The patient's perspective on the need for informed consent for minimal risk studies: Development of a survey-based measure-Reference-Cited by-同舟云学术

The patient's perspective on the need for informed consent for minimal risk studies: Development of a survey-based measure

Published:2016-04-02 Issue:2 Volume:7 Page:116-124
ISSN:2329-4515
Container-title:AJOB Empirical Bioethics
language:en
Short-container-title:AJOB Empirical Bioethics

Author:

Kaplan Sherrie H.,Gombosev Adrijana,Fireman Sheila,Sabin James,Heim Lauren,Shimelman Lauren,Kaganov Rebecca,Osann Kathryn E.,Tjoa Thomas,Huang Susan S.

Publisher

Informa UK Limited

Subject

Health Policy,Philosophy,Health (social science)

Link

http://www.tandfonline.com/doi/pdf/10.1080/23294515.2016.1161672

Reference46 articles.

1. What determines whether patients are willing to participate in resuscitation studies requiring exception from informed consent?

2. The Quality Improvement–Research Divide and the Need for External Oversight

3. Moving Comparative Effectiveness Research Into Practice: Implementation Science And The Role Of Academic Medicine

4. Extracting information from hospital records: what patients think about consent

5. The Real Problem Is Consent for Treatment, Not Consent for Research

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