Core Exercises and Their Effects on Sprint, Jump, Agility, and Balance in Amateur Soccer Players

April 24, 2025 updated by: University of Yalova

The Effects of Core Exercises on Change of Direction, Vertical Jump, Sprint, and Postural Sway: An Experimental Study

This study aimed to investigate the effects of a 4-week core exercise program on sprint, vertical jump, agility, and postural sway performance in amateur male soccer players aged 18-23. Participants were randomly assigned to an intervention group (core training) or a control group (regular training). Physical performance tests were conducted before and after the training program. The results are expected to help coaches and sports scientists better understand the performance benefits of core training.

Study Overview

Detailed Description

This randomized controlled study investigated the effects of a 4-week core exercise program on sprint, vertical jump, agility, and postural sway performance in amateur male soccer players aged 18 to 23. Thirty participants were randomly assigned to either a core training group (n=15) or a control group (n=15). The core training group performed additional core stability exercises three times per week, while the control group continued their regular training routine. All participants completed physical performance tests, including 10- and 20-meter sprint, change of direction test, countermovement jump (CMJ), and postural sway assessment using a force platform. Pre- and post-test comparisons were conducted to evaluate the intervention's effectiveness. Ethical approval was obtained from the Gazi University Ethics Committee (Approval No: 2024-1685). The study was designed to help coaches and sport scientists understand how core training may improve athletic performance parameters in amateur football players.

Study Type

Interventional

Enrollment (Actual)

30

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

    • Marmara
      • Yalova, Marmara, Turkey, 77100
        • Yalova 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

  • Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Male amateur soccer players aged 18 to 23 years
  • Actively participating in regular soccer training (minimum 3 sessions/week)
  • No musculoskeletal injuries within the last 6 months
  • Provided informed consent

Exclusion Criteria:

  • History of lower extremity surgery
  • Any neurological or vestibular disorders
  • Participation in core training within the past 3 months
  • Use of medication that may affect balance or neuromuscular performance

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: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Core Training Group
Participants in this group received a 4-week core training program in addition to their regular soccer training. The program included dynamic and static core stabilization exercises, performed 3 times per week, each session lasting approximately 25-30 minutes.
This intervention consists of a 4-week core training program including exercises like planks, side planks, bird-dogs, bridges, and dead bugs, performed 3 days per week alongside regular soccer training. Each session lasted approximately 25-30 minutes.
No Intervention: Control Group
Participants in this group continued their usual soccer training routine and did not receive any additional core training during the 4-week period.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change of Direction Performance (Illinois Test)
Time Frame: Baseline (Week 0) and Week 5 (immediately after the 4-week intervention)
Change of direction (COD) performance was measured using the Illinois Change of Direction Test. Participants completed the test before and after a 4-week core training intervention. COD time was recorded using infrared timing gates, and the best of two attempts was used for analysis. Lower completion time indicates better performance.
Baseline (Week 0) and Week 5 (immediately after the 4-week intervention)

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Selman Kaya, Phd, Yalova University

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)

November 15, 2024

Primary Completion (Actual)

December 20, 2024

Study Completion (Actual)

December 20, 2024

Study Registration Dates

First Submitted

April 16, 2025

First Submitted That Met QC Criteria

April 16, 2025

First Posted (Actual)

April 24, 2025

Study Record Updates

Last Update Posted (Actual)

April 29, 2025

Last Update Submitted That Met QC Criteria

April 24, 2025

Last Verified

April 1, 2025

More Information

Terms related to this study

Other Study ID Numbers

  • CORE2025-SK

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

IPD Plan Description

At this time, there is no definitive plan for individual participant data (IPD) sharing. The decision will depend on future institutional policies, ethical approvals, and data availability.

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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