Initial Steps in Creating a Patient-Centric Addendum to Clinical Trial Informed Consent Forms

被引:1
|
作者
King-Kallimanis, Bellinda L. [3 ,4 ]
Ferris, Andrea
Dropkin, Lisa [1 ]
Molina, Mariel [1 ]
Redway, Lydia [1 ]
Gerber, David E. [2 ]
Grant, Tracey L.
Roy, Upal Basu
机构
[1] Lungev Fdn, Chicago, IL USA
[2] Edge Res, Arlington, VA USA
[3] Univ Texas Southwestern Med Ctr, Harold C Simmons Comprehens Canc Ctr, Dallas, TX USA
[4] LUNGev Fdn, 6917 Arlington Rd,Suite 352, Bethesda, MD 20814 USA
来源
JTO CLINICAL AND RESEARCH REPORTS | 2023年 / 4卷 / 10期
关键词
INFORMATION;
D O I
10.1016/j.jtocrr.2023.100575
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Introduction: The purpose of the informed consent form (ICF) is to outline the risks and benefits of an interventional clinical trial to potential participants. The aim of this study was to explore the feasibility of a short addendum to the ICF, summarizing key points most relevant to potential participants.Methods: A sample of 20 ICFs was reviewed against the requirements of the U.S. federal regulation documents and assessed for readability. Alongside the ICF review, we con-ducted focus groups and one-on-one interviews with people with lung cancer (n 1/4 9) to learn what information was most important when considering participation in a clinical trial using a hypothetical phase 3 ICF. Results: The 20 ICFs reviewed were from phases 1 to 3, expanded-access, and single-patient trials covering pre-dominantly NSCLC; 60% were global. The mean length of the ICFs was 21 (range: 15-34) pages. The average reading level was tenth grade whereas the average U.S. reading level was eighth grade. Readability varied by section, the "pur -pose of the study" section had the highest reading level. In the qualitative research component, participants were "overwhelmed" by the hypothetical ICF. Participants were also asked to list information for the addendum; their suggestions broadly map to federal regulations. An addendum with reference to sections in the ICF for addi-tional details was well received. Conclusions: The variations in ICF architecture and read-ability make it difficult for patients to make an informed decision to participate in a clinical trial. Implications extend beyond lung cancer, highlighting key areas for ICF im-provements and providing a roadmap for developing a patient-centric addendum.(c) 2023 The Authors. Published by Elsevier Inc. on behalf of the International Association for the Study of Lung Cancer.This is an open access article under the CC BY-NC-ND li-cense (http://creativecommons.org/licenses/by-nc-nd/ 4.0/).
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页数:5
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