Public Health Sciences, Michigan State University + Henry Ford Health, 1 Ford Place, Suite 5E, Detroit, MI, 48202, United States, 1 3137997237.
College of Nursing, University of South Florida, Tampa, FL, United States.
JMIR Form Res. 2024 Nov 22;8:e59837. doi: 10.2196/59837.
BACKGROUND: Patient portals are being increasingly used by health systems in the United States. Although some patients use portals for clinical use, patient perspectives on using portals for research-related activities, to complete health screenings, and to request at-home self-test kits are unclear. OBJECTIVE: We aimed to understand patient perspectives on using electronic health portals for research; health-related screenings; and patient-initiated, home-based self-testing. METHODS: Patients (N=105) from the Patient Engaged Research Center at a large, urban, midwestern health system completed a 23-item web-based survey on patient portal (MyChart) use and willingness to use the patient portal for research, risk assessments, and self-test kits. Frequencies and percentages were generated. RESULTS: Almost all participants (102/105, 97.1%) had accessed MyChart at least once, with most (44/102, 43.1%) indicating they logged in at least once per month. Participants indicated logging into MyChart to check laboratory results or other health data (89/105, 84.8%), because they received a message to log in (85/105, 81%), and to message their health care professional (83/105, 79%). Fewer participants logged in to see what medications they had been prescribed (16/105, 15.2%) and to learn more about their health conditions (29/105, 27.6%). Most participants indicated logging into MyChart on a computer via a website (70/105, 66.7%) or on a smartphone via an app (54/105, 51.4%). When asked about how likely they would be to participate in different types of research if contacted via MyChart, most (90/105, 85.7%) said they would be likely to answer a survey, fill out a health assessment (87/105, 82.9%), or watch a video (86/105, 81.9%). Finally, participants would be willing to answer risk assessment questions on MyChart regarding sleep (74/101, 73.3%), stress (65/105, 61.9%), diabetes (60/105, 57.1%), anxiety (59/105, 56.2%), and depression (54/105, 51.4%) and would be interested in receiving an at-home self-test kit for COVID-19 (66/105, 62.9%), cholesterol (63/105, 60%), colon cancer (62/105, 59%), and allergies (56/105, 53.3%). There were no significant demographic differences for any results (all P values were >.05). CONCLUSIONS: Patient portals may be used for research recruitment; sending research-related information; and engaging patients to answer risk assessments, read about health information, and complete other clinical tasks. The lack of significant findings based on race and gender suggests that patient portals may be acceptable tools for recruiting research participants and conducting research. Allowing patients to request self-test kits and complete risk assessments in portals may help patients to take agency over their health care. Future research should examine if patient portal recruitment may help address persistent biases in clinical trial recruitment to increase enrollment of women and racial minority groups.
背景:患者门户在美国的医疗系统中被越来越多地使用。尽管一些患者将门户用于临床用途,但患者对使用门户进行研究相关活动、完成健康筛查以及请求在家进行自我检测试剂盒的看法尚不清楚。
目的:我们旨在了解患者对使用电子健康门户进行研究、健康相关筛查以及患者发起的、基于家庭的自我检测的看法。
方法:来自一家大型城市中西部医疗系统的患者参与研究中心的 105 名患者完成了一份关于使用患者门户(MyChart)进行研究、风险评估和自我检测试剂盒的意愿的 23 项网络调查。生成了频率和百分比。
结果:几乎所有参与者(105 名中的 102 名,97.1%)至少访问过一次 MyChart,其中大多数(44 名中的 43.1%)表示他们每月至少登录一次。参与者表示登录 MyChart 是为了查看实验室结果或其他健康数据(89/105,84.8%),因为他们收到了登录的消息(85/105,81%),并且向他们的医疗保健专业人员发送消息(83/105,79%)。较少的参与者登录是为了查看他们开了哪些药(16/105,15.2%)和了解更多关于他们的健康状况(29/105,27.6%)。大多数参与者表示他们通过网站(70/105,66.7%)或通过应用程序(54/105,51.4%)在计算机上登录 MyChart。当被问及如果通过 MyChart 联系他们,他们参与不同类型研究的可能性时,大多数(90/105,85.7%)表示他们可能会回答调查、填写健康评估(87/105,82.9%)或观看视频(86/105,81.9%)。最后,参与者愿意在 MyChart 上回答有关睡眠(74/101,73.3%)、压力(65/105,61.9%)、糖尿病(60/105,57.1%)、焦虑(59/105,56.2%)和抑郁(54/105,51.4%)的风险评估问题,并对 COVID-19(66/105,62.9%)、胆固醇(63/105,60%)、结肠癌(62/105,59%)和过敏(56/105,53.3%)的自我检测试剂盒感兴趣。所有结果的人口统计学差异均无统计学意义(所有 P 值均>.05)。
结论:患者门户可用于研究招募;发送与研究相关的信息;并让患者参与回答风险评估、阅读健康信息和完成其他临床任务。基于种族和性别没有显著发现表明,患者门户可能是招募研究参与者和进行研究的可接受工具。允许患者在门户中请求自我检测试剂盒并完成风险评估,可能有助于患者控制自己的医疗保健。未来的研究应研究患者门户招募是否有助于解决临床试验招募中持续存在的偏见,以增加女性和少数族裔群体的参与率。
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