CompletedNot Applicable

The YourMove Study: Optimizing Individualized and Adaptive mHealth Interventions Via Control Systems Engineering Methods

United States386 participantsStarted 2022-10-07

Plain-language summary

The purpose of this study is to determine the efficacy of a new digital health tool that uses a phone and smartwatch to encourage physical activity and increase weekly amounts of Moderate to Vigorous Physical Activity (MVPA) over 12 months among adults compared to a digital health intervention that mimics a standard of care corporate wellness program.

Who can participate

Age range25 Years – 80 Years

SexALL

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Age 25-80 years old * Intend to be available for a 12-month intervention * Willing and able to attend 3 measurement visits over 12-months * Willing and able to use a smartphone and text messaging * Willing and able to use the wearable and corresponding app * Willing and able to walk and engage in moderate-intensity physical activity * Healthy enough to participate based on the Physical Activity Readiness Questionnaire * BMI between 18-40 kg/m\^2 Exclusion Criteria: * Psychiatric or medical conditions that prohibit compliance with the study protocol * Enrolled in or planning to enroll in a physical activity program during the study period * Those with a mechanical medical implant, such as a pacemaker

What they're measuring

Change in minutes of moderate-to-vigorous physical activity (MVPA)

Timeframe: Baseline, 12-months

Trial details

NCT IDNCT05598996

SponsorUniversity of California, San Diego

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2025-11-08

View on ClinicalTrials.gov More Inactivity, Physical trials