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Investigating sexual health counseling with a problem-solving approach with online and face-to-face on sexual satisfaction of women with polycystic ovary syndrome

Investigating the effect of sexual health counseling with a problem-solving approach Online and face-to-face on the sexual satisfaction of women with polycystic ovary syndrome

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20230302057590N1
Enrollment
56
Registered
2023-03-25
Start date
2023-04-21
Completion date
Unknown
Last updated
2023-04-03

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

Conditions

Counseling on sexual satisfaction.

Interventions

Intervention 1: Intervention group: The first intervention in the face-to-face group is held in the form of 6 2-hour sessions at the diabetes clinic once a week by a senior student of counseling in mi

Sponsors

Yazd University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: Women with polycystic ovary syndrome according to the Rotterdam criteria and doctor's diagnosis Iranian and resident of Yazd city At least literate in reading and writing and speaking Persian language Completion of informed consent to participate in the research Ages 18-45 years Having Smart mobile phone Desire to install the messenger program Married To cross At least one year from the start of marriage

Exclusion criteria

Exclusion criteria: Using drugs that affect sexual performance (for example: blood lipid-lowering drugs, cimetidine, digoxin, progesterone, antidepressants, etc.) Consumption of alcohol and psychoactive substances according to the patient Simultaneous participation in similar studies People with known mental problems under medical treatment (such as depression, etc.) pregnancy Women who have recently given birth and have children less than 6 months old The occurrence of major stress in the last 6 months, including the loss of loved ones

Design outcomes

Primary

MeasureTime frame
Sexual satisfaction score in Larson's sexual satisfaction questionnaire. Timepoint: Before the start of the intervention, immediately after the end of the intervention and one month after the end of the intervention. Method of measurement: Larson sexual satisfaction questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactBehnaz Enjezab

Yazd University of Medical Sciences

enjezabbehnaz@yahoo.com009838241751

Outcome results

None listed

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