Advance Research Directives: Dementia Researchers' Views on a Prototype Directive and Implementation Strategies
Author:
Affiliation:
1. Professor of the Faculty of Law at the University of Technology Sydney
2. Research associate of the Faculty of Health and Medicine at the University of Newcastle, Australia, and Hunter Medical Research Institute
Funder
National Health and Medical Research Council
Hunter Medical Research Institute
Publisher
Wiley
Subject
Health(social science)
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/eahr.500091
Reference48 articles.
1. ‘Thinking about It for Somebody Else’: Alzheimer's Disease Research and Proxy Decision Makers' Translation of Ethical Principles into Practice;Dunn L. B.;American Journal of Geriatric Psychiatry,2013
2. Advance Directives for Research: How Do They Compare with Surrogates' Predictions of Older Adults' Preferences?;Hérault É.;IRB: Ethics & Human Research,2018
3. Shepherdet al. “Ethical Understandings of Proxy Decision Making.”
4. Assessing the Quality of Democratic Deliberation: A Case Study of Public Deliberation on the Ethics of Surrogate Consent for Research;De Vries R.;Social Science & Medicine,2010
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4. Making an Advance Research Directive: An Interview Study with Adults Aged 55 and Older with Interests in Dementia Research;Ethics & Human Research;2023-05
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