TMS-fNIRS Personalized Dosing

Recruiting N/A Interventional Study
Post Traumatic Stress Disorder Traumatic Brain Injury
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 – 70
Sex
Any
Study type
Interventional
Purpose
Other
Participants needed
60 (estimated)
Sponsor
Florida State University · Other
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About This Trial
The intent of this study is to establish technical feasibility in a clinical population (PTSD, with or without mild TBI) of personalized TMS-fNIRS technology. Thereby demonstrating the utility of transcranial magnetic stimulation - functional near-infrared spectroscopy (TMS-fNIRS) technology as a direct measure of frontal brain activity, potentially replacing the indirect motor threshold procedure…
Trial Locations
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Eligibility Criteria
Inclusion Criteria 1. Adults ages 18-70 years. 2. Eligible for consideration of treatment with TMS for PTSD. 3. Diagnosis of PTSD based on CAPS-5. 4. No changes in psychotropic medication (if taking psychotropic medication) and/or changes in supportive psychotherapy for 1 month prior to initial vis…
Contacts

Isabelle Taylor, MA

850-728-3881

fsun@med.fsu.edu

CONTACT

Kevin Johnson, PhD, RN

850-728-3881

fsun@med.fsu.edu

CONTACT