Expanding the Frame of "Voluntariness" in Informed Consent: Structural Coercion and the Power of Social and Economic Context
Kennedy Institute of Ethics Journal 23 (4):355-379 (2013)
Abstract
Whether intended or not, conceptions of informed consent are often rooted in archetypal notions of the researcher and prospective study participant. The former is assumed problematically to be a disinterested yet humanitarian individual who is well trained to conduct robust science. The latter is often characterized as being motivated by some altruistic notions about the contribution to science and society they are making even as they seek some personal benefit from the research. Cast in a dyad, the researcher has the responsibility to inform the participant thoroughly about the purpose of the research, the risks and benefits of participation, and any alternatives to research available, as well as the ..DOI
10.1353/ken.2013.0018
My notes
Similar books and articles
Procedural misconceptions and informed consent: Insights from empirical research on the clinical trials industry.Jill A. Fisher - 2006 - Kennedy Institute of Ethics Journal 16 (3):251-268.
Discrepancy between participants' understanding and desire to know in informed consent: are they informed about what they really want to know?Jiwon Koh, Eurah Goh, Kyung-Sang Yu, Belong Cho & Jeong Hee Yang - 2012 - Journal of Medical Ethics 38 (2):102-106.
Collective informed consent and decision power.Jukka Varelius - 2009 - Science and Engineering Ethics 15 (1):39-50.
Research without consent: Exception from and waiver of informed consent in resuscitation research.Michelle H. Biros - 2007 - Science and Engineering Ethics 13 (3):361-369.
Payment for research participation: a coercive offer?A. Wertheimer & F. G. Miller - 2008 - Journal of Medical Ethics 34 (5):389-392.
Argumentation and informed consent in the doctor–patient relationship.Jerome Bickenbach - 2012 - Journal of Argumentaion in Context 1 (1):5-18.
Money for research participation: Does it jeopardize informed consent?Christine Grady - 2001 - American Journal of Bioethics 1 (2):40 – 44.
Audit of the Informed Consent Process as a Part of a Clinical Research Quality Assurance Program.Pramod M. Lad & Rebecca Dahl - 2014 - Science and Engineering Ethics 20 (2):469-479.
Are research participants truly informed? Readability of informed consent forms used in research.James R. P. Ogloff & Randy K. Otto - 1991 - Ethics and Behavior 1 (4):239 – 252.
Understanding informed consent for participation in international health research.Ayodele S. Jegede - 2009 - Developing World Bioethics 9 (2):81-87.
Informed Consent: A Primer for Clinical Practice.Deborah Bowman - 2011 - Cambridge University Press.
The Limits of Consent: A Socio-Ethical Approach to Human Subject Research in Medicine.Oonagh Corrigan (ed.) - 2009 - Oxford University Press.
Analytics
Added to PP
2013-12-24
Downloads
87 (#142,534)
6 months
8 (#104,882)
2013-12-24
Downloads
87 (#142,534)
6 months
8 (#104,882)
Historical graph of downloads
Citations of this work
Serial Participation and the Ethics of Phase 1 Healthy Volunteer Research.Rebecca L. Walker, Marci D. Cottingham & Jill A. Fisher - 2018 - Journal of Medicine and Philosophy 43 (1):83-114.
Feeding and Bleeding: The Institutional Banalization of Risk to Healthy Volunteers in Phase I Pharmaceutical Clinical Trials.Jill A. Fisher - 2015 - Science, Technology, and Human Values 40 (2):199-226.
Research Payment and Its Social Justice Concerns.Jill A. Fisher - 2019 - American Journal of Bioethics 19 (9):35-36.
Ethical considerations of recruiting migrant workers for clinical trials.Bushra Zafreen Amin - 2021 - Journal of Medical Ethics 47 (6):434-436.
Ethics and etiquette in an emergency vaccine trial. The orchestration of compliance.Arsenii Alenichev - 2020 - Tandf: Global Bioethics 31 (1):13-28.