Breast Cancer. Malignant neoplasm of breast
Conditions
Interventions
Intervention 1: Intervention group: The intervention will be performed in the following steps: 1- describing the objectives of the study to the participants and obtaining their consent 2- Creating a
Sponsors
Esfahan University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
40 Years to 59 Years
Inclusion criteria
Inclusion criteria: Middle-aged women who have not had two breast cancer screening methods, including mammography or clinical breast examination, for at least the past two years. Minimum literacy No history of malignant breast disease in the person or close relatives Owning a laptop, mobile phone or tablet with the ability to access the Internet and install software Consent to participate in the study
Exclusion criteria
Exclusion criteria: Pregnant and breastfeeding women History of participating in training sessions related to breast cancer screening
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Motivation. Timepoint: 1- Before the intervention 2- Three months after the intervention program 3- Six months after the intervention program. Method of measurement: Questionnaire including factors related to the promotion of breast cancer screening behaviors.;Social support. Timepoint: 1- Before the intervention 2- Three months after the intervention program 3- Six months after the intervention program. Method of measurement: Questionnaire including factors related to the promotion of breast cancer screening behaviors.;Information seeking. Timepoint: 1- Before the intervention 2- Three months after the intervention program 3- Six months after the intervention program. Method of measurement: Questionnaire including factors related to the promotion of breast cancer screening behaviors.;Self-care. Timepoint: 1- Before the intervention 2- Three months after the intervention program 3- Six months after the intervention program. Method of measurement: Questionnaire including factors related to the promotion of breast cancer screening behaviors.;Stress management. Timepoint: 1- Before the intervention 2- Three months after the intervention program 3- Six months after the intervention program. Method of measurement: Questionnaire including factors related to the promotion of breast cancer screening behaviors.;Worry. Timepoint: 1- Before the intervention 2- Three months after the intervention program 3- Six months after the intervention program. Method of measurement: Questionnaire including factors related to the promotion of breast cancer screening behaviors. | — |
Secondary
| Measure | Time frame |
|---|---|
| Breast self-examination behavior. Timepoint: 1- Before the intervention 2- Three months after the intervention program 3- Six months after the intervention program. Method of measurement: Questionnaire including factors related to the promotion of breast cancer screening behaviors.;Clinical breast examination behavior. Timepoint: 1-Before the intervention 2- Three months after the intervention program 3- Six months after the intervention program. Method of measurement: Questionnaire including factors related to the promotion of breast cancer screening behaviors.;Mammography behavior. Timepoint: 1-Before the intervention 2- Three months after the intervention program 3- Six months after the intervention program. Method of measurement: Questionnaire including factors related to the promotion of breast cancer screening behaviors. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactBanafsheh Tavakoli
Esfahan University of Medical Sciences
Outcome results
None listed