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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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| Main Authors: | , |
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| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
BMJ Group
2006
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| Fag: | |
| Online adgang: | 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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