Emotion regulation skills training versus self-helper mood tracking software on female sexual modes, female sexual distress and husband’s sexual satisfaction in medical university students undergoing premenstrual dysphoric disorder

Not Applicable

• Conditions: Premenstural Dysphoric Disorder.; Mood disorder due to known physiological condition with depressive features; F06.31

• Registration Number: IRCT20220310054250N1
• Lead Sponsor: Yazd University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 4 April 2022

Recruitment & Eligibility

• Status: Pending
• Sex: Female
• Target Recruitment: 68

Inclusion Criteria

Married female students of Shahid Sadoughi University of Medical Sciences aged 19-49
Desire to participate in the study
Having an Android or iOS smartphone
History of diagnosis and treatment of premenstrual dysphoric disorder based on the seven criteria of DSM5 and in at least two consecutive cycles according to the calendar of premenstrual syndrome and clinical interviews, symptoms are still presence.
Having sex with spouse until the end of the study
Negative sexual modes
Having sexual distress
Low spouse sexual satisfaction

Exclusion Criteria

Pregnancy
Presence of sexual dysfunction disorder in first half of mensural cycle
Having systemic illness
Having sever mental disorder
Being alcohol or drug abuser
Simultaneously participation in other similar study

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Female sexual modes. Timepoint: Baseline, completion of intervention at week 8, follow-up at week 12 from baseline. Method of measurement: Female sexual modes questionnaire.;Female sexual distress. Timepoint: Baseline, completion of intervention at week 8, follow-up at week 12 from baseline. Method of measurement: Female Sexual Distress Scale.;Woman's opinion about her husband's sexual satisfaction. Timepoint: Baseline, completion of the intervention in week 8, follow-up of study completion in week 12 from baseline. Method of measurement: Visual Analogue Scale.