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Clinical Trial Summary

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.


Clinical Trial Description

Veterans and first responders diagnosed with PTSD will be studied to evaluate safety and efficacy of an EEG personalized TMS paradigm. All participants will undergo 2 days of extensive testing prior to eTMS application and 2 days of testing after. Testing will include MRI, OPM, EEG, behavioral tasks, questionnaires, and an EEG sleep study. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06294106
Study type Interventional
Source Virginia Polytechnic Institute and State University
Contact Jessica Florig, MPH
Phone 540-526-2261
Email jnw@vtc.vt.edu
Status Recruiting
Phase N/A
Start date June 10, 2024
Completion date April 2026

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