Sexual Need's Rehabilitation Framework (SNRF) model versus the Sexual rehabilitation Programme After Radiotherapy for gynecologic Cancer (SPARC) model on sexual distress, sexual well-being, and sexual quality of life in gynecological Cancers

Not Applicable

Recruiting

Conditions: Condition 1: Endometrial cancer. Condition 2: ovarian cancer. Condition 3: cervical cancer. Condition 4: Breast cancer.
Endometrial intraepithelial neoplasia [EIN]
Other ovarian dysfunction
Cervical root disorders, not elsewhere classified
Malignant neoplasm of breast
N85.02
E28.8
G54.2

Registration Number: IRCT20230121057170N1

Lead Sponsor: Yazd University of Medical Sciences

Brief Summary: Not available

Detailed Description: Not available

Recruitment & Eligibility

Status: Recruiting

Sex: Female

Target Recruitment: 84

Inclusion Criteria

Women with gynecological cancers (endometrium, ovary, cervix, breast)
In women under radiotherapy who have been at least one month after their radiotherapy and chemotherapy
Married and sexually active women
desire to participate in the study
Iranian nationality
Smartphone access
Ability to use a smartphone

Exclusion Criteria

Having mental disorders and being treated for mental disorders
Drug and alcohol addiction
Recurrence of cancer during sampling
pregnancy
Extensive pelvic surgeries
Prohibition of sexual intercourse for medical reasons

Study & Design

Study Type: interventional

Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Sexual distress (primary outcome variable). Timepoint: Baseline, completion of the intervention in the eighth week and follow-up at the end of the study in the twelfth week. Method of measurement: Female Sexual Distress questionnaire.

Secondary Outcome Measures

Name	Time	Method
Sexual well-being(Secondary outcome variable). Timepoint: Baseline, completion of the intervention in the eighth week and follow-up at the end of the study in the twelfth week. Method of measurement: Sexual well-being questionnaire.;Sexual quality of life(Secondary outcome variable). Timepoint: Baseline, completion of the intervention in the eighth week and follow-up at the end of the study in the twelfth week. Method of measurement: sexual quality of life-female questionnaire.