Cardiac rehabilitation
Conditions
Interventions
Not applicable.
Sponsors
Isala Zwolle
Eligibility
Inclusion criteria
Inclusion criteria: In order to be eligible to participate in this study, a subject must meet all of the following criteria: - Patients of 65 years or older who have accepted CR - Signed written informed consent - One of the following criteria: o Patients with an ACS, including MI and/or revascularisation within 3 months prior to the start of the CR programme o Patients that underwent a PCI within 3 months prior to the start of the CR programme o Patients that received CABG within 3 months prior to the start of the CR programme o Patients who were treated surgically or percutaneously for valvular heart disease (including TAVI) within 3 months prior to the start of the CR programme o Patients with a stable angina with documented significant CAD (defined by standard non-invasive or invasive methods)
Exclusion criteria
Exclusion criteria: A potential subject who meets any of the following criteria will be excluded from participation in this study: - Contraindication to CR - Mental impairment leading to inability to cooperate - Severe impaired ability to exercise - Signs of severe cardiac ischemia and/or a positive exercise testing on severe cardiac ischemia - Insufficient knowledge of the native language - Implanted cardiac device (CRT-P, ICD)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Difference in peak oxygen uptake (VO2peak) between the end of CR programme (T1) and baseline (T0). | — |
Secondary
| Measure | Time frame |
|---|---|
| - Difference in VO2peak between 12 months (T2) and T0 - Difference in VO2peak between T2 and T1 - Traditional risk factors for CVD - Major Adverse Cardiovascular Events (MACE) - General health - Care utilisation - Costs of care utilisation - Adherence - Compliance | — |
Contacts
Public ContactLeonie Prins
Diagram B.V.
Outcome results
None listed