Condition 1: colon cancer. Condition 2: Rectum cancer. Malignant neoplasm of colon Malignant neoplasm of rectum
Conditions
Interventions
Intervention 1: The participants of intervention group receives health belief model-based training content within Multimedia tool. For follow up,the subjects will receive in every two week one phone
Prevention
The participants of intervention group receives health belief model-based training content within Multimedia tool. For follow up,the subjects will receive in every two week one phone contact, also th
The participants of intervention group receives Motivation-protection-based training content within Multimedia tool. For follow up,the subjects will receive in every two week one phone contact, also
control group receives clinical routine education
Sponsors
Vice chancellor for research of Bushehr University of Medical Sciences
Eligibility
Sex/Gender
All
Age
49 Years to 79 Years
Inclusion criteria
Inclusion criteria: The inclusion criteria are: older than 50 years; having the ability to read and write; not having colorectal cancer or other types of cancers; not having family history of colorectal cancer; residence in Boushehr city; having ability to work with the appropriate tool for viewing multimedia. Exclusion criteria are: dissatisfaction to participate in the study; not seeing Multi Media; unwillingness to Continue participation in the study at any time.
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Preventive Nutrition pattern. Timepoint: Before education and 3 months later. Method of measurement: three-day recall alimentary questionnaire. | — |
Secondary
| Measure | Time frame |
|---|---|
| Perceived sensitivity. Timepoint: Before study, a week after the intervention and Three Months after intervention. Method of measurement: Researcher-made perceived sensitivity questionnaire.;Perceived severity. Timepoint: Before study, a week after the intervention and Three Months after intervention. Method of measurement: Researcher-made perceived severity questionnaire.;Perceived benefits. Timepoint: Before study, a week after the intervention and Three Months after intervention. Method of measurement: Researcher-made perceived benefits questionnaire.;Perceived barriers. Timepoint: Before study, a week after the intervention and Three Months after intervention. Method of measurement: Researcher-made perceived barriers questionnaire.;Perceived self-efficacy. Timepoint: Before study, a week after the intervention and Three Months after intervention. Method of measurement: Researcher-made perceived self-efficacy questionnaire.;Awareness. Timepoint: Before study, a week after the intervention and Three Months after intervention. Method of measurement: Researcher-made perceived awareness questionnaire.;Perceived rewards are incompatible behavior. Timepoint: Before study, a week after the intervention and Three Months after intervention. Method of measurement: Researcher-made perceived Perceived rewards are incompatible behaviorquestionnaire.;Fear. Timepoint: Before study, a week after the intervention and Three Months after intervention. Method of measurement: Researcher-made fear questionnaire.;Effectiveness of the perceived response. Timepoint: Before study, a week after the intervention and Three Months after intervention. Method of measurement: Researcher-made Effectiveness of the perceived responsequestionnaire.;Perceived cost. Timepoint: Before study, a week after the intervention and Three Months after intervention. Method of measurement: Researcher-made Perceived cost questionnaire.;Intent. Timepoint: Before study, a week after the intervention and Three Mont | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactAzita Noroozi
Bushehr University of Medical Sciences, Bushehr
Outcome results
None listed