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Aerobic Interval Training in Cardiac Rehabilitation

This study has been completed.
Sponsor:
Collaborator:
St. Olavs Hospital
Information provided by (Responsible Party):
Norwegian University of Science and Technology
ClinicalTrials.gov Identifier:
NCT00964067
First received: August 21, 2009
Last updated: March 20, 2017
Last verified: March 2017
August 21, 2009
March 20, 2017
September 2009
April 2011   (Final data collection date for primary outcome measure)
VO2peak [ Time Frame: baseline, after 12 weeks and after 1 year ]
Same as current
Complete list of historical versions of study NCT00964067 on ClinicalTrials.gov Archive Site
quality of life [ Time Frame: baseline, 12 weeks and 1 year ]
Same as current
Not Provided
Not Provided
 
Aerobic Interval Training in Cardiac Rehabilitation
Effect of High Intensity Aerobic Interval Training in Cardiac Rehabilitation
The purpose of the study is to compare home-based aerobic interval training with supervised interval training performed in groups or on a treadmill at the hospital.
Cardiac rehabilitation is usually first offered in hospitals, but there are several studies that show that home-based rehabilitation is equally efficient. How this comes out when exercise is organized as aerobic interval training is not known.
Interventional
Not Provided
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
  • Myocardial Infarction
  • Coronary Artery Disease
Other: Exercise training
Interval training at 90% of max heart rate. Warm-up of 10-15 minutes up to 70% of HRmax, then 4 minutes of exercise at 90%. 3 minutes of active pause between the intervals. Total 45 minutes of exercise. Twice a week.
  • Active Comparator: Treadmill group
    Interval exercise performed on treadmills, supervised
    Intervention: Other: Exercise training
  • Active Comparator: Exercise groups
    Supervised and organised in groups of ten
    Intervention: Other: Exercise training
  • Active Comparator: home-based exercise
    Interval training at home, free choice of modality
    Intervention: Other: Exercise training

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
90
July 2012
April 2011   (Final data collection date for primary outcome measure)

Inclusion Criteria:

  • coronary artery disease
  • age over 18
  • referred to cardiac rehabilitation
  • exercise tolerance demonstrated

Exclusion Criteria:

  • severe arrhythmia
  • heart failure
  • drug abuse
  • pregnancy
Sexes Eligible for Study: All
18 Years to 80 Years   (Adult, Senior)
No
Contact information is only displayed when the study is recruiting subjects
Norway
 
 
NCT00964067
HJERTEREHAB2009
No
Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
Not Provided
Norwegian University of Science and Technology
Norwegian University of Science and Technology
St. Olavs Hospital
Study Director: Asbjørn Støylen, PhD Norwegian University of Science and Technology
Norwegian University of Science and Technology
March 2017

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP