Clinical Trial

TMS + Exposure Therapy for Pediatric OCD

Study acronym: NExT
Active, Not Recruiting
View on ClinicalTrials.gov →
Summary
The goal of this clinical trial is to compare different forms of transcranial magnetic stimulation (TMS) for improving the outcomes of Exposure with Response Prevention (ERP) in youth and young adults with Obsessive-Compulsive Disorder (OCD). Researchers will compare three groups: ERP with one of two different active ("real") forms of TMS vs. ERP with sham ("fake") TMS. The main questions this study aims to answer are: 1) whether TMS normalizes functioning in brain circuits that contribute to compulsive behavior, and 2) whether TMS reduces compulsions during ERP. Participants will: * Complete clinical interviews, questionnaires, and computerized tasks * Complete two MRIs (brain scans) * Receive daily TMS followed by ERP for two weeks (10 sessions)
Protocol Amendment History 2 changes
notable Primary completion pushed: 2026-06-30 -> 2029-08-31 2026-07-25
minor Completion pushed: 2026-07-31 -> 2029-10-31 2026-07-25
Trial Details
NCT Number NCT05931913
Lead Sponsor Bradley Hospital
Collaborators: University of Minnesota, Butler Hospital
Conditions Obsessive-Compulsive Disorder
Enrollment 50 participants
Start Date 2024-03-20
Primary Completion 2029-08-31 (estimated)
Study Completion 2029-10-31 (estimated)
Updated on ClinicalTrials.gov 2026-07-24