The effect of Mindfulness counseling on sexual satisfaction and function in women with polycystic ovary syndrome

Not Applicable

Recruiting

• Conditions: F52.9; Polycystic ovary syndrome.; Unspecified sexual dysfunction not due to a substance or known physiological condition

• Registration Number: IRCT20201101049216N1
• Lead Sponsor: Ahvaz University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 22 February 2021

Recruitment & Eligibility

• Status: Recruiting
• Sex: Female
• Target Recruitment: 54

Inclusion Criteria

Age 18 to 55 years
Married
Have a minimum literacy rate
BMI less than 30
Diagnosis of polycystic ovary syndrome based on Rotterdam criteria (oligomenorrhea / amenorrhea, ultrasound evidence, clinical signs such as acne, hirsutism, and laboratory signs of hyperandrogenism (also recorded and diagnosed by a gynecologist)
Score less than 26.5 from the Sexual Function Questionnaire(FSFI)
Score less than 75 on the Sexual Satisfaction Questionnaire(ISS)
6 months have passed since the start of treatment
Do not be treated with infertility drugs

Exclusion Criteria

Having a specific physical and mental illness
Addiction to alcohol, drugs and other psychotropic drugs
Having sexual dysfunction in yourself and your spouse
Pregnancy and lactation

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Sexual function. Timepoint: Evaluation of sexual function and satisfaction before the intervention and in week 8 and week 12 after the intervention. Method of measurement: FSFI Sexual Function Questionnaire(FSFI).;Sexual Satisfaction Questionnaire. Timepoint: Evaluation of sexual function and satisfaction before the intervention and in week 8 and week 12 after the intervention. Method of measurement: Larson Sexual Satisfaction Questionnaire.