Improved informed consent documents for biomedical research do not increase patients’ understanding but reduce enrolment: a study in real settings

AIMS: The aim was to evaluate the comprehension of participants of an improved informed consent document (ICD). METHOD: This was a randomized controlled French multicentre study performed in real conditions. Participants were adult patients undergoing screening for enrolment in biomedical research s...

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Publicat a:Br J Clin Pharmacol
Autors principals: Paris, Adeline, Deygas, Béatrice, Cornu, Catherine, Thalamas, Claire, Maison, Patrick, Duale, Christian, Kane, Maty, Hodaj, Enkelejda, Cracowski, Jean-Luc
Format: Artigo
Idioma:Inglês
Publicat: John Wiley & Sons, Ltd 2015
Matèries:
Clinical Trials
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC4631174/
https://ncbi.nlm.nih.gov/pubmed/26147763
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/bcp.12716
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