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Effect of Training Intensity on Microvascular Function

Not Applicable
Completed
Conditions
Vascular Remodeling
Sedentary Behavior
Hemodynamic Rebound
Registration Number
NCT07237854
Lead Sponsor
Université Libre de Bruxelles
Brief Summary

The aim of this trial is to investigate the effect of aerobic training intensity on muscle vascular function: continuous versus interval.

Detailed Description

This trial will compare the hemodynamic effects of aerobic training on muscle microvascular function between participants randomly assigned to one of two groups: a continuous training group and an high-intensity interval training group.

All data concerning the primary and secondary outcomes will be obtained at the start and repeated at the end of 8 weeks aerobic training.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
25
Inclusion Criteria
  • Healthy female or male between 18 and 45 years
  • Be sedentary
  • Able to cycle
  • Able to provide written informed consent
Exclusion Criteria
  • Have a pathology that may impact vascular function as :

    • cardiac pathology
    • pneumological pathology
    • metabolic pathology
  • Smoke

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
Percutaneous muscle biopsies of the vastus lateralisAt baseline and after completion of the 8-week intervention

Muscle tissue samples obtained from the vastus lateralis were processed using optical clearing and immunohistochemical staining techniques to visualize the microvascular network. Confocal microscopy was employed to acquire high-resolution three-dimensional images of arterioles, capillaries, and venules. Quantitative assessments included:

1. Internal diameter measurements, based on endothelial cell boundaries (intima layer)

2. External diameter measurements, based on smooth muscle cells and pericytes (media layer)

3. Capillary density, determined by counting the number of capillaries per sample volume

Secondary Outcome Measures
NameTimeMethod
Cardiopulmonary Exercise Testing (CPET)At baseline and after completion of the 8-week intervention

VO₂max was determined using a graded, incremental exercise test performed on a cycle ergometer until volitional exhaustion. Throughout the test, respiratory gases were continuously measured using a metabolic cart (e.g., COSMED K5), which provided breath-by-breath analysis.

The following parameters were recorded :

1. VO₂ (oxygen uptake) in mL/min

2. VCO₂ (carbon dioxide production) in mL/min

3. Minute ventilation (VE) in L/min

Maximal Cardiac Output Measurement Using Inert Gas Rebreathing (Innocor)At baseline and after completion of the 8-week intervention

Innocor is a medical device that estimates cardiac output using the inert gas rebreathing technique, a validated non-invasive method. During the procedure, the participant inhales a gas mixture containing nitrous oxide (N₂O) and sulfur hexafluoride (SF₆) through a closed circuit. These inert gases are absorbed and eliminated at rates proportional to pulmonary blood flow. By analyzing the washout kinetics of these gases during a brief rebreathing period, Innocor calculates pulmonary blood flow, which is then used to estimate cardiac output. This measurement is typically performed at rest or at peak exercise intensity, such as during the final stage of a cardiopulmonary exercise test (CPET).

The system provides real-time data on:

1. Cardiac output (L/min)

2. Stroke volume (ml/min)

3. Heart rate (bpm)

4. Pulmonary blood flow (L/min)

Trial Locations

Locations (1)

Université Libre de Bruxelles, Faculté des Sciences de la motricité, Laboratoire de kinésithérapie

🇧🇪

Brussels, Anderlecht, Belgium

Université Libre de Bruxelles, Faculté des Sciences de la motricité, Laboratoire de kinésithérapie
🇧🇪Brussels, Anderlecht, Belgium

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