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Clinical Trials/NCT02265432
NCT02265432
Unknown
Not Applicable

iFit-Study: Using Mobile Technology to Promote Physical Activity

Dr Falk Mueller-Riemenschneider1 site in 1 country74 target enrollmentOctober 2014

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Physical Activity
Sponsor
Dr Falk Mueller-Riemenschneider
Enrollment
74
Locations
1
Primary Endpoint
average daily step counts
Last Updated
10 years ago

Overview

Brief Summary

The purpose of this study is to test an intervention which uses a personalized mobile-technology based approach that aims to promote physical activity and reduce sedentary behaviour in inactive working Singaporean adults.

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: 1. General physical activity educational materials 2. Wearable activity tracking devices to enable the intervention participants to self-monitor their physical activity behavior and receive real-time feedback 3. Access to an online map of Singapore providing location based information about leisure time physical activity opportunities 4. 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.

Registry
clinicaltrials.gov
Start Date
October 2014
End Date
September 2016
Last Updated
10 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Dr Falk Mueller-Riemenschneider
Responsible Party
Sponsor Investigator
Principal Investigator

Dr Falk Mueller-Riemenschneider

Assistant Professor

National University of Singapore

Eligibility Criteria

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

Outcomes

Primary Outcomes

average daily step counts

Time Frame: 6 months

Secondary Outcomes

  • time spent in minutes per week on moderate- to vigorous- intensity physical activity measured by accelerometer(6 months)
  • time spent in sedentary activities per day(6 months)
  • level of physical activity(measured by accelerometer and self-report) determined in MET minutes per week(6 months)
  • time spent in vigorous-, moderate- and light- intensity activities will be determined.(6 months)

Study Sites (1)

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