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TerminatedNCT00226733Updated May 18, 2010

Training Intensity After Coronary Bypass Grafting

A Phase 2 interventional study of Exercise training and Exercise training in Coronary Artery Bypass, sponsored by Norwegian University of Science and Technology. Terminated at 1 site in Norway. Per ClinicalTrials.gov, last updated 2010-05-18.

Sponsored by Norwegian University of Science and Technology · Phase 2, Interventional, and Treatment

Phase
Phase 2
Study type
Interventional
Enrollment
60
Allocation
Randomized
Sex
All
01

Study summary

The purpose of this study is to investigate the effect of high and moderate intensity exercise training after coronary bypass surgery. The subjects are randomised to training at either 60-70% or 85-95% of their maximal capacity daily for four weeks. Primary outcome measure is change in maximal aerobic capacity, measured as change in maximal oxygen consumption, after the training period. Secondary outcome measures are change in quality of life, heart rate variability, ultrasound measures of the heart and blood variables, including endothelian markers.

Read the detailed description

The exercise part of cardiac rehabilitation today is often composed of low to moderate intensity training. Several studies have found interval training with high intensity to be more effective in improving physical capacity in healthy subjects and also in different patient populations. We therefore wish to compare high intensity interval training with moderate intensity training in patients operated with coronary bypass surgery. Maximal oxygen consumption is shown to be the best indicator of how many years you life, both in healthy persons and in cardiac patients.

The subjects in this study is attending a four week rehabilitation program at an residential institution in Norway. They are randomised to do either a moderate or a high intensity aerobic training session each day.

The hypothesis in advance, was that high intensity interval training lead to a greater improvement in maximal oxygen consumption than training with moderate intensity. We also hypothesised that there would be no difference between the two groups after 6 months, since then the patients had to administer their own exercise training.

02

Conditions studied

  • Coronary Artery Bypass

Keywords

  • Coronary Artery Bypass (E04.928.220.520.220)
  • Exercise Test [E01.370.370.380.250]
  • Echocardiography [E01.370.370.380.220]
  • Quality of Life [K01.752.400.750]
03

In context

Lead sponsor

Norwegian University of Science and Technology is the lead sponsor of 487 studies on the registry; 52 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Coronary Artery Grafting (4-12 weeks ago)

Exclusion criteria

Exclusion Criteria:

  • Not able to exercise on a treadmill
  • Left ventricle ejection fraction \< 30%
  • hemodynamic significant valve deficit (> NYHA classification II)
05

Study design

Phase
Phase 2
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
60 participants

Study arms

  • Experimental
    A

    Interval exercise training with high intensity

    Behavioral: Exercise training

  • Active comparator
    B

    Exercise training with moderate intensity

    Behavioral: Exercise training

Interventions

  • BehavioralExercise training

    Interval exercise training with high intensity five days per week for four weeks.

  • BehavioralExercise training

    Exercise training with moderate intensity, five days per week for four weeks.

06

What researchers measure

Primary outcomes

  1. Oxygen Consumption

Secondary outcomes

  1. Quality of life

  2. Pulse

  3. Blodverdier

  4. Ekkokardiografiske parametre

07

Study locations

1 site
  • Norwegian University of Science and Technology
    Trondheim, 7489, Norway
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 18, 2010, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT00226733
Lead sponsor
Norwegian University of Science and Technology
Collaborators
Stiftelsen Helse og Rehabilitering, Landsforeningen for hjerte og lungesyke (LHL), Røros Rehabiliteringssenter, St. Olavs Hospital
First posted
Sep 27, 2005
Start date
Mar 2004
Primary completion
Mar 2007
Completion
Mar 2007
Last update
May 18, 2010

Study contacts

Stig A Slørdahl, Dr.med
study chair · NTNU, Institutt for sirkulasjon og bildediagnostikk
Trine T Moholdt, MS
principal investigator · NTNU, Institutt for sirkulasjo og bildediagnostikk

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

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This study is terminated, as verified in Apr 2008. You cannot join it, but the record below documents what was studied.

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