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Efficacy of sexual counseling on sexual behaviors in women with endometriosis, candidates for laparoscopic surgery.

Efficacy of sexual counseling on sexual behaviors in women with endometriosis, candidates for laparoscopic surgery.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20180130038567N1
Enrollment
60
Registered
2018-08-04
Start date
2018-08-23
Completion date
Unknown
Last updated
2018-09-11

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

Conditions

Endometriosis. Endometriosis, Unspecified

Interventions

Intervention 1: Intervention group: Intervention group will receive three 45-minute PLISSIT based (the first three stages) individual sexual counseling sessions weekly. Stage1: Permission Stage 2: Lim

Sponsors

Iran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
15 Years to 50 Years

Inclusion criteria

Inclusion criteria: Not pregnant Sexually active Heterosexual Sexual dysfunction or dyspareunia during last 6 months Diagnosis of endometriosis by clinical symptoms (dysmenorrhea, dyspareunia, dysuria, dyschezia, pelvic pain, infertility, hematuria, etc.) clinical examinations examination, and imaging methods(ultrasound, MRI,…), Pelvic pain associated with endometriosis Negative history of hormonal medications (contraceptive pill, gonadotropins, etc.) during the last 3 months. No gynecologic malignancy Negative history of underlying diseases such as cardiovascular, respiratory, renal, hematological, liver, rheumatologic and neurological diseases, psychological disorders in women and spouses Negative history of psychiatric drugs by couple Interested in collaborating in research

Exclusion criteria

Exclusion criteria: Failure to prove endometriosis by surgery The unwillingness of endometriosis women to participate in the study

Design outcomes

Primary

MeasureTime frame
Sexual behaviors. Timepoint: Before intervention, 3 and 6 months after intervention. Method of measurement: Using sexual behavior questionnaires (Female Sexual Function Index, sexual distress, Sexual satisfaction scale for women, Multi- dimensional sexual self-concept).

Secondary

MeasureTime frame
Quality Life. Timepoint: Before and 6 months after intervention. Method of measurement: The endometriosis health profile questionnaire-30.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactShahla chaichian

Iran University of Medical Sciences

shahlachaichian@yahoo.com+98 21 64351

Outcome results

None listed

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