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Different Endurance Training Protocols in Cardiac Rehabilitation

Phase 4
Completed
Conditions
Coronary Artery Disease
Interventions
Other: Endurance training with constant work load
Other: Pyramid-Training
Other: High-intensity interval training
Registration Number
NCT01493193
Lead Sponsor
Paracelsus Medical University
Brief Summary

It is the aim of the study to compare the effects of 6 weeks of either high-intensity interval training (HIT; carried out at correctly assessed 85-95% of maximal heart rate), pyramid, or continuous endurance training, on changes of physical exercise capacity in cardiac patients.

The three exercise arms (isocaloric) are composed as follows:

Endurance training (n=15): 31min at 65-75% HRmax; HIT (n=15): 4x4min intervals at 85-95% HRmax divided by 3x3min of active recovery at 60-70% HRmax, making it a total of 25min; Pyramids (n=15): One Pyramid consists of 8 one-minute blocks. Those are grouped starting with one block of 70-75% HRmax, followed by one block at 75-80% HRmax and another one at 80-85% HRmax. The top of the pyramid are 2 blocks of 85-90% HRmax. Intensity is lowered afterwards with one block at 80-85% HRmax, followed by one block at 75-80% HRmax and last one at 70-75% HRmax. Two more pyramids follow, each divided by 2min of active recovery at 65-70% HRmax, making it a total of 28min.

All protocols are initiated by 5min of warm-up and end with 5min of cool-down, both at 60-70% HRpeak.

Primary Outcome: Individual maximum power output in watt (Pmax). Secondary Outcome: Change of power output in watt at lactate thresholds at 2 and 4 mmol/l.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
60
Inclusion Criteria

At least one of the following diagnoses within the previous 3 months:

  • acute coronary syndrome (STEMI)
  • acute coronary syndrome (NSTEMI)
  • aortocoronary bypass surgery
  • PCI
  • stable coronary heart disease
Exclusion Criteria
  • Unstable angina pectoris
  • Heart failure (NYHA IV)
  • Acute endomyocarditis or other acute infections
  • Pulmonary artery embolism or phlebothrombosis within the previous 6 months
  • Hemodynamically unstable arrhythmia
  • Hypertrophic cardiomyopathy
  • participation in another study within the previous 6 months
  • Medical conditions which prevent patients from complying with the exercise program

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Endurance training with constant work loadEndurance training with constant work load-
Pyramid-TrainingPyramid-Training-
High-intensity interval trainingHigh-intensity interval training-
Primary Outcome Measures
NameTimeMethod
Individual maximum power output in watt (Pmax)6 weeks

Change of individual maximum power output in watt (Pmax) on a bicycle ergometer after the training intervention of controlled physical activity within 6 weeks

Secondary Outcome Measures
NameTimeMethod
Power output in watt at lactate threshold of 2 and 4 mmol/l6 weeks

Change of power output in watt at lactate thresholds at 2 and 4 mmol/l

Trial Locations

Locations (1)

Department of Sports Medicine, Prevention and Rehabilitation Paracelsus Medical University

🇦🇹

Salzburg, Austria

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