MedPath

actofem and sexual functio

Phase 3
Recruiting
Conditions
Depression.
Major depressive disorder, single episode
Registration Number
IRCT20160524028038N14
Lead Sponsor
Yasouj University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Female
Target Recruitment
104
Inclusion Criteria

Age 18-45 years
Reading and writing literacy
Obtaining a score of less than twenty and diagnosing mild to moderate depression on the Hamilton scale
For at least 4 weeks, be treated with anti-depressants that affect sexual function
Marriage
Having sex at least once a month
Having an emotionally satisfying relationship with a stable and sexually active spouse for at least one year
Desire to participation

Exclusion Criteria

The unwillingness of the research unit during sampling, which will lead to his withdrawal from the study
Having speech or hearing problems
Addiction to drugs and alcohol in a person or his spouse
Getting women's diseases and vaginitis and sexual disorders with organic background according to the statement of the research unit
Sexual problem before taking antidepressants
symptoms of psychosis
Loss of relatives, acquaintances or friends during the last six months
Known sexual problem in men
Current pregnancy and breastfeeding
Suffering from internal diseases such as cardiovascular, thyroid, arthritis, diabetes, epilepsy, kidney infection
Taking birth control pills
Taking drugs that affect sexual performance, such as blood pressure reducers, antihistamine H2 blockers, barbiturates).

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Sexual function. Timepoint: Before the intervention and three months after the intervention. Method of measurement: Female sexual function index.;Depression severity. Timepoint: Before the intervention and three months after the intervention. Method of measurement: Beck depression questionnaire.
Secondary Outcome Measures
NameTimeMethod
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