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The objective of this study is to assess by what physiological mechanisms patients with heart failure benefit from exercise. Effects of an exercise intervention will be assessed for both central (heart and lungs) and peripheral (muscle fiber and mitochondria) factors.
A randomized, non-blinded prospective intervention trial. Patients randomized to exercise intervention will undergo supervised aerobic training on ergometer cycle for 12 weeks whilst control group receives standard care. Before and after the intervention, all participants will undergo cardiac magnetic resonance imaging (cardiac MR) examinations, Ventilation/Perfusion Single Photon Emission Computed Tomography (V/P SPECT), Cardiopulmonary exercise tests, muscle biopsies and blood sampling.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Supervised exercise | Experimental | The exercise intervention will include 2 supervised sessions of ergometer cycling with a warm up period of 10 minutes and 20 minutes of cycling at the aerobic intensity below the anaerobic threshold as determined from baseline results. Patients in the exercise arm will have 1 unsupervised exercise session where the participants walk or bicycle for 30 minutes at an intensity experienced as somewhat hard (Borg 13) according to the Borg Rating of Perceived Exertion Scale. |
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| Standard of Care | No Intervention | The control group will receive advise to continue to live as usual. After 4 and 8 weeks, participants in the control group will be contacted by telephone for inquiry of general wellbeing. No other interventions will be performed in the control group. |
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Supervised Exercise | Other | 12 weeks of supervised aerobic exercise individually adapted to exercise capacity according to a VO2 peak test |
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| Measure | Description | Time Frame |
|---|---|---|
| Maximal oxygen uptake (VO2peak) | a change in maximal oxygen uptake (VO2 peak) of 2 ml/min/kg | 12 weeks intervention |
| Measure | Description | Time Frame |
|---|---|---|
| Health related quality of life | Change in Health related quality of life assessed with Kansas City Cardiomyopathy Questionnaire (KCCQ). KCCQ scores are scaled from 0 to 100 and summarized in 25-point ranges, where scores represent health status as follows: 0 to 24: very poor to poor; 25 to 49: poor to fair; 50 to 74: fair to good; and 75 to 100: good to excellent. | 12 weeks intervention |
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Inclusion Criteria:
Exclusion criteria:
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Skåne University Hospital Lund | Lund | 22158 | Sweden |
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| Cardiac volumes and function | Change in cardiac volumes and function assessed using Cardiac MR indicating effects of the exercise intervention as compared to the control group | 12 weeks intervention |
| Perfusion gradients on Ventilation / Perfusion Single Photon Emission Computed Tomography (V/P SPECT) | Change in pulmonary congestion quantified by V/P SPECT | 12 weeks intervention |
| Mitochondrial function | Change in mitochondrial number and function using respirometry indicating effects of the exercise intervention as compared to the control group | 12 weeks intervention |