CHU de Saint-Etienne
Saint-Etienne, 42055, France
NCT Number: NCT05013021
The present study aims to analyse first, the acute effects generated by a single bout of Sprint Interval Training (SIT) and, secondly, the effects of a long-term intervention on sedentary participants.
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Notify Me18 year–40 year
All sexes
Interventional
Not applicable
Saint-Etienne, 42055, France
The main goal is to determine the optimal dose of high-intensity exercise that enhances the best physiological adaptations.
The cumulative effects of SIT, will be assessed by a series of measures placed throughout the time-course (before, after the 1st , the 2nd and the 3rd block of SIT). Those measures consist of physiological measurements (VO2max), neuromuscular capacities (force-velocity profile) the autonomic nervous system responses (heart rate variability) and blood markers (lactate, Creatine phosphoKinase (CK), cytokinases, µRNA). Acute effects will be measured in the familiarisation sessions (after short (8 sprints) and long (14 sprints) sets) by performing a battery of neuromuscular, perceptual, and autonomic nervous system tests before and after the single session of SIT.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
The Sprint Interval Training (SIT) training consists of 3 successive blocks of 5 training sessions each. The sessions are 24 to 48 hours apart.
. One block lasts two weeks. After the end of one block, the following block begins the day after.
The Sprint Interval Training lasts 6 weeks.
Each session consists of a series of sprints, the number of which varies from 8 to 14. Thus a session will last from 30 to 45 min approximately
So, the time frame of this study is Baseline, Block 1, Block 2 and Block 3 (Not in day or week or month)
Time frame: At the end of the 1st, 2nd and 3rd block : Each block = 2 weeks; each block is 1 day apart
consumption oxygen uptake (VO2max) measured on a cycle ergometer
The main objective is to determine at which time frame of sprint interval training blocks, the endurance performance (VO2max) is best.
Time frame: At the end of the 1st, 2nd and 3rd block : Each block = 2 weeks; each block is 1 day apart
It is measured thanks to the force-speed profile using two sprints of 7s with braking forces of 0 , 4 and 0.7 N.kg-1 respectively.
Time frame: At the end of the 1st, 2nd and 3rd block : Each block = 2 weeks; each block is 1 day apart
It is measured thanks to the force-speed profile using two sprints of 7s with braking forces of 0 , 4 and 0.7 N.kg-1 respectively.
Time frame: At the end of the 1st, 2nd and 3rd block : Each block = 2 weeks; each block is 1 day apart
It is measured thanks to the force-speed profile using two sprints of 7s with braking forces of 0 , 4 and 0.7 N.kg-1 respectively.
Time frame: At the end of the 1st, 2nd and 3rd block : Each block = 2 weeks; each block is 1 day apart
It is measured by means of a voluntary maximum contraction test in which the maximum force generated voluntarily is compared to that voluntarily generated force will be compared to that evoked using electrical stimulation of the femoral nerve.
Time frame: At the end of the 1st, 2nd and 3rd block : Each block = 2 weeks; each block is 1 day apart
Time frame: At the end of the 1st, 2nd and 3rd block : Each block = 2 weeks; each block is 1 day apart
Blood sample
Time frame: At the end of the 1st, 2nd and 3rd block : Each block = 2 weeks; each block is 1 day apart
Blood sample
Time frame: At the end of the 1st, 2nd and 3rd block : Each block = 2 weeks; each block is 1 day apart
Blood sample
Time frame: At the end of the 1st, 2nd and 3rd block : Each block = 2 weeks; each block is 1 day apart
Blood sample
Centre Hospitalier Universitaire de Saint Etienne
Other
Sprint Interval Training (SIT) on the Endurance, Strength and Velocity Capacities of Healthy Sedentary Subjects
Acronym: BénéfiSIT
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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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