“Uninformed consent” in clinical trials with cancer patients: A qualitative analysis of patients’ and support persons’ communication experiences and needs

URN to cite this document:: urn:nbn:de:bvb:355-epub-578891
DOI to cite this document:: 10.5283/epub.57889

Bernardi, Christine ; Wolff, Daniel

; Lüke, Florian

; Hies, Johannes ; Hallowell, Nina ; Horn, Ruth ; Seitz, Frederike ; Heudobler, Daniel

; Hermann-Johns, Anne

License: Creative Commons Attribution 4.0
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Date of publication of this fulltext: 12 Mar 2024 10:49

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Abstract

Objective Cancer patients are often overwhelmed when being informed about clinical trials. However, there is a lack of evidence-based strategies to improve physician-patient communication in this area. This study assessed the experiences and needs of cancer patients and their support persons (SPs) during the informed consent (IC) process prior to participation in clinical trials. Methods 17 ...