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Home based cardiac rehabilitation

A study on the effectiveness of a comprehensive home based cardiac rehabilitation intervention on the health promotion of patient with coronary heart disease

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016022926820N1
Enrollment
240
Registered
2016-08-09
Start date
2016-07-09
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

Coronary heart disease. Acute myocardial infarction

Interventions

Intervention 1: Intervention group will be given three sessions of educational program (for half an hour each) on physical activity. Comparably, control group will receive routine training before disc
Lifestyle
Intervention group will be given three sessions of educational program (for half an hour each) on physical activity. Comparably, control group will receive routine training before discharge.
Intervention group will be given three sessions of educational program (for half an hour each) on stress management. Comparably, control group will receive routine training before discharge.
Intervention group will be given three sessions of educational program (for half an hour each) on healthy diet. Comparably, control group will receive routine training before discharge.
Intervention group will be given three sessions of educational program (for half an hour each) on smoking cessation for current smokers. Comparably, control group will receive routine training before

Sponsors

National Institute for Medical Research Development (NIMAD)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Inclusion criteria: having coronary heart disease. Exclusion criteria: dementia; unstable angina; cardiac arrhythmia's

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Quality of life. Timepoint: Before and 6 months after intervention. Method of measurement: Quality of life questionnaire for cardiac patients.;Depression. Timepoint: Before and 6 months after intervention. Method of measurement: Beck Depression Inventory.;Physical activity. Timepoint: Before and 6 months after intervention. Method of measurement: Godin Leisure Time Physical Activity Questionnaire.;Blood pressure. Timepoint: Before and 6 months after intervention. Method of measurement: Using mercury sphygmomanometer on millimeters of mercury scale.;BMI. Timepoint: Before and 6 months after intervention. Method of measurement: The person's weight in kilograms divided by the square of height in meters.;Lipid profile. Timepoint: Before and 6 months after intervention. Method of measurement: Using rlated laboratory kits.

Secondary

MeasureTime frame
Recurrent cardiovascular events. Timepoint: A year after the intervention. Method of measurement: Individual medical records.;Mortality due to cardiovascular disease. Timepoint: A year after the intervention. Method of measurement: Individual medical records.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactHassan Okatialiabad

Zahedan University of Medical Sciences

okati_h@yahoo.com+98 54 3329 5837

Outcome results

None listed

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