是否愿意通过患者门户网站接受健康筛查、研究招募以及用于健康监测的居家自我检测试剂盒:试点定量调查。

IF 2 Q3 HEALTH CARE SCIENCES & SERVICES JMIR Formative Research Pub Date : 2024-11-22 DOI:10.2196/59837
Elizabeth Lockhart, Jordan Gootee, Leah Copeland, DeAnne Turner
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引用次数: 0

摘要

背景:美国的医疗系统越来越多地使用患者门户网站。尽管一些患者使用门户网站进行临床治疗,但患者对使用门户网站进行研究相关活动、完成健康筛查以及申请家庭自我检测试剂盒的看法尚不明确:我们旨在了解患者对使用电子健康门户网站进行研究、健康相关筛查以及由患者发起的家庭自我检测的看法:来自一家大型中西部城市医疗系统患者参与研究中心的患者(人数=105)完成了一项包含 23 个项目的网络调查,内容涉及患者门户网站(MyChart)的使用情况以及使用患者门户网站进行研究、风险评估和自我检测包的意愿。调查结果显示了频率和百分比:几乎所有参与者(102/105,97.1%)都至少访问过一次 MyChart,其中大多数人(44/102,43.1%)表示每月至少登录一次。参与者表示登录 "我的医疗图表 "是为了查看化验结果或其他健康数据(89/105,84.8%),因为他们收到了登录信息(85/105,81%),以及给医护人员留言(83/105,79%)。为查看处方药物(16/105,15.2%)和了解更多健康状况(29/105,27.6%)而登录的参与者较少。大多数参与者表示是在电脑上通过网站登录 MyChart(70/105,66.7%)或在智能手机上通过应用程序登录 MyChart(54/105,51.4%)。当被问及如果通过 MyChart 与他们联系,他们有多大可能参与不同类型的研究时,大多数人(90/105,85.7%)表示他们有可能回答调查问卷、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%)和抑郁症(54/105,51.4%),并有兴趣接受 COVID-19 (66/105,62.9%)、胆固醇(63/105,60%)、结肠癌(62/105,59%)和过敏症(56/105,53.3%)的居家自测包。所有结果均无明显的人口统计学差异(所有 P 值均大于 0.05):结论:患者门户网站可用于研究招募、发送研究相关信息、吸引患者回答风险评估、阅读健康信息和完成其他临床任务。基于种族和性别的研究结果并不明显,这表明患者门户网站可能是招募研究参与者和开展研究的可接受工具。允许患者在门户网站上申请自我检测试剂盒和完成风险评估可能有助于患者掌握自己的医疗保健。未来的研究应探讨患者门户网站的招募是否有助于解决临床试验招募中持续存在的偏见,以增加妇女和少数种族群体的参与人数。
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Willingness to Be Contacted via a Patient Portal for Health Screening, Research Recruitment, and at-Home Self-Test Kits for Health Monitoring: Pilot Quantitative Survey.

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.

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来源期刊
JMIR Formative Research
JMIR Formative Research Medicine-Medicine (miscellaneous)
CiteScore
2.70
自引率
9.10%
发文量
579
审稿时长
12 weeks
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