Characterization of Hamstring and Quadriceps Neuromuscular Fatigue After Soccer Game
QIF
1 other identifier
interventional
15
1 country
1
Brief Summary
This is a monocentric study comparing hamstring and quadriceps neuromuscular fatigue after simulated soccer game, anaerobic and aerobic training sessions. The purpose of this study was:
- 1.To quantify the decrease of isometric force immediately after a simulate soccer game.
- 2.To characterize peripheral and central fatigue between hamstring and quadriceps muscles and described the kinetics of recovery after specific tasks of soccer training.
- 3.To compare the level neuromuscular fatigue induced by anaerobic and aerobic training.
- 4.To highlight correlation between neuromuscular fatigue and performance markers.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for phase_2
Started Nov 2021
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
June 2, 2021
CompletedFirst Posted
Study publicly available on registry
June 29, 2021
CompletedStudy Start
First participant enrolled
November 4, 2021
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 1, 2023
CompletedStudy Completion
Last participant's last visit for all outcomes
July 1, 2023
CompletedApril 27, 2022
April 1, 2022
1.7 years
June 2, 2021
April 19, 2022
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Difference in maximal isometric hamstring strength before and immediately after exercise (i.e., pre vs. immediate post exercise) expressed as a percentage (%).
Before and immediately post exercise (i.e., during the first minute after cessation of exercise)
Secondary Outcomes (11)
Relative difference (in %) in maximum isometric hamstring strength before and after exercise (i.e., pre- vs. post-exercise), relative to pre-exercise strength across different test types.
Before and immediately post exercise, 5, 10, 15, 30-minutes and 24 and 48-hours post-exercise
Relative difference (in %) in maximal isometric quadriceps strength before and after exercise (i.e., pre vs. post exercise), related to preexercise strength according to the different types of tests.
Before and immediately post exercise, 5, 10, 15, 30-minutes and 24 and 48-hours post-exercise
Relative difference (%) in maximum isometric hamstring and quadriceps strength for each test type at the different times of interest.
Before and immediately post exercise, 5, 10, 15, 30-minutes and 24 and 48-hours post-exercise
Difference in pre- and post-exercise (i.e., pre- vs. post-exercise) hamstring potentiated jerk amplitude (N) relative to pre-exercise amplitude by event type at different times of interest.
Before and immediately post exercise, 5, 10, 15, 30-minutes and 24 and 48-hours post-exercise
Difference in pre- and post-exercise (i.e., pre- vs. post-exercise) potentiated jerk amplitude (N) of the quadriceps, relative to pre-exercise amplitude, by test type at different times of interest.
Before and immediately post exercise, 5, 10, 15, 30-minutes and 24 and 48-hours post-exercise
- +6 more secondary outcomes
Study Arms (1)
Physical exercices arm
EXPERIMENTALthree randomizations will be used to determine the order of the tests that will be proposed to the subjects: on the one hand for the exercise modalities (match, anaerobic, aerobic) and, on the other hand, for the exercise modalities included in the anaerobic and aerobic exercise families: Anaerobic agility / anaerobic - linear sprints Aerobic - shuttle / aerobic - linear
Interventions
surface EMG: surface electrodes will be positioned on the muscles to evaluate the level of muscle activation non invasive muscular neurostimulations : application of a percutaneous electrical stimulation of the motor nerve of the considered muscle and a direct electrical stimulation of the muscle
Eligibility Criteria
You may qualify if:
- male
- age limits: minimum: 16 ; maximum: 40 years old
- to be a soccer player, licensed to the French Football Federation
- affiliation to the social health insurance scheme
- signing an informed consent form
You may not qualify if:
- impossibility to give the subject enlightened information (subject in emergency situation, difficulties in understanding the study, …)
- subject under the protection of justice
- subject under guardianship or curatorship
- lower limbs musculotendinous or articular problems
- smoker or having been a smoker in the last 5 years
- subject wearing a pacemaker
- drug treatment in progress and impossibility to stop it within 7 days before the beginning of the study.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Hopitaux Universitaires de Strasbourg
Strasbourg, 67091, France
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- phase 2
- Allocation
- NA
- Masking
- NONE
- Purpose
- BASIC SCIENCE
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
June 2, 2021
First Posted
June 29, 2021
Study Start
November 4, 2021
Primary Completion
July 1, 2023
Study Completion
July 1, 2023
Last Updated
April 27, 2022
Record last verified: 2022-04