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Effect of theory–based intervention program on promoting screening behavior of breast cancer in employed women

Design, Implementation and Evaluation of theory–based intervention program on promoting screening behavior of breast cancer in employed women University of Medical Sciences

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20171224038026N1
Enrollment
160
Registered
2018-04-27
Start date
2018-09-11
Completion date
Unknown
Last updated
2018-05-21

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

Conditions

Increased screening. Encounter for screening for malignant neoplasm of breast

Interventions

Intervention 1: "Intervention group": 3 training sessions for 90 minutes, 2 sessions, 60 minutes workshop, one instruction book, one instructional film, 3 pamphlets, 1 posters, 3 photo clips and e-lea

Sponsors

Hamedan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 69 Years

Inclusion criteria

Inclusion criteria: Having ages 61-20 years Not having breast cancer Having the consent to participate in the study

Exclusion criteria

Exclusion criteria: Age less than 20 years Having breast cancer discontent to participate in the study

Design outcomes

Primary

MeasureTime frame
Doing behavior Screening. Timepoint: Before the intervention and one month and three months after the intervention. Method of measurement: Report behavior screening Through the questionnaire.

Secondary

MeasureTime frame
Screening behavior. Timepoint: Before the intervention one month and three months after the intervention. Method of measurement: questionnaire.;Knowledge. Timepoint: Before and one and three months after the intervention. Method of measurement: questionnaire.;Perceived sensitivity. Timepoint: Before and one and three months after the intervention. Method of measurement: questionnaire.;Perceived severity. Timepoint: Before and one and three months after the intervention. Method of measurement: questionnaire.;Reward. Timepoint: Before and one and three months after the intervention. Method of measurement: questionnaire.;Response Costs. Timepoint: Before and one and three months after the intervention. Method of measurement: questionnaire.;Fear. Timepoint: Before and one and three months after the intervention. Method of measurement: questionnaire.;Self Efficacy. Timepoint: Before and one and three months after the intervention. Method of measurement: questionnaire.;Response Efficacy. Timepoint: Before and one and three months after the intervention. Method of measurement: questionnaire.;Treat Appraisal. Timepoint: Before and one and three months after the intervention. Method of measurement: questionnaire.;Coping Appraisal. Timepoint: Before and one and three months after the intervention. Method of measurement: questionnaire.;Motivation. Timepoint: Before and one and three months after the intervention. Method of measurement: questionnaire.;Health Promotion. Timepoint: Before and one and three months after the intervention. Method of measurement: questionnaire.;Screening Behavior of Breast Cancer. Timepoint: Before and one and three months after the intervention. Method of measurement: questionnaire.;Social Support Theory. Timepoint: Before and one and three months after the intervention. Method of measurement: questionnaire.;Emotional Support. Timepoint: Before and one and three months after the intervention. Method of measurement: questionnaire.;Information Support

Countries

Iran (Islamic Republic of)

Contacts

Public Contactmitra dogonchi

Hamedan University of Medical Sciences

dogonchi.mitra@yahoo.com+98 17 3452 1398

Outcome results

None listed

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