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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04010409
Other study ID # 201809069RINA
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date January 8, 2019
Est. completion date December 31, 2024

Study information

Verified date December 2022
Source National Taiwan University Hospital
Contact Yi Ling Chien, M.D., Ph.D.
Phone 886-2-2312-3456
Email ylchien@hotmail.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This study aims to investigate the ability of reading emotions by the Eyes task in adults with ASD, and examine the gazing pattern and frontal activation during the task. We plan to recruit 50 adults with ASD and 50 typically-developing adults. Eye-tracking and frontal activation (measured by functional near-infrared spectroscopy) will be examined during the Eyes task.


Description:

Autism spectrum disorder (ASD) is a clinical syndrome characterized by mindreading deficits, or Theory of Mind deficits. The Reading the Mind in the Eyes task (abbreviated as the Eyes task) was developed to assess the mindreading deficits as a hallmark of social deficits of ASD. This study aims to investigate the ability of reading emotions by the Eyes task in adults with ASD, and examine the gazing pattern and frontal activation during the task. We plan to recruit 50 adults with ASD and 50 typically-developing adults. All the participants will complete clinical measures and the Eyes task. Eye-tracking and frontal activation (measured by functional near-infrared spectroscopy) will be examined during the Eyes task.


Recruitment information / eligibility

Status Recruiting
Enrollment 60
Est. completion date December 31, 2024
Est. primary completion date December 31, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 20 Years to 50 Years
Eligibility Inclusion Criteria: - Adult aged between 20 and 50 years who had a diagnosis of ASD based on DSM-5. - Had a full-scale IQ > 70 on WAIS-IV. Exclusion Criteria: - A history of major mental illness (e.g., bipolar affective disorder, schizophrenia) or neurological diseases. - Visual impairment and that would preclude participation.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
no intervention
no intervention

Locations

Country Name City State
Taiwan National Taiwan University Hospital Taipei

Sponsors (1)

Lead Sponsor Collaborator
National Taiwan University Hospital

Country where clinical trial is conducted

Taiwan, 

Outcome

Type Measure Description Time frame Safety issue
Primary eye tracking indicators eye tracking indicators 30 min
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