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This is a single-centre open randomized parallel-group study. Patients will be selected at random to be included in group 1: eccentric rehabilitation or group 2: conventional rehabilitation.
In addition, a group of healthy volunteers aged between 20 and 85 years will also be recruited. This group will make it possible to evaluate, during the two exercise sessions, mechanisms of adaptation linked to eccentric exercise vs concentric exercise.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Patients with chronic heart failure | Experimental |
| |
| Controls | Other |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| initial evaluation | Other |
| ||
| Period of cardiac rehabilitation |
| Measure | Description | Time Frame |
|---|---|---|
| Evolution of performance in the 6-minute walk test between the initial assessment and the final assessment of a reconditioning programme | 12 weeks |
| Measure | Description | Time Frame |
|---|---|---|
| Evolution of functional and physiological capacities and tolerance criteria | 12 weeks |
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Inclusion Criteria:
Patients :
Healthy volunteers:
Exclusion Criteria:
Patients:
associated chronic motor deficit of a neurological origin (example: sequelae of a cerebrovascular accident), an osteo-articular origin (example: impairment due to Rheumatoid arthritis), of a peripheral vascular disease (example: peripheral artery disease, venous disease, lymphedema) will not be included in the exclusion criteria provided thay are compatible with the level of physical ability defined in the inclusion criteria. The presence of an implantable pacemaker and/or defibrillator will not be an exclusion criterion
Healthy volunteers:
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| CHU de Dijon | Dijon | 21079 | France |
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| Other |
|
| final evaluation | Other |
|
| Concentric and eccentric exercise sessions | Other |
|