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Using Mobile Technology to Promote Physical Activity

iFit-Study: Using Mobile Technology to Promote Physical Activity

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02265432
Enrollment
74
Registered
2014-10-16
Start date
2014-10-31
Completion date
2016-09-30
Last updated
2015-11-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Physical Activity

Keywords

Physical activity, Sedentary behavior

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.

Interventions

BEHAVIORALGeneral physical activity educational materials
DEVICEWearable activity tracking devices (fitbit)
OTHERonline map

Sponsors

Dr Falk Mueller-Riemenschneider
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
25 Years to 65 Years
Healthy volunteers
Yes

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

Design outcomes

Primary

MeasureTime frame
average daily step counts6 months

Secondary

MeasureTime frame
time spent in minutes per week on moderate- to vigorous- intensity physical activity measured by accelerometer6 months
time spent in sedentary activities per day6 months
level of physical activity(measured by accelerometer and self-report) determined in MET minutes per week6 months
time spent in vigorous-, moderate- and light- intensity activities will be determined.6 months

Other

MeasureTime frame
Recall, use and perceived usefulness of intervention and intervention components6 months
Knowledge, attitudes and perceived barriers to physical activity6 months
Quality of life6 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)6 months

Countries

Singapore

Contacts

Primary ContactFalk Mueller-Riemenschneider Falk <falk.mueller-riemenschneider, MBBS,MSc,MD
falk.mueller-riemenschneider@nuhs.edu.sg+65 66013122

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026