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Effect of Repetitive Transcranial Magnetic Stimulation approved by FDA (rTMS-FDA) versus Repetitive Transcranial Magnetic Stimulation with concentration on Mirror Neuron System (rTMS-MNS) on emotion and mood regulation in patients with major depressive disorder

Phase 2
Conditions
Major depression.
Severe depressive episode with psychotic symptoms
Registration Number
IRCT201610209014N123
Lead Sponsor
Vice-chancellor for Research the Technology, Hamadan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
30
Inclusion Criteria

major depressive disorder; age of 18 to 65 years; receiving standard anti-depression drugs.
Exclusion criteria: pregnancy; drug abuse during the last month; drug addiction during the last six months; neurologic disease or convulsion; having metal implant; using lorazepam, benzodiazepines, monoamine oxidase enzyme inhibitors or bupropion in the last month.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Assessing excitement regulation. Timepoint: before and 2 and 4 weeks after intervention. Method of measurement: using excitement adequacy ranking scale.;Assessing mood regulation. Timepoint: before and 2 and 4 weeks after intervention. Method of measurement: using POMS criteria.;Assessing social perception. Timepoint: before and 2 and 4 weeks after intervention. Method of measurement: by reading mind in the eyes.
Secondary Outcome Measures
NameTimeMethod
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