Sexual satisfaction and quality counseling. Counseling related to sexual attitude
Conditions
Interventions
Intervention group: The intervention in the test group is counseling with a solution-oriented approach, which will be presented in 8 sessions in the Sky Room. The intervention (counseling with a solut
Sponsors
Yazd University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
18 Years to 45 Years
Inclusion criteria
Inclusion criteria: Willingness to participate in the study History of at least one failure of assisted reproductive techniques in infertile women with polycystic ovary syndrome according to the Rotterdam criteria and registered in the medical file of the Research Institute of Reproductive Sciences Being Iranian Ability to understand and speak Persian language and cooperate in doing assignments Having an Android or IOS smart phone Sharing bed with husband
Exclusion criteria
Exclusion criteria: Participating in concurrent sexual health-related intervention studies Having children Use of any drug or hormone affecting sexual performance within 60 days before the intervention Existence of various types of severe mental disorders (psychosis, schizophrenia, etc.) under medical treatment based on the information of the medical record or her statements The presence of chronic diseases such as overt diabetes, hypertension, cardiovascular disease, thyroid disease, kidney disease, etc. Use of tobacco, drugs and alcohol according to the patient Existence of stressful events during the last 6 months such as immigration, death of relatives, divorce
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Measuring the quality of sexual life in women with polycystic ovary syndrome using fertility failure techniques. Timepoint: In the baseline, week 8 and in follow-up at the end of the study in week 12 in both groups. Method of measurement: Sex life quality questionnaire (Simond et al.). | — |
Secondary
| Measure | Time frame |
|---|---|
| Measuring sexual life satisfaction in women with polycystic ovary syndrome with a history of failure of assisted reproductive techniques. Timepoint: In the baseline, week 8 and in the follow-up study completion in week 12. Method of measurement: Larson sexual satisfaction questionnaire. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactMahshid Bokaei
Yazd University of Medical Sciences
Outcome results
None listed