A Study on the Efficacy and Safety of Accelerated Transcranial Magnetic Stimulation for Obsessive-Compulsive Disorder and Its Underlying Neurological Mechanisms

Status: Recruiting
Location: See location...
Intervention Type: Other
Study Type: Interventional
Study Phase: Not Applicable
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
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 60
Healthy Volunteers: f
View:

• 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;

• Normal vision or corrected vision;

• Capacity to complete protocol-specified tests.

Locations
Other Locations
China
Shanghai Pudong New Area Mental Health Centre
RECRUITING
Shanghai
Contact Information
Primary
Yijie Zhao
yj_zhao@tongji.edu.cn
+86 13585960699
Time Frame
Start Date: 2025-07-03
Estimated Completion Date: 2027-12-31
Participants
Target number of participants: 20
Treatments
Experimental: rTMS
individualized rTMS targeting IFC, with symptom provocation
Related Therapeutic Areas
Sponsors
Leads: Shanghai Pudong New Area Mental Health Center, School of Medicine, Tongji University

This content was sourced from clinicaltrials.gov