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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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| Опубликовано в: : | BMC Med Res Methodol |
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| Главные авторы: | , , , |
| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
BioMed Central
2017
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| Предметы: | |
| Online-ссылка: | 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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