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

Abstract 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...

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Bibliographic Details
Main Authors: Pia Dellson, Christina Carlsson, Mef Nilbert, Helena Jernström
Format: Article
Language:English
Published: BMC 2019-05-01
Series:Trials
Subjects:
Online Access:http://link.springer.com/article/10.1186/s13063-019-3416-2