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

The effectiveness comparison of sexual need's rehabilitation framework (SNRF) model versus the Sexual rehabilitation Programme After Radiotherapy for gynecological Cancer (SPARC) model on sexual distress, sexual well-being, and sexual quality of life in gynecological Cancers .

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20230121057170N1

Enrollment

Registered

2023-08-26

Start date

2023-09-21

Completion date

Unknown

Last updated

2023-10-16

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

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

Interventions

Intervention 1: The first intervention group: The first group will receive the sexual rehabilitation model based on the needs framework (SNRF) in the form of 8 online and consecutive sessions, once a

Eligibility

Sex/Gender

Female

Inclusion criteria

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

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

Design outcomes

Primary

Measure	Time frame
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

Measure	Time frame
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.	—

Measure

Time frame

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.

—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactTahmineh Farajkhoda

Yazd University of Medical Sciences

farajkhoda_t@yahoo.com+98 35 1751 3824

Outcome results

None listed

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