IPS TMS for Patients with PTSD | Clinical Research Studies Listing

Recruiting

18 years - 60 years

All

Phase 1

120 participants needed

1 Location

Brief description of study

This study will be the first of its kind to explore the impact of continuous theta burst stimulation (cTBS) to the intraparietal sulcus (IPS) on arousal symptoms among patients with posttraumatic stress disorder (PTSD). We will demonstrate that IPS cTBS results in significant target engagement in the form of reduction in anxiety-potentiated startle (APS) compared to sham cTBS and will identify the ideal dose of cTBS.

Eligibility of study

You may be eligible for this study if you meet the following criteria:

Conditions: PTSD
Age: 18 years - 60 years
Gender: All

Male or Female, Age 18-60, Diagnosed with PTSD, right-handed, no metal implants, not pregnant, no history of seizures/seizure disorders, ability to read and write in English

Updated on 02 Jul 2025. Study ID: 21-0951

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