177 通过赋予参与者发言权,将参与者的经历置于改进研究的中心位置

IF 2.1 Q3 MEDICINE, RESEARCH & EXPERIMENTAL Journal of Clinical and Translational Science Pub Date : 2024-04-03 DOI:10.1017/cts.2024.168
Rhonda Kost, Ranee Chatterjee, Ann Dozier, Daniel Ford, Joseph Andrews, Nancy Green, Paul A. Harris, Alex Cheng
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引用次数: 0

摘要

目标/目的:赋予参与者话语权(EPV)是一项由洛克菲勒领导的 6 CTSA 合作项目,旨在开发定制的 REDCap 基础设施,以便使用经过验证的研究参与者感知调查(RPPS)收集参与者的反馈意见,在使用案例中展示其价值,并将其推广开来供广泛采用。方法/研究对象:EPV 团队制定了数据和调查实施标准,以及仪表板和多语言 RPPS/REDCap 项目 XML 文件的规格。VUMC 定制了一个 "一目了然 "仪表盘外部模块,用于显示 "顶部方框 "得分(最佳答案百分比),并通过条件格式化帮助分析,以及回复率/完成率。结果将填充到医疗点仪表板中,并汇总到多医疗点仪表板中进行基准比较。结果可按参与者/研究特征进行筛选。各站点利用当地的基础设施、倡议和利益相关者的意见,开发了各自的使用案例。设计了基础设施和指南,以便通过公共网站进行传播。结果/预期结果:五个站点通过电子邮件、患者门户网站或短信发送了 23797 份调查问卷。4133名(19%)不同年龄、种族和民族的参与者返回了回复。各医疗点对数据进行了分析,并根据所选结果采取了行动,改善了招募、沟通和受重视感。感觉被倾听和尊重的总得分很高(90%);感觉同意程序准备充分的得分较低(57-77%),需要采取行动。有些小组的体验比其他小组好。各地区在某些评分方面差异很大。目前正在传播 EPV。在 EPV 团队的建议下,可免费下载基础设施和指南。2023 年,第六个站点开始试用低识字率调查版本,并将数据同步到联盟仪表板。讨论/意义:EPV RPPS/REDCap 基础设施使各站点能够收集参与者的反馈意见,确定可操作的调查结果,并与同行进行比较。利益相关者和合作者设计并测试了地方倡议,以提高响应度和多样性、解决差异问题并发现更好的做法。
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177 Placing Participant Experiences at the Center of Improving Research by Empowering the Participant Voice
OBJECTIVES/GOALS: Empowering the Participant Voice (EPV) is a 6-CTSA Rockefeller-led collaboration to developcustom REDCap infrastructure to collect participant feedback using the validated Research Participant Perception Survey (RPPS), demonstrate its value in use cases, and disseminate it for broad adoption. METHODS/STUDY POPULATION: The EPV team developed data and survey implementation standards, and specifications for the dashboard and multi-lingual RPPS/REDCap project XML file. The VUMC built a custom At-a-Glance Dashboard external module that displays Top Box scores (percent best answer), with conditional formatting to aid analysis, and response/completion rates. Results populate site dashboards, and aggregate to a multi-site dashboard for benchmarking. Results can be filtered by participant/study characteristics. Sites developed individual use cases, leveraging local infrastructure, initiatives and stakeholder input. Infrastructure and guides were designed for dissemination through public websites. RESULTS/ANTICIPATED RESULTS: Five sites sent 23,797surveys via email, patient portal or SMS. 4,133 (19%) participants diverse in age, race, and ethnicity, returned responses. Sites analyzed their data and acted on selected findings, improving recruitment, communication and feeling valued. Aggregate scores for feeling listened to and respected were hight (>90%%); scores for feeling prepared by the consent process were lower (57-77%) and require action. Some groups experiences were better than others. Sites differed significantly in some scores. Dissemination of EPV is underway. Infrastructure and guides are downloadable free of charge, with advice from the EPV team. In 2023, a sixth site began piloting a lower literacy survey version and syncing data to the consortium dashboard. DISCUSSION/SIGNIFICANCE: The EPV RPPS/REDCap infrastructure enabled sites to collect participant feedback, identify actionable findings and benchmark with peers. Stakeholders and collaborators designed and tested local initiatives to increase responses and diversity, address disparities, and discover better practices.
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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
期刊最新文献
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