- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07577362
Core Training in Amateur Soccer Players
May 3, 2026 updated by: Musa Güneş, Karabuk University
The Effect of Core Muscle Strengthening Training on Performance in Soccer Players
The core region is a part of the body composed of axes surrounding the torso and plays a crucial role in maintaining stability.
Therefore, it is considered important for maintaining athletic performance in athletes.
This study aims to investigate the effects of core strength training, in addition to routine training programs, on jumping, agility, speed, balance, and shooting speed performance in amateur football players.
Study Overview
Status
Recruiting
Conditions
Intervention / Treatment
Detailed Description
The core region, consisting of muscles that surround the torso, plays a crucial role in maintaining stability in the body.
Therefore, it is considered essential for maintaining athletic performance in athletes.
It is known that the core region is activated before extremity movements in achieving athletic performance.
For this reason, core training plays an important role in maintaining optimal extremity movement and improving performance.
Furthermore, the importance of core stabilization in preventing injuries is emphasized.
Although various studies have been conducted on the importance of core training in athletes, the lack of standardization still makes this issue significant.
In this context, this study aims to examine the effect of core strength training, in addition to routine training programs, on jumping, agility, speed, balance, and shooting speed performance in amateur football players.
Study Type
Interventional
Enrollment (Estimated)
40
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 Contact
- Name: Musa Güneş, PhD
- Phone Number: 03704789081
- Email: musagunes@karabuk.edu.tr
Study Locations
-
-
-
Karabük, Turkey (Türkiye)
- Recruiting
- Karabuk University, Physiotherapy and Rehabilitation Application and Research Center
-
Contact:
- Musa Güneş, PhD
- Phone Number: 03704189081
- Email: musagunes@karabuk.edu.tr
-
Principal Investigator:
- Furkan Arslan
-
-
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:
- Being between 18-35 years old
- Being able to communicate in Turkish
- Willing to participate in the training.
- Being a licensed football player
Exclusion Criteria:
- Body mass index of 30 kg/m² or higher
- History of lower extremity surgery in the last 6 months
- Cardiac, musculoskeletal, vestibular, and neurological problems
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: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Triple
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Core training group
The core training group will receive progressive exercises designed to strengthen core muscles, 3 days a week for 8 weeks.
|
The core training group will receive progressive exercises designed to strengthen core muscles, 3 days a week for 8 weeks.
|
|
Other: Control Group
The control group will continue with their routine training programs.
|
The control group will continue with their routine training programs.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Jumping performance
Time Frame: Baseline, After intervention (eight week later)
|
A mobile application compatible with the My Jump video camera system will be used to measure participants' vertical jump heights.
|
Baseline, After intervention (eight week later)
|
|
Balance performance
Time Frame: Baseline, After intervention (eight week later)
|
Participants' dynamic balance will be assessed using the modified Star Excursion Balance Test (SEBT).
Measurements will be taken in three directions: anterior, posteromedial, and posterolateral.
The better the reach, the better the balance performance.
|
Baseline, After intervention (eight week later)
|
|
Agility
Time Frame: Baseline, After intervention (eight week later)
|
Agility will be assessed using the T-shaped agility test, which consists of four cones.
Agility increases as the time decreases.
|
Baseline, After intervention (eight week later)
|
|
Speed
Time Frame: Baseline, After intervention (eight week later)
|
The 20-meter speed test will be used to determine the athlete's speed.
Measurements will be taken using photocells placed at the beginning and end of the 20-meter running distance.
|
Baseline, After intervention (eight week later)
|
|
Core endurance
Time Frame: Baseline, After intervention (eight week later)
|
For core endurance testing, trunk extensor endurance (Sorenson test), trunk flexor endurance, and trunk oblique muscle endurance tests will be performed.
|
Baseline, After intervention (eight week later)
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Musa Güneş, PhD, Karabuk University
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)
May 1, 2026
Primary Completion (Estimated)
October 30, 2026
Study Completion (Estimated)
December 30, 2026
Study Registration Dates
First Submitted
May 3, 2026
First Submitted That Met QC Criteria
May 3, 2026
First Posted (Actual)
May 11, 2026
Study Record Updates
Last Update Posted (Actual)
May 11, 2026
Last Update Submitted That Met QC Criteria
May 3, 2026
Last Verified
May 1, 2026
More Information
Terms related to this study
Other Study ID Numbers
- Karabuk-005
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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