I70 I10
Conditions
Interventions
Group 1: Intervention: The intervention-group, to test the primary endpoint of the study, trains once a week in the conventional cardiac rehabilitation group, but also trains once a week in an individ
Sponsors
Präventive und Rehabilitative Sportmedizin
Klinikum rechts der Isar/ Technische Universität München (TUM)
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Participation in secondary outpatient cardiac rehabilitation Written informed consent Physian approval of supervised physical activity Exercise capacity < 1.4 Watt/kgBW measured within 12 weeks before beginning participation in the study
Exclusion criteria
Exclusion criteria: Maximum exercise capacity > 1.4 Watt/kg BW Contraindication for regular supervised exercise High-grade aortic valve stenosis NYHA IV Heart Failure Uncontrolled hypertension Uncontrolled diabetes Hospitalisation for cardiac symptoms within six weeks Acute systemic disease/ fever Chronic drug/ alcohol abuse Inability/unwillingness to understand/participate in all aspects of the study Rejection of participant by the study center
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Change in exercise capacity after six months, measured as maximal watts achieved during exercise testing per kilogram of body weight (Watt/kgBW). | — |
Secondary
| Measure | Time frame |
|---|---|
| Cardiovascular risk-profile (6 and 12 months after beginning the intervention) Quality of Life (QoL) (6 and 12 months after beginning the intervention ) Safety (SAE/AE) (6 and 12 months after beginning the intervention) Physical Activity Level (PAL) (6 and 12 months after beginning the intervention) | — |
Countries
Germany
Contacts
Public ContactJeffrey Wilcox Christle
Präventive und Rehabilitative Sportmedizin Klinikum recht der Isar/Technische Universität München (TUM)
Outcome results
None listed