Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT06107452

Customization of Cardiac Readaptation Based on Force-velocity Profile and Heart Rate Variability

Led by Centre Hospitalier Universitaire de Saint Etienne · Updated on 2025-07-10

110

Participants Needed

1

Research Sites

116 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

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

CONDITIONS

Official Title

Customization of Cardiac Readaptation Based on Force-velocity Profile and Heart Rate Variability

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age over 18 years
  • Acute Coronary Syndrome treated within the last 6 months
  • Medical revascularization by angioplasty with or without stenting, or surgical coronary artery bypass
  • Initial cardiopulmonary exercise test maximum power output of at least 60 watts for women and 80 watts for men
  • Able to understand French
  • Provided informed consent
Not Eligible

You will not qualify if you...

  • Significant other health conditions that limit the ability to practice physical activity

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Chu Saint-Etienne

Saint-Etienne, France

Actively Recruiting

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Research Team

D

David HUPIN, MD

CONTACT

H

Hélène RAINGARD, CRA

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

OTHER

Number of Arms

2

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