Clin2
NCT05916417Possibly a fitActive, not recruiting

Personalized TMS dosing for PTSD using brain monitoring

Post Traumatic Stress DisorderTraumatic Brain Injury

Part of Brain & nervous system, Injuries & trauma, Mental health clinical trials.

This study tests a “personalized dosing” approach for transcranial magnetic stimulation (TMS) in adults with PTSD. It aims to see whether using brain measurements to guide the TMS settings can improve treatment while keeping participants safe.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Enrollment
60 people
Ages
18 years to 70 years
Study type
Interventional

Who can take part

  • Be between 18 and 70 years old
  • Have a confirmed PTSD diagnosis based on the CAPS-5 assessment
  • Have not changed PTSD-related meds or supportive therapy (or your care plan) in the last month, and be able to keep it steady during the study
  • Be able to understand the study, follow visit instructions, and sign consent
  • Not have medical issues that make brain stimulation unsafe, such as certain metal in the head or a seizure disorder
  • Be able to complete MRI (for example, not have metal that blocks MRI and can tolerate the scan)

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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