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Effect of Educational Package on Doing Preventive Behaviors of Cardiovascular disease

The Effect of Educational Package Based on Health Belief Model for People at Risk of Cardiovascular Disease to Modify Unhealthy Behaviors.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201201238803N1
Enrollment
100
Registered
2012-09-29
Start date
2011-07-23
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

Condition 1: Acude myocardial infarction. Condition 2: Subsequent myocardial infarction. Condition 3: Certain current complications following acute. Condition 4: Other acute ischaemic heart diseases. Condition 5: Chronic ischaemic heart disease. Condition 6: Angina pectoris. Acude myocardial infarction Subsequent myocardial infarction Certain current complications following acute myocardial infarction Other acute ischaemic heart diseases Chronic ischaemic heart disease Angina pectoris

Interventions

Intervention 1: Intervention Group Will Receive Educational Package (5 Educational Booklets). Intervention 2: Control Group Are Expose Usual Educations(Mass Media,..).
Prevention
Intervention Group Will Receive Educational Package (5 Educational Booklets)
Control Group Are Expose Usual Educations(Mass Media,..)

Sponsors

Shahid Sadoughi University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 65 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria:30-65 years old; having at least one Risk Factor of Cardiovascular Disease; Free of Diagnosed Heart Disease & Free of Mental Disorders exclusion criteria : Being Illiterate; Unable to read

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Preventive behaviors. Timepoint: At first of study and 2 months after intervention. Method of measurement: Questionare.

Secondary

MeasureTime frame
Knowledge. Timepoint: At the first of study & 2 months after intervention. Method of measurement: Questionnare.;Perceived susceptibility. Timepoint: At first of study $ 2 months after intervention. Method of measurement: Questionnare.;Perceived severity. Timepoint: At first of study & 2 montha after intervention. Method of measurement: Questionnare.;Perceived benefits. Timepoint: At first of study & 2 months after intervention. Method of measurement: Questionnare.;Perceived barriers. Timepoint: At first of study & 2 months after intervention. Method of measurement: Questionnare.;Self efficacy. Timepoint: At first of study & 2 months after intervention. Method of measurement: Questionnare.;Cues to action. Timepoint: At first of study & 2 months after intervention. Method of measurement: Questionnare.

Countries

Iran (Islamic Republic of)

Contacts

Public Contacttahereh rahimdel

shahid sadoughi university of medical sciences

rahimdell@yahoo.com+98 35 1726 6711

Outcome results

None listed

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