Fitbit One and Text Messaging Prompts to Promote Physical Activity in Overweight/Obese Adults
- Conditions
- ObesityHealth Behavior
- Interventions
- Behavioral: SMS Text Messages & Fitbit OneBehavioral: Fitbit One Only
- Registration Number
- NCT02188875
- Lead Sponsor
- University of California, San Diego
- Brief Summary
Previous studies suggest self-regulatory techniques including self-monitoring, and SMS text-messaging as an intervention modality, can modify health behaviors including physical activity (PA). The primary purpose of this study was to examine change in objectively measured PA in a randomized controlled pilot trial that tested a wearable sensor/device (Fitbit One) for self-monitoring and SMS text-messaging prompts to promote PA in overweight/obese adults. In a 2-group design, 67 participants were provided the Fitbit One and half were randomized to receive 3 daily SMS-based PA prompts. A Fitbit One was provided to facilitate self-monitoring with a wearable tracker for instant feedback and website of daily PA summaries. Outcome measures were number of steps and minutes of PA by intensity-level using two accelerometers: Actigraph GT3X+ (primary) at baseline and 6-week follow-up and Fitbit One (secondary) at baseline and weeks 1-6. The main hypothesis was that text messaging plus the Fitbit One would show a greater increase in steps and minutes of PA compared to only the Fitbit One at 6-week follow-up.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 67
- 18-69 years of age
- overweight or obese (otherwise healthy)
- does not meet recommended levels of PA (>150 min/wk of MVPA)
- owns a personal mobile phone and able to use SMS text-messaging
- owns a personal computer, has access to Internet, able to operate the Fitbit One
- fluent in English
Not provided
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description SMS Text Messages & Fitbit One SMS Text Messages & Fitbit One All study participants were provided a Fitbit One to facilitate self-monitoring of PA. Those who were randomly assigned to the intervention group were asked to indicate 3 preferred times of the day to receive text message prompts to do PA throughout the 6-week study period. Fitbit One Only Fitbit One Only An active control group was also provided the Fitbit One to facilitate self-monitoring of PA throughout the 6-week study period.
- Primary Outcome Measures
Name Time Method steps per day (Actigraph GT3X+) up to 6 weeks Number of steps per day was measured using Actigraph GT3X+ at baseline and 6-week follow-up
- Secondary Outcome Measures
Name Time Method Minutes per week of physical activity by intensity level (Actigraph GT3X+) up to 6 weeks Moderate-to-vigorous intensity physical activity (MVPA) (min/wk) and total PA (min/wk) were assessed using Actigraph GT3X+ at baseline week and 6-week follow-up
Trial Locations
- Locations (1)
UCSD Moores Cancer Center
🇺🇸La Jolla, California, United States