Experiences and lessons learned from a patient-engagement service established by a national research consortium in the U.S. Veterans Health Administration

IF 2.6 Q2 HEALTH POLICY & SERVICES Learning Health Systems Pub Date : 2024-04-16 DOI:10.1002/lrh2.10421
Tracy L. Sides, Agnes C. Jensen, Malloree M. Argust, Erin C. Amundson, Gay R. Thomas, Rebecca Keller, Mallory Mahaffey, Erin E. Krebs
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Abstract

Introduction

Meaningful engagement of patients in the research process has increased over the past 20 years. Few accounts are available of engagement infrastructure and processes used by large research organizations. The Pain/Opioid Consortium of Research (Consortium) is a U.S. Department of Veterans Affairs (VA) research network that provides infrastructure to accelerate health research and implementation of evidence-based health care. The Consortium's key activities include facilitating Veteran-engaged research and building community between Veterans and VA researchers. This report sought to describe experiences and lessons learned from the first 3 years of a national research engagement service, featuring a Veteran Engagement (VE) Panel, established by the Consortium.

Methods

We gathered authors' experiences to describe development and operation of the Consortium's VE Panel. Engagement staff collected program evaluation data about partners (Veterans and researchers), projects about which the VE Panel consulted, and meeting attendance during operation of the engagement service.

Results

We created a 12-member VE Panel; all of whom had lived experience with chronic pain, prescription opioid medication use, or opioid use disorder. Engagement staff and VE Panel members implemented an engagement service operational model designed to continuously learn and adapt. The panel consulted on 48 projects spanning the research process. Seventy-eight percent of panel members, on average, attended each monthly meeting. VE Panel members and participating researchers reported high satisfaction with the quality, ease, and outcomes of their engagement service experiences.

Conclusions

This work provides an illustrative example of how a national research consortium facilitated Veteran-engaged research and built community between Veterans and VA researchers by developing and operating an ongoing engagement consulting service, featuring a VE Panel. The service, designed as a learning community, relied on skilled engagement staff to cultivate high quality experiences and outcomes for all partners.

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美国退伍军人健康管理局全国研究联盟建立的患者参与服务的经验和教训
在过去 20 年中,患者有意义地参与研究过程的情况越来越多。关于大型研究机构所使用的参与基础设施和流程,目前鲜有报道。疼痛/阿片类药物研究联盟(联盟)是美国退伍军人事务部(VA)的一个研究网络,为加快健康研究和循证医疗的实施提供了基础设施。联盟的主要活动包括促进退伍军人参与的研究以及在退伍军人和退伍军人事务部研究人员之间建立社区。本报告旨在介绍退伍军人参与联盟设立的退伍军人参与(VE)小组在开展全国性研究参与服务的前三年中取得的经验和教训。参与人员收集了有关合作伙伴(退伍军人和研究人员)、退伍军人参与小组咨询的项目以及参与服务运行期间会议出席情况的项目评估数据。参与员工和自愿者小组成员实施了旨在不断学习和调整的参与服务运营模式。小组在整个研究过程中为 48 个项目提供了咨询服务。平均有 78% 的小组成员参加了每次月度会议。退伍军人参与小组成员和参与研究人员对其参与服务体验的质量、便捷性和成果表示高度满意。这项工作提供了一个实例,说明国家研究联盟如何通过开发和运营以退伍军人参与小组为特色的持续参与咨询服务,促进退伍军人参与研究,并在退伍军人和退伍军人事务部研究人员之间建立社区。这项服务被设计成一个学习社区,依靠技术娴熟的参与人员为所有合作伙伴提供高质量的体验和成果。
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来源期刊
Learning Health Systems
Learning Health Systems HEALTH POLICY & SERVICES-
CiteScore
5.60
自引率
22.60%
发文量
55
审稿时长
20 weeks
期刊最新文献
Issue Information Envisioning public health as a learning health system Thanks to our peer reviewers Learning health systems to implement chronic disease prevention programs: A novel framework and perspectives from an Australian health service The translation-to-policy learning cycle to improve public health
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