Improving the quality of consent to randomised controlled trials by using continuous consent and clinician training in the consent process

Objective: To assess whether continuous consent, a process in which information is given to research participants at different stages in a trial, and clinician training in that process were effective when used by clinicians while gaining consent to the Total Body Hypothermia (TOBY) trial. The TOBY t...

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Bibliographic Details
Authors: Allmark, P. (Author) ; Mason, S. (Author)
Format: Electronic Article
Language:English
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Published: BMJ Publ. 2006
In: Journal of medical ethics
Year: 2006, Volume: 32, Issue: 8, Pages: 439-443
Online Access: Presumably Free Access
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