NCT06107452Completed
Customization of Cardiac Readaptation Based on Force-velocity Profile and Heart Rate Variability
Customization of Cardiac Readaptation Based on Force-velocity Profile and Heart Rate Variability: A Controlled and Randomized Study
Source: ClinicalTrials.gov · Last updated 17 Sept 2026
Brief summary (registry, in English)
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 aerobic capacity, muscular strength, and cardiovascular parameters among patients who were trained based on their PFVP. Guided training utilizing heart rate variability (HRV) is also garnering increasing interest as a means to optimize training load and promote recovery
- Status (registry)
- Completed
- Study type
- Interventional
- Enrollment
- 102 (actual)
- First submitted
- 11 Oct 2023
- Start date
- 5 Feb 2024
- Primary completion date
- 12 Sept 2025
- Lead sponsor
- Centre Hospitalier Universitaire de Saint Etienne
- Diseases
- Coronary artery disease
- NCT number
- NCT06107452
What you commit to
- Study type: Interventional
- Participants enrolled: 102
- From 5 Feb 2024 to the primary completion date, 12 Sept 2025
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Other
- \- Significant co-morbidities limited practice of physical activity
Who the study is looking for
- \>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
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| CHU Saint-Etienne Coordinator of this site? Confirm its status | Saint-Etienne | France | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.