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The effect of educational intervention program on performing mammography in women referring to health centers

Designing, Implementing and Evaluating the Effect of Educational Intervention Program Using Combination of Health Belief Model and Theory of Planned Behavioral on Mammography in Women Referring to Khorramabad Health Centers

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20190407043188N1
Enrollment
140
Registered
2019-06-19
Start date
2018-04-19
Completion date
Unknown
Last updated
2019-08-26

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

Conditions

The effect of educational intervention program using combination of health belief model and theory of planned behavior on performing mammography in women referring to health centers. Special screening examination for neoplasm of breast

Interventions

Intervention 1: Using the results of the pre-test, the training classes were considered for this group. Intervention 2: Control group: There was no intervention for this group. After the collection of

Sponsors

Yazd University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
50 Years to 70 Years

Inclusion criteria

Inclusion criteria: Having ages 50 to 70 years old Not having a mammogram history over the past year Not having a history of breast cancer in one person or first-degree relatives (sister, mother, daughter)

Exclusion criteria

Exclusion criteria: Unwillingness to cooperate No participation in training sessions more than two sessions No participation in training sessions more than two sessions No participation in post-test

Design outcomes

Primary

MeasureTime frame
Perform of mammography. Timepoint: Before the intervention and 3 months after the end of the intervention. Method of measurement: Questionnaire.;Perceived Sensitivity and severity. Timepoint: Before the intervention and 3 months after the end of the intervention. Method of measurement: Questionnaire.;Perceived Benefits. Timepoint: Before the intervention and 3 months after the end of the intervention. Method of measurement: Questionnaire.;Perceived Barriers. Timepoint: Before the intervention and 3 months after the end of the intervention. Method of measurement: Questionnaire.;Perceived Self-efficacy. Timepoint: Before the intervention and 3 months after the end of the intervention. Method of measurement: Questionnaire.;Cues to action. Timepoint: Before the intervention and 3 months after the end of the intervention. Method of measurement: Questionnaire.;Attitude. Timepoint: Before the intervention and 3 months after the end of the intervention. Method of measurement: Questionnaire.;Normative beliefs. Timepoint: Before the intervention and 3 months after the end of the intervention. Method of measurement: Questionnaire.;Perceived behavioral control. Timepoint: Before the intervention and 3 months after the end of the intervention. Method of measurement: Questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactZahra khazir

Yazd University of Medical Sciences

zahrakhazir@gmail.com+98 35 3820 9114

Outcome results

None listed

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