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

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

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20201101049216N1
Enrollment
54
Registered
2021-02-08
Start date
2021-02-12
Completion date
Unknown
Last updated
2021-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Polycystic ovary syndrome. Unspecified sexual dysfunction not due to a substance or known physiological condition

Interventions

Intervention 1: Intervention group: The experimental group will receive 8 sessions of cognitive counseling based on group mindfulness for 120 minutes once a week on a specific day. The sessions will b

Sponsors

Ahvaz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 55 Years

Inclusion criteria

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

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

Design outcomes

Primary

MeasureTime frame
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.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMitra Tadayon

Ahvaz University of Medical Sciences

tadayon-m@ajums.ac.ir+98 61 3336 1968

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026