Département de Médecine Physique et Réadaptation
Montpellier, 34295, France
NCT Number: NCT05727774
The goal of this clinical trial is to compare the efficiency of water biking training in hot (35°C) versus neutral (25°C) temperature water to elicite heat acclimation in healthy recreative athletes.
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Notify Me18 year–60 year
All sexes
Interventional
Not applicable
Montpellier, 34295, France
The goal of this clinical trial is to compare the efficiency of water biking training in hot (35°C) versus neutral (25°C) temperature water to elicite heat acclimation in healthy recreative athletes. The main questions it aims to answer are:
Participants will have to do pre and post training tests in both normal environment (cardiorespiratory stress test, force/velocity profile test, echocardiography) and artificially hot and humid indoor environment (time trial). The training protocols consists in 10 sessions of 1 hour of water bike aerobic training (5 times a week for 2 weeks) at an intensity based on the heart rate corresponding to the 1st respiratory threshold, in hot (interventional group IG: 35°C) versus neutral (control group CG: 25°C) water.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Training protocol includes 10 water biking sessions in hot water temperature (35°C) for this group
Training protocol includes 10 water biking sessions in neutral water temperature (25°C) for this group
Time frame: The 1st Time Trial will be performed the week preceding the program training. The 2nd Time Trial will be performed the week following the program training
The participant has to perform the longer distance possible in 30 min on a stationary bike in hot and humid atmosphere (environmental room). The change of distance (measured in meter) will be assessed before and after the 2 weeks training program.
Time frame: The 1st maximal cardiorespiratory test will be performed the week preceding the program training. The 2nd maximal cardiorespiratory test will be performed the week following the program training
The participant has to perform a maximal cardiorespiratory test on a stationary bike in normal environment. The change in VO2 Max (measured in ml/kg/min) will be assessed before and after the 2 weeks training program.
Time frame: The 1st maximal cardiorespiratory test will be performed the week preceding the program training. The 2nd maximal cardiorespiratory test will be performed the week following the program training
The participant has to perform a maximal cardiorespiratory test on a stationary bike in normal environment. The change in Maximal Aerobic Power (measured in Watts) will be assessed before and after the 2 weeks training program.
Time frame: The 1st echocardiography will be performed the week preceding the program training. The 2nd echocardiography will be performed the week following the program training
The participant has to pass an echocardiography with specific measurment of "global longitudinal strain of left ventricule" (united in %). The change will be assessed before and after the 2 weeks training program.
Time frame: The 1st Time Trial will be performed the week preceding the program training. The 2nd Time Trial will be performed the week following the program training
Central temperature will be measured during Time Trial in hot and humid atmosphere (environmental room). The change on central temperature (measured in °C) will be assessed before and after the 2 weeks training program.
Time frame: The 1st Time Trial will be performed the week preceding the program training. The 2nd Time Trial will be performed the week following the program training
Cutaneous temperature will be measured during Time Trial in hot and humid atmosphere (environmental room). The change on cutaneours temperature (measured in °C) will be assessed before and after the 2 weeks training program.
Time frame: The 1st Time Trial will be performed the week preceding the program training. The 2nd Time Trial will be performed the week following the program training
Sweat quality will be measured during Time Trial in hot and humid atmosphere (environmental room). The change of Na concentration (measured in mmol/l) will be assessed before and after the 2 weeks training program.
Time frame: The 1st measure of body weight will be performed the week preceding the program training. The 2nd measure of body weight will be performed the week following the program training
Body weight loss will be measured before and after Time Trial in hot and humid atmosphere (environmental room). The change of the body weight (measured in Kg) will be assessed between before and after the 2 weeks training program.
Time frame: The sleep self-questionnaire will be performed immediately after the first training session (Day 1) and immediately after the last training session (Day 10) of water biking
Sleep quality will be measured after the first and the last training session using a specific sleep self-questionnaire (PSQI) to detect the effect of hot or neutral water training during the 2 weeks training program.
PSQI : Pittsburgh Sleep Quality Index. Qualitative questionnaire, no score measured.
Time frame: The 1st measure of force/velocity power will be performed the week preceding the program training. The 2nd measure of force/velocity power will be performed the week following the program training
The participant has to perform a maximal force/velocity test to measure the force/velocity power on a specific fitness testing cycle (Monark 818 E). The change of force/velocity power (measured in N/m) will be assessed between before and after the 2 weeks training program.
Time frame: The 1st measure of CRP will be performed the week preceding the program training. The 2nd measure of CRP will be performed the week following the program training
A blood test will be performed to measure the change of CRP concentration (measured in mg/l) between before and after the 2 weeks training program.
Time frame: The 1st measure of haematocrit will be performed the week preceding the program training. The 2nd measure of haematocrit will be performed the week following the program training
A blood test with complete blood count will be performed to measure the change of haematocrit (which is expressed in %) between before and after the 2 weeks training program.
Time frame: The 1st measure of hemoglobin level will be performed the week preceding the program training. The 2nd measure of hemoglobin level will be performed the week following the program training
A blood test with complete blood count will be performed to measure the change of hemoglobin level (measured in g/100ml) between before and after the 2 weeks training program.
Time frame: The 1st Time Trial will be performed the week preceding the program training. The 2nd Time Trial will be performed the week following the program training
The Borg Rating of Perceived Exertion (RPE) will be used to measure physical activity intensity level. The scale is from 6 to 20. The higher the score is, the higher the perception of effort is.
RPE will be measured after the first Time Trial and after the second Time Trial (post training protocol).
University Hospital, Montpellier
Other
Effect of Hot Versus Neutral Water for Heat Acclimatation and Sport Performance During a Water Biking Training Protocol : Controlled Randomised Study
Acronym: THERMIDOR
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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