Researchers who enroll patients in clinical trials - only 24% would enroll themselves
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Researchers who enroll patients in clinical trials - only 24% would enroll themselves
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概要
Fewer than one in four rural physicians and research coordinators surveyed in 2015 said they would personally enroll in a clinical trial, despite obtaining consent from patients every week - what does that gap between practice and personal choice reveal about informed consent and the system that depends on it? Could decades of ethical failures and uneven training explain why many who obtain consent for others refuse it for themselves?
In this episode, we trace a path from a 2015 University of Montana survey to the postwar origins of modern research ethics, laying out what the study measured and why the findings matter for everyday clinical practice - can informed consent mean the same thing when those who administer it are reluctant to accept it?
Person: Ann Cook and Freeman Hoas
Date: 2015
Location: rural America; University of Montana Department of Psychology
Sample size: 80 respondents
Setting: hospital or hospital-clinic for 90% of respondents
- 24% of respondents said they would personally enroll in a clinical trial, and only with conditions.
- 34 of the 80 respondents were physicians or active researchers.
- 46 of the 80 respondents were research coordinators.
- 66% of research coordinators reported some research methods training; 53% of physicians reported the same.
- 59% of coordinators had ethics training versus 17% of physicians.
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