MedPath

Effect of Cognitive Behavioral Therapy on premenstrual syndrome

Phase 2
Conditions
Premenstrual Syndrome.
Premenstrual tension syndrome
Registration Number
IRCT2015062822960N1
Lead Sponsor
Vicechancellor for research, Shahid Chamran University of Midical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
40
Inclusion Criteria

having regular menstrual cycles (24-35days); do not taking hormonal, psychotropic, vitamins, oral contraceptives at the time; not being pregnant or lactating; not experiencing stressors such as marriage, surgery, death of relatives, and etc. during the previous three months; not being under any kind of treatment to relieve the symptoms during the study and not having internal, gynecological, and psychiatric disorders.
Exclusion criteria: Absence of the above conditions.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Health Related Quality of Life. Timepoint: Before intervention, 70 days after the start of intervention, 2month after the end of intervention. Method of measurement: Health Related Quality of Life Questionaire.
Secondary Outcome Measures
NameTimeMethod
Premenstrual Syndrome. Timepoint: before intervention, 70 days after the start of intervention, 2 month after the end of intervention. Method of measurement: Daily Record of Severity of Problems.
© Copyright 2025. All Rights Reserved by MedPath