TMS for Veterans Attending a 2-week Intensive Outpatient Program for PTSD

Part of paid clinical trials in Chicago, Illinois.

Sponsor
Rush University Medical Center
Study ID
NCT06271733
Status
Completed

Conditions

Eligibility Criteria

Sex
ALL
Age
18 Years - 65 Years
Healthy Volunteers
Not accepted

Interventions

  • TMS — DEVICE
    2 sessions of iTBS per day for 5 days

Study Details

The goal of this study is to determine whether complementing regular intensive PTSD treatment with intermittent theta burst stimulation (iTBS) applied to the right dorsolateral prefrontal cortex (DLPFC) can improve treatment response for individuals attending a 2-week intensive outpatient program (IOP) for PTSD.

Key Dates

Start date
Jan 11, 2022
Status verified
Feb 2026
Primary completion
Jun 27, 2025
Completion
Oct 27, 2025

Study Design

Enrollment
6 participants (actual)
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT

Arms

  • Experimental: TMS

Primary Outcome Measure

PTSD Checklist for DSM-5 (PCL-5) [ Time Frame: 1 month-follow up ]

Locations (1)

FacilityCityStateZIPSite coordinators
Rush University Medical CenterChicagoIllinois60612-

Find similar trials in Chicago, IL

By condition
PTSD (post-traumatic stress disorder)
By specialty
PsychiatryMental healthBehavioral health
By research site
Rush University Medical Center· Chicago, IL

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