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The effectiveness of the intervention program based on the 5A self-management model on Promoting Sexual Function in women with Endometriosis

Investigating the effectiveness of the intervention program based on the 5A self-management model compared to routine care on Promoting Sexual Function in Women with Endometriosis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20160224026756N9
Enrollment
68
Registered
2025-07-18
Start date
2025-07-29
Completion date
Unknown
Last updated
2025-07-21

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

Conditions

Sexual function in women with endometriosis. Sexual dysfunction, not caused by organic disorder or disease

Interventions

Intervention 1: Intervention group: In the intervention group, an intervention program based on the 5A self-management model will be implemented for each woman diagnosed with endometriosis with the in

Sponsors

Esfahan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
19 Years to 45 Years

Inclusion criteria

Inclusion criteria: Iranian nationality Consent to participate in the study Primary education level or higher Having primary school education and higher Within reproductive age (19 to 45 years old) Married and sexually active Being the only wife of her husband Diagnosis of endometriosis by a gynecologist Currently undergoing medical treatment for endometriosis and not candidates for surgery during the intervention period and up to one month after the intervention's completion Obtaining a score less than 28 on the standard Female Sexual Function Index (FSFI) questionnaire.

Exclusion criteria

Exclusion criteria: Presence of pregnancy or breastfeeding Women undergoing assisted reproductive techniques History of known mental disorders requiring medication History of substance or alcohol abuse in the participant or her husband Husbands of participants not suffering from premature ejaculation or erectile dysfunction as self-reported by the participant History of participation in educational courses focused on sexual health education History of surgery in the study participants or their husbands, such as prostatectomy, mastectomy, and other breast surgeries (identified through participant questioning and medical record review) History of stressful events in the past 6 months, such as parental death, etc Presence of any disease in the study participants or their husbands that affects sexual function, including systemic diseases such as liver, kidney, and lung failure Cardiovascular diseases Malignant diseases (cancers) Mental illnesses Mood disorders (depression, anxiety) Ulcerative colitis Vasculitis Thyroid and adrenal cortex diseases Diabetes Hypertension Central nervous system disorders Infectious and sexually transmitted diseases (identified through participant questioning and medical record review) Consumption of medications that affect sexual function by the study participants or their husbands, including Psychotropic medications,Cardiac and antihypertensive medications,Thiazide diuretics,Antidepressants,Anticonvulsants,Hypnotics (sleeping pills),Narcotic medications ,Hormonal medications ,Antihistamines,Anti-cancer medications ,Sexual performance-enhancing medications

Design outcomes

Primary

MeasureTime frame
Sexual function in women with endometriosis. Timepoint: At the beginning of the study (before the intervention ) and one month after the end of the intervention. Method of measurement: Female Sexual Function Index (FSFI).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMahnaz Noroozi

Esfahan University of Medical Sciences

noroozi@nm.mui.ac.ir+98 31 3792 7570

Outcome results

None listed

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