Evaluation of Informed Consent Documents used in Critical Care Trials

Evaluation of Informed Consent Documents used in Critical Care Trials

The literature suggests that informed consent documents (ICDs) are not well understood by research participants. The patient decision aid model may suggest improvements for the informed consent process, particularly in the critical care setting (ICU) because of patient capacity issues. Our goal was...

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Bibliographic Details
Main Author: ATWERE, PEARL
Other Authors: BREHAUT, JAMIE
Language:en
Published: Université d'Ottawa / University of Ottawa 2015
Subjects:
INFORMED CONSENT
INFORMED CONSENT DOCUMENT
CRITICAL CARE
CRITICAL CARE TRIALS
INTENSIVE CARE
RECOMMENDATIONS
documentation
consent forms
ethics
third-party consent
proxy
clinical trials
biomedical research
vulnerable populations
critical illness
cognition disorders
DECISION SUPPORT
DECISION AIDS
GUIDELINES
DECISION SUPPORT STANDARDS
Online Access:http://hdl.handle.net/10393/33356
http://dx.doi.org/10.20381/ruor-4033

Internet

http://hdl.handle.net/10393/33356
http://dx.doi.org/10.20381/ruor-4033

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