Status:

RECRUITING

The Effects of Very Brief Exposure on PTSD in U.S. Combat Veterans

Lead Sponsor:

Children's Hospital Los Angeles

Conditions:

Post Traumatic Stress Disorder

Eligibility:

All Genders

18-50 years

Phase:

NA

Brief Summary

The goal of this clinical trial is to develop a new behavioral treatment for U.S. combat veterans with post-traumatic stress disorder (PTSD), very brief exposure to combat-related stimuli. The main qu...

Detailed Description

The prevailing treatment for Post-traumatic Stress Disorder (PTSD) is exposure: the confrontation of traumatic memories, in one form or another. Although exposure therapies are effective for combat re...

Eligibility Criteria

Inclusion

  • Patient Population
  • Males and females ages 18-50
  • Diagnostic and Statistical Manual of Mental Disorders Fifth Edition (DSM-5) diagnosis of PTSD
  • Traumatic event is a combat-based experience (e.g., being injured, watching a buddy be killed)
  • Minimum score of 18 on the Combat Experience Scale (CES)
  • Minimum score of 3 or more on Primary Care (PC)-PTSD-5
  • Participants with other cooccurring psychiatric disorders (e.g., anxiety, ADHD) will be included to ensure a representative sample.
  • Healthy Population
  • • Males and Females, ages 18-50

Exclusion

  • Patient Population
  • Treatment for PTSD, substance abuse, or mental health concerns in the past 6 months
  • 10 or more years since the combat trauma
  • Acute intoxication
  • Severe level of Substance Dependence (6 or more DSM-V symptoms)
  • Prior diagnosis of Autistic Spectrum Disorders
  • Current or past psychotic disorders or active psychotic symptoms
  • Current Bipolar I Disorder
  • Dementia
  • Neurological or serious medical conditions (e.g., stroke, epilepsy/ seizure disorder, cancer, Lupus, HIV+);
  • Traumatic brain injury
  • Healthy Population
  • Ferromagnetic implants (e.g., pacemaker), metal braces, retainers, tattoos or permanent make up w/ metallic content, transdermal medicinal patches that cannot be removed
  • Neurological or serious medical conditions (e.g., stroke, epilepsy/ seizure disorder, cancer, Lupus, HIV+);
  • Lifetime Diagnosis of PTSD, Tourette's Syndrome, Bipolar Disorder, Substance Dependence, Eating Disorder, Autism Spectrum Disorder, a psychotic disorder, Acute Stress Disorder
  • Lifetime history of traumatic event defined as a life-threatening event involving physical attack, guns, fire or explosion (i.e the kinds of traumatic events combat veterans are likely to experience)
  • Traumatic Brain Injury
  • Birth at less than 37 weeks gestational age
  • Claustrophobia
  • Anxiety Disorder, Mood Disorder, Substance Abuse Disorder, Adjustment Disorder in past 2 years
  • Treatment for mental health concern in past 2 years
  • Pregnant Females

Key Trial Info

Start Date :

March 22 2024

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

July 1 2027

Estimated Enrollment :

80 Patients enrolled

Trial Details

Trial ID

NCT06218381

Start Date

March 22 2024

End Date

July 1 2027

Last Update

December 18 2025

Active Locations (1)

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Brain Imaging Lab

Los Angeles, California, United States, 90027