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Effect of Exercise After Heart Transplantation

Phase 2
Completed
Conditions
Heart Transplantation
Interventions
Other: Interval-based aerobic exercise
Registration Number
NCT01091194
Lead Sponsor
Oslo University Hospital
Brief Summary

This is a randomized controlled trial which will include approximately 50 heart transplant recipients 1-8 years after heart transplantation. The intervention and follow up period is 1 year. The primary purpose is to investigate if systematic, high intensity, interval-based aerobic exercise training results in a greater improvement of exercise capacity (measured by VO2peak) than previously shown in heart transplant recipients.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
51
Inclusion Criteria
  • Norwegian heart transplanted patients > 18 years of age
  • 1-8 years after heart transplantation
  • Optimal medical treatment
  • Stable condition
  • Written informed consent
  • Must have access to a physical therapist or personal trainer in their hometown
  • Motivation for exercise
Exclusion Criteria
  • Unstable condition
  • In need of revascularization or other invention
  • Infections, open wounds or skin diseases
  • Physical disabilities which prevent participation
  • Other diseases, illnesses or conditions which contradict exercise

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
ExerciseInterval-based aerobic exerciseInterval-based aerobic exercise
Primary Outcome Measures
NameTimeMethod
Peak oxygen uptake (VO2peak)Before and after the intervention period of 1 year
Secondary Outcome Measures
NameTimeMethod
Isokinetic muscle strength of quadriceps and hamstringsBefore and after the intervention period of 1 year
Quality of life measured by questionnairesBefore and after the intervention period of 1 year
Myocardial function measured by echocardiographyBefore and after the intervention period of 1 year
Reinnervation as judged by autonomic nervous control (Heart Rate Variability)Before and after the intervention period of 1 year
Progression on coronary atherosclerosis measured by intra vascular ultrasound (IVUS)Before and after the intervention period of 1 year
Vascular tone and compliance measured by tonometryBefore and after the intervention period of 1 year
Analysis of isolated muscle cells from myocardial biopsyBefore and after the intervention period of 1 year
Regular blood screening, lipid profile, inflammatory status, nerve growth factor, biochemical markers for endothelial function, prothrombotic factor, factors connected to vascularization: NT-proBNP and gene expression analysis.Before and after the intervention period of 1 year

Trial Locations

Locations (1)

Department of Cardiology, Oslo University Hospital, Rikshospitalet

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Oslo, Norway

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