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NCT05931913 · ClinicalTrials.gov registry record · NA

TMS + Exposure Therapy for Pediatric OCD

A NA study of Obsessive - Compulsive Disorder, sponsored by Bradley Hospital.

Recruiting
Registry status
NA
Development phase
60
Enrollment target
2
Study locations

NCT05931913 is a NA study of Obsessive - Compulsive Disorder that is actively recruiting participants, run by Bradley Hospital. The registered enrollment target is 60 participants, below the 2,064-participant average among 84 other Obsessive - Compulsive Disorder trials with a reported enrollment target (97% lower). The trial reports 2 study locations across 2 states.

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The verdict

NCT05931913, a NA study of Obsessive - Compulsive Disorder, is actively recruiting participants, sponsored by Bradley Hospital.

RECRUITING
Registry status
NA
Development phase
60 participants
Enrollment target
2
Study locations

Study 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)

Interventions

  • DEVICE Transcranial Magnetic Stimulation: intermittent theta burst to dorsolateral prefrontal cortex
  • BEHAVIORAL Exposure with Response Prevention
  • DEVICE Transcranial Magnetic Stimulation: Sham
  • DEVICE Transcranial Magnetic Stimulation: continuous theta burst to pre supplementary motor area

Study Locations (2)

Minnesota

  • University of Minnesota - Minneapolis

Rhode Island

  • Emma Pendleton Bradley Hospital - Riverside

Trial Details

FieldValue
Enrollment Target 60 participants
Start Date 2024-03-20
Est. Completion 2026-07-31
Phase NA

Sponsor

Bradley Hospital

12 total trials

What the Registry Record Tells You About NCT05931913

The ClinicalTrials.gov registry entry for NCT05931913 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 60 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 2,064-participant average among 84 other Obsessive - Compulsive Disorder trials with a reported enrollment target (97% lower). The listed sponsor is Bradley Hospital, which has 12 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Obsessive - Compulsive Disorder appearing as the primary indexed condition, and to 4 interventions - of which Transcranial Magnetic Stimulation: intermittent theta burst to dorsolateral prefrontal cortex is the first listed.

NCT05931913 reports 2 study locations spanning 2 distinct geographic areas - top geographies include Minnesota, Rhode Island.

Frequently Asked Questions

What is clinical trial NCT05931913 about?

NCT05931913 is a clinical study titled "TMS + Exposure Therapy for Pediatric OCD". 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 tw...

What is the current status of trial NCT05931913?

This trial is currently recruiting. It is a NA study. The enrollment target is 60 participants. The study started on 2024-03-20. Estimated completion is 2026-07-31.

What conditions does trial NCT05931913 study?

This clinical trial studies the following conditions: Obsessive - Compulsive Disorder.

What interventions are being tested in trial NCT05931913?

The interventions under investigation include: Transcranial Magnetic Stimulation: intermittent theta burst to dorsolateral prefrontal cortex (DEVICE), Exposure with Response Prevention (BEHAVIORAL), Transcranial Magnetic Stimulation: Sham (DEVICE), Transcranial Magnetic Stimulation: continuous theta burst to pre supplementary motor area (DEVICE).

Who is sponsoring clinical trial NCT05931913?

This trial is sponsored by Bradley Hospital, which has 12 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05931913 being conducted?

This trial has 2 study locations across Minnesota, Rhode Island. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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