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The effect of educational intervention on lifestyle and clinical outcomes of patients with myocardial infarction

The effect of educational intervention, based on Pender's health promotion model on lifestyle and clinical outcomes of patients with myocardial infarction

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT201607236909N1
Enrollment
100
Registered
2016-09-21
Start date
2014-07-19
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

Myocardial Infarction. Acute myocardial infarction

Interventions

Intervention 1: Intervention group: eight training sessions lasting 45 minutes, twice a week, including: two sessions about the nature of cardiovascular disease, risk factors and treatment options, on
Lifestyle
Intervention group: eight training sessions lasting 45 minutes, twice a week, including: two sessions about the nature of cardiovascular disease, risk factors and treatment options, one sessions about
Control group: routine training (education about medications, nutrition and authorized activity)

Sponsors

Gonabad University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 60 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: patients who have no history of previous myocardial infarction, with the age between 30 and 60 years, at least an elementary school education and the ejection fraction above 40 percent (according to doctor's approval); Exclusion criteria: participation in rehabilitation programs in the control group and failure to participate in training sessions in the intervention group

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Lifestyle. Timepoint: Befor and three months after intervention. Method of measurement: Health Promotion Lifestyle Profile (HPLP).;Lipid profile. Timepoint: Befor and three months after intervention. Method of measurement: Blood sample by auto analyzer BT3000.;Blood pressure. Timepoint: Befor and three months after intervention. Method of measurement: Measuring arterial blood pressure by mercury sphygmomanometer.;Ejection fraction. Timepoint: Befor and three months after intervention. Method of measurement: Echocardiography.;Fasting blood level of glucose. Timepoint: Befor and three months after intervention. Method of measurement: Measuring blood glucose by glucometer before breakfast.

Secondary

MeasureTime frame
Cardiac knowledge. Timepoint: Befor and three months after the end of intervention. Method of measurement: Cardiac knowledge questionnaire.;Perceive benefits to behavior. Timepoint: Befor and three months after the end of intervention. Method of measurement: Perceive Benefits to Behavior (PBB) questionnaire.;Perceive barrier to behavior. Timepoint: Befor and three months after the end of intervention. Method of measurement: Perceive Barrier to Behavior (PBB) questionnaire.;Perceived self-efficacy. Timepoint: Befor and three months after the end of intervention. Method of measurement: Perceived Self-Efficacy questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFatemeh Mohammadipour

Lorestan University of Medical Sciences

mohammadipourf@gmail.com+98 66 3312 0195

Outcome results

None listed

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