PTSD Trial, Recruiting NCT06544408 Sponsor: Florida State University Condition: PTSD
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PTSD Trial, Recruiting

NCT06544408
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:

  • Adults between 18 and 65 years of age.
  • People who have been diagnosed with PTSD according to standard diagnostic criteria, with a symptom checklist score above 33.
  • People who have not changed their psychiatric medications or supportive talk therapy in the month before their first visit, and for whom it is medically appropriate to keep that treatment stable for the whole trial.
  • People who are able to understand what the study involves, agree to take part in writing, and follow the study procedures for its full duration.

Who may not be able to join:

  • People who have a medical reason that makes brain stimulation treatment unsafe, such as metal fragments in the head, a history of seizures, a brain tumour, stroke, brain aneurysm, or multiple sclerosis.
  • People who have had an active substance use disorder in the last 3 months, or whose current substance use puts them at increased risk or causes significant problems in daily life.
  • People with dementia or another condition affecting thinking and memory that would prevent them from engaging in the treatment.
  • People with a history or diagnosis of schizophrenia, schizoaffective disorder, delusional disorder, or another psychotic illness that would make safe participation in the trial not possible.
  • People assessed as being at significant risk of suicide, as determined by the clinical team.
  • People for whom obsessive-compulsive disorder (OCD) is their primary diagnosis (though people with some OCD symptoms alongside PTSD may still be considered).
  • People who cannot stop taking medications that significantly lower the seizure threshold, such as certain older antidepressants or clozapine.
  • People who are currently pregnant, planning to become pregnant, or where pregnancy is suspected.
  • People with unstable medical conditions that could make it unsafe to receive the brain stimulation treatment used in this trial.
  • People with a severe traumatic brain injury.
  • People who do not speak English, as rapid communication during treatment delivery is required for safety.
  • People involved in significant ongoing legal cases or compensation claims that the research team determines could affect the study, particularly where mental health is being assessed as part of those proceedings.
  • People who have previously received active brain stimulation (TMS) to specific areas of the front of the brain, or who have previously had electroconvulsive therapy (ECT).

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 27 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: Frank A Kozel, MD, Florida State University

Phone: 850-644-2824

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
Florida State University
Registry
ClinicalTrials.gov
Start date
6 November 2024
Est. completion
30 June 2028

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Clinician-Administered PTSD Scale for DSM-V (CAPS-V) to determine left dl-PFC accel-TMS efficacy; Clinician-Administered PTSD Scale for DSM-V (CAPS-V) to determine dm-PFC accel-TMS efficacy; Clinician-Administered PTSD Scale for DSM-V (CAPS-V) to determine superior symptom reduction

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: 27 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