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Effect of omega-3-fatty acids versus placebo on clinical symptoms of patients with major depressive disorder

Phase 2
Conditions
Major depressive disorder.
Severe depressive episode without psychotic symptoms
Registration Number
IRCT201705249014N164
Lead Sponsor
Vice-chancellor for Research and Technology, Hamadan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
60
Inclusion Criteria

Age of 18 to 65 years; major depressive disorder
Exclusion criteria: Pregnancy or breastfeeding; narcotic addiction; psychosis.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Depressive symptoms. Timepoint: before intervention and 6 and 12 weeks after intervention. Method of measurement: using standard questionnaire.;Sleep disorder. Timepoint: before intervention and 6 and 12 weeks after intervention. Method of measurement: using standard questionnaire.;Social competencies. Timepoint: before intervention and 6 and 12 weeks after intervention. Method of measurement: using standard questionnaire.;Physical activity. Timepoint: before intervention and 6 and 12 weeks after intervention. Method of measurement: using standard questionnaire.;Cognitive performance. Timepoint: before intervention and 6 and 12 weeks after intervention. Method of measurement: using standard questionnaire.
Secondary Outcome Measures
NameTimeMethod
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