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The effect of IT interventions in cardiac rehabilitation patients

Not Applicable
Recruiting
Conditions
Condition 1: Per-cutaneous coronary angioplasty. Condition 2: Coronary artery bypass surgery. Condition 3: Heart valve surgery. Condition 4: Cardiac transplantation.
Presence of coronary angioplasty implant and graft
Presence of aortocoronary bypass graft
Presence of other heart-valve replacement
Registration Number
IRCT20180730040643N1
Lead Sponsor
Mashhad University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
300
Inclusion Criteria

The patient or immediately family has smart phones.
Patients under coronary angioplasty
Patients undergo coronary artery bypass surgery
Patients undergo heart valve surgery
Patients undergo cardiac transplantation
Patients who have completed informed consent and are willing to enter the study.

Exclusion Criteria

Primary phase after acute coronary syndrome (up to two days)
Untreated arrhythmia
Acute heart failure
Uncontrolled hypertension (systolic upper than 200 or diastolic over 100)
Advanced coronary artery blockage
Acute Myocarditis and pericarditis
Congenital heart failure and cardiomyopathy
Acute systemic diseases (creatinine more than 3 and liver enzymes more than 3 times)
Uncontrolled Diabetes
There is a clot in the heart
VTE
AF with uncontrolled response
Patients who are not able to study information or are unable to complete questionnaires
Patients who cannot attend the study for any reason (such as psychiatric disorder, dementia, life-threatening concomitant illness, motor disability).
Patients who have received cardiac rehab in the last 12 months.
Patients who have received intracardiac defibrillator (ICD) or Cardiac Resynchronization Therapy (CRT) or a combination of both within the last 6 months.

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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