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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: ClinicalTrials.gov
Last refreshed on: 12 December 2020
Main ID:  NCT01280812
Date of registration: 23/11/2010
Prospective Registration: Yes
Primary sponsor: University of California, San Francisco
Public title: Applying Mobile Persuasive Technologies to Increase Physical Activity in Women
Scientific title: Applying Mobile Persuasive Technologies to Increase Physical Activity in Women
Date of first enrolment: February 2011
Target sample size: 210
Recruitment status: Completed
URL:  https://clinicaltrials.gov/show/NCT01280812
Study type:  Interventional
Study design:  Allocation: Randomized. Intervention model: Parallel Assignment. Primary purpose: Prevention. Masking: Single (Outcomes Assessor).  
Phase:  N/A
Countries of recruitment
United States
Contacts
Name:     Yoshimi Fukuoka, Ph.D.
Address: 
Telephone:
Email:
Affiliation:  University of California, San Francisco
Key inclusion & exclusion 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



Age minimum: 25 Years
Age maximum: 69 Years
Gender: Female
Health Condition(s) or Problem(s) studied
Sedentary Lifestyle
Physical Activity
Intervention(s)
Behavioral: Control (pedometer only)
Behavioral: Mobile phone based physical activity intervention with maintenance plus
Behavioral: Mobile phone based physical activity intervention with maintenance regular
Primary Outcome(s)
Accelerometer (Omron Active Style Pro HJA-350IT) Measured Moderate to Vigorous Physical Activity (Minutes Per Day) [Time Frame: Baseline, 3 and 9 months]
Accelerometer (Omron Active Style Pro HJA-350IT) Measured Daily Steps [Time Frame: Baseline, 3, and 9 months]
Secondary Outcome(s)
Self-reported Physical Activity Measured by the 7-day Physical Activity Recall (PAR) [Time Frame: Baseline, 3 and 9 months]
Social Support for Physical Activity (Friends) [Time Frame: Baseline, 3 and 9 months]
Modified Self-Efficacy for Physical Activity Survey [Time Frame: Baseline, 3 and 9 months]
Social Support for Physical Activity (Family) [Time Frame: Baseline, 3 and 9 months]
Secondary ID(s)
5R01HL104147-02
P0031274
Source(s) of Monetary Support
Please refer to primary and secondary sponsors
Secondary Sponsor(s)
American Heart Association
National Heart, Lung, and Blood Institute (NHLBI)
Ethics review
Results
Results available: Yes
Date Posted: 23/09/2020
Date Completed:
URL: https://clinicaltrials.gov/ct2/show/results/NCT01280812
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