Study of Repetitive Transcranial Magnetic Stimulation Efficacy on Obsessive Compulsive Disorder (OCD) (TMS-TOC)
Primary Purpose
Obsessive-Compulsive Disorder
Status
Completed
Phase
Phase 2
Locations
France
Study Type
Interventional
Intervention
rTMS
Sham Comparator
Sponsored by
About this trial
This is an interventional treatment trial for Obsessive-Compulsive Disorder focused on measuring Repetitive Transcranial Magnetic Stimulation, Supplementary Motor Area, Obsessive-Compulsive Disorder, Sham rTMS, Placebo-controlled, Randomized, Double-blind, fMRI, DSM-IV Obsessive-Compulsive Disorder
Eligibility Criteria
Inclusion Criteria:
- signed patient informed consent;
- primary obsessive compulsive disorder;
- current YBOCS score at least 15 with or without drug (or obsessive/compulsive subscores of at least 10);
- males/females 18-65yrs;
- treated with at least two adequate dose of SRI at least 8 weeks at some stage of illness;
- currently using adequate, stable dose of SSRI at least 8 weeks but not responding.
Exclusion Criteria:
- schizophrenia, other psychotic disorders, bipolar I, current major depressive disorder (MADRS>20), substance/alcohol dependence within last 6 months;
- severe axis II;
- significant suicide risk;
- metallic implant in cranium;
- severe/unstable medical conditions;
- ECT in the last month;
- pregnancy or breastfeeding ;
- history epilepsy; neurological disorder leading to increased intracranial pressure; severe cardiac disorder/intracardiac lines, pacemakers; Gilles de la Tourette syndrome;
- current structured psychotherapy;
- current drug treatment of bipolar disorder.
Sites / Locations
- Pitie Salpetriere Hospital
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
1
2
Arm Description
Outcomes
Primary Outcome Measures
Yale-Brown Obsessive Compulsive Scale (YBOCS)
Secondary Outcome Measures
Clinical Global Impression - Severity (CGI-S)
- Clinical Global Impression - Improvement (CGI-I)
Global Assessment of Functioning (GAF)
- Montgomery Asberg Depression Rating Scale (MADRS)
Brief Anxiety Scale (BAS
Sheehan Disability Scale (SDS)
Hospital Anxiety and Depression (HAD) scale
Maudsley Obsessional Inventory (MOCI)
LPO scale
Full Information
NCT ID
NCT00822601
First Posted
January 13, 2009
Last Updated
July 30, 2012
Sponsor
Assistance Publique - Hôpitaux de Paris
1. Study Identification
Unique Protocol Identification Number
NCT00822601
Brief Title
Study of Repetitive Transcranial Magnetic Stimulation Efficacy on Obsessive Compulsive Disorder (OCD)
Acronym
TMS-TOC
Official Title
A Controlled Study of rTMS Over Supplementary Motor Area (SMA) in Obsessive Compulsive Disorder
Study Type
Interventional
2. Study Status
Record Verification Date
January 2009
Overall Recruitment Status
Completed
Study Start Date
November 2008 (undefined)
Primary Completion Date
April 2012 (Actual)
Study Completion Date
April 2012 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Assistance Publique - Hôpitaux de Paris
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Our study's purpose is to show the efficacy of the transcranial magnetic stimulation (a non invasive method of cerebral modulation) in patients suffering from chronic obsessive compulsive disorder (OCD). This new method will be applied in 20 patients during 4 weeks (5 sessions each week), and its effects on OCD symptoms will be compared to those of a "sham" (=placebo) stimulation applied with the same process in 20 other patients, randomly assigned to the comparison group. The maintenance of the therapeutic effects will be explored during 8 weeks following the end of the treatment. In addition to classical scales used to measure the treatment effects, all patients will be examined using a functional magnetic resonance imaging (fMRI) before and after treatment to explore the cerebral effects of rTMS
Detailed Description
Repetitive Transcranial Magnetic Stimulation (rTMS) has been shown to be an effective therapeutic tool for the treatment of several neuropsychiatric disorders including major depression and hallucinations in schizophrenia but, to date, studies exploring the effects of rTMS in Obsessive Compulsive Disorder (OCD) have produce negative or conflicting results, especially those applying the stimulation to the prefrontal cortex as for the treatment of depression. However, a promising result has been obtained in a study in which the rTMS was applied to the Supplementary Motor Area (SMA), but in a small size and heterogeneous sample. The SMA has connections with areas of the brain, especially motor areas and subcortical-limbic circuitry, implicated in OCD.
