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弗雷明汉心脏研究中现场与远程移动设备支持的比较:基于观察性研究设计的数字化随访中使用健康电子心研究:随机试点研究。

Comparison of On-Site Versus Remote Mobile Device Support in the Framingham Heart Study Using the Health eHeart Study for Digital Follow-up: Randomized Pilot Study Set Within an Observational Study Design.

机构信息

Section of Endocrinology, Diabetes, Nutrition, and Weight Management, Boston University School of Medicine, Boston, MA, United States.

Framingham Heart Study, Framingham, MA, United States.

出版信息

JMIR Mhealth Uhealth. 2019 Sep 30;7(9):e13238. doi: 10.2196/13238.

Abstract

BACKGROUND

New electronic cohort (e-Cohort) study designs provide resource-effective methods for collecting participant data. It is unclear if implementing an e-Cohort study without direct, in-person participant contact can achieve successful participation rates.

OBJECTIVE

The objective of this study was to compare 2 distinct enrollment methods for setting up mobile health (mHealth) devices and to assess the ongoing adherence to device use in an e-Cohort pilot study.

METHODS

We coenrolled participants from the Framingham Heart Study (FHS) into the FHS-Health eHeart (HeH) pilot study, a digital cohort with infrastructure for collecting mHealth data. FHS participants who had an email address and smartphone were randomized to our FHS-HeH pilot study into 1 of 2 study arms: remote versus on-site support. We oversampled older adults (age ≥65 years), with a target of enrolling 20% of our sample as older adults. In the remote arm, participants received an email containing a link to enrollment website and, upon enrollment, were sent 4 smartphone-connectable sensor devices. Participants in the on-site arm were invited to visit an in-person FHS facility and were provided in-person support for enrollment and connecting the devices. Device data were tracked for at least 5 months.

RESULTS

Compared with the individuals who declined, individuals who consented to our pilot study (on-site, n=101; remote, n=93) were more likely to be women, highly educated, and younger. In the on-site arm, the connection and initial use of devices was ≥20% higher than the remote arm (mean percent difference was 25% [95% CI 17-35] for activity monitor, 22% [95% CI 12-32] for blood pressure cuff, 20% [95% CI 10-30] for scale, and 43% [95% CI 30-55] for electrocardiogram), with device connection rates in the on-site arm of 99%, 95%, 95%, and 84%. Once connected, continued device use over the 5-month study period was similar between the study arms.

CONCLUSIONS

Our pilot study demonstrated that the deployment of mobile devices among middle-aged and older adults in the context of an on-site clinic visit was associated with higher initial rates of device use as compared with offering only remote support. Once connected, the device use was similar in both groups.

摘要

背景

新的电子队列(e-Cohort)研究设计为收集参与者数据提供了资源有效的方法。目前尚不清楚,如果在没有直接的面对面接触的情况下实施电子队列研究,是否能够达到成功的参与率。

目的

本研究的目的是比较 2 种不同的设置移动健康(mHealth)设备的入组方法,并评估电子队列试点研究中设备使用的持续情况。

方法

我们将弗雷明汉心脏研究(Framingham Heart Study,FHS)的参与者共同纳入弗雷明汉心脏研究-健康电子心脏(FHS-Health eHeart,HeH)试点研究,这是一个具有收集 mHealth 数据基础设施的数字队列。有电子邮件地址和智能手机的 FHS 参与者被随机分配到我们的 FHS-HeH 试点研究中的 2 个研究臂之一:远程支持与现场支持。我们对老年人(年龄≥65 岁)进行了抽样,目标是将我们样本的 20%作为老年人。在远程臂中,参与者收到一封包含注册网站链接的电子邮件,注册后,他们会收到 4 个可与智能手机连接的传感器设备。现场臂中的参与者被邀请到现场 FHS 设施,并获得注册和连接设备的现场支持。设备数据至少跟踪 5 个月。

结果

与拒绝的人相比,同意我们试点研究的人(现场,n=101;远程,n=93)更有可能是女性、受过高等教育和年轻。在现场臂中,设备的连接和初始使用比远程臂高出≥20%(活动监测器的平均百分比差异为 25%[95%CI 17-35],血压袖带为 22%[95%CI 12-32],秤为 20%[95%CI 10-30],心电图为 43%[95%CI 30-55]),现场臂的设备连接率为 99%、95%、95%和 84%。一旦连接,在 5 个月的研究期间,研究臂之间的设备使用情况相似。

结论

我们的试点研究表明,在现场诊所就诊的情况下,向中年和老年人部署移动设备与更高的初始设备使用率相关,而仅提供远程支持则相反。一旦连接,两组的设备使用情况相似。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b94/6792023/d94a56c638ea/mhealth_v7i9e13238_fig1.jpg

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