Why we should not seek individual informed consent for participation in health services research
نویسندگان
چکیده
منابع مشابه
Why we should not seek individual informed consent for participation in health services research.
Ethics committees now require that individuals give informed consent to much health services research, in the same way as for clinical research. This is misguided. Existing ethical guidelines do not help us decide how to seek consent in these cases, and have allowed managerial experimentation to remain largely unchecked. Inappropriate requirements for individual consent can institutionalise hea...
متن کامل(Why) should we require consent to participation in research?
It is widely accepted that informed consent is a requirement of ethical biomedical research. It is less clear why this is so. As an argumentative strategy the article asks whether it would be legitimate for the state to require people to participate in research. This article argues that the consent requirement cannot be defended by appeal to any simple principle, such as not treating people mer...
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People living in rural areas far from health care centers are more likely to require health care services due to their long distances services and poverty(1). Tele-rehabilitation is considered as one of the rapidly emerging and growing areas of telemedicine and a precious model for providing clinical services like assessment, treatment and follows up as well as reducing the length of time for h...
متن کاملResearch Ethics and Informed Consent : Not Applicable
Copyright and reuse: The Warwick Research Archive Portal (WRAP) makes this work of researchers of the University of Warwick available open access under the following conditions. Copyright © and all moral rights to the version of the paper presented here belong to the individual author(s) and/or other copyright owners. To the extent reasonable and practicable the material made available in WRAP ...
متن کاملVoluntary participation and informed consent to international genetic research.
OBJECTIVES We compared voluntary participation and comprehension of informed consent among individuals of African ancestry enrolled in similarly designed genetic studies of hypertension in the United States and Nigeria. METHODS Survey questionnaires were used to evaluate factors associated with voluntariness (the number of people volunteering) and understanding of the study's genetic purpose....
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ژورنال
عنوان ژورنال: Journal of Medical Ethics
سال: 2002
ISSN: 0306-6800
DOI: 10.1136/jme.28.5.313