Getting the Most out of Consent: Patient‐Centered Consent for an Acute Stroke Trial-Reference-Cited by-同舟云学术

Getting the Most out of Consent: Patient‐Centered Consent for an Acute Stroke Trial

Published:2022-02-26 Issue:2 Volume:44 Page:33-40
ISSN:2578-2355
Container-title:Ethics & Human Research
language:en
Short-container-title:Ethics & Human Research

Author:

Dickert Neal W.¹,Metz Kathleen²,Deeds S. Iris³,Linke Michael J.⁴,Mitchell Andrea R.⁵,Speight Candace D.⁶,Adeoye Opeolu M.⁷

Affiliation:

1. Associate professor in the Department of Medicine at the Emory University School of Medicine and in the Department of Epidemiology at the Emory University Rollins School of Public Health

2. Resident in the Department of Emergency Medicine at Emory University School of Medicine

3. Project manager in the Department of Emergency Medicine at the Washington University School of Medicine

4. Adjunct professor and IRB chair at the University of Cincinnati College of Medicine

5. Senior research administrative coordinator in the Department of Medicine at the Emory University School of Medicine

6. Data analyst in the Department of Medicine at the Emory University School of Medicine

7. Professor and the chair of the Department of Emergency Medicine at the Washington University School of Medicine

Funder

Greenwall Foundation

National Institute of Neurological Disorders and Stroke

Patient-Centered Outcomes Research Institute

Agency for Healthcare Research and Quality

National Institutes of Health

National Center for Advancing Translational Sciences

Publisher

Wiley

Subject

Health (social science)

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/eahr.500122

Reference21 articles.

1. The accuracy of surrogate decision makers: informed consent in hypothetical acute stroke scenarios

2. Emergency Consent: Patients’ and Surrogates’ Perspectives on Consent for Clinical Trials in Acute Stroke and Myocardial Infarction

3. Partnering With Patients to Bridge Gaps in Consent for Acute Care Research

4. Understanding and Improving Informed Consent for Clinical Trials during Health Emergencies

5. Adaptive Clinical Trials

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