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Patients’ and physicians’ disagreement on patients’ understanding of clinical cancer trial information: a pairwise pilot study of mirroring subjective assessments compared with objective measurements

BACKGROUND: Informed consent is a prerequisite for patients included in clinical trials. Trial design, inclusion criteria and legal requirements are increasingly complex. This complexity challenges design and delivery of written and oral trial information to ensure understandable information. To eva...

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Pubblicato in:Trials
Autori principali: Dellson, Pia, Carlsson, Christina, Nilbert, Mef, Jernström, Helena
Natura: Artigo
Lingua:Inglês
Pubblicazione: BioMed Central 2019
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Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC6542135/
https://ncbi.nlm.nih.gov/pubmed/31142346
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13063-019-3416-2
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