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Development and evaluation of decision aids for people considering taking part in a clinical trial: a conceptual framework
Ethical requirements of informed consent stipulate that patients approached to participate in a clinical trial be provided with written information that must cover key aspects of the trial. For consent to be deemed “informed”, potential participants should be provided with a range of information abo...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
BioMed Central
2019
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6612082/ https://www.ncbi.nlm.nih.gov/pubmed/31277693 http://dx.doi.org/10.1186/s13063-019-3489-y |