PTSD Trial, Recruiting NCT06294106 Sponsor: Virginia Polytechnic Institute and State University Condition: PTSD
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PTSD Trial, Recruiting

NCT06294106
Recruiting Not Applicable

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • You are a veteran or a first responder (such as a police officer, firefighter, or paramedic)
  • You have been diagnosed with post-traumatic stress disorder (PTSD) and scored 31 or higher on a standard PTSD symptom checklist called the PCL-5

Who may not be able to join:

  • You have claustrophobia (fear of enclosed spaces)
  • You have any reason you cannot safely have an MRI scan (such as certain metal implants or devices in your body)
  • You are currently pregnant
  • You have medical, psychological, or neurological conditions that are not well controlled or stable
  • Your brain wave (EEG) activity cannot be measured in a specific way needed for the study (confirm with trial site)
  • You have previously had electroconvulsive therapy (ECT) or repetitive transcranial magnetic stimulation (rTMS), which are types of brain stimulation treatments
  • You have a history of a brain lesion or increased pressure inside the skull
  • You have had a stroke
  • You have a history of other conditions affecting the brain or nervous system
  • You or a family member have a history of epilepsy or seizures
  • You are taking certain medications that may interfere with the study (confirm with trial site for specific medications)

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 21 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Principal Investigator: Wynn Legon, PhD, Virginia Polytechnic Institute and State University

Phone: 540-526-2261

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Not Applicable
Sponsor
Virginia Polytechnic Institute and State University
Registry
ClinicalTrials.gov
Start date
10 June 2024
Est. completion
1 June 2028

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Adverse Events; Report of Symptoms

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 21 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov