Investigating sexual health counseling with a problem-solving approach with online and face-to-face on sexual satisfaction of women with polycystic ovary syndrome
- Conditions
- Counseling on sexual satisfaction.
- Registration Number
- IRCT20230302057590N1
- Lead Sponsor
- Yazd University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- Female
- Target Recruitment
- 56
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
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
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 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.
- Secondary Outcome Measures
Name Time Method