- 0022339020
- Cross-cultural communication: The special case of interpreters in health care
- (1985) JAMA , vol.254 , pp. 3344-3348
- Putsch III, R.W.¹

28
- 0029206626
- Caring for patients in cross-cultural settings
- (1995) Hastings Cent Rep , vol.25 , pp. 6-14
- Jecker, N.S.¹ Carrese, J.A.² Pearlman, R.A.³

29
- 0026613627
- Ethics are local: Engaging cross-cultural variation in the ethics for clinical research
- (1992) Soc Sci Med , vol.35 , pp. 1079-1091
- Christakis, N.A.¹

30
- 0024563435
- DNA sampling and informed consent
- (1989) CMAJ , vol.140 , pp. 1023-1028
- Knoppers, B.M.¹ Laberge, C.²

31
- 0034153572
- Involving study populations in the review of genetic research
- (2000) J Law Med Ethics , vol.28 , pp. 41-51
- Sharp, R.R.¹ Foster, M.W.²

32
- 0006523706
- I-DNA-Fication, personal privacy, and social justice
- (1999) Chicago-Kent Law Rev , vol.74 , pp. 101-122
- Juengst, E.T.¹

33
- 0034149801
- Commentary: What a community review can and cannot do
- (2000) J Law Med Ethics , vol.28 , pp. 52-54
- Juengst, E.T.¹

34
- 0033194471
- Protecting communities in research: Philosophical and pragmatic challenges
- (1999) Camb Q Healthc Ethics , pp. 501-513
- Weijer, C.¹

35
- 0030997240
- Hypertension prevalence in seven populations of African origin
- (1997) Am J Public Health , vol.87 , pp. 160-168
- Cooper, R.¹ Rotimi, C.² Ataman, S.³

36
- 0029917006
- Polymorphisms of renin-angiotensin genes among Nigerians, Jamaicans, and African Americans
- (1996) Hypertension , vol.27 , pp. 558-563
- Rotimi, C.N.¹ Puras, A.² Cooper, R.³

37
- 0031949444
- Determinism and mass-media portrayals of genetics
- (1998) Am J Hum Genet , vol.62 , pp. 979-984
- Condit, C.M.¹ Ofulue, N.² Sheedy, K.M.³

38
- 0031714589
- Ethics, epidemiology and the thrifty gene: Biological determinism as a health hazard
- (1998) Soc Sci Med , vol.47 , pp. 1189-1195
- McDermott, R.¹

39
- 0033001537
- Novel hMLH1 and hMSH2 germline mutations in African Americans with colorectal cancer
- (1999) JAMA , vol.281 , pp. 2316-2320
- Weber, T.K.¹ Chin, H.-M.² Rodriguez-Bigas, M.³

40
- 85031481196
- Associated Press Jul 1
- (1999) Gene links cancer risk to blacks
- Thompson, C.¹

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