N/A
N=210
Applying Mobile Persuasive Technologies to Increase Physical Activity in Women
Sedentary Lifestyle · Physical Activity
Bottom Line
View on ClinicalTrials.gov: NCT01280812 ↗Enrolled (actual)
210
Serious AEs
2.4%
Results posted
Sep 2020
Primary outcome: Primary: Accelerometer (Omron Active Style Pro HJA-350IT) Measured Daily Steps — 5837; 5063; 5384; 8709 Steps/Day
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- Mobile phone based physical activity intervention with maintenance plus (Behavioral); Mobile phone based physical activity intervention with maintenance regular (Behavioral); Control (pedometer only) (Behavioral)
- Age
- Adult, Older Adult · 25+ yrs
- Sex
- Female
- Sponsor
- University of California, San Francisco
- Primary completion
- Apr 2015
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Accelerometer (Omron Active Style Pro HJA-350IT) Measured Daily Steps |
5837; 5063; 5384; 8709; 8096; 6608 | — |
| PRIMARY Accelerometer (Omron Active Style Pro HJA-350IT) Measured Moderate to Vigorous Physical Activity (Minutes Per Day) |
43.5; 38.0; 45.7; 67.6; 61.6; 53.0 | — |
| SECONDARY Self-reported Physical Activity Measured by the 7-day Physical Activity Recall (PAR) |
33.1; 32.9; 32.9; 34.5; 34.8; 33.7 | — |
| SECONDARY Modified Self-Efficacy for Physical Activity Survey |
19.0; 19.8; 18.8; 18.1; 18.0; 19.1 | — |
| SECONDARY Social Support for Physical Activity (Family) |
32.8; 31.5; 32.0; 34.8; 35.6; 31.6 | — |
| SECONDARY Social Support for Physical Activity (Friends) |
31.8; 31.5; 31.1; 34.7; 35.1; 31.1 | — |
Summary
The primary purpose of this study is to assess the efficacy of the mobile phone-based physical activity intervention on increasing physical activity compared to the control group.
Eligibility Criteria
Inclusion Criteria
- Sedentary lifestyle at work and/or during leisure time
- Intend to be physically active
- Female, age >25 to 69
- Access to a home telephone or a mobile phone
- Speak and read English
Exclusion Criteria
- Known medical conditions or other physical problems that need special attention in an exercise program
- Plan a trip abroad during the first 4 months of the study period.
- Pregnant/Delivered a baby during the last 6 months
- Known severe hearing or speech problem
- Body Mass Index (BMI) > 43.0 kg/m2
- Currently participate in lifestyle modification programs or research studies that may potentially confound the results of the study
- History of bariatric surgery or future plans for bariatric surgery in the next 12 months
Data sourced from ClinicalTrials.gov (NCT01280812). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.