PTSD Trial, Recruiting
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:
- People who are between 18 and 80 years of age
- People who are at least 3 months past the event that caused their mild traumatic brain injury (mTBI)
- People who have a confirmed history of mild traumatic brain injury, either with or without PTSD, as determined through specific standardised assessment tools used by the trial team
- People who report at least a moderate level of difficulty with at least one of four thinking or memory-related complaints, as measured by a specific symptom questionnaire (the Neurobehavioral Symptom Inventory)
Who may not be able to join:
- People who are currently taking part in another research study
- People who are not fluent in English, both in speaking and reading
- People who had epilepsy before their brain injury
- People who have been receiving treatment for active seizures in the past 6 months
- People who are currently taking medications that can lower the seizure threshold, including certain antipsychotics, trazodone, or tramadol
- People who have had surgery on blood vessels in the brain or on heart valves
- People who have a history of bleeding in the brain, blood vessel conditions affecting the brain, or degenerative brain disorders
- People who have a current or past diagnosis of a psychotic spectrum disorder, such as bipolar disorder or schizophrenia
- People with significant heart disease, as determined by a doctor reviewing their medical records
- People who are pregnant at the time of joining or at any point during the study
- People with reasons they cannot safely have an MRI or a type of brain stimulation treatment (called TMS/iTBS), such as claustrophobia or metal in the eyes, face, or brain
- People who have implanted medical devices such as a cardiac pacemaker or defibrillator, cochlear implant, nerve stimulator, or metal clips in the brain
- People diagnosed with a moderate or severe traumatic brain injury (for example, loss of consciousness lasting more than 30 minutes, or extended memory loss after the injury)
- People whose prescribed mental health medications have been changed — including starting, stopping, or adjusting the dose — within the 30 days before the study screening
- People who are taking prescribed central nervous system (CNS) stimulant medications and are not willing to stop taking them during the study
- People who test positive for opioids without a valid prescription, or people on prescribed opioids taking more than the equivalent of 200 mg of morphine per day
- People whose results on a memory and validity test suggest the answers may not be a reliable reflection of their actual abilities, as assessed by a neuropsychologist on the research team
- People who are actively suicidal with a plan to cause harm or a recent attempt, as identified through a structured clinical interview
- People showing signs of increased pressure in the brain, detected through an eye examination or a baseline MRI scan
- People with moderate or severe cannabis use disorder, defined by 4 or more specific symptoms on a clinical assessment tool
- People with severe alcohol use disorder, defined by 6 or more specific symptoms on a clinical assessment tool
- People with a resting systolic blood pressure of 170 or higher at baseline
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.
Contact this trial
Principal Investigator: Theresa LB Pape, Dr.PH, Northwestern University
Phone: 708-878-0578
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
Where this trial is recruiting
Primary endpoints
Change in the Mayo Portland Adaptability Inventory (MPAI)
Can't join this trial?
Data last synced from ClinicalTrials.gov: 26 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.