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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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Detalhes bibliográficos
Main Authors: Allmark, P, Mason, S
Formato: Artigo
Idioma:Inglês
Publicado em: BMJ Group 2006
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2563382/
https://ncbi.nlm.nih.gov/pubmed/16877621
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jme.2005.013722
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