Effects of psychotherapy on brain function in PTSD
Official title: The Effects of Trauma-focused Psychotherapy on Reward Circuitry Function and Information Encoding
Run by University of Texas at Austin · NCT06096740 · Data updated 2026-11-12
This study is testing whether trauma-focused therapy can change how the brain processes rewards in people with chronic PTSD to see if it helps them feel more positive emotions.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years to 65 Years |
| Sex | All |
| Enrollment | 120 (estimated) |
| Sponsor | University of Texas at Austin Academic / other |
| Drugs / interventions | radiation |
| Locations | 1 site (Austin, Texas) |
| Status | Recruiting |
| Started | June 1, 2024 |
| Main results expected | March 1, 2029 |
| Study ends | May 1, 2029 |
| Registry record updated | May 1, 2026 |
| Trial ID | NCT06096740 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are individuals with chronic PTSD who have experienced a qualifying traumatic event and can undergo fMRI assessments.
✕Probably not a fit
Patients with a history of psychosis, bipolar disorder, or active substance dependence may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This study aims to explore how trauma-focused psychotherapy, specifically cognitive processing therapy (CPT), influences brain circuitry related to reward processing in individuals with chronic PTSD. By utilizing functional magnetic resonance imaging (fMRI), the researchers will assess changes in reward circuit function under both safe and threatening conditions. The study will involve 120 participants who will undergo clinical assessments and neurobiological evaluations before being randomized into immediate or delayed treatment groups. The goal is to understand how these changes correlate with improvements in the ability to experience positive emotions following therapy.
Why it matters
Potential benefit: If successful, this study could enhance therapeutic approaches for PTSD by providing insights into how psychotherapy can improve emotional processing.
How similar studies have gone: Previous studies have shown promising results in using psychotherapy to improve emotional processing in PTSD, suggesting this approach may be effective.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * English as primary language, and comprehension suitable to understand experimenter instructions. * Current and chronic syndromic PTSD, defined as being exposed to a DSM-5 Criterion A traumatic event, with the presence DSM-5 qualifying PTSD symptoms for at least 3 months, as assessed by the Clinician-Administered PTSD Scale for DSM-5. * Able and willing to undergo functional magnetic resonance imaging (fMRI). * Willingness to participate in repeated assessments and as part of a delayed treatment group. Exclusion Criteria: * Evidence of current or prior history of psychosis or bipolar disorder as evidenced by self-report or clinical interview. * Active substance dependence within the past 6 months as evidenced by clinical interview. * Current regular psychiatric medication use (i.e. antidepressants), except for as-needed benzodiazepine or opiate medication no more than three times per week, on average, or for short-duration stimulant medication for attention deficit hyperactivity disorder that can be skipped within 24 hours of study visits. * A recent (\<6 months) suicide attempt or current active ideation with intent. * Unremovable ferrous metal in body. * History of neurological disorder, stroke, seizures/convulsions (except febrile seizures in childhood), epilepsy, brain surgery, electroconvulsive or radiation treatment, brain hemorrhage or tumor, or thyroid disorder. * Anyone who is pregnant or trying to become pregnant. * Current or past year (\> 3 sessions), psychotherapy with a prominent exposure or cognitive restructuring component. * Previous or current (es)ketamine treatment and/ or brain stimulation/neuromodulation treatment. * Other ongoing treatment that is likely to confound experimental effects. * Previous penetrating head injury/traumatic brain injury. Mild-to-moderate traumatic brain injury without penetrating injury is allowable.
Where it's running
-
Health Discovery Building (HDB), 1601 Trinity St., Bldg B., Z0600
Austin, Texas, United States Recruiting
Study contacts
- Principal investigator: Gregory A Fonzo, PhD — The University of Texas at Austin
- Study coordinator: Lauren Enten, B.S.A
- Email: fonzolab@austin.utexas.edu
- Phone: 512-495-5856
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
-
Non-invasive vagus nerve stimulation (gammaCore) for PTSD
This study will test whether the handheld gammaCore device, which delivers mild electrical stimulation to the vagus nerve through the neck, can help adults with PTSD reduce their symptoms.
-
Non‑trauma PTSD treatment for veterans and service members with mild or moderate TBI
This pilot will test a non‑trauma psychotherapy program to help veterans and service members with mild or moderate traumatic brain injury who have PTSD.
-
Psilocybin-assisted therapy for PTSD after sexual assault
This trial will test whether a single 25 mg oral dose of psilocybin combined with therapy helps cisgender women who have PTSD from a sexual assault.
-
Short-term therapy for PTSD symptoms
This study is testing a week-long therapy to see if it can help adults with PTSD feel better and reduce their symptoms.
-
Augmented reality-enhanced exposure therapy for PTSD in U.S. military personnel
This tests whether adding augmented reality to standard exposure therapy helps U.S. military veterans and active-duty adults with PTSD.
-
Working memory training to improve fear extinction in veterans with PTSD
This study is testing if a special memory training program can help veterans with PTSD learn to manage their fears better.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.