- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07323550
Single-Dual Task Performance in Children With Autism Spectrum Disorder and Typically Developing Children
February 5, 2026 updated by: Gamze Demircioğlu, Atlas University
Comparing Single and Dual Task Effects in Children With Autism Spectrum Disorder and Typically Developing Children
This study aims to compare the effects of single-task and dual-task conditions on motor performance and postural control in children with Autism Spectrum Disorder (ASD) and typically developing children.
Participants' performance under single-task and dual-task conditions involving cognitive load will be evaluated to examine how cognitive demands affect physical task performance in both groups.
Study Overview
Status
Completed
Intervention / Treatment
Study Type
Observational
Enrollment (Actual)
90
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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Ordu, Turkey (Türkiye)
- Moren Language, Speech, and Development Center
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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
Yes
Sampling Method
Non-Probability Sample
Study Population
The study population consists of children aged 5 to 16 years, including children diagnosed with mild to moderate Autism Spectrum Disorder and age- and sex-matched typically developing children.
All participants are able to follow basic instructions and complete single-task and dual-task motor assessments.
Written informed consent is obtained from the legal guardians of all participants prior to enrollment.
Description
Inclusion Criteria:
- Autism Spectrum Disorder (ASD) Group:
- Aged between 5 and 16 years
- Diagnosed with mild to moderate Autism Spectrum Disorder based on Childhood Autism Rating Scale (CARS) scores
- Ability to understand basic visual, auditory, and verbal instructions
- Sufficient cognitive capacity to follow dual-task instructions
Typically Developing Control Group:
- Age- and sex-matched with the ASD group
- No history of neurological, psychiatric, sensory, orthopedic, or developmental disorders
- No acute or chronic medical conditions
- No pain complaints during assessment
- Written informed consent obtained from a legal guardian
Exclusion Criteria:
Both Groups:
- History of neurological disorders, epilepsy, or seizures
- Orthopedic or musculoskeletal conditions affecting balance
- Visual or hearing impairments (except corrected vision or hearing with glasses or hearing aids)
- Use of assistive devices for walking or balance
- Use of medications affecting balance or motor performance
- Presence of comorbid psychiatric disorders
- Inability to cooperate adequately during assessment
- Absence from more than two consecutive assessment sessions
- Participation in another intervention program during the study period
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
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
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Autism Spectrum Disorder
The diagnosis of Autism Spectrum Disorder was made by child and adolescent psychiatrists in accordance with the Diagnostic and Statistical Manual of Mental Disorders - Fifth Edition (DSM-5) diagnostic criteria.
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Participants will perform motor tasks under single-task and dual-task conditions.
In the dual-task condition, a concurrent cognitive task will be added to the motor task to increase cognitive load.
Performance during these conditions will be assessed to examine the effects of cognitive load on motor performance and postural control.
No therapeutic intervention, medication, or device is applied.
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Typically developing child
A control group consisting of children with normal development, matched to the OSB group in terms of age and gender variables, was included.
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Participants will perform motor tasks under single-task and dual-task conditions.
In the dual-task condition, a concurrent cognitive task will be added to the motor task to increase cognitive load.
Performance during these conditions will be assessed to examine the effects of cognitive load on motor performance and postural control.
No therapeutic intervention, medication, or device is applied.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Postural control performance
Time Frame: Day 3
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Postural control will be assessed using the Nintendo Wii Balance Board under both single-task and dual-task conditions.
The mean value of center of pressure sway in the medio-lateral and anterior-posterior directions will be calculated during a 30-second quiet standing task with eyes open.
Values will be expressed in millimeters (mm).
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Day 3
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Walking Performance
Time Frame: Day 3
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Gait performance will be assessed under single-task and dual-task conditions using a sensor-based mobile gait analysis application.
The mean walking speed will be calculated during a 6-meter walking task performed at a self-selected comfortable pace.
Walking speed values will be expressed in meters per second (m/s).
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Day 3
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Motor Performance
Time Frame: Day 3
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Motor performance will be assessed under single-task and dual-task conditions using the Sit-to-Stand App.
During a 30-second sit-to-stand test, the mean vertical power will be calculated based on average vertical velocity normalized to body weight.
Mean power values will be expressed in watts (W) and used as an indicator of lower extremity muscle performance.
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Day 3
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Childhood Autism Rating Scale
Time Frame: Day 1
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The Childhood Autism Rating Scale (CARS) was used to assess autism spectrum disorder and rate its severity.
The CASR is an observation-based assessment tool developed by Schopler, Reichler, and Renner in 1980.The scale consists of 15 items and covers behavioral areas such as social relationships, imitation, emotional responses, physical movements, adaptation, visual and auditory responses, olfactory responses, language communication, and intelligence .
In the scoring of the test, 15-29 points indicate no signs of autism, 30-37 points indicate mild to moderate levels, and 38-60 points indicate severe levels of autistic traits .
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Day 1
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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)
September 1, 2025
Primary Completion (Actual)
October 1, 2025
Study Completion (Actual)
February 5, 2026
Study Registration Dates
First Submitted
December 23, 2025
First Submitted That Met QC Criteria
December 23, 2025
First Posted (Actual)
January 7, 2026
Study Record Updates
Last Update Posted (Actual)
February 6, 2026
Last Update Submitted That Met QC Criteria
February 5, 2026
Last Verified
February 1, 2026
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2024-ATLAS-MSEHF-003
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
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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