Aerobic Interval Training in Cardiac Rehabilitation

Sponsor
Norwegian University of Science and Technology (Other)
Overall Status
Completed
CT.gov ID
NCT00964067
Collaborator
St. Olavs Hospital (Other)
90
1
3
34
2.6

Study Details

Study Description

Brief Summary

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.

Condition or Disease Intervention/Treatment Phase
  • Other: Exercise training
N/A

Detailed Description

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.

Study Design

Study Type:
Interventional
Actual Enrollment :
90 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Effect of High Intensity Aerobic Interval Training in Cardiac Rehabilitation
Actual Study Start Date :
Sep 1, 2009
Actual Primary Completion Date :
Apr 1, 2011
Actual Study Completion Date :
Jul 1, 2012

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Treadmill group

Interval exercise performed on treadmills, supervised

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: Exercise groups

Supervised and organised in groups of ten

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: home-based exercise

Interval training at home, free choice of modality

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.

Outcome Measures

Primary Outcome Measures

  1. VO2peak [baseline, after 12 weeks and after 1 year]

Secondary Outcome Measures

  1. quality of life [baseline, 12 weeks and 1 year]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 80 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • coronary artery disease

  • age over 18

  • referred to cardiac rehabilitation

  • exercise tolerance demonstrated

Exclusion Criteria:
  • severe arrhythmia

  • heart failure

  • drug abuse

  • pregnancy

Contacts and Locations

Locations

Site City State Country Postal Code
1 St.Olavs University Hospital Trondheim Norway 7006

Sponsors and Collaborators

  • Norwegian University of Science and Technology
  • St. Olavs Hospital

Investigators

  • Study Director: Asbjørn Støylen, PhD, Norwegian University of Science and Technology

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Norwegian University of Science and Technology
ClinicalTrials.gov Identifier:
NCT00964067
Other Study ID Numbers:
  • HJERTEREHAB2009
First Posted:
Aug 24, 2009
Last Update Posted:
Mar 22, 2017
Last Verified:
Mar 1, 2017
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Norwegian University of Science and Technology
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 22, 2017