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Patients’ beliefs regarding informed consent for low-risk pragmatic trials

BACKGROUND: The requirement to obtain written informed consent may undermine the potential of pragmatic randomized clinical trials (pRCTs) to improve evidence-based care. This requirement could compromise trials statistical power or even force it to close them down prematurely. However, recent data...

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Pubblicato in:BMC Med Res Methodol
Autori principali: Dal-Ré, Rafael, Carcas, Antonio J., Carné, Xavier, Wendler, David
Natura: Artigo
Lingua:Inglês
Pubblicazione: BioMed Central 2017
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Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC5604493/
https://ncbi.nlm.nih.gov/pubmed/28923007
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12874-017-0424-3
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