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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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Detalhes bibliográficos
Publicado no:Trials
Main Authors: Dellson, Pia, Carlsson, Christina, Nilbert, Mef, Jernström, Helena
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2019
Assuntos:
Acesso em linha: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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