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Return of Genetic Research Results to Participants and Families: IRB Perspectives and Roles.
- Source :
- Journal of Law, Medicine & Ethics; Fall2015, Vol. 43 Issue 3, p502-513, 12p, 6 Charts
- Publication Year :
- 2015
-
Abstract
- We surveyed IRB chairs' perspectives on offering individual genetic research results to participants and families, including family members of deceased participants, and the IRB's role in addressing these issues. Given a particular hypothetical scenario, respondents favored offering results to participants but not family members, giving choices at the time of initial consent, and honoring elicited choices. They felt IRBs should have authority regarding the process issues, but a more limited role in medical and scientific issues. [ABSTRACT FROM AUTHOR]
- Subjects :
- GENETIC research & ethics
TISSUE banks
ATTITUDE (Psychology)
AUTHORITY
FAMILIES
HEALTH services administration
INFORMED consent (Medical law)
POLICY sciences
QUESTIONNAIRES
RESEARCH funding
RESEARCH ethics
RESPONSIBILITY
SOCIAL role
ETHICAL decision making
INSTITUTIONAL review boards
DISCLOSURE
ACCESS to information
HUMAN research subjects
ETHICS
Subjects
Details
- Language :
- English
- ISSN :
- 10731105
- Volume :
- 43
- Issue :
- 3
- Database :
- Complementary Index
- Journal :
- Journal of Law, Medicine & Ethics
- Publication Type :
- Academic Journal
- Accession number :
- 110404943
- Full Text :
- https://doi.org/10.1111/jlme.12292