MedPath

Social network-based CBT for PMS

Phase 3
Conditions
Premenstrual Syndrome.
N94.3
Premenstrual tension syndrome
Registration Number
IRCT20180218038789N4
Lead Sponsor
Qazvin University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
140
Inclusion Criteria

Moderate to severe premenstrual syndrome
Internet access
having smart phone
Willingness to participate in the study

Exclusion Criteria

Diagnosis of psychosis or bipolar disorder
Diagnosis of eating disorder
Diagnosis of moderate to severe depression
Participate in psychotherapy for premenstrual symptoms now or in the past
Acute suicidal tendencies
Childbirth or breastfeeding during the last three months
Pregnancy
Gynecological diseases (hysterectomy, oophorectomy, cervical cancer, polycystic ovary syndrome, endometriosis, infertility)
Initiation or change in the use of antidepressants, benzodiazepines, antipsychotics, oral contraceptives or hormones over the past three months

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Severity of PMS symptoms. Timepoint: Before the intervention, immediately and two months after the intervention. Method of measurement: Daily record of premenstrual syndrome symptoms.
Secondary Outcome Measures
NameTimeMethod
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