nified Trans diagnostic Treatment

Not Applicable

Recruiting

• Conditions: Premenstrual syndrome.; Premenstrual tension syndrome; N94.3

• Registration Number: IRCT20201128049518N1
• Lead Sponsor: Shahid Beheshti University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 5 January 2021

Recruitment & Eligibility

• Status: Recruiting
• Sex: Female
• Target Recruitment: 40

Inclusion Criteria

Diagnosis of premenstrual syndrome based on diagnostic and Statistical Manual of Mental Disorders (DSM)
Lack of mental retardation
No use of psychiatric drugs before the study

Exclusion Criteria

Dissatisfaction to participate in study
Psychiatric comorbidity
Drug allergy

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Symptoms of Premenstrual. Timepoint: At the first of study (before the intervention), 4 and 8 week after starting psychotherapy sessions in experimental and control group premenstrual symptoms are evaluated. Method of measurement: Premenstrual Syndrome Screening (PSST).;Quality of sleep. Timepoint: At the first of study (before the intervention), 4 and 8 week after starting psychotherapy sessions in experimental and control group quality of sleep is evaluated. Method of measurement: Iowa Sleep Disturbances Inventory (ISDI).;????? ?????? ?????. Timepoint: At the first of study (before the intervention), 4 and 8 week after starting psychotherapy sessions in experimental and control group cognitive emotion regulation is evaluated. Method of measurement: Cognitive Emotion Regulation Questionnaire (CERQ).