The Effect of Futsal Training on Physical Fitness in Amateur Futsal Players

May 17, 2024 updated by: Bilal Deniz Aydos, Istanbul Medipol University Hospital

The Effect of Classical Futsal Training Program on Physical Fitness Level of University Amateur Futsal Players

The goal of this observational study is to examine the effects of classical futsal training on physical fitness in amateur futsal players. The main question[s] it aims to answer are:

• Does classical futsal training have any effect on the physical fitness level of futsal players? Participants will be taken to the classical futsal training program for 8 weeks. Before and after 8 weeks, players will be evaluated for their physical fitness.

Study Overview

Status

Not yet recruiting

Conditions

Intervention / Treatment

Detailed Description

The study was planned to be carried out as a non-randomized clinical study with 30 athletes in the university futsal team.

All athletes will be evaluated at the beginning of the training and will continue their classical futsal training for 8 weeks.

The program to be applied in addition to routine training 2 times a week;

  • It will begin with a 10-minute standard futsal workout warm-up. warm-up program; It will consist of light aerobic exercises and dynamic stretching of large muscle groups.
  • After the warm-up period, all groups will participate in the standard 45-minute futsal training.
  • Finally, the training will end with 5 minutes of cool-down exercises (dynamic stretching).

The first evaluation will be made 2 days before the athletes' routine training, and the next evaluations will be made at least 2 days after the last training.

Study Type

Observational

Enrollment (Estimated)

30

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

  • Turkey
      • Istanbul, Turkey
        • Bİlal Deniz Aydos

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

  • Adult

Accepts Healthy Volunteers

No

Sampling Method

Probability Sample

Study Population

Male athletes between the ages of 18-25, who are in the Istanbul Medipol University Futsal team, will be included in the study.

Description

Inclusion Criteria:

  • be between the ages of 18-25
  • Playing in Istanbul Medipol University futsal team
  • 2 days a week, 2 hours training for futsal or 1 game a week and 2 hours a week, 2 days a week

Exclusion Criteria:

  • History of lower extremity injury or surgery within 6 months prior to the test
  • Injury three months before the study,
  • Failure to heal or complete rehabilitation of previous injury,
  • Physical or mental conditions that prevent them from participating in technical and tactical futsal training and/or experimental training programs
  • Two or more missed training sessions

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

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in balance after 8-week training program
Time Frame: 8 Week
Y Balance Test
8 Week
Change in muscle strenght after 8-week training program
Time Frame: 8 week
Myometer Measurement
8 week
Change in anaerobic capacity after 8-week training program
Time Frame: 8 week
Running Based Anaerobic Sprint Test
8 week
Change in flexibility after 8-week training program
Time Frame: 8 week
Sit and Reach Test
8 week
Change in stability after 8-week training program
Time Frame: 8 week
Closed kinetic chain lower extremity stability test
8 week

Collaborators and Investigators

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

Sponsor

Istanbul Medipol University Hospital

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 (Estimated)

May 20, 2024

Primary Completion (Estimated)

May 20, 2024

Study Completion (Estimated)

May 31, 2024

Study Registration Dates

First Submitted

February 25, 2024

First Submitted That Met QC Criteria

May 1, 2024

First Posted (Actual)

May 6, 2024

Study Record Updates

Last Update Posted (Actual)

May 17, 2024

Last Update Submitted That Met QC Criteria

May 17, 2024

Last Verified

May 1, 2024

More Information

Terms related to this study

Keywords

Other Study ID Numbers

  • E-10840098-604.01.01-1310

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

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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