Randomized Clinical Trial for optimal Cardiac Rehabilitation: A traditional Dutch Cardiac Rehabilitation Program versus a Canadian High Efficiency Cardiac Rehabilitation Program
Completed
- Conditions
- coronary syndromeheart attack10028593
- Registration Number
- NL-OMON36989
- Lead Sponsor
- niversitair Medisch Centrum Sint Radboud
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 210
Inclusion Criteria
- Patients suitable for cardiac rehabilitation
- Signed written informed consent
- One of the following criteria:
* Patients with an acute coronary syndrome, including myocardial infarction (MI) within 3 months prior to inclusion
* Patients that underwent a percutaneous coronary intervention (PCI) within 3 months prior to inclusion
* Patients that received coronary artery bypass grafting (CABG) within 3 months prior to inclusion
Exclusion Criteria
- Mental impairment leading to inability to cooperate
- Severe impaired ability to exercise of other than cardiovascular causes
- Signs of cardiac ischemia and/or a positive exercise testing on cardiac ischemia
- Insufficient knowledge of the Dutch language
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <p>Physical capacity (peak oxygen uptake)</p><br>
- Secondary Outcome Measures
Name Time Method