RECRUITING

eTMS for Veterans and First Responders With PTSD

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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.

Official Title

Electroencephalogram (EEG) Personalized Transcranial Magnetic Stimulation (eTMS) for Post-Traumatic Stress Disorder (PTSD)

Quick Facts

Study Start:2024-06-10
Study Completion:2026-04
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06294106

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years to 65 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Veteran or first responder
  2. * diagnosed with post-traumatic stress disorder with PCL-5 cutoff of 31 or above
  1. * Claustrophobia
  2. * Contraindications to MRI
  3. * Pregnant
  4. * Uncontrolled medical, psychological, or neurological conditions
  5. * Unable to calculate EEG alpha frequency
  6. * History of ECT or rTMS
  7. * History of intracranial lesion or increased intracranial pressure
  8. * History of stroke
  9. * History of other neurologic conditions
  10. * Family history of epilepsy
  11. * Personal history of epilepsy
  12. * certain medications

Contacts and Locations

Study Contact

Jessica Florig, MPH
CONTACT
540-526-2261
jnw@vtc.vt.edu

Principal Investigator

Wynn Legon, PhD
PRINCIPAL_INVESTIGATOR
Virginia Polytechnic Institute and State University

Study Locations (Sites)

Fralin Biomedical Research Institute
Roanoke, Virginia, 24016
United States

Collaborators and Investigators

Sponsor: Virginia Polytechnic Institute and State University

  • Wynn Legon, PhD, PRINCIPAL_INVESTIGATOR, Virginia Polytechnic Institute and State University

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2024-06-10
Study Completion Date2026-04

Study Record Updates

Study Start Date2024-06-10
Study Completion Date2026-04

Terms related to this study

Additional Relevant MeSH Terms

  • Post Traumatic Stress Disorder