Nurse Navigation Program Based On Health Belief Model In Breast Cancer Screening (NaHeB-CaS) (NaHeB-CaS)
Breast Cancer

About this trial
This is an interventional prevention trial for Breast Cancer focused on measuring Syrian woman, Nurse navigation program, Early screening, Cancer, Health blief Model
Eligibility Criteria
Inclusion Criteria:
- Being between the ages of 40-69.
- Being a woman.
- Not having been diagnosed with breast cancer.
- Not doing BSE on a regular basis every month.
- Not having had CME and mammography in the last three years.
- Not to be pregnant, breastfeeding or postpartum.
- No history of breast cancer.
- Not having received training on breast cancer.
- To agree to participate in the research.
- Absence of a mental illness.
- Being literate, accessible and communicative.
- Not having a communication barrier
- Being registered with Sultanbeyli Empowered Migrant Health Center
Exclusion Criteria:
- Having a problem with breast cancer before.
- Having BSE, CBE or Mammography at regular intervals.
- Having had a mastectomy for any reason.
Sites / Locations
- Sultanbeyli Empowered Migrant Health Center
Arms of the Study
Arm 1
Arm 2
Experimental
No Intervention
Intervention Group
Control Group
Intervention Group First, pre-tests were applied to the women in the experimental group. A 4-week training program created by taking into account the cultural characteristics of Syrian women; Explaining breast health, Explaining breast structure, Cancer, Breast cancer, Early diagnosis and its importance, BSE application, CBE and mammography, Barriers on breast cancer, Cancer Early Diagnosis, Screening and Education Center. A 'Nurse-directed screening counseling telephone support line' will be established for the women in the experimental group. Then, motivational interviews will be applied to the women in the experimental group by the researcher, who emphasizes the importance of early diagnosis in line with the health belief model. Reminders will be made by phone every week in the 3rd month. The final tests will be held 4 months after the end of the training.
Pre-tests will be applied to the women in the control group. No intervention will be applied to the women in this group and post-tests will be performed 4 months after the pre-test.