In our study, 40 adult outpatients with OCD, who have been insufficiently responsive to at least two recognized drug treatments, will be randomly assigned to one of two treatment groups (active low frequency (1 Hz, 100% of the motor threshold) rTMS or sham-placebo) applied to the SMA daily for up to four weeks. An individual MRI-guided neuronavigation will be used to precisely define the target stimulation site in each patient. Rating scales for symptom change will be obtained at baseline, during the rTMS course, at the end of 4 weeks of treatment, and after a 2-month follow-up period. The main outcome measure will be the Yale-Brown Obsessive Compulsive scale, and secondary outcome measure will include the CGI scales, the LPO scale, the MOCI, and the SDS. Brain activity changes in fMRI before and after active/sham treatment will be compared between groups, with rest measures and provocation tasks.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Obsessive-Compulsive Disorder
Keywords
Repetitive Transcranial Magnetic Stimulation, Supplementary Motor Area, Obsessive-Compulsive Disorder, Sham rTMS, Placebo-controlled, Randomized, Double-blind, fMRI, DSM-IV Obsessive-Compulsive Disorder
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantOutcomes Assessor
Allocation
Randomized
Enrollment
40 (Actual)
8. Arms, Groups, and Interventions
Arm Title
1
Arm Type
Experimental
Arm Title
2
Arm Type
Placebo Comparator
Intervention Type
Device
Intervention Name(s)
rTMS
Intervention Description
Arm 1 (experimental) : rTMS, 4 weeks of stimulation with RMT frequency 1Hz, intensity 100% of RMT for 20 minutes (1500 pulses), 5 minutes of trains with 2 minutes of intra-train intervals to both SMA. Treatment will be given 5 times a week for 4 weeks.
Intervention Type
Device
Intervention Name(s)
Sham Comparator
Intervention Description
sham rTMS (using a placebo coil), 4 weeks of stimulation, will mimic the active treatment mentioned above.
Primary Outcome Measure Information:
Title
Yale-Brown Obsessive Compulsive Scale (YBOCS)
Time Frame
week 1, 2, 3, 4, 5, 7, 9, 11, 13
Secondary Outcome Measure Information:
Title
Clinical Global Impression - Severity (CGI-S)
Time Frame
week 1, 2, 3, 4, 5, 7, 9, 11, 13
Title
- Clinical Global Impression - Improvement (CGI-I)
Time Frame
week 1, 2, 3, 4, 5, 7, 9, 11, 13
Title
Global Assessment of Functioning (GAF)
Time Frame
week 5, 13
Title
- Montgomery Asberg Depression Rating Scale (MADRS)
Time Frame
week 5, 13
Title
Brief Anxiety Scale (BAS
Time Frame
week 5, 13
Title
Sheehan Disability Scale (SDS)
Time Frame
, week 5, 13
Title
Hospital Anxiety and Depression (HAD) scale
Time Frame
week 1, 2, 3, 4, 5, 7, 9, 11, 13
Title
Maudsley Obsessional Inventory (MOCI)
Time Frame
week 5, 13
Title
LPO scale
Time Frame
week 5, 13
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
signed patient informed consent;
primary obsessive compulsive disorder;
current YBOCS score at least 15 with or without drug (or obsessive/compulsive subscores of at least 10);
males/females 18-65yrs;
treated with at least two adequate dose of SRI at least 8 weeks at some stage of illness;
currently using adequate, stable dose of SSRI at least 8 weeks but not responding.
Exclusion Criteria:
schizophrenia, other psychotic disorders, bipolar I, current major depressive disorder (MADRS>20), substance/alcohol dependence within last 6 months;
severe axis II;
significant suicide risk;
metallic implant in cranium;
severe/unstable medical conditions;
ECT in the last month;
pregnancy or breastfeeding ;
history epilepsy; neurological disorder leading to increased intracranial pressure; severe cardiac disorder/intracardiac lines, pacemakers; Gilles de la Tourette syndrome;
current structured psychotherapy;
current drug treatment of bipolar disorder.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Antoine Pelissolo, MD, PhD
Organizational Affiliation
Assistance Publique - Hôpitaux de Paris
Official's Role
Principal Investigator
Facility Information:
Facility Name
Pitie Salpetriere Hospital
City
Paris
ZIP/Postal Code
75013
Country
France
12. IPD Sharing Statement
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Study of Repetitive Transcranial Magnetic Stimulation Efficacy on Obsessive Compulsive Disorder (OCD)
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