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

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
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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