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Motor Function Assessment and VR-based Motor Training in Adults With Autism Spectrum Disorder

Motor Function Assessment and VR-based Motor Training in Adults With Autism Spectrum Disorder

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07134569
Enrollment
200
Registered
2025-08-21
Start date
2023-12-15
Completion date
2027-07-31
Last updated
2026-01-12

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

Conditions

Autism

Keywords

Virtual Reality, motor training

Brief summary

The goal of this clinical trial is to learn if autism affect motor functions, including muscle strength, balance, and motor control? Additionally, understanding the motor functions, cognitive functions, and brain activation in individuals with autism, and verifying whether motor training can effectively improve muscle strength, balance, and motor control. The main questions aim to answer are: \[primary hypothesis or outcome measure 1\]? \[primary hypothesis or outcome measure 2\]? If there is a comparison group: Researchers will compare \[arm information\] to see if \[insert effects\]. Participants will \[describe the main tasks participants will be asked to do, interventions they'll be given and use bullets if it is more than 2 items\].

Interventions

Six weeks, twice per week.

Sponsors

National Taiwan University Hospital
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 45 Years
Healthy volunteers
Yes

Inclusion criteria

\> The ASD Group Inclusion criteria: * young adult aged between 18 and 45 years who had a diagnosis of ASD from a licensed mental health or medical professional based on DSM-5. * was motivated to complete the 6-week VR-based motor function training. * had a full-scale IQ \> 70 on the WAIS-IV.

Exclusion criteria

* a history of major mental illness (e.g., bipolar affective disorder, schizophrenia, or psychosis), neurological diseases (e.g., stroke, lumbar radiculopathy, or spinal cord injury) that hamper walking function, or neurosurgery. * visual impairment and/or hearing impairment that would preclude participation in motor assessment or training. * The Non-ASD control group Inclusion criteria: * young adult aged between 18 and 45 years who do not have a diagnosis of ASD. * had a full-scale IQ \> 70 on the WAIS-IV.

Design outcomes

Primary

MeasureTime frameDescription
The performance of movement operational assessment40 minutesParticipants will take movement operational assessment, which composed of different tests, such as Timed Up and Go Test (TUG), the 10-meter walk test (10MWT) and the 6-minute walk test (6WMT)
The performance of motor coordination control1 hour, twicethe performance recorded with Vicon, an motion capture system, and Single Leg Stance Test

Secondary

MeasureTime frame
The N-back Task performance40 minutes
The performance of Timed Up and Go Test (TUG)1 minute, twice
The performance of the 10-meter walk test (10MWT)1 minute, twice
The performance of 6-minute walk test (6WMT)6 minutes, twice

Countries

Taiwan

Contacts

Primary ContactYi Ling Chien, Clinical Professor
ntuh.peers@gmail.com+886 2-23123456

Outcome results

None listed

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