TrialPath
← Back to searchRecruiting

Targeted Accelerated TMS for Post-Traumatic Stress Disorder

NCT07245641 · Brigham and Women's Hospital
In plain English

Click the button to translate this study into plain language — what it is, who qualifies, and what participation looks like.

About this study
In a recent study in Nature Neuroscience, the investigators analyzed three independent datasets to derive a brain circuit causally linked to PTSD in military veterans. Investigators found that brain lesions that reduce the probability of developing PTSD (n=193) were connected to the same brain circuit based on the functional connectivity profiles of individual patients with PTSD using fMRI (n=180). Finally, investigators demonstrated that scalp-targeted TMS to our circuit rapidly improved PTSD symptoms (n=20). Separately, the investigators partnered with a private clinic to administer open-label, circuit-targeted aTMS to patients with PTSD (n=8). Investigators found that the treatment was safe and tolerable. Response and remission rates were 75% and 63%, respectively. Of note, these response and remission rates assess outcomes up to 4 weeks after the treatment ends. This approach captures individual variability in response trajectory and aligns with our own data from aTMS treatment of TRD. The strength of these findings has inspired us to launch a pilot randomized controlled aTMS trial in which the investigators prospectively target our PTSD circuit using each patient's neuroimaging data in combination with the accelerated TMS treatment protocol.
Eligibility criteria
Inclusion Criteria * Age 18-65 * DSM-5 diagnosis of PTSD per PTSD Checklist for DSM-5 (CAPS-5) * At least moderate symptoms of PTSD per PCL-5 (≥21) * English proficiency sufficient to understand risks/benefits * No new medications or medication increases before, during, or after aTMS * Primary clinician (e.g. psychiatrist, therapist, psychologist, APRN, PA, etc.) responsible for psychiatric care before, during, and after the trial * Agreement to lifestyle considerations: * Abstain from becoming pregnant from screening to one-month after treatment (the MRI visit) * Continue usual intake patterns of caffeine- or xanthine-containing products (e.g. coffee, tea, soft drinks, chocolate) throughout treatment * No changes to routine intake of alcohol, tobacco, and recreational drugs if patients are using them at baseline for at least 24 hours before the start of each MRI and TMS session
Study design
Enrollment target: 40 participants
Allocation: randomized
Masking: quadruple
Age groups: adult, older_adult
Timeline
Starts: 2025-12-15
Estimated completion: 2028-01
Last updated: 2026-02-02
Interventions
Procedure: Transcranial Magnetic Stimulation
Primary outcomes
  • PTSD Checklist with Criterion A for DSM-5 (PCL-5) (Before treatment to 1-month post treatment)
Sponsor
Brigham and Women's Hospital · other
With: Mass General Home Base Program
Contacts & investigators
ContactInterventional Psychiatry Research Group · contact · bwhtap@mgb.org · 6175253526
All locations (1)
Brigham and Women's HospitalRecruiting
Boston, Massachusetts, United States
Targeted Accelerated TMS for Post-Traumatic Stress Disorder · TrialPath