Qualitative assessment of proposed visual key information pages for informed consent.

IF 2.1 Q3 MEDICINE, RESEARCH & EXPERIMENTAL Journal of Clinical and Translational Science Pub Date : 2024-11-21 eCollection Date: 2024-01-01 DOI:10.1017/cts.2024.662
Krista E Cooksey, Eliana Goldstein, Clara Lee, Jessica Mozersky, Kimberly A Kaphingst, Victor Catalan Gallegos, Mary C Politi
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Abstract

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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对拟议的用于知情同意的视觉关键信息页面进行定性评估。
2018年共同规则修订旨在通过推荐简明的关键信息(KI)部分来改进知情同意,但对如何描述KI提供了很少的指导。我们开发了创新的视觉KI模板,注重健康素养和视觉设计原则。我们探讨了可能影响可视化KI页面实现的最终用户的态度、信念和制度政策。材料和方法:从2023年10月到2024年4月,我们对主要研究者、研究人员、机构审查委员会(IRB)人员(包括监督/管理人员)和社区合作伙伴进行了半结构化访谈。来自三个学术机构(中西部、东南部和西部山区)的40名参与者查看了KI示例页面并完成了访谈。我们根据能力、机会和改变行为的动机(COM-B)框架,归纳和演绎地对书面记录进行编码。采用内容分析法对数据进行分析,并按主题组织。结果:参与者对视觉KI示例反应积极。他们讨论了潜在的好处,包括改善信息处理和对研究程序的理解、研究的多样性、对研究的信任和研究工作流程。他们还描述了在广泛实施之前需要考虑的潜在挑战:IRB对联邦指导方针的解释,对IRB提交过程的可能影响,开发视觉效果所需的努力/技能,以及简洁地传达研究风险的困难。关于在同意期间何时使用视觉KI没有达成共识,有些人怀疑它们是否适用于所有研究类型。讨论:Visual KI为长期存在的知情同意挑战提供了一个有希望的解决方案。未来的工作可以探索资源和培训,以应对挑战并促进广泛使用。
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来源期刊
Journal of Clinical and Translational Science
Journal of Clinical and Translational Science MEDICINE, RESEARCH & EXPERIMENTAL-
CiteScore
2.80
自引率
26.90%
发文量
437
审稿时长
18 weeks
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