eFHS Messaging Trial
NCT03516019 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 650
Last updated 2021-02-11
Summary
In this research the investigators will develop and test an innovative scalable mobile health and digital cardiovascular monitoring system within a longitudinal deeply characterized cohort with three components: 1) smartphone application (app) designed to promote adherence, integrate digital and mHealth information, and facilitate communication with participants and researchers; 2) smartwatch activity monitoring using the Apple iWatch; and 3) home blood pressure (BP) monitoring using the Withings blood pressure device.
The objective of the messaging trial is to test the effect of messaging strategies on improving participants' long-term use of and engagement with our selected mobile health technologies and on increasing response rate of survey data collection.
Conditions
Interventions
- OTHER
-
personalized notices
The personalized notices take into account if data were received over the previous week, and accordingly encourages the participant to use the device and send her data, or encourages the participant to continue using the device and sending data. A library of personalized notices with alternative motivational content was developed. Each time a notification is sent, it will be drawn at random from the library.
- OTHER
-
standard notices
The standard notices which are neutral and invite participants to wear the watch daily and to measure their blood pressure weekly.
- OTHER
-
am notices
notifications sent at 7 am.
- OTHER
-
pm notices
notifications sent at 7 pm.
- OTHER
-
weekday notices
notifications sent on Wednesday
- OTHER
-
weekend notices
notifications sent on Saturday
Sponsors & Collaborators
-
Robert Wood Johnson Foundation
collaborator OTHER -
Boston University
lead OTHER
Principal Investigators
-
Joanne Murabito, MD ScM · Framingham Heart Study
Study Design
- Allocation
- RANDOMIZED
- Purpose
- PREVENTION
- Masking
- SINGLE
- Model
- FACTORIAL
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2018-05-19
- Primary Completion
- 2019-03-23
- Completion
- 2019-03-23
Countries
- United States
Study Locations
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