在一家学术医疗中心实施 MyChart 招聘。

IF 2.1 Q3 MEDICINE, RESEARCH & EXPERIMENTAL
Journal of Clinical and Translational Science Pub Date : 2024-10-14 eCollection Date: 2024-01-01 DOI:10.1017/cts.2024.605
Carrie Dykes, Cody Gardner, Jack Chang, David Pinto, Karen Wilson, Martin S Zand, Ann Dozier
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引用次数: 0

摘要

导言:招募研究参与者仍然是研究人员关注的主要问题。利用临床团队来识别潜在的合格患者可能会造成很大的障碍。为了克服这一问题,我们利用电子病历的现有功能,实施了一个使用患者门户网站(MyChart)的流程,作为新的机构招募选项:为了简化机构审批流程,我们成立了一个由人类受试者保护、信息技术和隐私等方面的代表组成的工作小组,并与许多利益相关者共同审核了我们的流程。我们对研究审批的具体流程进行了描述,首先是与我们的临床和转化科学奖资助的招募和保留职能部门进行协商:从咨询到发送第一条信息的时间从 84 天到 442 天不等,随着时间的推移略有下降。患者对 MyChart 有关现有研究的信息的总体回复率为 23%,其中三分之一的患者表示有兴趣了解更多信息。黑人和西班牙裔患者的回复率约为白人患者的 50%:结论:任何医学专科的许多不同类型的研究都能通过该选项成功找到感兴趣的患者。研究团队需要支持来定义适当的纳入/排除标准,以确定电子健康记录中的相关人群,他们还需要协助以通俗易懂的语言撰写研究说明。使用 MyChart 进行招募解决了这一关键障碍,并为研究团队提供了提供全面招募咨询的机会,以确定研究团队不会考虑的其他招募渠道。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Implementation of MyChart for recruitment at an academic medical center.

Introduction: Recruitment of participants into research studies remains a major concern for investigators. Using clinical teams to identify potentially eligible patients can present a significant barrier. To overcome this, we implemented a process for using our patient portal, called MyChart, as a new institutional recruitment option utilizing our electronic health record's existing functionality.

Methods: To streamline the institutional approval process, we established a working group comprised of representatives from human subject protection, information technology, and privacy and vetted our process with many stakeholder groups. Our specific process for study approval is described and started with a consultation with our recruitment and retention function funded through our Clinical and Translational Science Award.

Results: The time from consultation to the first message(s) sent ranged from 84 to 442 days and declined slightly over time. The overall patient response rate to MyChart messages about available research studies was 23% with one third of those saying they were interested in learning more. The response rate for Black and Hispanic patients was about 50% that of White patients.

Conclusions: Many different types of studies from any medical specialty successfully identified interested patients using this option. Study teams needed support in defining appropriate inclusion/exclusion criteria to identify the relevant population in the electronic health records and they needed assistance writing study descriptions in plain language. Using MyChart for recruitment addressed a critical barrier and opened up the opportunity to provide a full recruitment consultation to identify additional recruitment channels the study teams would not have considered otherwise.

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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
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