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Digital Health Tool for Physical Activity (YourMove Trial)

N/A
Recruiting
Led By Daniel Rivera, PhD
Research Sponsored by University of California, San Diego
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up baseline, 12 months
Awards & highlights

YourMove Trial Summary

This trial tests a digital health tool to help adults become more physically active over 12 months.

Who is the study for?
This trial is for adults aged 25-80 who are healthy enough to be active, can use a smartwatch and app, and have a BMI of 18-40. They must commit to a year-long program and attend three check-ups. It's not for those in other activity programs, with conditions affecting participation or with devices like pacemakers.Check my eligibility
What is being tested?
The study tests a new mobile health tool that pairs with your phone and watch to boost physical activity over the course of a year. It will be compared against standard digital wellness programs to see if it helps people do more moderate-to-vigorous exercise.See study design
What are the potential side effects?
Since this trial involves increasing physical activity through technology, side effects might include typical exercise-related issues such as muscle soreness or strain but should otherwise have minimal risks.

YourMove Trial Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~baseline, 12 months
This trial's timeline: 3 weeks for screening, Varies for treatment, and baseline, 12 months for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Change in minutes of moderate-to-vigorous physical activity (MVPA)
Secondary outcome measures
Anxiety
Change in Body Mass Index (BMI)
Gait
+27 more
Other outcome measures
Alcohol Use Disorder
Smoke

YourMove Trial Design

2Treatment groups
Experimental Treatment
Active Control
Group I: COT-Based InterventionExperimental Treatment1 Intervention
The COT-based intervention will include the following to improve both steps/day (move more), and improving minutes/week of MVPA (exercise): adaptive daily steps/day goal-setting plus feedback; positive reinforcement (i.e., points, which translate to gift cards), self-monitoring of both steps/day and min/week MVPA; education about MVPA sent via text message in both conditions; planning support for scheduling bouts of MVPA via SMS in both conditions; and motivational messages sent via SMS in both conditions, and the use of a self-experimentation tool (REFLECT), developed based on prior successful pilot efforts, focused on fostering effective self-regulatory capacities of individuals.
Group II: ControlActive Control1 Intervention
The non-COT approach was designed to be an equivalent to emerging standard of care options for digital health worksite wellness programs to increase PA (control) for a 12-month study period. Participants assigned to the non-COT-based (control) group will receive the latest Fitbit Versa smartwatch and will download the Fitbit smartphone app. Unlike the intervention group, the daily step goal and the accompanying number of points will be static (10,000 steps/day; 150 points/day, respectively). The goal will be delivered to participants via the standard Fitbit app features and points will be communicated via email. Participants will also receive a weekly PA goal (150 minutes of MVPA/per week) and the same accompanying motivational and informative texts that the intervention group receives. Control participants will not complete the physical activity and exercise reflection and planning exercise (Reflect).

Find a Location

Who is running the clinical trial?

National Cancer Institute (NCI)NIH
13,717 Previous Clinical Trials
40,952,978 Total Patients Enrolled
5 Trials studying Sedentary Lifestyle
173 Patients Enrolled for Sedentary Lifestyle
Small Steps Labs, LLCUNKNOWN
2 Previous Clinical Trials
718 Total Patients Enrolled
Arizona State UniversityOTHER
286 Previous Clinical Trials
109,187 Total Patients Enrolled

Media Library

COT-Based Intervention Clinical Trial Eligibility Overview. Trial Name: NCT05598996 — N/A
Sedentary Lifestyle Research Study Groups: COT-Based Intervention, Control
Sedentary Lifestyle Clinical Trial 2023: COT-Based Intervention Highlights & Side Effects. Trial Name: NCT05598996 — N/A
COT-Based Intervention 2023 Treatment Timeline for Medical Study. Trial Name: NCT05598996 — N/A
~157 spots leftby Jun 2025
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