Actively Recruiting

Phase Not Applicable
Age: 12Years - 17Years
All Genders
NCT05423444

Neural Connectivity During Therapy for Adolescent PTSD

Led by The University of Texas Health Science Center at San Antonio · Updated on 2026-01-13

180

Participants Needed

1

Research Sites

221 weeks

Total Duration

On this page

Sponsors

T

The University of Texas Health Science Center at San Antonio

Lead Sponsor

N

National Institute of Mental Health (NIMH)

Collaborating Sponsor

AI-Summary

What this Trial Is About

Posttraumatic stress disorder in adolescence impairs neurobiological networks underlying cognitive, social and emotional skills. Neuroimaging research that seeks to identify the neural mechanisms of treatments for PTSD could lead to novel treatments, but progress has been slow using current methods. The proposed study uses an innovative approach to identify neural mechanisms of specific phases of trauma-focused therapy for youth with PTSD, allowing a new understanding of brain changes associated with the process of therapy.

CONDITIONS

Official Title

Neural Connectivity During Therapy for Adolescent PTSD

Who Can Participate

Age: 12Years - 17Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Ages 12 to 17 years and Tanner stage 2 or above
  • History of interpersonal trauma
  • PTSD symptoms with a rating of 2 or higher on at least one symptom from each of the 4 clusters using the Clinician-Administered PTSD Scale for Children and Adolescents
  • PTSD symptoms lasting at least one month
Not Eligible

You will not qualify if you...

  • Current or past use of psychiatric medications
  • Severe suicidal or homicidal ideation
  • Current hospitalization
  • Receiving other psychotherapy or previous treatment with TF-CBT
  • History of head injury with loss of consciousness longer than 5 minutes
  • IQ below 85
  • Major medical illness
  • MRI contraindications such as metal in the body or braces on teeth
  • Diagnosis of psychosis, bipolar 1, autism, developmental disorder, or panic disorder
  • First-degree family member with psychosis or bipolar I disorder
  • Substance dependence within past 3 months or frequent current drug use

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

UT Health Department of Psychiatry

San Antonio, Texas, United States, 78229

Actively Recruiting

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Research Team

A

Amy Garrett, PhD

CONTACT

N

Natalia Gomez-Giulilani

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

BASIC_SCIENCE

Number of Arms

2

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