Recovery Kinetics After the Use of Small Sided Games With a Small and Large Number of Players and Large Pitch Area

March 18, 2020 updated by: Ioannis G. Fatouros, University of Thessaly

Investigation on Recovery Kinetics After the Use of Small Sided Games With a Small and Large Number of Players and Large Pitch Area

Soccer is an intermittent sport in which the aerobic and anaerobic capacity of the players are both essential. Elite football players perform an average of 150-250 short and intense movements during a match, demonstrating the significant contribution of the anaerobic energy system. Sided-games is a tool to enhance the performance of the aerobic and anaerobic system. This training includes actions such as sprinting, changes of direction, accelerations, decelerations, jumps, and shooting, characterized by a strong eccentric component. Eccentric actions are associated with exercise-induced muscle damage (EIMD). Nevertheless, to date, EIMD responses following a session of sided games training have not yet been investigated. Therefore, the present study aims to examine the speed of recovery after training with a large-dimension pitch area with a small and large number of athletes in football.

Study Overview

Detailed Description

Football is an intermittent sport that includes actions of variable intensities and combines elements of physical fitness with technical and tactical skills. The game is characterized by a combination of several short-term movements such as jumps and change of direction. Typically, a player in a soccer game changes his kinetic situation every 4-6 seconds. The mean and maximum heart rate during the fight is approximately 85% and 98% of the maximum heart rate, respectively, while the average oxygen uptake is 70% of the maximum, proving that the aerobic system contributes significantly during the game. In addition, the lactic acid value in the blood ranges from 2 to 14 mM, which proves that also the anaerobic energy system contributes significantly during a game. Based on the above, the training of soccer players must meet the physiological and physiological requirements of the game.

There are two approaches to developing fitness. In the first, there is a distinction between fitness training technical skills and tactics, while the second attempts to achieve all of them at the same time, and for that purpose, the sided games are used. The first approach refers to the literature as a traditional form of physical fitness training and contains the ball and run exercises. It is part of the training unit and separates the physical conditioning from the technique and tactics, resulting in longer training time. Moreover, although this training achieves the necessary physiological adaptations, the piece of game specialization is missing. For this reason, coaches have been interested in the sided games with restrictions, combining physical, technical, and tactical elements. The coach can modify these games to achieve the training goal each time. During training with racing blocks, a similar or even higher heart rate has been observed on soccer players compared with the short-term intermittent exercise. The intensity of the exercise on the sided games is controlled by several variables that the coach can modify according to the training goal. Many variables can affect the training load such as pitch area, the number of players, and other restrictions (e.g., goalkeepers, contact limitation, etc.). In the application of sided games with large dimension and a small number of players, the maximum heart rate can reach 84-90% while with a large number of players it can reach 84-88%. There is a lack of references regarding rehabilitation after the implementation of sided games, and especially after the execution of large-dimension pitch area with a small and large number of athletes. The aim of the proposed study is, therefore, to examine the speed of recovery after training with a large-dimension pitch area with a small and large number of athletes in football.

Study Type

Interventional

Enrollment (Actual)

10

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

      • Trikala, Greece, 42100
        • SmArT LABORATORY, SCHOOL OF PHYSICAL EDUCATION & SPORTS SCIENCES, UNIVERSITY OF THESSALY

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

18 years to 25 years (Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

Male

Description

Inclusion Criteria:

  1. Absence of any musculoskeletal injury for at least 6 months prior to the study
  2. No use of any drugs or ergogenic supplements for at least 6 months prior to the study
  3. Absence of regular soccer training for the last 3 years

Exclusion Criteria:

  1. Any recent incidence of musculoskeletal injury
  2. Use of any drugs or ergogenic supplements for the last 6 months
  3. Regular soccer training for the last 3 years-

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: Screening
  • Allocation: Randomized
  • Interventional Model: Crossover Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Small Number of Players training protocol A
Small Sided Game: 4 vs 4
8 participants each side game (4vs4), size of pitch area 25*20 m. In total, 6 consecutive 4-minutes bouts interspersed by a 3-minutes rest between each bout will be executed.
Experimental: Large Number of Players training protocol B
Small Sided Game: 8 vs 8
16 participants each side game (8vs8), size of pitch area 25*20 m. In total, 3 consecutive 8-minutes bouts interspersed by a 1-minutes rest between each bout will be executed.
No Intervention: Control
No training protocol will be performed, the participants will perform only the measurements for performance and muscle damage and neuromuscular fatigue

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Differences in changes in delayed onset of muscle soreness (DOMS) between the two training protocols
Time Frame: Pre-protocol, Day 1, Day 2, Day 3
Delayed onset of muscle soreness (DOMS) is a muscle damage marker
Pre-protocol, Day 1, Day 2, Day 3
Differences in changes in maximal concentric strength between the two training protocols
Time Frame: Baseline, Day 1, Day 2, Day 3
Maximal concentric strength is used as a muscle damage marker
Baseline, Day 1, Day 2, Day 3
Differences in changes in maximal eccentric strength between the two training protocols
Time Frame: Baseline, Day 1, Day 2, Day 3
Maximal eccentric strength is used as a muscle damage marker
Baseline, Day 1, Day 2, Day 3
Differences in changes in creatine kinase (CK) between the two training protocols
Time Frame: Pre-protocol, Day 1, Day 2, Day 3
Creatine kinase (CK) is a muscle damage marker
Pre-protocol, Day 1, Day 2, Day 3

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Differences in changes in countermovement jump between the two training protocols
Time Frame: Baseline, Day 1, Day 2, Day 3
Countermovement jump is used as a performance marker
Baseline, Day 1, Day 2, Day 3
Differences in changes in Repeated Sprint Ability (RSA) between the two training protocols
Time Frame: Baseline, Day 1, Day 2, Day 3
Repeated Sprint Ability (RSA) is a performance marker
Baseline, Day 1, Day 2, Day 3
Differences in changes in maximal concentric strength between the two training protocols
Time Frame: Baseline, Day 1, Day 2, Day 3
Maximal concentric strength is used as a performance marker
Baseline, Day 1, Day 2, Day 3
Differences in changes in maximal eccentric strength between the two training protocols
Time Frame: Baseline, Day 1, Day 2, Day 3
Maximal eccentric strength is used as a performance marker
Baseline, Day 1, Day 2, Day 3
Differences in changes in maximal isometric strength between the two training protocols
Time Frame: Baseline, Hour 1, Hour 2, Hour 3
Maximal isometric strength is used as a neuromuscular fatigue marker
Baseline, Hour 1, Hour 2, Hour 3

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Ioannis G Fatouros, PhD, DPESS, School of Physical Education, Sport & Dietetics, University of Thessaly

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the 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)

August 30, 2019

Primary Completion (Anticipated)

August 30, 2020

Study Completion (Anticipated)

September 30, 2020

Study Registration Dates

First Submitted

May 29, 2019

First Submitted That Met QC Criteria

May 30, 2019

First Posted (Actual)

May 31, 2019

Study Record Updates

Last Update Posted (Actual)

March 20, 2020

Last Update Submitted That Met QC Criteria

March 18, 2020

Last Verified

March 1, 2020

More Information

Terms related to this study

Other Study ID Numbers

  • REKI-SSG

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

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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