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breast screening behaviors

The education effect base on health belief model on screening behaviors in high risk women

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201101015525N1
Enrollment
100
Registered
2011-06-20
Start date
2010-01-10
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

breast screening brehaviours. c50

Interventions

Intervention 1: In intervention group all educations will be given based on Health Belief Model in order to behaviour change.The sassions will be held in 10-15 people groups assisting lecture,slide, p
Early detection
Treatment - Drugs
In intervention group all educations will be given based on Health Belief Model in order to behaviour change.The sassions will be held in 10-15 people groups assisting lecture,slide, posters and film

Sponsors

Reproductive HealthResearch Center of Shaid Beheshti Medical Science University
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

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

Exclusion criteria:

Design outcomes

Secondary

MeasureTime frame
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.

Primary

MeasureTime frame
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.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactHamid Reza Mirzaei

Shohada Tajrish Hospital

mirzaei65@yahoo.com+98 21 2271 8081

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026