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Clinical Trial Summary

The aim of this study was to examine the effects of high intensity aerobic interval training (AIT) versus moderate continuous training (CON) in heart transplant recipients.


Clinical Trial Description

Clinically stable heart transplant recipients > 12 month or more after HTx, age > 18 years, willing and capable of giving written informed consent for study participation and anticipated to be able to participate in the study for 12 months were included from the Heart Centre, Rigshospitalet, Copenhagen University Hospital. Patients were excluded due to unstable condition or postoperative complications, recent severe rejection episodes (>H1R < 3 month), physical disabilities which prevent participation and re-transplantation or multi-organtransplantation. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT01914406
Study type Interventional
Source Bispebjerg Hospital
Contact
Status Completed
Phase N/A
Start date January 2011
Completion date October 2013

See also
  Status Clinical Trial Phase
Completed NCT02077764 - The GRAFT Study: Evaluation of Graft Function, Rejection and Cardiac Allograft Vasculopathy in First Heart Transplant Recipients. N/A
Terminated NCT01278745 - Prevention of Cardiac Allograft Vasculopathy Using Rituximab (Rituxan) Therapy in Cardiac Transplantation Phase 2
Recruiting NCT06190171 - Respiratory Strength Training in Heart Transplant Recipients N/A
Completed NCT01912248 - Acute Effect of Strength Training on Blood Pressure in Cardiac Patients N/A
Active, not recruiting NCT01759966 - Autonomic Cardiovascular Control After Heart Transplantation
Completed NCT01796379 - High Intensity Training in de Novo Heart Transplant Recipients in Scandinavia N/A
Completed NCT02213770 - Long Term Effect of High-intensity Training After Heart Transplantation N/A
Completed NCT03662789 - Intravenous Iron Supplement for Iron Deficiency in Cardiac Transplant Recipients Phase 2/Phase 3