Partnering With Patients to Bridge Gaps in Consent for Acute Care Research
Neal W. Dickert,Amanda Michelle Bernard,JoAnne M. Brabson,Rodney J. Hunter,Regina McLemore,Andrea R. Mitchell,Stephen Palmer,Barbara Reed,Michele Riedford,Raymond T. Simpson,Candace D. Speight,Tracie Steadman &Rebecca D. Pentz
Abstract
Clinical trials for acute conditions such as myocardial infarction and stroke pose challenges related to informed consent due to time limitations, stress, and severe illness. Consent processes shou...Other Versions
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References found in this work
Reframing Consent for Clinical Research: A Function-Based Approach.Scott Y. H. Kim,David Wendler,Kevin P. Weinfurt,Robert Silbergleit,Rebecca D. Pentz,Franklin G. Miller,Bernard Lo,Steven Joffe,Christine Grady,Sara F. Goldkind,Nir Eyal &Neal W. Dickert -2017 -American Journal of Bioethics 17 (12):3-11.
False Hopes and Best Data: Consent to Research and the Therapeutic Misconception.Paul S. Appelbaum,Loren H. Roth,Charles W. Lidz,Paul Benson &William Winslade -1987 -Hastings Center Report 17 (2):20-24.
Misunderstanding in Clinical Research: Distinguishing Therapeutic Misconception, Therapeutic Misestimation, & Therapeutic Optimism.Sam Horng &Christine Grady -2003 -IRB: Ethics & Human Research 25 (1):11.
Readability of consent form templates: a second look.M. K. Paasche-Orlow,F. L. Brancati,H. A. Taylor,S. Jain,A. Pandit &M. S. Wolf -2013 -IRB: Ethics & Human Research 35 (4):12-19.
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