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The effect of the training program on mammography behavior

Comparison of the Effect of Educational Intervention based on Web and Manual on Mammography Use in Women: An Application of Health Belief Model

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20190708044157N1
Enrollment
126
Registered
2019-08-09
Start date
2019-08-21
Completion date
Unknown
Last updated
2019-10-07

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

Conditions

Breast cancer screening.

Interventions

Intervention 1: Intervention group: After extracting the names of women aged 40 years and over, the electronic records are reviewed to evaluate some of the criteria for entering the study. For the web

Sponsors

Boushehr University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
40 Years to No maximum

Inclusion criteria

Inclusion criteria: Information recorded in Health Care centers Having reading and writing skills & the ability to communicate verbally Age 40 and over Suitable physical conditions to answer questions and participate in the study having access to the internet and the knowledge to use it Having computer and smartphone Inclination to participate in the research Failure to do mammograms in the last two years

Exclusion criteria

Exclusion criteria: Having breast cancer Pregnancy Lactation Having chest disease history A history of breast cancer in a first degree family Drop out of the study

Design outcomes

Primary

MeasureTime frame
Breast cancer screening behavior. Timepoint: Before intervention and two months after intervention. Method of measurement: Questionnaire.

Secondary

MeasureTime frame
Awareness. Timepoint: Before intervention and two months after intervention. Method of measurement: Questionnaire.;Perceived Benefits. Timepoint: Before intervention and two months after intervention. Method of measurement: Questionnaire.;Perceived Barriers. Timepoint: Before intervention and two months after intervention. Method of measurement: Questionnaire.;Perceived Susceptibility. Timepoint: Before intervention and two months after intervention. Method of measurement: Questionnaire.;Perceived Severity. Timepoint: Before intervention and two months after intervention. Method of measurement: Questionnaire.;Health Motivation. Timepoint: Before intervention and two months after intervention. Method of measurement: Questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactHemameddin Javadzade

Boushehr University of Medical Sciences

sh.javadzadeh@bpums.ac.ir+98 77 3345 0084

Outcome results

None listed

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