Repetitive Transcranial Magnetic Stimulation (rTMS) in the Treatment of Obsessive Compulsive Disorder

Sponsor
Shanghai Mental Health Center (Other)
Overall Status
Recruiting
CT.gov ID
NCT03649685
Collaborator
RenJi Hospital (Other), Shanghai 10th People's Hospital (Other)
120
1
4
33.5
3.6

Study Details

Study Description

Brief Summary

This study will evaluate the possible therapeutic effects of repetitive transcranial magnetic stimulation(rTMS) in obsessive-compulsive disorder (OCD) in OCD patients who have not fully responded to pharmacotherapy, and the underlying neural mechanism by EEG.

Condition or Disease Intervention/Treatment Phase
  • Device: Continuous theta burst stimulation (cTBS)
  • Device: shame rTMS
N/A

Detailed Description

The purpose of study is to examine the efficacy of rTMS over different brain areas, including the bilateral supplement motor Area (SMA), the right dorsal lateral prefrontal cortex (DLPFC) and SMA+DLPFC in the treatment of OCD. 120 OCD patients will be randomized into four groups. Continuous theta burst stimulation (cTBS) stimulation will be performed once a day, five times a week, for four weeks. The investigators will assess improvement after four weeks of cTBS. Though the study, Yale-Brown Obsessive Compulsive Scale(Y-BOCS), the Dimensional Yale-Brown Obsessive-Compulsive Scale (DY-BOCS), the Barratt Impulsiveness Scale-11 (BIS-11), the Beck Depression Inventory-II(BDI-II), the Beck Anxiety Inventory (BAI), Perceived Stress Scale(PSS), Pittsburgh sleep quality index(PSQI), the Obsessive-Compulsive Inventory-Revised(OCI-R) and side effects will be obtained by a trained investigator. The patients will also receive magnetic resonance imaging scan and electroencephalography (EEG).

Study Design

Study Type:
Interventional
Anticipated Enrollment :
120 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Triple (Participant, Investigator, Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
A Randomized Clinical Trial of Repetitive Transcranial Magnetic Stimulation (rTMS) Treatment for Obsessive-Compulsive Disorder
Actual Study Start Date :
Jul 15, 2019
Anticipated Primary Completion Date :
Dec 31, 2021
Anticipated Study Completion Date :
Apr 30, 2022

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Group1: rTMS(bilateral SMA)

Continuous theta burst stimulation (cTBS) stimulation will be applied over the bilateral SMA once a day, 5 days/week, for 4 weeks.

Device: Continuous theta burst stimulation (cTBS)
50Hz of 90% MT for 3 pulses train over will be repeated at 200ms for the 40s, 600 pulses

Experimental: Group2: rTMS(right DLPFC)

Continuous theta burst stimulation (cTBS) stimulation will be applied over the right DLPFC once a day, 5 days/week, for 4 weeks.

Device: Continuous theta burst stimulation (cTBS)
50Hz of 90% MT for 3 pulses train over will be repeated at 200ms for the 40s, 600 pulses

Experimental: Group3: rTMS(right DLPFC+bilateral SMA)

Continuous theta burst stimulation (cTBS) stimulation will be applied over the right DLPFC and bilateral SMA once a day, 5 days/week, for 4 weeks.

Device: Continuous theta burst stimulation (cTBS)
50Hz of 90% MT for 3 pulses train over will be repeated at 200ms for the 40s, 600 pulses

Sham Comparator: Group4: shame rTMS

The sham rTMS will be applied over the bilateral SMA once a day, 5 days/week, for 4 weeks.

Device: shame rTMS
The sham coil has been specifically developed to mimic the real one but is not associated with a stimulus sensation compared to the coil delivering real stimulation cTBS.

Outcome Measures

Primary Outcome Measures

  1. Symptom improvement assessed by the Yale-Brown Obsessive Compulsive Scale [Up to 6 months]

    The responder on Y-BOCS is defined as a Y-BOCS decrease at least 25% from the baseline at post-treatment

Secondary Outcome Measures

  1. The Dimensional Yale-Brown Obsessive-Compulsive Scale (DY-BOCS) [Up to 6 months]

    The DY-BOCS self-report is composed of an 88-item self-report checklist, designed to provide a detailed description of obsessions and compulsions that are divided into six different OC symptom dimensions.

  2. The Barratt Impulsiveness Scale-11 (BIS-11) [Up to 6 months]

    It is is an important tool for measuring impulsivity.

  3. The Beck Depression Inventory-II(BDI-II) [Up to 6 months]

    It is a 21-item self-report measure scored on a 4-point Likert-type scale to summarize recent symptoms of depression.

  4. The Beck Anxiety Inventory (BAI) [Up to 6 months]

    It is a 21-item self-report inventory that is used for measuring the severity of anxiety.

  5. State-trait Anxiety Inventory(STAI) [Up to 6 months]

    It has 20 items for assessing trait anxiety and 20 for state anxiety.

  6. Perceived Stress Scale(PSS) [Up to 6 months]

    It is to measure the degree to which situations in one's life are appraised as stressful.

  7. Pittsburgh sleep quality index(PSQI) [Up to 6 months]

    It is a self-report questionnaire that assesses sleep quality over a 1-month time interval.

  8. The Obsessive-Compulsive Inventory-Revised(OCI-R) [Up to 6 months]

    It's a self-report designed to measure the principal dimensions which characterise obsessive-compulsive disorder.

  9. side effects [Up to 6 months]

    It measures side effects including dizziness, headache, itching and so on.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • age>18 years old;

  • DSM-5 criteria for OCD;

  • Y-BOCS total score > or = 16, despite treatment with an adequate trial of a serotonin reuptake inhibitor (SRI) and currently using adequate, stable dose of SRI at least 4 weeks. An adequate SRI trial is defined as treatment for at least 12 weeks on the SRI, that meets or exceeds the recommended dosage level for OCD;

  • or=9 yrs education

Exclusion Criteria:
  • any additional current psychiatric comorbidity, except for obsessive-compulsive personality disorder

  • serious suicide risk;

  • the inability to receive rTMS because of metallic implants, or history of seizures,or history of head injury, or history of neurosurgery;

  • any major medical disease;

  • pregnancy or nursing of an infant;

  • participation in current clinical study;

  • current use of any investigational drug;

  • TMS/DBS treatment at any point in their lifetime;

  • history of long-time use of benzodiazepines

Contacts and Locations

Locations

Site City State Country Postal Code
1 Shanghai Mental Health Center Shanghai Shanghai China 200030

Sponsors and Collaborators

  • Shanghai Mental Health Center
  • RenJi Hospital
  • Shanghai 10th People's Hospital

Investigators

  • Principal Investigator: Zhen Wang, PhD,MD, Shanghai Mental Health Center

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Zhen Wang, vice-president, Shanghai Mental Health Center
ClinicalTrials.gov Identifier:
NCT03649685
Other Study ID Numbers:
  • SMHC-OCD-003
First Posted:
Aug 28, 2018
Last Update Posted:
Sep 14, 2021
Last Verified:
Sep 1, 2021
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Sep 14, 2021