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AutismNCT07323550

Single-Dual Task Performance in Children With Autism Spectrum Disorder and Typically Developing Children

An observational study of Autism and Dual Task, run by Atlas University at 1 site in Turkey (Türkiye).

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

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. Read more about this study

Who is it for?
Ages 5 to 16 yearsHealthy volunteers can take part
Conditions the study is for
Autism, Dual Task
What is being tested?
Single- and Dual-Task Condition Assessment
How many people
90 participants
Where
1 siteTurkey (Türkiye)
Study dates
1 Sep 2025to 5 Feb 2026
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 5 to 16 years
  • All sexes
  • Healthy volunteers accepted
  • Child

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.

Who may be able to join

  • 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:
Show all 11Show fewer
  • 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

Who cannot join

  • 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
Show all 10Show fewer
  • 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

Trial locations and contacts

1 site in 1 country.

Turkey (Türkiye)1 site
  • Moren Language, Speech, and Development Center

    Ordu

Other trials in Turkey (Türkiye)

About this study

Official title: 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.

Conditions
Autism, Dual Task
Being tested
Single- and Dual-Task Condition Assessment
Medical subject headings
Autistic Disorder

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Single- and Dual-Task Condition AssessmentOther

    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.

Study groups in NCT07323550
Study groupRoleWhat they receive
Autism Spectrum DisorderThe 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.
Receives: Other: Single- and Dual-Task Condition Assessment
Typically developing childA control group consisting of children with normal development, matched to the OSB group in terms of age and gender variables, was included.
Receives: Other: Single- and Dual-Task Condition Assessment

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Postural control performance

    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).

    Measured: Day 3

Secondary outcomes (3)
  1. Walking Performance

    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).

    Measured: Day 3

  2. Motor Performance

    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.

    Measured: Day 3

  3. Childhood Autism Rating Scale

    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 .

    Measured: Day 1

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted7 Jan 2026
  2. Study start1 Sep 2025
  3. Primary completion1 Oct 2025
  4. Study completion5 Feb 2026

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Cross-sectional
Enrolment
90 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07323550
Sponsor's protocol ID
2024-ATLAS-MSEHF-003
Status last verified
Feb 2026
First submitted
23 Dec 2025
Last updated
6 Feb 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

An observational study of Autism and Dual Task, run by Atlas University at 1 site in Turkey (Türkiye).

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 11 inclusion and 10 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 6 Feb 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Turkey (Türkiye). Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Postural control performance (time frame: Day 3). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 6 Feb 2026.

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