- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06203379
Efficacy of Neuromuscular Training in Youth Soccer Players
August 15, 2024 updated by: hazal genc, Istanbul Medipol University Hospital
Effects of Preseason Neuromuscular Training Improves , Youth, Male Soccer Players
Soccer stands as one of the most widespread sports that ensures active participation .
It has continued to grow and develop since its inception in all societies
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Footballers suffer injuries in various ways during training sessions and matches throughout the season due to excessive strain.
Hence, numerous studies have investigated the injury sites and frequencies of footballers.
According to these findings, it has been determined that young footballers experience more lower extremity injuries compared to professional footballers.
Study Type
Interventional
Enrollment (Actual)
41
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Istanbul, Turkey
- Bahçehir University
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
Accepts Healthy Volunteers
Yes
Description
Inclusion criteria:
- Being between the ages of 15-16
- Playing amateur football for at least 2 years
- Being a male athlete
- Voluntarily participate in the study
- Obtaining informed consent from them
Exclusion criteria:
- Bone fractures, fractures, ligament and muscle tears in the body.
- Has a systemic disease
- Having a serious injury in the last 3 months.
- Having any neurological problem
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: Exercise Training
|
Exercise Training
|
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Experimental: Neuromuscular Exercise Training
|
Neuromuscular Exercise Training
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
vertical jump height
Time Frame: 8 weeks
|
Optojump device was used for the assessment of jump height.
Optojump is an optical sensor system used for sports and performance analysis.
It accurately assesses athletes' fundamental parameters like jumping, speed, agility, and vertical leap to measure and enhance their physical abilities.
The device uses a series of sensors and specialized software to monitor athletes' performance, enabling them to plan more effective training and continuously improve their performance.
|
8 weeks
|
|
jump duration (flight time)
Time Frame: 8 weeks
|
Optojump device was used for the assessment of jump duration (flight time).
Optojump is an optical sensor system used for sports and performance analysis.
It accurately assesses athletes' fundamental parameters like jumping, speed, agility, and vertical leap to measure and enhance their physical abilities.
The device uses a series of sensors and specialized software to monitor athletes' performance, enabling them to plan more effective training and continuously improve their performance.
|
8 weeks
|
|
Y Balance Test
Time Frame: 8 weeks
|
The Y Balance Test evaluates an individual's dynamic balance, flexibility, and overall neuromuscular control.
Commonly used in physiotherapy, sports medicine, and rehabilitation, it involves a series of movements where an individual maintains balance on one leg while reaching as far as possible with the other leg in various directions, forming a Y shape.
Health professionals obtain valuable information about lower limb strength and stability by measuring the reached distances and assessing the ability to control multi-directional movements.
|
8 weeks
|
|
Fatigue Severity Scale
Time Frame: 8 weeks
|
this scale comprises nine items.
Participants rate their agreement with each statement on a scale from 1 to 7, where 1 indicates strong disagreement and 7 indicates strong agreement.
A score of 4 or higher generally indicates severe fatigue
|
8 weeks
|
|
The Shuttle Run Test
Time Frame: 8 weeks
|
It increases in difficulty as participants try to cover the specified distance within shorter intervals between shuttles.
The number of completed shuttles reflects the individual's aerobic endurance level, serving as a common too for adjusting training programs and monitoring endurance levels for athletes and sports teams.
|
8 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
January 14, 2024
Primary Completion (Actual)
March 14, 2024
Study Completion (Actual)
August 15, 2024
Study Registration Dates
First Submitted
January 2, 2024
First Submitted That Met QC Criteria
January 11, 2024
First Posted (Actual)
January 12, 2024
Study Record Updates
Last Update Posted (Actual)
August 16, 2024
Last Update Submitted That Met QC Criteria
August 15, 2024
Last Verified
August 1, 2024
More Information
Terms related to this study
Other Study ID Numbers
- E-10840098-772.02-7993
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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