- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07446530
Research on the Impact of Gamification Movement on Children With Sensory Integration Disorders
February 28, 2026 updated by: Guang Yang, Prof. Dr., Northeast Normal University
A Randomized Controlled Trial on the Impact of Gamification Movement on the Motor Skills of Children With Sensory Integration Disorders
This study aims to investigate the impact of gamified exercise intervention on the sensory integration ability and basic motor skills of children with sensory integration dysfunction.
A randomized controlled trial design will be adopted, recruiting 48 children with sensory integration dysfunction and randomly assigning them to three groups: the gamified exercise group, the sensory integration training group, and the regular physical education curriculum group.
Study Overview
Status
Enrolling by invitation
Conditions
Study Type
Interventional
Enrollment (Estimated)
48
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
-
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Jilin
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Changchun, Jilin, China, 130022
- Faculty of Sports Science
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-
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
- Child
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- According to the Developmental Rating Scale for Sensory Integration Abilities in Children, the subject's score in any of the tests for vestibular sense, proprioception, and tactile sense is less than 40; they are willing to participate in this study; and their guardian has signed the informed consent form.
Exclusion Criteria:
- Individuals with abnormal physical appearance; individuals with severe illnesses; individuals with severe cognitive impairments.
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: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Triple
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Gamified exercise
|
Students in the gamification group will undergo a 12-week gamification exercise program, with interventions conducted three times a week, each lasting 60 minutes.
The main components include warm-up, game segment, and cool-down.
Participants' attendance and adherence will be recorded during the intervention period.
|
|
Active Comparator: Sensory Integration Training Group
|
Students in the sensory integration training group will undergo a 12-week sensory integration training program, with interventions conducted three times a week for 60 minutes each time.
The main components include warm-up, sensory integration training, and relaxation.
Participants' attendance and compliance will be recorded during the intervention period.
|
|
Active Comparator: Regular physical education courses
|
Students in the regular physical education curriculum group will undergo a 12-week regular physical education program, with interventions conducted three times per week for 60 minutes each time.
The main components include warm-up, physical activities, and relaxation.
Participants' attendance and adherence will be recorded during the intervention period.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Sensory integration ability
Time Frame: month 3
|
The sensory integration ability of young children was evaluated by measuring their scores on the sensory integration scale before and after the intervention.
|
month 3
|
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Basic motor skills
Time Frame: month 3
|
The level of basic motor skills development in young children was evaluated by measuring their performance in completing 13 actions before and after the intervention.
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month 3
|
|
physical fitness
Time Frame: Three months
|
By measuring the seven physical indicators of the participants before and after the intervention, including height (in centimeters), 10-meter shuttle run (seconds), standing long jump (centimeters), tennis throw distance (meters), consecutive double jumps (seconds), sit-and-reach test (centimeters), and walking on a balance beam (seconds), their physical health status can be evaluated.
|
Three months
|
|
Pediatric Balance Scale,PBS
Time Frame: Three months
|
The balance ability of the participants was evaluated by measuring their scores in the balance test before and after the intervention.
|
Three months
|
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 (Estimated)
March 1, 2026
Primary Completion (Estimated)
May 25, 2026
Study Completion (Estimated)
June 20, 2026
Study Registration Dates
First Submitted
January 23, 2026
First Submitted That Met QC Criteria
February 28, 2026
First Posted (Actual)
March 3, 2026
Study Record Updates
Last Update Posted (Actual)
March 3, 2026
Last Update Submitted That Met QC Criteria
February 28, 2026
Last Verified
February 1, 2026
More Information
Terms related to this study
Other Study ID Numbers
- CCEE202603
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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