Premenstrual Syndrome. Premenstrual tension syndrome
Conditions
Interventions
Intervention 1: Intervention group: Cognitive-behavioral therapy based on social networks. Intervention 2: Control group: No intervention.
Sponsors
Qazvin University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
20 Years to 45 Years
Inclusion criteria
Inclusion criteria: Moderate to severe premenstrual syndrome Internet access having smart phone Willingness to participate in the study
Exclusion criteria
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
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 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
| Measure | Time frame |
|---|---|
| General self-efficacy. Timepoint: Before the intervention, immediately and two months after the intervention. Method of measurement: General self-efficacy questionnaire.;Professional QoL. Timepoint: Before the intervention, immediately and two months after the intervention. Method of measurement: Professional QoL questionnaire.;The impact of premenstrual syndrome on daily life. Timepoint: Before the intervention, immediately and two months after the intervention. Method of measurement: PMS-Impact Questionnaire.;Coping with premenstrual symptoms. Timepoint: Before the intervention, immediately and two months after the intervention. Method of measurement: Coping with premenstrual symptoms Scale.;Anxiety and Depression. Timepoint: Before the intervention, immediately and two months after the intervention. Method of measurement: Hospital Anxiety and Depression Scale.;Fear of covid. Timepoint: Before the intervention, immediately and two months after the intervention. Method of measurement: Fear of Covid-19 scale. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactZainab Alimoradi
Qazvin University of Medical Sciences
Outcome results
None listed