Determining the Impact of the Health Promotion Program for Women with Breast Cancer on the Quality of Life, Hope and Family Support During Surgery and Chemotherapy
Phase 3
Recruiting
- Conditions
- Breast Cancer.Malignant Neoplasm of Breast
- Registration Number
- IRCT20230510058141N1
- Lead Sponsor
- Mashhad University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Female
- Target Recruitment
- 304
Inclusion Criteria
The patient is a new case of breast cancer.
She is a candidate for mastectomy surgery or a candidate for a chemotherapy protocol.
The patient is female.
The patient must be between 25 and 65 years old.
Be an Iranian patient.
The patient should be able to read and write in Persian language.
Exclusion Criteria
Does not Agree to Participate in the Research.
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The score obtained from the EORCT QLQ30 quality of life questionnaire. Timepoint: In surgery patients: at times (discharge day) 0 and 6 weeks after surgery and in chemotherapy patients at times 0 (first session of chemotherapy), one week later and 3 months later. Method of measurement: EORCT quality of life QLQ c30 questionnaire.;Hope: the score obtained from the Hearth Hope Index tool. Timepoint: In surgery patients: at times (discharge day) 0 and 6 weeks after surgery and in chemotherapy patients at times 0 (first session of chemotherapy), one week later and 3 months later. Method of measurement: Hearth Hope Index tool.;Family support: score obtained from the ICE-FPSQ Perceived Family Support Questionnaire. Timepoint: In surgery patients: at times (discharge day) 0 and 6 weeks after surgery and in chemotherapy patients at times 0 (first session of chemotherapy), one week later and 3 months later. Method of measurement: ICE-FPSQ Perceived Family Support Questionnaire.
- Secondary Outcome Measures
Name Time Method