Effects of TDCS on improvement of obsessive compulsive symptoms in patients with obsessive-compulsive disorder

Phase 3

Recruiting

• Conditions: Obsessive-compulsive disorder; obsessive-compulsive disorder.

• Registration Number: IRCT20200518047492N1
• Lead Sponsor: Ardabil University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 7 September 2020

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 30

Inclusion Criteria

Age 18 to 40
literacy to read and write
OCD according to DSM-5 criteria
Willingness to participate in the study

Exclusion Criteria

severe mental illness,
History of stroke,
serious neurologic symptoms including seizures, Brain Surgery, Brain tumor, CSF shunt in the brain, snail planting,
physical tools in the body,
serious physical illness

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Obsessive compulsive symptoms. Timepoint: Before the intervention, after the intervention and one months after the intervention. Method of measurement: Yale Brown Questionnaire.;Quality of life. Timepoint: Before the intervention, after the intervention and one months after the intervention. Method of measurement: quality of life Questionnaire.;Depression. Timepoint: Before the intervention, after the intervention and one months after the intervention. Method of measurement: Beck-II Questionnaire.;Cognitive functions. Timepoint: Before the intervention, after the intervention and one months after the intervention. Method of measurement: Wisconsin cards.;Quantitative Electroencephalographic Changes (QEEG). Timepoint: Before the intervention, after the intervention and one months after the intervention. Method of measurement: Quantitative Electroencephalographic.