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Designing a sexual health promotion program for women with hysterectomy and implementing an intervention based on results

Designing a sexual health promotion program for women with hysterectomy and implementing an intervention based on results: an exploratory sequential mixed method Study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20201222049797N3
Enrollment
70
Registered
2023-07-31
Start date
2024-09-19
Completion date
Unknown
Last updated
2023-08-21

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

Conditions

Hysterectomy women due to gynecological and obstetric problems.

Interventions

Intervention 1: Intervention group: Intervention group: The group whose study intervention included the presentation of sexual health promotion program to hysterectomy women will receive 60-90 minutes

Sponsors

Yazd University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Women who underwent hysterectomy due to gynecological diseases and obstetric issues (fibroids, adenomyosis, endometrial hyperplasia, postpartum hemorrhages, etc.) and other than women's concerts At least three months and at most three years have passed since the hysterectomy. having sexual dysfunction (getting a score of 28 and above from the questionnaire of women's sexual function) Being Iranian Being married and being the only spouse of a person Having a common bed with your wife Having informed online consent to participate in the study

Exclusion criteria

Exclusion criteria: Participating in interventional studies related to sexual health at the same time Suffering from chronic diseases such as diabetes, chronic hypertension, heart disease, etc. Existence of various types of severe mental disorders (psychosis, schizophrenia, etc.) under medical treatment based on medical record information or statements Smoking, drugs and alcohol Using any drug or hormone affecting sexual performance within 60 days before the intervention Existence of stressful events during the last 6 months such as immigration, death of relatives and financial problems Perform oophorectomy

Design outcomes

Primary

MeasureTime frame
Change in mean scores of sexual function measured by the Female Sexual Function Questionnaire (FSFI). Timepoint: Female sexual function questionnaires will be completed by the participants before, immediately after the intervention and one month after the intervention. Method of measurement: Female sexual function is based on the FSFI questionnaire of Razon et al., which measures this variable in 6 areas.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Fateme ZareMobini

Yazd University of Medical Sciences

fatemehzaremobini@yahoo.com+98 35 3824 1751

Outcome results

None listed

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