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
Tracy L. Sides, Agnes C. Jensen, Malloree M. Argust, Erin C. Amundson, Gay R. Thomas, Rebecca Keller, Mallory Mahaffey, Erin E. Krebs
{"title":"Experiences and lessons learned from a patient-engagement service established by a national research consortium in the U.S. Veterans Health Administration","authors":"Tracy L. Sides,&nbsp;Agnes C. Jensen,&nbsp;Malloree M. Argust,&nbsp;Erin C. Amundson,&nbsp;Gay R. Thomas,&nbsp;Rebecca Keller,&nbsp;Mallory Mahaffey,&nbsp;Erin E. Krebs","doi":"10.1002/lrh2.10421","DOIUrl":null,"url":null,"abstract":"<div>\n \n \n <section>\n \n <h3> Introduction</h3>\n \n <p>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.</p>\n </section>\n \n <section>\n \n <h3> Methods</h3>\n \n <p>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.</p>\n </section>\n \n <section>\n \n <h3> Results</h3>\n \n <p>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.</p>\n </section>\n \n <section>\n \n <h3> Conclusions</h3>\n \n <p>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.</p>\n </section>\n </div>","PeriodicalId":43916,"journal":{"name":"Learning Health Systems","volume":"8 3","pages":""},"PeriodicalIF":2.6000,"publicationDate":"2024-04-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/lrh2.10421","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Learning Health Systems","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/lrh2.10421","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"HEALTH POLICY & SERVICES","Score":null,"Total":0}
引用次数: 0

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.

Abstract Image

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。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
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
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信