Promoting Lifestyle Change via Tailored mHealth Feedback
common.study.values.description
“Promoting Lifestyle Change Via Tailored mHealth Feedback to Improve Health”
The overall purpose of this randomized clinical trial is to examine the effect and efficacy of the individualized, real-time, smartphone-based feedback of diet and physical activity self-monitoring on subsequent weight-control behaviors, weight loss outcomes and sustainability of patient engagement. Participants will be randomized to one of 2 groups: (1) Self-Monitoring -similar to what many people do on their own, subjects will self-monitor diet, physical activity using Fitbit and weight using a Bluetooth-enabled scale, and (2) Self-Monitoring +Feedback-participants will self-monitor as described for the Self-Monitoring group but also will receive tailored Feedback messages. The Self-Monitoring +Feedback participants will receive up to 4 daily discrete pop-up Feedback messages on the participant's smartphone delivered at random times during waking hours and tailored to content of recorded entries in the subjects' smartphone-based diaries and a weekly summary Feedback message about the participant's weight.
common.study.values.location
participant.ui.study.affiliations-map.online-study.header-virtual
participant.ui.study.affiliations-map.online-study.text
common.study.values.methods


Behavioral - One-on-one Session
Participants will receive a 45-minute one-on-one behavioral lifestyle program for a healthful lifestyle and weight loss.
Behavioral - Self-monitoring
Participants will receive an orientation on how to self-monitor using the smartphone and other devises
Behavioral - Feedback
Participants will receive up to 4 daily feedback messages based on progress in attaining target behavior. The feedback messages will be delivered on a variable ratio schedule and tailored to data in subjects' dietary recordings
participant.views.study.view.additional
participant.views.study.view.scientific-title
12 Months Weight Loss Study Using Feedback Messages Delivered Via Smartphone
common.study.values.clinical-trial-id
NCT03367936
participant.views.study.view.id
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