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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
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

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
CHU Saint-Etienne
Coordinator of this site? Confirm its status
Saint-EtienneFranceUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.