Design and implementation of community consultation for research conducted under exception from informed consent regulations for the PreVent and the PreVent 2 trials: Changes over time and during the COVID-19 pandemic

IF 2.2 3区 医学 Q3 MEDICINE, RESEARCH & EXPERIMENTAL Clinical Trials Pub Date : 2024-04-27 DOI:10.1177/17407745241243045
Tom Gugel, Karen Adams, Madelon Baranoski, N David Yanez, Michael Kampp, Tesheia Johnson, Ani Aydin, Elaine C Fajardo, Emily Sharp, Aartee Potnis, Chanel Johnson, Miriam M Treggiari
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Abstract

Introduction:Emergency clinical research has played an important role in improving outcomes for acutely ill patients. This is due in part to regulatory measures that allow Exception From Informed Consent (EFIC) trials. The Food and Drug Administration (FDA) requires sponsor-investigators to engage in community consultation and public disclosure activities prior to initiating an Exception From Informed Consent trial. Various approaches to community consultation and public disclosure have been described and adapted to local contexts and Institutional Review Board (IRB) interpretations. The COVID-19 pandemic has precluded the ability to engage local communities through direct, in-person public venues, requiring research teams to find alternative ways to inform communities about emergency research.Methods:The PreVent and PreVent 2 studies were two Exception From Informed Consent trials of emergency endotracheal intubation, conducted in one geographic location for the PreVent Study and in two geographic locations for the PreVent 2 Study. During the period of the two studies, there was a substantial shift in the methodological approach spanning across the periods before and after the pandemic from telephone, to in-person, to virtual settings.Results:During the 10 years of implementation of Exception From Informed Consent activities for the two PreVent trials, there was overall favorable public support for the concept of Exception From Informed Consent trials and for the importance of emergency clinical research. Community concerns were few and also did not differ much by method of contact. Attendance was higher with the implementation of virtual technology to reach members of the community, and overall feedback was more positive compared with telephone contacts or in-person events. However, the proportion of survey responses received after completion of the remote, live event was substantially lower, with a greater proportion of respondents having higher education levels. This suggests less active engagement after completion of the synchronous activity and potentially higher selection bias among respondents. Importantly, we found that engagement with local community leaders was a key component to develop appropriate plans to connect with the public.Conclusion:The PreVent experience illustrated operational advantages and disadvantages to community consultation conducted primarily by telephone, in-person events, or online activities. Approaches to enhance community acceptance included partnering with community leaders to optimize the communication strategies and trust building with the involvement of Institutional Review Board representatives during community meetings. Researchers might need to pivot from in-person planning to virtual techniques while maintaining the ability to engage with the public with two-way communication approaches. Due to less active engagement, and potential for selection bias in the responders, further research is needed to address the costs and benefits of virtual community consultation and public disclosure activities compared to in-person events.
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设计和实施社区咨询,为 PreVent 和 PreVent 2 试验中根据知情同意例外规定进行的研究提供咨询:随着时间推移和在 COVID-19 大流行期间的变化
导言:急诊临床研究在改善急症患者预后方面发挥了重要作用。这部分归功于允许知情同意例外(EFIC)试验的监管措施。美国食品和药物管理局(FDA)要求申办者-研究者在启动知情同意例外试验之前,必须开展社区咨询和公开披露活动。社区咨询和公开披露的方法多种多样,并根据当地情况和机构审查委员会 (IRB) 的解释进行了调整。方法:PreVent 和 PreVent 2 研究是两项紧急气管插管知情同意例外试验,PreVent 研究在一个地区进行,PreVent 2 研究在两个地区进行。结果:在两项 PreVent 试验的 "例外知情同意 "活动实施的 10 年间,公众对 "例外知情同意 "试验的概念和紧急临床研究的重要性总体上表示支持。社区关注的问题很少,而且联系方法也没有太大差别。采用虚拟技术联系社区成员的出席率更高,与电话联系或现场活动相比,总体反馈更为积极。不过,远程现场活动结束后收到的调查回复比例要低得多,受访者中受教育程度较高的比例更高。这表明,在完成同步活动后,受访者的参与积极性较低,可能存在较大的选择偏差。重要的是,我们发现与当地社区领袖的接触是制定与公众联系的适当计划的关键要素。结论:PreVent 的经验说明了主要通过电话、现场活动或在线活动进行社区咨询的操作优缺点。提高社区接受度的方法包括与社区领袖合作以优化沟通策略,以及在社区会议期间让机构审查委员会代表参与进来以建立信任。研究人员可能需要从现场规划转向虚拟技术,同时保持与公众进行双向交流的能力。由于参与的积极性较低,而且可能会出现选择偏差,因此需要进一步研究虚拟社区咨询和公开披露活动与现场活动相比的成本和效益。
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来源期刊
Clinical Trials
Clinical Trials 医学-医学:研究与实验
CiteScore
4.10
自引率
3.70%
发文量
82
审稿时长
6-12 weeks
期刊介绍: Clinical Trials is dedicated to advancing knowledge on the design and conduct of clinical trials related research methodologies. Covering the design, conduct, analysis, synthesis and evaluation of key methodologies, the journal remains on the cusp of the latest topics, including ethics, regulation and policy impact.
期刊最新文献
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