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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Detalles Bibliográficos
Autores principales: Dellson, Pia, Carlsson, Christina, Nilbert, Mef, Jernström, Helena
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6542135/
https://www.ncbi.nlm.nih.gov/pubmed/31142346
http://dx.doi.org/10.1186/s13063-019-3416-2

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6542135/
https://www.ncbi.nlm.nih.gov/pubmed/31142346
http://dx.doi.org/10.1186/s13063-019-3416-2

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