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Patient representatives’ views on patient information in clinical cancer trials

BACKGROUND: Patient enrolment into clinical trials is based on oral information and informed consent, which includes an information sheet and a consent certificate. The written information should be complete, but at the same time risks being so complex that it may be questioned if a fully informed c...

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Библиографические подробности
Опубликовано в: :BMC Health Serv Res
Главные авторы: Dellson, Pia, Nilbert, Mef, Carlsson, Christina
Формат: Artigo
Язык:Inglês
Опубликовано: BioMed Central 2016
Предметы:
Online-ссылка:https://ncbi.nlm.nih.gov/pmc/articles/PMC4736467/
https://ncbi.nlm.nih.gov/pubmed/26831330
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12913-016-1272-2
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