- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06942676
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
Status
Completed
Intervention / Treatment
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.
Sponsor
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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