- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02265432
Using Mobile Technology to Promote Physical Activity
iFit-Study: Using Mobile Technology to Promote Physical Activity
Study Overview
Status
Conditions
Detailed Description
Considering the increasing burden in type 2 diabetes mellitus and other chronic diseases, the promotion of physical activity and reduction of sedentary behavior have an important role to improve population health.
Primarily, potential participants will be identified and recruited among participants from the Singapore Health Study (SHS) 2014 based on pre-specified selection criteria . SHS is a cross-sectional study of adults between 18 and 79 years which is conducted annually to monitor health, health behavior and health determinants among the Singapore general population.
All eligible participants will be randomized with a 1:1 ratio to intervention and control group.
Intervention group participants will receive a personalized mobile-technology based intervention to promote physical activity. It consists of four components:
- General physical activity educational materials
- Wearable activity tracking devices to enable the intervention participants to self-monitor their physical activity behavior and receive real-time feedback
- Access to an online map of Singapore providing location based information about leisure time physical activity opportunities
- Personalized text messages which include, educational information, tailored theory-based motivational messages, as well as compliance enhancing reminders
Control group participants will receive general physical activity educational materials, identical in content to that of the general educational materials of intervention group participants.
All participants will be assessed at baseline, 6 months and 12 months after the intervention by accelerometry and self-reported questionnaires.
Study Type
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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-
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Singapore, Singapore
- Recruiting
- National Univeristy of Singapore
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Men and women 25 to 65 years of age
- Physically inactive
- Working full-time for at least one more year after inclusion
- Signed written informed consent for the intervention study
- Willing to wear the activity tracker, fitbit all the time every day for 6 months
Exclusion Criteria:
- severe medical conditions prohibiting participation in physical activity
- pregnant women
- insufficient English language skills
- Participants who have already activity tracker device
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Mobile technology intervention
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Other: Control
1.General physical activity educational materials
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
average daily step counts
Time Frame: 6 months
|
6 months
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
time spent in minutes per week on moderate- to vigorous- intensity physical activity measured by accelerometer
Time Frame: 6 months
|
6 months
|
time spent in sedentary activities per day
Time Frame: 6 months
|
6 months
|
level of physical activity(measured by accelerometer and self-report) determined in MET minutes per week
Time Frame: 6 months
|
6 months
|
time spent in vigorous-, moderate- and light- intensity activities will be determined.
Time Frame: 6 months
|
6 months
|
Other Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Quality of life
Time Frame: 6 months
|
6 months
|
proportion of participants being physical active according to current recommendations (at least 150 minutes of moderate intensity activity or an appropriate equivalent of vigorous activity)
Time Frame: 6 months
|
6 months
|
Recall, use and perceived usefulness of intervention and intervention components
Time Frame: 6 months
|
6 months
|
Knowledge, attitudes and perceived barriers to physical activity
Time Frame: 6 months
|
6 months
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Falk Mueller-Riemenschneider Falk <falk.mueller-riemenschneider, MSc, MD, Saw Swee Hock School of Public Health, National University of Singapore
Study record dates
Study Major Dates
Study Start
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- R -608-000-071-112
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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-
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