Using Mobile Technology to Promote Physical Activity

November 12, 2015 updated by: Dr Falk Mueller-Riemenschneider

iFit-Study: Using Mobile Technology to Promote Physical Activity

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.

Study Overview

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.

Study Type

Interventional

Enrollment (Anticipated)

74

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Singapore, Singapore
        • Recruiting
        • National Univeristy of Singapore

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

25 years to 65 years (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

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

This section provides details of the study plan, including how the study is designed and what the study is measuring.

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
  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
Other: Control
1.General physical activity educational materials

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

This is where you will find people and organizations involved with this study.

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

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

October 1, 2014

Primary Completion (Anticipated)

April 1, 2016

Study Completion (Anticipated)

September 1, 2016

Study Registration Dates

First Submitted

October 9, 2014

First Submitted That Met QC Criteria

October 15, 2014

First Posted (Estimate)

October 16, 2014

Study Record Updates

Last Update Posted (Estimate)

November 16, 2015

Last Update Submitted That Met QC Criteria

November 12, 2015

Last Verified

November 1, 2015

More Information

Terms related to this study

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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