Comparison of the effectiveness of the PLISSIT model with the Sexual health model on quality of life and sexual behavior among women with breast cancer
- Conditions
- breast cancer.Malignant neoplasm: Overlapping lesion of breast
- Registration Number
- IRCT2016083025431N2
- Lead Sponsor
- Zanjan university medical sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 75
Study inclusion criteria:
1. Having a wife and sexually active individual reports
2. age between 20 and 50 years
3. Other breast cancer and non-cancer
4. Sexual Distress Scale score above 11
5. fiftieth percentile score means lower sexual behavior of women of reproductive age.
6. treatment of patients with surgery or chemotherapy or both
7. After at least 3 months of treatment,
8. do not receive formal education about sexual issues during the last 6 months
9. no history of mental illness in the past year at least
10. No drugs or alcohol
Exclusion criteria Study:
1. relapse
2. intervention during hospitalization
3. Pregnancy
4. Start the field of psychiatric medications
5. participate in therapy sessions over a meeting
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Sexual behavior/ quality of life. Timepoint: befor intervention/ 6 week after intervention/ 12 week after intervention. Method of measurement: DemoDemographic questionnaire, the questions related illness and treatments, native standardized questionnaire and sexual distress, sexual function questionnaire to determine the type of sexual dysfunction, native questionnaire to assess sexual behavior in women of childbearing age and quality of life questionnaire in patients with breast cancer.;Sexual behavior/ quality of life. Timepoint: befor intervention/ 6 week after intervention/ 12 week after intervention. Method of measurement: Demographic questionnaire, the questions related illness and treatments, native standardized questionnaire and sexual distress, sexual function questionnaire to determine the type of sexual dysfunction, native questionnaire to assess sexual behavior in women of childbearing age and quality of life questionnaire in patients with breast cancer.
- Secondary Outcome Measures
Name Time Method Sexual Fanction. Timepoint: befor intrvention/ 6 week intervention/ 12 week intervention. Method of measurement: Femal sexual function scale.