From Subject to Participant: Ethics and the Evolving Role of Community in Health Research

被引:59
作者
Bromley, Elizabeth [1 ,2 ]
Mikesell, Lisa [3 ,4 ]
Jones, Felica [5 ]
Khodyakov, Dmitry [6 ]
机构
[1] Univ Calif Los Angeles, Dept Psychiat & Biobehav Sci, Ctr Hlth Serv & Soc, Semel Inst, Los Angeles, CA 90024 USA
[2] Los Angeles VA Healthcare Syst, VA Mental Illness Res Educ & Clin Ctr, Los Angeles, CA USA
[3] Rutgers State Univ, Sch Commun & Informat, Commun Dept, New Brunswick, NJ 08903 USA
[4] Rutgers State Univ, Inst Hlth Hlth Care Policy & Aging Res, New Brunswick, NJ 08903 USA
[5] Hlth African Amer Families II, Los Angeles, CA USA
[6] RAND Corp, Santa Monica, CA USA
关键词
ENGAGED RESEARCH; INVOLVEMENT; PRINCIPLES; PROMOTION; PEOPLE; TRUST;
D O I
10.2105/AJPH.2014.302403
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Belmont Report principles focus on the well-being of the research subject, yet community-engaged investigators often eschew the role of subject for that of participant. We conducted semistructured interviews with 29 community and academic investigators working on 10 community-engaged studies. Interviews elicited perspectives on ethical priorities and ethical challenges. Interviewees drew on the Belmont Report to describe 4 key principles of ethical community-engaged research (embodying ethical action, respecting participants, generalizing beneficence, and negotiating justice). However, novel aspects of the participant role were the source of most ethical challenges. We theorize that the shift in ethical focus from subject to participant will pose new ethical dilemmas for community-engaged investigators and for other constituents interested in increasing community involvement in health research.
引用
收藏
页码:900 / 908
页数:9
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