eTMS for Veterans and First Responders With PTSD
Recruiting now · Not applicable · Has a placebo group
Conditions studied: Post Traumatic Stress Disorder
In brief
A battery of physiological and behavioral data will be collected before and after application of eTMS. Participants will be veterans or first responders diagnosed with PTSD. Study will be a double-blind, sham-controlled, parallel group, randomized clinical trial.
Key facts
- Study ID
- NCT06294106
- Run by
- Virginia Polytechnic Institute and State University
- People needed
- 20
- Starts
- 2024-06-10
- Expected to finish
- 2028-09-01
- Last updated by the study team
- 2026-07-02
Who can join
Age: 18 and older, up to 65. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Veteran or first responder
- diagnosed with post-traumatic stress disorder with PCL-5 cutoff of 31 or above
You may not qualify if…
- 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 is running
- Fralin Biomedical Research Institute — Roanoke, Virginia, United States (enrolling)
Full record on ClinicalTrials.gov
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