Informed consent in randomised controlled trials: development and preliminary evaluation of a measure of Participatory and Informed Consent (PIC)

BACKGROUND: Informed consent (IC) is an ethical and legal prerequisite for trial participation, yet current approaches evaluating participant understanding for IC during recruitment lack consistency. No validated measure has been identified that evaluates participant understanding for IC based on th...

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Publicado en:Trials
Main Authors: Wade, Julia, Elliott, Daisy, Avery, Kerry N. L., Gaunt, Daisy, Young, Grace J., Barnes, Rebecca, Paramasivan, Sangeetha, Campbell, W Bruce, Blazeby, Jane M., Birtle, Alison J, Stein, Rob C., Beard, David J, Halliday, Alison W, Donovan, Jenny L.
Formato: Artigo
Idioma:Inglês
Publicado: BioMed Central 2017
Assuntos:
Research
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC5513045/
https://ncbi.nlm.nih.gov/pubmed/28716064
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13063-017-2048-7
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