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Ensayo clínico

TMS + Exposure Therapy for Pediatric OCD: Second Phase

NCT: NCT07859683 · NOT_YET_RECRUITING

ID NCTNCT07859683
EstadoNOT_YET_RECRUITING
Fecha de inicio2026-10-01
Finalización2029-10-31
SponsorBradley Hospital (OTHER)
First posted
Last updated

Resumen breve

The goal of this clinical trial is to test 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 two groups: ERP with active ("real") TMS vs. ERP with sham ("fake") TMS. The first phase of this study found that active TMS+ERP normalized functioning in brain circuits that contribute to compulsive behavior. This second phase will test whether TMS-induced brain changes lead to improvements in OCD symptom severity. 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)

Fuente oficial

Ver en ClinicalTrials.gov →

Datos obtenidos de la API de ClinicalTrials.gov. Para conocer el estado más reciente, consulte el registro oficial.

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