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breast screening behaviors

Not Applicable
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

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

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
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
NameTimeMethod
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.
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