Qualitative assessment of proposed visual key information pages for informed consent

被引:1
作者
Cooksey, Krista E. [1 ]
Goldstein, Eliana [1 ]
Lee, Clara [2 ]
Mozersky, Jessica [3 ]
Kaphingst, Kimberly A. [4 ,5 ]
Gallegos, Victor Catalan [2 ]
Politi, Mary C. [1 ]
机构
[1] Washington Univ, Dept Surg, Div Publ Hlth Sci, Sch Med, St Louis, MO 63130 USA
[2] Univ North Carolina Chapel Hill, Dept Surg, Div Plast & Reconstruct Surg, Sch Med, Chapel Hill, NC USA
[3] Washington Univ, Dept Med, Div Gen Med & Geriatr, Sch Med, St Louis, MO USA
[4] Univ Utah, Dept Commun, Salt Lake City, UT USA
[5] Univ Utah, Huntsman Canc Inst, Salt Lake City, UT USA
关键词
Informed consent; health literacy; visual design; key information section; Common Rule;
D O I
10.1017/cts.2024.662
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Introduction: The 2018 Common Rule revision intended to improve informed consent by recommending a concise key information (KI) section, yet provided little guidance about how to describe KI. We developed innovative, visual KI templates with attention to health literacy and visual design principles. We explored end users' attitudes, beliefs, and institutional policies that could affect implementing visual KI pages.Materials and methods: From October 2023 to April 2024, we conducted semi-structured interviews with principal investigators, research staff, and Institutional Review Board (IRB) personnel, including those in oversight/management, and community partners. Forty participants from three academic institutions (in the Midwest, Southeast, and Mountain West) viewed example KI pages and completed interviews. We coded written transcripts inductively and deductively based on the capability, opportunity, and motivation to change behavior (COM-B) framework. Data were analyzed using content analysis and organized thematically.Results: Participants responded positively to the visual KI examples. They discussed potential benefits, including improving information processing and understanding of study procedures, diversity in research, trust in research, and study workflow. They also described potential challenges to consider before widespread implementation: IRBs' interpretations of federal guidelines, possible impacts on IRB submission processes, the effort/skill required to develop visuals, and difficulty succinctly communicating study risks. There was no consensus about when to use visual KI during consent, and some wondered if they were feasible for all study types.Discussion: Visual KI offers a promising solution to long-standing informed consent challenges. Future work can explore resources and training to address challenges and promote widespread use.
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页数:11
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