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The Effects of Core Stabilization Exercises on Physical Performance, Balance, and Coordination in Young Football Players (CORE-U17)

14 giugno 2026 aggiornato da: Nida Afet Kansu, European University of Lefke

This study aims to examine the effects of a 6-week core stabilization exercise program on balance, coordination, and core endurance parameters in young soccer players. Soccer is a sport that requires multifaceted skills such as balance, agility, and endurance, and it is well-known that stabilization of the lumbopelvic region (core) plays a critical role in enhancing performance and reducing the risk of injury.

The study will include male volunteer athletes aged 14-17 years from the Alayköy Football Club Under-17 team in Cyprus. Participants will be randomly assigned to an exercise group (n=10) and a control group (n=10). The exercise group will undergo a progressive core stabilization program (plank, side plank, dead bug, etc.) twice a week for 6 weeks in addition to their routine training, while the control group will continue only with routine soccer training. Data will be collected using the Y-Balance Test, Pro-Agility Test, Squat Repetition Test, McGill Core Endurance Tests (Flexion and Lateral Bridge), and Prone Extension Test. Data analysis will be performed using Statistical Package for the Social Sciences version 27.0; the Wilcoxon test will be used for within-group changes, and the Mann-Whitney U test will be used for between-group comparisons. Ethical committee approval was obtained from the Scientific Research and Publication Ethics Committee (BAYEK) of the European University of Lefke, and informed consent forms will be collected from participants and their parents.

Panoramica dello studio

Tipo di studio

Interventistico

Iscrizione (Effettivo)

20

Fase

  • Non applicabile

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Luoghi di studio

    • Nicosia
      • Nicosia, Nicosia, Cipro
        • Alayköy Football Club

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

  • Bambino

Accetta volontari sani

Descrizione

Inclusion Criteria:

Be a member of the Alayköy Football Club Under-17 football team Be between the ages of 14 and 17 years Be a male football player Be able to participate in training sessions both in person and online Be able to demonstrate regular soccer training participation of at least three days per week Have participated in regular soccer training for at least one year Not have suffered a serious injury, acute health problem, or surgical intervention in the last three months that would prevent sports participation Agree to participate in the study voluntarily Have written informed consent signed by both the participant and parent or guardian

Exclusion Criteria:

Not be a member of the Alayköy Football Club Under-17 football team Be unable to participate in training sessions in person or online Have a history of lower or upper extremity surgical intervention, neurological disease, or serious musculoskeletal system injury within the last six months Demonstrate absenteeism that would interfere with participation in the exercise program or test protocols Fail to complete the test battery due to lack of motivation or cooperation issues during the evaluation process Be enrolled in a structured exercise or rehabilitation program outside the study protocol during the intervention period

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Altro
  • Assegnazione: Randomizzato
  • Modello interventistico: Assegnazione parallela
  • Mascheramento: Nessuno (etichetta aperta)

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: Core Stabilization Exercise Group
Participants in this group will perform a six-week progressive core stabilization exercise program in addition to their regular soccer training.
A progressive six-week core stabilization training program performed twice per week in addition to regular soccer training. The program includes exercises such as planks, side planks, dead bugs, Russian twists, and mountain climbers. The duration and difficulty will be gradually increased over the six-week period. Each session will last approximately 60 minutes including warm-up and cool-down. Exercises will be performed in four phases: warm-up exercises (pelvic tilt, cat-cow, dynamic side steps), stabilization-focused exercises (plank, side plank, dead bug, glute bridge), strength-focused exercises (Russian twists, mountain climbers, leg raises, hollow body hold), and cool-down exercises (child's pose, seated forward bend, cobra stretch).
Nessun intervento: Control Group
Participants in this group will continue their routine soccer training without additional core stabilization exercises.

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Dynamic Balance Performance
Lasso di tempo: 6 week
Dynamic balance will be assessed using the Y-Balance Test (Star Excursion Balance Test), a reliable field-based measure of lower extremity neuromuscular control, postural stability, and functional symmetry. Participants will stand on a single leg at the center of a Y-shaped device and reach with the contralateral leg in three directions: anterior, posteromedial, and posterolateral. Each reach direction will be performed three times. The mean of the three reach distances will be calculated and used as the dynamic balance score. Measurements will be performed at baseline and after the 6-week intervention period.
6 week

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Agility and Coordination
Lasso di tempo: 6 week
Agility and change-of-direction speed will be evaluated using the Pro-Agility Test (5-10-5 shuttle run). Participants will start from a central line, sprint 5 meters to one side, touch the line, change direction and sprint 10 meters to the opposite side, touch the line, and sprint 5 meters back to the starting point. The time to complete the course will be recorded in seconds using a stopwatch. Each participant will perform multiple trials. Measurements will be conducted at baseline and after the 6-week intervention period.
6 week
Lower Extremity Performance
Lasso di tempo: 6 week
Lower extremity muscular performance will be assessed using a bodyweight squat repetition test. Participants will stand with feet shoulder-width apart and perform squats to approximately 90-degree knee flexion while maintaining proper trunk alignment. The number of correctly performed repetitions within a 30-second time interval will be recorded. Measurements will be performed at baseline and after the 6-week intervention period.
6 week
Core Flexor Endurance
Lasso di tempo: 6 week
Core flexor endurance will be assessed using the McGill Core Endurance Test flexor endurance test. Participants will maintain a static sit-up position with the trunk supported at approximately 60 degrees and the knees flexed at 90 degrees while the lower body is stabilized. The time the position is held without loss of posture will be recorded in seconds. Measurements will be performed at baseline and after the 6-week intervention period.
6 week
Core Extensor Endurance
Lasso di tempo: 6 week
Core extensor endurance will be assessed using the Prone Extension Test (Superman Test). Participants will be positioned prone on a flat surface. The upper extremities will be placed in shoulder flexion with elbows fully extended and lifted at head level while the lower extremities are maintained in neutral hip position. Participants will be instructed to simultaneously lift the trunk to sternum level and raise the lower extremities from the ground to achieve a full trunk extension position. The time sustained in the correct position will be recorded in seconds using a stopwatch. Measurements will be performed at baseline and after the 6-week intervention period.
6 week
Lateral Core Endurance
Lasso di tempo: 6 week
Lateral core endurance will be assessed using the McGill Core Endurance Test lateral bridge test. Participants will support their body on one forearm and the side of the foot, maintaining a straight line from head to feet. The holding time in seconds for each side will be recorded. Measurements will be taken at baseline and after the 6-week intervention period.
6 week

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Investigatori

  • Direttore dello studio: Beraat Alptuğ, MD, PhD, European University of Lefke

Pubblicazioni e link utili

La persona responsabile dell'inserimento delle informazioni sullo studio fornisce volontariamente queste pubblicazioni. Questi possono riguardare qualsiasi cosa relativa allo studio.

Pubblicazioni generali

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Effettivo)

17 aprile 2026

Completamento primario (Effettivo)

29 maggio 2026

Completamento dello studio (Effettivo)

5 giugno 2026

Date di iscrizione allo studio

Primo inviato

10 giugno 2026

Primo inviato che soddisfa i criteri di controllo qualità

14 giugno 2026

Primo Inserito (Effettivo)

16 giugno 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

16 giugno 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

14 giugno 2026

Ultimo verificato

1 giugno 2026

Maggiori informazioni

Termini relativi a questo studio

Altri numeri di identificazione dello studio

  • BAYEK060.13

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

NO

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

No

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

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