Patients' beliefs regarding informed consent for low-risk pragmatic trials
Patients' beliefs regarding informed consent for low-risk pragmatic trials
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Publisher
England: BioMed Central Ltd
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Language
English
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England: BioMed Central Ltd
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Contents
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 from the U.S. and Spain suggest that a majority of the public...
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Patients' beliefs regarding informed consent for low-risk pragmatic trials
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TN_cdi_doaj_primary_oai_doaj_org_article_50bd29ce9e5e492f9301843645886452
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https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_50bd29ce9e5e492f9301843645886452
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ISSN
1471-2288
E-ISSN
1471-2288
DOI
10.1186/s12874-017-0424-3