增强特殊人群的代表性:在VA临床试验中纳入女性退伍军人的方法。

IF 2 3区 医学 Q3 MEDICINE, RESEARCH & EXPERIMENTAL
Karen M. Goldstein , Elizabeth M. Yano , Paula P. Schnurr , Lori A. Bastian , Susan Alton Dailey , Alyssa Pomernacki , Diane Carney , Jennifer M. Gierisch , Alison B. Hamilton , Andrea Nevedal , Dawne Vogt , Susan M. Frayne
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引用次数: 0

摘要

临床试验对历史上边缘化人群的招募不足,阻碍了公平纳入可能从医疗保健创新中受益的个体,并限制了结果的普遍性。几十年来,退伍军人健康管理局(VA)进行了大量的临床试验,影响了退伍军人和平民的临床指南。在退伍军人事务部,女性在数量上是少数,招募这些人参加试验面临着性别特定的护理结构、独特的人口特征和虐待的挑战,比如退伍军人事务部的性创伤和性骚扰率更高。我们描述了我们通过为退伍军人合作研究项目开发的退伍军人事务部女性强化招募计划(WERP)加强女性退伍军人参与临床试验的方法。这一信息与临床试验团队寻求将女性退伍军人纳入他们的试验有关。我们的研究结果也对其他寻求公平地增加边缘化人群参与的研究人员有启示,以便研究结果可以推广到更广泛的人群。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Enhancing representation of special populations: An approach to the inclusion of women veterans in VA clinical trials
The under-recruitment of historically marginalized populations into clinical trials thwarts equitable inclusion of individuals who could benefit from healthcare innovations and limits the generalizability of results. For decades, the Veterans Health Administration (VA) has conducted large clinical trials that impact clinical guidelines for veterans and civilians alike. Within the VA, women are a numeric minority, and recruitment of this population into trials is challenged by gender-specific care structures, distinct demographic characteristics, and mistreatment such as higher rates of military sexual trauma and harassment on VA grounds. We describe our approach to enhancing the inclusion of women veterans in clinical trials through the VA Women's Enhanced Recruitment Program (WERP) as developed for the VA Cooperative Studies Program. This information is relevant to clinical trial teams seeking to include women veterans in their trials. Our findings also have implications for other researchers seeking equitably increase participation of marginalized populations so that findings are generalizable to broader populations.
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来源期刊
CiteScore
3.70
自引率
4.50%
发文量
281
审稿时长
44 days
期刊介绍: Contemporary Clinical Trials is an international peer reviewed journal that publishes manuscripts pertaining to all aspects of clinical trials, including, but not limited to, design, conduct, analysis, regulation and ethics. Manuscripts submitted should appeal to a readership drawn from disciplines including medicine, biostatistics, epidemiology, computer science, management science, behavioural science, pharmaceutical science, and bioethics. Full-length papers and short communications not exceeding 1,500 words, as well as systemic reviews of clinical trials and methodologies will be published. Perspectives/commentaries on current issues and the impact of clinical trials on the practice of medicine and health policy are also welcome.
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