Customization of Cardiac Readaptation Based on Force-velocity Profile and Heart Rate Variability
Recruiting
N/A
Interventional Study
Acute Coronary Syndrome
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 and older
- Sex
- Any
- Study type
- Interventional
- Purpose
- Other
- Participants needed
- 110 (estimated)
- Sponsor
- Centre Hospitalier Universitaire de Saint Etienne · Other
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About This Trial
Cardiac readaptation aims to mitigate cardiovascular risks and enhance the quality of life among coronary patients. Our research laboratory has an international expertise in training optimization in top-athletes and a previous study has demonstrated the efficacy of optimizing cardiac rehabilitation through the power-force-velocity profile (PFVP). The findings exhibited significant improvements in …
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* \>18
* Acute Coronary Syndrome treated in the last 6 months
* Medical revascularization (angioplasty ± stenting) or surgical (coronary artery bypass)
* Initial CPETt: MPA ≥ 60w in women and ≥80w in men
* French
* Informed consent
Exclusion Criteria:
\- Significant co-morbidi…
Contacts