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The effect of an intervention program on the sexual health of women with endometriosis

Developing and evaluating an interventional program based on the needs and strategies for improving the sexual health of women with endometriosis: A mixed method Study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20220620055229N2
Enrollment
70
Registered
2023-03-07
Start date
2023-12-06
Completion date
Unknown
Last updated
2023-07-25

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

Conditions

endometriosis. Endometriosis of uterus

Interventions

Intervention 1: Intervention group: For the intervention group, in addition to providing routine treatment for endometriosis, an intervention was designed (it should be noted that the content of the i

Sponsors

Yazd University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Women with endometriosis based on the diagnosis of a gynecologist Being Iranian Being married Having sex with your wife Having informed online consent to participate in the study

Exclusion criteria

Exclusion criteria: Being pregnant Participating in concurrent sexual health-related intervention studies Having cancer or chronic diseases Existence of various types of severe mental disorders (psychosis, schizophrenia) under medical treatment based on medical record information or statements Drug and alcohol addiction 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, divorce and acute financial problems

Design outcomes

Primary

MeasureTime frame
Quality of sex life. Timepoint: Before the intervention, immediately and two months after the intervention. Method of measurement: Questionnaire of the quality of sexual life of Simond women.

Secondary

MeasureTime frame
Women's sexual performance. Timepoint: Before the intervention, immediately and two months after the intervention. Method of measurement: Rozen Women's Sexual Performance Questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFatemeh ZareMobini

Yazd University of Medical Sciences

fatemehzaremobini@yahoo.com+98 35 2438 1751

Outcome results

None listed

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