- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04593199
Physical Activity Promotion in Children Using a Novel Smartphone Game: A Pilot Randomized Controlled Trial
October 28, 2021 updated by: Sam Liu, University of Victoria
Increasing physical activity is critical for children's overall health.
Smartphone apps using gamification has shown promise to increasing physical activity using game techniques.
This study is a 4-week randomized controlled trial using a gamified smartphone app to determine acceptability and preliminary effectiveness to increase physical activity in children.
Study Overview
Status
Recruiting
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Anticipated)
160
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 Contact
- Name: Sam Liu, PhD
- Phone Number: 2507218392
- Email: samliu@uvic.ca
Study Contact Backup
- Name: Sam Lapusniak, Masters
- Phone Number: 2508094655
- Email: samlapusniak@uvic.ca
Study Locations
-
-
British Columbia
-
Victoria, British Columbia, Canada, V8W2Y2
- Recruiting
- University of Victoria
-
-
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
8 years to 14 years (Child)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Children aged 8-14 years old
- Not meeting the recommended Canadian physical activity guidelines of 60min per day of moderate-to-vigorous physical activity
- English-literate
- Normal to corrected vision
Exclusion Criteria:
- Diagnosis or injury that prevents physical activity participation
- No access to a smartphone or tablet
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 |
|---|---|
|
Sham Comparator: Physical Activity Tracking App Only
Over a four week period, participants were asked to use the Fitbit app to track their daily physical activity.
|
Participants were asked to use the Fitbit app to track and sync their daily physical activity.
Other Names:
|
|
Active Comparator: Physical Activity Tracking + Gamified Smartphone App
Over a four week period, participants were asked to use the Fitbit app to track their daily physical activity.
Additionally, they were asked to use the gamified smartphone app, Draco, during the intervention period.
|
The primary objective was to determine the acceptability and satisfaction of the Draco app among children.
Secondary objective was to evaluate if the Draco app could improve physical activity levels (steps, and moderate-to-vigorous physical activity) and intrinsic motivation for physical activity in children.
The gamified smartphone app, Draco, is a virtual pet simulator where you care for a pet by exercising, walking, and answering healthy lifestyle questions.
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
User satisfaction with gamified smartphone app
Time Frame: 4 weeks
|
User satisfaction was measured using an adapted version of the short form Intrinsic Motivation Inventory used by Ahn, Johnsen & Ball, 2019.
Items pertained to the enjoyment, satisfaction of using the app and if the experience was unenjoyable.
Scores are rated on a 5 point Likert scale where 1 is the lowest score and 5 is the highest. 1 = Not true for me; 2 = Not really true for me; 3 = Sometimes true for me; 4 = Often true for me; 5 = Very true for me.
|
4 weeks
|
|
Acceptability with gamified smartphone app
Time Frame: 4 weeks
|
Exit interviews were performed after the intervention period to determine satisfaction and acceptability.
Questions related to their experience using the app, their physical activity behavior (before, during, and after the intervention period) and recommendations for app content
|
4 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Steps
Time Frame: 4 weeks
|
Steps were collected using a Fitbit over the intervention period.
Fitbit is a previously validated and reliable instrument to measure physical activity (Feehan et al., 2018).
|
4 weeks
|
|
Physical activity minutes
Time Frame: 4 weeks
|
Minutes of physical activity engaged in by the participants were collected using a Fitbit device worn by participants.
The device is worn while the participant is engaging in physical activity.
The intensity of exercise is calculated by heartrate.
Fitbit is a previously validated and reliable instrument to measure physical activity (Feehan et al., 2018).
|
4 weeks
|
|
Motivation for physical activity
Time Frame: 4 weeks
|
Motivation for physical activity was measured using an adapted version of the Intrinsic Motivation Inventory used by Ahn, Johnsen & Ball, 2019.
Questions related to perceived competence to physical activity, perceived autonomy to physical activity and perceived relatedness to the app.
The items addressed perceived competence, perceived autonomy, and relatedness.
Scores are rated on a 5 point Likert scale where 1 is the lowest score and 5 is the highest. 1 = Not true for me; 2 = Not really true for me; 3 = Sometimes true for me; 4 = Often true for me; 5 = Very true for me.
|
4 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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 (Actual)
January 28, 2019
Primary Completion (Anticipated)
March 1, 2022
Study Completion (Anticipated)
April 15, 2022
Study Registration Dates
First Submitted
October 13, 2020
First Submitted That Met QC Criteria
October 13, 2020
First Posted (Actual)
October 19, 2020
Study Record Updates
Last Update Posted (Actual)
November 5, 2021
Last Update Submitted That Met QC Criteria
October 28, 2021
Last Verified
October 1, 2021
More Information
Terms related to this study
Other Study ID Numbers
- UVic181243
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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