breast screening behaviors
- Conditions
- breast screening brehaviours.c50
- Registration Number
- IRCT201101015525N1
- Lead Sponsor
- Reproductive HealthResearch Center of Shaid Beheshti Medical Science University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 100
inclusion criteria: every woman who is at risk of breast cancer (because of family history of breast malignancy in her first degree relative i.e mother,sister, daughter) but has not been diagnosed for any kind of malignancy and /or suspicios pathologic of breast tumor can be rectuited for intervention if she has been not diagnosed for breast cancer . Meanwhile having general well being and health to attending at indtructive sessions .
exclusion criteria: every woman with any kind of malignancy , unabling ti attending at instuctive sessions due to illness, dwelling out of Tehran
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Breast self examination. Timepoint: before and 3 months after intervention. Method of measurement: chech list and questionnaire.;Clinical examination. Timepoint: before and 3 months after intervention. Method of measurement: check list and questionnaire.;Mamography. Timepoint: before and 3 months after intervention. Method of measurement: chech list and questionnaire.
- Secondary Outcome Measures
Name Time Method Knowledge. Timepoint: before and 3 months after intervention. Method of measurement: questionnaire.;Perceived severity. Timepoint: before and 3 months after intervention. Method of measurement: questionnaire.;Perceived benefits. Timepoint: before and 3 months after intervention. Method of measurement: questionnaire.;Perceived barriers. Timepoint: before and 3 months after intervention. Method of measurement: questionnaire.;Perceived sucseptibility. Timepoint: befoer and 3 months after intervention. Method of measurement: questionnaire.;Self efficacy. Timepoint: before and 3 months after intervention. Method of measurement: questionnaire.