Using eTMS to treat PTSD in veterans and first responders
Official title: Electroencephalogram (EEG) Personalized Transcranial Magnetic Stimulation (eTMS) for Post-Traumatic Stress Disorder (PTSD)
Run by Virginia Polytechnic Institute and State University · NCT06294106 · Data updated 2026-11-12
This study is testing a new brain treatment called eTMS to see if it can help veterans and first responders with PTSD feel better.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years to 65 Years |
| Sex | All |
| Enrollment | 20 (estimated) |
| Sponsor | Virginia Polytechnic Institute and State University Academic / other |
| Locations | 1 site (Roanoke, Virginia) |
| Status | Recruiting |
| Started | June 10, 2024 |
| Main results expected | June 2028 |
| Study ends | September 2028 |
| Registry record updated | July 2, 2026 |
| Trial ID | NCT06294106 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates for this study are veterans or first responders who have been diagnosed with PTSD.
✕Probably not a fit
Patients with contraindications to MRI, uncontrolled medical conditions, or a history of certain neurological issues 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 clinical trial evaluates the safety and efficacy of an EEG personalized Transcranial Magnetic Stimulation (eTMS) approach for veterans and first responders diagnosed with PTSD. Participants will undergo extensive physiological and behavioral testing before and after the eTMS application, including MRI, EEG, and various behavioral assessments. The study is designed as a double-blind, sham-controlled, parallel group, randomized trial to ensure robust results.
Why it matters
Potential benefit: If successful, this treatment could significantly improve PTSD symptoms in veterans and first responders.
How similar studies have gone: While the approach of using eTMS is innovative, similar studies have shown promise in treating PTSD with neuromodulation techniques.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Veteran or first responder * diagnosed with post-traumatic stress disorder with PCL-5 cutoff of 31 or above Exclusion Criteria: * Claustrophobia * Contraindications to MRI * Pregnant * Uncontrolled medical, psychological, or neurological conditions * Unable to calculate EEG alpha frequency * History of ECT or rTMS * History of intracranial lesion or increased intracranial pressure * History of stroke * History of other neurologic conditions * Family history of epilepsy * Personal history of epilepsy * certain medications
Where it's running
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Fralin Biomedical Research Institute
Roanoke, Virginia, United States Recruiting
Study contacts
- Principal investigator: Wynn Legon, PhD — Virginia Polytechnic Institute and State University
- Study coordinator: Jessica Florig, MPH
- Email: jnw@vtc.vt.edu
- Phone: 540-526-2261
Similar studies
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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.