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Research on Autistic Children Based on Eye Tracking and Magnetic Resonance Imaging

Development of a social gaze improvement system for children with autism based on augmented reality eye tracking - Research on Autistic Children Based on Eye Tracking and Magnetic Resonance Imaging

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500095342
Enrollment
Unknown
Registered
2025-01-06
Start date
2025-01-10
Completion date
Unknown
Last updated
2025-01-13

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

Conditions

Autism Spectrum Disorder

Interventions

Experimental group:The social gaze improvement system was intervened for 1 month. The intervention was carried out 5 days a week, 3 times a day, each time for about 15 minutes, and the intervention in
Control group:The social gaze improvement system was involved in sham intervention for 1 month, and after 1 month, the social gaze improvement system intervention was applied for 1 month. The interven

Sponsors

Chinese PLA General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
3 Years to 12 Years

Inclusion criteria

Inclusion criteria: (1) Has been professionally evaluated and meets the diagnostic criteria for autism spectrum disorders; (2) Aged between 3 to 12 years old; (3) The results of the Autism Diagnostic Observation Schedule, 2nd edition (ADOS-2) meet the standard cut-off for autism spectrum disorders; (4) The guardian of the subject voluntarily participated in the intervention, was able to cooperate in completing the intervention and signed an informed consent form.

Exclusion criteria

Exclusion criteria: (1) A diagnosis of comorbid psychotic symptoms according to DSM-IV or DSM-V that meets the diagnostic criteria for other mental disorders, such as schizophrenia, schizoaffective disorder, and bipolar disorder; (2) Self-injury or suicidal behavior within the last year; (3) Contraindications to EGT such as the presence of metal foreign bodies in the body or any other electronic equipment implanted in the body; (4) Having neurological diseases or medical history such as epilepsy, traumatic brain injury; and (5) Have severe visual, auditory or motor impairments that prevent them from cooperating with examinations and interventions; and (6) Have severe hepatic or renal dysfunction or other serious physical illnesses; (7) Have received neuromodulation interventions such as EGT, transcranial electrical stimulation, transcranial focused ultrasound, etc. within 3 months prior to enrollment; (8) Those who are participating in other clinical research trials.

Design outcomes

Primary

MeasureTime frame
Transcranial stimulation data;Fixation Duration on the Region of Interest;

Secondary

MeasureTime frame
Autism Diagnostic Observation Schedule Score, Second Edition;The Diagnostic and Statistical Manual of Mental Disorders-V Score;

Countries

China

Contacts

Public ContactShijun Li

Chinese PLA General Hospital

shijunli07@yeah.net+86 10 6693 7564

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026