Actively Recruiting

Phase Not Applicable
Age: 12Years - 18Years
All Genders
ID05185128

Neural Basis of Social Cognition Deficits in Youth With Autism and Schizophrenia

Led by Loma Linda University · Updated on 2026-02-04

90

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Social difficulties are common in neuropsychiatric disorders like autism spectrum disorder (ASD) and schizophrenia spectrum disorder (SSD). This research investigates the shared and unique brain mechanisms behind these social challenges in adolescents with ASD and SSD. The study aims to understand how a targeted 16-week social skills program may influence brain networks involved in social understanding and improve social outcomes in these groups compared to typically developing peers. Participants include 30 adolescents with ASD and 30 with SSD who will undergo the Program for the Education and Enrichment of Relational Skills (PEERS), a parent-assisted intervention involving weekly 90-minute sessions over 16 weeks. This program focuses on improving friendship quality and social skills through teaching communication, humor, conflict resolution, and friendship development. A control group of 30 typically developing adolescents will undergo the same MRI and behavioral assessments 16 weeks apart without receiving the intervention. Throughout the study, all participants will complete MRI scans including functional MRI and magnetic resonance spectroscopy before and after the intervention period. Behavioral and social cognition assessments will be conducted to measure changes in social skills and brain activity. Researchers will analyze brain connectivity, activation, and neurochemical changes to understand treatment effects and relate these findings to improvements in social behavior. The study duration includes pre- and post-intervention assessments spanning 16 weeks, aiming to identify neural biomarkers linked to social skills improvements.

CONDITIONS

Brief Title

Neural Basis of Social Cognition Deficits

Who Can Participate

Age: 12Years - 18Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adolescents aged 12 to 18 years
  • Diagnosis of autism spectrum disorder or schizophrenia spectrum disorder confirmed by clinical assessments
  • Verbal and full-scale IQ of 70 or higher
  • Ability to participate in MRI scanning and behavioral assessments
  • Typically developing adolescents without psychiatric history for control group
Not Eligible

You will not qualify if you...

  • History of significant medical or neurological conditions affecting brain imaging (e.g., epilepsy, brain tumor)
  • Any psychiatric history in typically developing control participants
  • Presence of MRI contraindications such as metal fragments, metal implants, or nonremovable braces
  • Inability to undergo MRI scanning safely or complete study procedures

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Outpatient Treatment

Duration - 16 weeks

Participants with autism spectrum disorder (ASD) or schizophrenia spectrum disorder (SSD) undergo the 16-week PEERS social skills intervention, consisting of weekly 90-minute sessions focused on improving social communication and friendship skills. Typically developing control participants do not receive the intervention but participate in assessments.

Weekly visits for 16 weeks

Outpatient Treatment

Duration - Pre- and post-intervention assessments spanning 16 weeks

Participants complete cognitive assessments and MRI imaging before and after the 16-week intervention period to evaluate treatment effects and compare with typically developing controls.

2 visits (in-person) for MRI and cognitive assessments

Trial Site Locations

Total: 1 location

1

Loma Linda U

Loma Linda, California, United States, 92354

Actively Recruiting

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Research Team

A

Aarti Nair, PhD

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NON_RANDOMIZED

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

2

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