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Clinical Trials/NCT01246570
NCT01246570CompletedNot Applicable

Supported Home-based Exercise Training Versus Usual Care After Cardiac Rehabilitation. A Randomized Controlled Study

Norwegian University of Science and Technology1 site in 1 country48 target enrollmentStarted: November 1, 2010Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
48
Locations
1
Primary Endpoint
Peak oxygen uptake

Study Overview

Brief Summary

It is known that organized cardiac rehabilitation is effective in improving exercise capacity in coronary heart disease patients. Less is known about the long-term results after cardiac rehabilitation. Earlier studies have shown that many patients quit exercising when no longer attending formal rehabilitation. The investigators wish to investigate the effect of a maintenance program after ending a rehabilitation program, and to compare this to usual care. The investigators hypothesis is that the maintenance program will result in higher exercise capacity and more physical activity compared to usual care.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
35 Years to 80 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • coronary heart disease patients

Exclusion Criteria

  • unstable angina pectoris
  • hemodynamic significant valve disease (> New York Heart Association class II)
  • pregnancy
  • left ventricular ejection fraction <30%
  • kidney failure (creatinin > 140)
  • uncontrolled hypertension

Arms & Interventions

Maintenance program

Experimental

Patients will attend a "motivational exercise session" once monthly. They will also be tested (exercise test with measurement of peak oxygen uptake) every third months.

Intervention: Exercise training (Behavioral)

Control

Active Comparator

Usual care. The patients will receive the usual care provided by the hospital and community health services

Intervention: Control (Other)

Outcomes

Primary Outcomes

Peak oxygen uptake

Time Frame: baseline and 12 months

The change in peak oxygen uptake from baseline to 12 months after baseline. In the intervention group, the peak oxygen uptake will be measured also every 3 months during the intervention period, and this will be reported

Secondary Outcomes

  • Blood markers(baseline and 12 months)
  • Death(baseline and 12 months)
  • Endothelial function(baseline and 12 months)
  • Quality of life(baseline and 12 months)
  • Myocardial infarction(baseline and 12 months)
  • Hospital readmission(baseline and 12 months)
  • Physical activity(baseline and 12 months)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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