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Recruiting NCT07198594

NCT07198594 Accelerated rTMS Therapeutic Approach for Refractory Obsessive-Compulsive Disorder

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Clinical Trial Summary
NCT ID NCT07198594
Status Recruiting
Phase
Sponsor Shanghai Pudong New Area Mental Health Center, School of Medicine, Tongji University
Condition Obsessive Compulsive Disorder (OCD)
Study Type INTERVENTIONAL
Enrollment 20 participants
Start Date 2025-07-03
Primary Completion 2026-12-31

Trial Parameters

Condition Obsessive Compulsive Disorder (OCD)
Sponsor Shanghai Pudong New Area Mental Health Center, School of Medicine, Tongji University
Study Type INTERVENTIONAL
Phase N/A
Enrollment 20
Sex ALL
Min Age 18 Years
Max Age 60 Years
Start Date 2025-07-03
Completion 2026-12-31
Interventions
rTMS

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Brief Summary

The goal of this clinical trial is to learn if individualized accelerated repetitive transcranial magnetic stimulation (rTMS) targeting the inferior frontal cortex combined with symptom provocation works to treat obsessive-compulsive disorders (OCD) in adults. It will also learn about the safety of rTMS over right IFC. The main questions it aims to answer are: * Does rTMS using a new individualized IFC target relieve participants' OCD symptoms? * What medical problems do participants have when taking rTMS? Participants will: * Take rTMS six times per day for 5 consecutive days * Visit the clinic once at baseline, the day and four weeks after treatment for checkups and tests

Eligibility Criteria

Inclusion Criteria: * Volunteer subjects with Obsessive Compulsive Disorders (OCD) according to the Diagnostic and Statistical Manual of Mental Disorders (DSM V) criteria * without associated tics ("Gilles de la Tourette" Syndrome) * Age 18-60 years, right-handed * Disease severity: Yale-Brown Obsessive Compulsive Scale score ≥16 for OCD patients * Medication stable for at least 4 weeks * Resistant patients to standard treatments: partial but insufficient response (reduction of Y-BOCS score \< 35%) or lack of response to previous well conducted treatment including: optimal tolerated dose and adequate duration (\> 12 weeks) of at least 2 Serotonin Reuptake Inhibitors (selective serotonin reuptake inhibitors, clomipramine), or 1 Serotonin Reuptake Inhibitors + 1 augmentation strategy (adjunction of an antipsychotic - such as risperidone or olanzapine or aripiprazole - or lithium or buspirone) * No systematic rTMS therapy in the past six months; * Signature of informed consent form; * Nor

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