The effectiveness of educational intervention for performing colorectal cancer screening

The effectiveness of educational intervention base on Preventive Health Model for performing colorectal cancer screening in 30-50 years old population referred to health center of Karoon city in 2018

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20180909040980N1

Enrollment

160

Registered

2019-02-04

Start date

2018-09-16

Completion date

Unknown

Last updated

2019-02-25

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

Conditions

Colorectal cancer. Malignant neoplasm of rectosigmoid junction

Interventions

Intervention 1: One group in the study will receive educational intervention. Educational content provided to the intervention group includes an app that is designed based on preventive health model,

Eligibility

Sex/Gender

All

Age

30 Years to 50 Years

Inclusion criteria

Inclusion criteria: Age 30 to 50 years Inclination to participate in research Diploma and higher education The absence of a person or primary relatives with colorectal cancer No history of colorectal screening People without any clinical symptoms (asymptomatic) Having informed consent

Exclusion criteria

Exclusion criteria: Not having Android mobile phone to install educational content Having physical limitation

Design outcomes

Primary

Measure	Time frame
Perceived self-efficacy. Timepoint: 2 months after the beginning of the study. Method of measurement: Colorectal screening questionnaire.;Perceived sensitivity. Timepoint: 2 months after the beginning of the study. Method of measurement: Colorectal screening questionnaire.;Worries and fears. Timepoint: 2 months after the beginning of the study. Method of measurement: Colorectal screening questionnaire.;Screening Effectiveness. Timepoint: 2 months after the beginning of the study. Method of measurement: Colorectal screening questionnaire.;Social support. Timepoint: 2 months after the beginning of the study. Method of measurement: Colorectal screening questionnaire.;Behavioral intention. Timepoint: 2 months after the beginning of the study. Method of measurement: Colorectal screening questionnaire.	—

Measure

Time frame

Perceived self-efficacy. Timepoint: 2 months after the beginning of the study. Method of measurement: Colorectal screening questionnaire.;Perceived sensitivity. Timepoint: 2 months after the beginning of the study. Method of measurement: Colorectal screening questionnaire.;Worries and fears. Timepoint: 2 months after the beginning of the study. Method of measurement: Colorectal screening questionnaire.;Screening Effectiveness. Timepoint: 2 months after the beginning of the study. Method of measurement: Colorectal screening questionnaire.;Social support. Timepoint: 2 months after the beginning of the study. Method of measurement: Colorectal screening questionnaire.;Behavioral intention. Timepoint: 2 months after the beginning of the study. Method of measurement: Colorectal screening questionnaire.

—

Secondary

Measure	Time frame
Screening behavior. Timepoint: 2 months after the beginning of the study. Method of measurement: Colorectal screening questionnaire.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFatemeh Fayazi

Ahvaz University of Medical Sciences

fatemeh.fayazi200@gmail.com+98 61 3553 1822

Outcome results

None listed

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