Assessment of efficacy of neuronavigated theta burst stimulation in obsessive compulsive disorder patient
Phase 3
- Conditions
- Health Condition 1: F422- Mixed obsessional thoughts and acts
- Registration Number
- CTRI/2019/07/020366
- Lead Sponsor
- Central institute of psychiatry
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1.Diagnosis of Obsessive-Compulsive Disorder using Diagnostic Criteria for Research (DCR) of International Classification of Disease-10th edition (ICD-10, World Health Organization,1992)
2.Age between 18- 60 years of either sex
3.Right handed
4.Patients giving written informed consent
Exclusion Criteria
1.OCD with severe depression as measured by HAM D score > 23
2.Presence of co-morbid neurological or other psychiatric disorder(s).
3.Patient with co morbid substance dependence, except nicotine and caffeine.
4.Patient on any psychotropic medications.
5.Having any metallic implants/parts in body.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Primary outcome of the study in change in severity of obsession and compulsion assessed at 0 week and at the end of 3 week of Theta Burst stimulation with the specially designed score sheet.Timepoint: YBOCS, HAM-D, HAM-A, CGI will be applied at the starting of intervention followed by assessment at 3 weeks and finally on follow up at 8 weeks
- Secondary Outcome Measures
Name Time Method Changes in levels of psychopathology as measured by HAM-D, HAM-A and CGITimepoint: Baseline, 03 weeks and 08 weeks post intervention