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Accepted for/Published in: JMIR mHealth and uHealth

Date Submitted: Mar 22, 2019
Open Peer Review Period: Mar 25, 2019 - Apr 27, 2019
Date Accepted: Jul 19, 2019
(closed for review but you can still tweet)

The final, peer-reviewed published version of this preprint can be found here:

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

Spartano N, Lin H, Sun F, Lunetta K, Trinquart L, Valentino M, Manders E, Pletcher M, Marcus G, McManus D, Benjamin E, Fox C, Olgin J, Murabito J

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

JMIR Mhealth Uhealth 2019;7(9):e13238

DOI: 10.2196/13238

PMID: 31573928

PMCID: 6792023

Comparison of on-site versus remote support in a mobile-device randomized pilot study: A collaboration between the Framingham Heart Study and Health eHeart Study (FHS-HeH)

  • Nicole Spartano; 
  • Honghuang Lin; 
  • Fangui Sun; 
  • Kathryn Lunetta; 
  • Ludovic Trinquart; 
  • Maureen Valentino; 
  • Emily Manders; 
  • Mark Pletcher; 
  • Gregory Marcus; 
  • David McManus; 
  • Emelia Benjamin; 
  • Caroline Fox; 
  • Jeffrey Olgin; 
  • Joanne Murabito

ABSTRACT

Background:

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

Objective:

To compare two distinct implementation strategies for co-enrolling participants from the Framingham Heart Study (FHS) into the FHS-Health eHeart (HeH) Pilot Study, a digital cohort with infrastructure for collecting mHealth data.

Methods:

FHS participants who had an email address and smartphone were randomized to our FHS-HeH pilot study into one of two study arms: remote vs. on-site support. We over-sampled older adults (≥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 four 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 was tracked for at least 5 months.

Results:

Compared to individuals that declined, individuals that consented to our pilot study (n=101 on-site, n=93 remote) were more likely to be women, highly educated, and younger. In the on-site arm, connection and initial use of devices was ≥20% higher than the remote arm (mean percent difference 25% [95% confidence interval, 17-35] for activity monitor, 22% [12-32] for blood pressure cuff, 20% [10-30] for scale, and 43% [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 study arms. Although recruitment of older adults ≥65 years was less efficient than adults <65 years (we consented 50% of those recruited ≥65 years vs. 75% of <65 years), rates of device connection and continued use of devices for 5 months was >70% across devices.

Conclusions:

Our pilot study demonstrated that 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 to offering only remote support. Once connected, device use was similar in both groups.


 Citation

Please cite as:

Spartano N, Lin H, Sun F, Lunetta K, Trinquart L, Valentino M, Manders E, Pletcher M, Marcus G, McManus D, Benjamin E, Fox C, Olgin J, Murabito J

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

JMIR Mhealth Uhealth 2019;7(9):e13238

DOI: 10.2196/13238

PMID: 31573928

PMCID: 6792023

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