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Effect of M-Health on secondary prevention of coronary artery disease patients

Not Applicable
Conditions
Coronary Artery disease.
125.0
125.1
Registration Number
IRCT20221016056204N1
Lead Sponsor
Tehran University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
1544
Inclusion Criteria

History of CAD defined as history of myocardial infarction, percutaneous coronary intervention, coronary artery bypass graft surgery, coronary angiography confirming stenosis>50% in at least one of the major epicardial coronary arteries or their main branches.
Having at least one uncontrolled risk factor including: uncontrolled hypertension, uncontrolled dyslipidemia and current cigarette smoking for =12 months.
Aged between 25 to 75 years
Inclination to staying in study for two years
Having and ability of using smart phone by the participant or one of his/her trustworthy relatives who lives near him/her
Willing to control the risk factors using App
Provides informed consent to participate in the study

Exclusion Criteria

Mental retardation
Individuals with prohibitive morbidity that requires close face-to-face monitoring.
End stage chronic disease such as: hepatic and/or renal failure, heart failure, active cancer

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Smoking Cessation. Timepoint: Three months post-randomization. Method of measurement: Self-report for quitting smoking.;Blood pressure control to less than 130/80 mm Hg. Timepoint: Three months post-randomization. Method of measurement: Sphygmomanometer/Blood pressure measurement by the physician in the clinic.;Dyslipidemia control with the target of low-density lipoprotein cholesterol (LDL-C) less than 55 mg/dL. Timepoint: Three months post-randomization. Method of measurement: Lab test to measure low-density lipoprotein cholesterol.
Secondary Outcome Measures
NameTimeMethod
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