Actively Recruiting

Phase Not Applicable
Age: 8Years - 14Years
All Genders
ID06904508

Electrophysiological Correlates of Anxiety-related Improvements Following Cognitive Behavioral Therapy for Autistic Youth in High-Need Communities

Led by Montclair State University · Updated on 2025-06-25

60

Participants Needed

2

Research Sites

N/A

Total Duration

On this page

Sponsors

M

Montclair State University

Lead Sponsor

C

Children's Hospital of Philadelphia

Collaborating Sponsor

AI-Summary

What this Trial Is About

This research aims to understand how brain activity relates to anxiety symptoms in autistic youth aged 8 to 14 from underserved communities. It investigates whether changes in brain activity align with improvements in anxiety after a cognitive behavioral therapy called Facing Your Fears (FYF). The study also explores how brain activity connects with other anxiety-related factors such as handling uncertainty and managing emotions. Participants are randomly assigned to one of two groups. One group receives the FYF intervention immediately, which is a 12-14 week outpatient group therapy involving weekly 90-minute sessions for autistic youth and their caregivers. The other group continues their usual treatment during a waitlist period and can participate in the FYF program afterward. The FYF program focuses on psychoeducation and cognitive behavioral techniques to help manage anxiety. Throughout the study, participants will undergo assessments including brain activity measurements using EEG, anxiety symptom questionnaires completed by youth and parents, and other tools measuring behavior and emotional regulation. These assessments occur before treatment and within two weeks after the intervention ends. Researchers will also monitor treatment adherence during each session. The total participation spans up to approximately 14 weeks from the first intervention session.

CONDITIONS

Brief Title

Brain Activity Changes After Cognitive Behavioral Therapy for Anxiety in Autistic Youth From High-Need Communities

Who Can Participate

Age: 8Years - 14Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Between the ages of 8 and 14
  • Significant deficits in reciprocal social behavior as shown by a score of 11 or above on the parent-report SCQ questionnaire
  • Verbally fluent in English to participate in specific ADOS-2 modules
  • Estimated verbal IQ of 70 or above as measured by the KBIT-2
  • Clinically significant anxiety symptoms based on parent-report SCARED or PRAS-ASD questionnaires
  • Have a legal guardian who can provide consent and participate in the intervention or allow another caregiver to participate alongside the child
Not Eligible

You will not qualify if you...

  • Failure to meet any of the inclusion criteria
  • Presence of severe medical or psychiatric impairments requiring intensive treatment, such as psychosis or severe aggression, as determined by the research team

AI-Screening

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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 - 12 to 14 weeks

Participants in the treatment group attend weekly 90-minute group sessions focused on cognitive behavioral therapy techniques to address anxiety.

Weekly visits for up to 14 weeks

Follow-up

Duration - Up to 2 weeks

Participants complete assessments within 2 weeks after the treatment ends to evaluate changes in anxiety symptoms and brain activity.

1 visit (in-person)

Trial Site Locations

Total: 2 locations

1

Montclair State University

Montclair, New Jersey, United States, 07043

Actively Recruiting

2

Drexel University

Philadelphia, Pennsylvania, United States, 19104

Actively Recruiting

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Research Team

E

Erin Kang, PhD

A

Arabella Peters, B.A.

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

BASIC_SCIENCE

Number of Arms

2

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