Intervention program to increase colorectal cancer screening

Design, implementation and evaluation of an educational intervention to increase colorectal cancer screening: An application of intervention mapping approach

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT2015041821822N1

Enrollment

244

Registered

2015-06-28

Start date

2015-09-06

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

Colorectal cancer. Malignant neoplasm of colon and rectum

Interventions

Intervention 1: Intervention group1: Interventions included holding educational sessions, distribution of educational aids tools such as pamphlet, film and free access to fecal occult blood test. Inte

Prevention

Intervention group1: Interventions included holding educational sessions, distribution of educational aids tools such as pamphlet, film and free access to fecal occult blood test

Intervention group2: Interventions included holding educational sessions, distribution of educational aids tools such as pamphlet and film

Intervention group3: free access to fecal occult blood test

Control group: For the control group will not perform any of the action that will be taken for the intervention group.

Eligibility

Sex/Gender

All

Age

40 Years to 75 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Residing in Hamadan; In the age group over 40 years; Lack of screening (fecal occult blood test and colonoscopy) and Exclusion criteria: Failure to cooperate with researchers; moved to another city during the study period

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
Perceived severity. Timepoint: Before and 4 months after intervention. Method of measurement: Questionnaire.;Knowledge. Timepoint: Before and 4 months after intervention. Method of measurement: Questionnaire.;Perceived susceptibility. Timepoint: Before and 4 months after intervention. Method of measurement: Questionnaire.;Intention. Timepoint: Before and 4 months after intervention. Method of measurement: Questionnaire.;Perceived barriers. Timepoint: Before and 4 months after intervention. Method of measurement: Questionnaire.;Social support. Timepoint: Before and 4 months after intervention. Method of measurement: Questionnaire.;Self efficacy. Timepoint: Before and 4 months after intervention. Method of measurement: Questionnaire.;Perceived benefits. Timepoint: Before and 4 months after intervention. Method of measurement: Questionnaire.	—

Measure

Time frame

Perceived severity. Timepoint: Before and 4 months after intervention. Method of measurement: Questionnaire.;Knowledge. Timepoint: Before and 4 months after intervention. Method of measurement: Questionnaire.;Perceived susceptibility. Timepoint: Before and 4 months after intervention. Method of measurement: Questionnaire.;Intention. Timepoint: Before and 4 months after intervention. Method of measurement: Questionnaire.;Perceived barriers. Timepoint: Before and 4 months after intervention. Method of measurement: Questionnaire.;Social support. Timepoint: Before and 4 months after intervention. Method of measurement: Questionnaire.;Self efficacy. Timepoint: Before and 4 months after intervention. Method of measurement: Questionnaire.;Perceived benefits. Timepoint: Before and 4 months after intervention. Method of measurement: Questionnaire.

—

Secondary

Measure	Time frame
FOBT. Timepoint: After intervention. Method of measurement: Stool Test.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFereshteh Besharati

Hamadan University of Medical Sciences

f.besharati@umsha.ac.irfereshteh.besharati@yahoo.com+98 81 3838 0292

Outcome results

None listed

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