Characterization of Hamstring and Quadriceps Neuromuscular Fatigue After Soccer Game
NCT ID: NCT04943510
Last Updated: 2022-04-27
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
UNKNOWN
PHASE2
15 participants
INTERVENTIONAL
2021-11-04
2023-07-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
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.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Differents Intensities of Passive Stretching on ROM, Neuromuscular and Performance in Soccer Players: A Blinded RCT
NCT03150563
Comparison of Post Isometric Relaxation and Post Facilitation Stretching on Hamstring Muscle Flexibility
NCT05727501
Relation Between Rectus Femoris Muscle Tension and Hamstring Strength and Activity in Healthy Sprinters
NCT04344691
The Effect of the Reverse Nordic Curl Exercise on Quadriceps Femoris Muscles Injury Rate Among Soccer Players
NCT04674072
Stretching vs Foam-rolling
NCT03573895
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
NA
SINGLE_GROUP
* 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
BASIC_SCIENCE
NONE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Physical exercices arm
three 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
Physical exercices
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
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Physical exercices
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
Other Intervention Names
Discover alternative or legacy names that may be used to describe the listed interventions across different sources.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* 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
Exclusion Criteria
* 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.
16 Years
40 Years
MALE
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
University Hospital, Strasbourg, France
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Hopitaux Universitaires de Strasbourg
Strasbourg, , France
Countries
Review the countries where the study has at least one active or historical site.
Facility Contacts
Find local site contact details for specific facilities participating in the trial.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
8168
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.