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Clinical Trials/KCT0008504
KCT0008504
Not Yet Recruiting
N/A

An Exploratory Clinical Trial Study to Evaluate the Effectiveness of Metaverse and Online Social Intervention Program for Improving Sociality in Children with High Functioning Autism Spectrum

Seoul National University Hospital0 sites60 target enrollmentTBD

Overview

Phase
N/A
Intervention
Not specified
Conditions
Mental and behavioural disorders
Sponsor
Seoul National University Hospital
Enrollment
60
Status
Not Yet Recruiting
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional Study
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • (1\) Children who meet the criteria for autism or autism spectrum based on the ADOS\-2 test within the last two years
  • (2\) If there is no test result within the last two years to determine the condition of (1\) above, the ADOS\-2 diagnostic test will be performed if the ASSQ score for screening is 14 or higher. Then, the child can be included if the test result meets the condition of (1\) above.
  • (3\) Children with a full\-scale IQ higher than 70 and { (at least one of the VCI or PRI subscore of 80 or higher) or (at least two of the VCI , VSI, and FRI subscore of 80 or higher) }.
  • (4\) Children who do not plan to change the number and content of other ongoing treatments such as physical therapy, cognitive therapy, speech therapy, and medication during the study period.
  • (5\) Both the child and their caregivers have consented to the study.

Exclusion Criteria

  • \- Children with a history of congenital/acquired brain damage such as cerebral palsy
  • \- Children with severe developmental delays or behavioral problems which would make it difficult for them to cooperate with activities on the metaverse.
  • \- Children participating in the social skills intervention program of the Rudolph Institute for Children's Social Development during the study period
  • \- Children who refuse to participate in the study

Outcomes

Primary Outcomes

Not specified

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