Pre- and Post-Training Assessment of Sprint Performance, Agility, Balance and Body Awareness in Football Players Regarding Hamstring Injury
30 juillet 2026 mis à jour par: Ezgi Türkmen, Health Institutes of Turkey
Aim of the study is to examine the impact of a history of hamstring injury on athletes by determining and comparing the pre- and post-training levels of sprint performance, agility, dynamic balance, and body awareness in football players with and without a history of hamstring injury.
Aperçu de l'étude
Statut
Recrutement
Les conditions
Description détaillée
The aim of this study is to compare sprint performance (10-meter sprint test (10mST) and 30-meter sprint test (30mST)), agility (T-Test of Agility), dynamic balance (Y-Balance Test), and body awareness (Body Awareness Questionnaire) levels in licensed football players with and without a history of hamstring injury, before and after training, in order to reveal the effect of a history of hamstring injury on functional performance and acute fatigue response.
Capturing acute changes with pre- and post-training measurements and comparing these between groups with and without a history of injury has the potential to make visible "intra-day/intra-training performance fluctuations" that may be overlooked upon returning to the field.
This research study is designed as an observational and cross-sectional evaluation study.
Type d'étude
Observationnel
Inscription (Estimé)
50
Contacts et emplacements
Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.
Coordonnées de l'étude
- Nom: Ezgi Türkmen
- Numéro de téléphone: 0090 216 547 26 00
- E-mail: turkmnezgi@gmail.com
Lieux d'étude
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Istanbul, Turquie (Türkiye)
- Recrutement
- Haliç Üniversitesi
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Contact:
- Ayşenur Çetinkaya
- Numéro de téléphone: 0090 212 924 24 44
- E-mail: aysenurcetinkaya@halic.edu.tr
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Critères de participation
Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.
Critère d'éligibilité
Âges éligibles pour étudier
- Adulte
Accepte les volontaires sains
Oui
Méthode d'échantillonnage
Échantillon non probabiliste
Population étudiée
Licensed Football Players Aged 18-35 with and without a History of Hamstring Injury
La description
Inclusion Criteria:
- Being a licensed male football player aged 18-35.
- Having played football actively for at least 2 years.
- Having attended training sessions regularly within the last 6 months.
- Having a history of hamstring injury (n=25).
- Not having a history of hamstring injury (n=25).
- Voluntarily agreeing to participate in the study.
Exclusion Criteria:
- Having a current history of a diagnosed musculoskeletal injury in the lower extremities.
- Having undergone lower extremity surgery within the last 6 months.
- Having a diagnosis of any neurological, orthopedic, or systemic disorder.
- Having a diagnosis of any systemic disease affecting balance.
- Having any significant physical limitations that would prevent the application of the tests.
- Having a diagnosed psychological disorder that would hinder communication.
Plan d'étude
Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.
Comment l'étude est-elle conçue ?
Détails de conception
Cohortes et interventions
Groupe / Cohorte |
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Group I
Football players with a history of hamstring injury
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Group II
Football players without a history of hamstring injury
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Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
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Sprint Performance (10-meter and 30-meter Sprint Tests)
Délai: Before and immediately after training
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To evaluate the acceleration and maximum sprint performance of the football players, 10-meter and 30-meter sprint tests will be conducted.
The 10-meter sprint test will be used to assess acceleration and explosive power capacity over short distances.
Participants will stand in a semi-prone position behind the starting line and will begin a 10-meter run at maximum speed upon receiving the starting command.
The time will be recorded in seconds.
The 30-meter sprint test will be used to evaluate maximum running speed, sprint performance, and anaerobic capacity.
Similarly, participants will begin a 30-meter run at maximum speed upon receiving the starting command.
The time will be recorded in seconds.
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Before and immediately after training
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T-Test of Agility
Délai: Before and immediately after training
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This test will be administered to assess participants' agility, speed of change of direction, coordination, and reaction capacity.
The test course is arranged in a 'T' shape using cones, with 10 meters forward from the starting point and 5 meters to the right and left.
Participant runs forward from the starting point to the midpoint, then moves sideways to the right and left as quickly but steadily as possible, and finally runs back to the starting point.
The test duration is recorded in seconds using a stopwatch.
Shorter test times indicate a higher level of agility and neuromuscular control.
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Before and immediately after training
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Y Balance Test
Délai: Before and immediately after training
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The YBT requires the athlete to balance on one leg whilst simultaneously reaching as far as possible with the other leg in three separate directions: anterior, posterolateral, and posteromedial.
Therefore, this test measures the athlete's strength, stability and balance in various directions.
The YBT composite score is calculated by summing the three reach directions and normalising the results to the lower limb length.
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Before and immediately after training
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Body Awareness Questionnaire (BAQ)
Délai: Before and immediately after training
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BAQ is an 18-item self-report scale designed to measure how attentive you are to normal, non-emotional internal bodily processes.
It evaluates your sensitivity to everyday bodily cycles (like sleep and hunger), ability to detect subtle changes, and capacity to anticipate physical reactions.
Typically takes about 3 to 5 minutes.
Items are generally rated on a 1 to 7 scale, with higher total scores indicating greater perceived conKdence and accuracy in monitoring your physical state over time.
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Before and immediately after training
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Collaborateurs et enquêteurs
C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.
Parrainer
Dates d'enregistrement des études
Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.
Dates principales de l'étude
Début de l'étude (Réel)
30 juillet 2026
Achèvement primaire (Estimé)
1 août 2026
Achèvement de l'étude (Estimé)
1 août 2026
Dates d'inscription aux études
Première soumission
24 juillet 2026
Première soumission répondant aux critères de contrôle qualité
24 juillet 2026
Première publication (Réel)
30 juillet 2026
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
31 juillet 2026
Dernière mise à jour soumise répondant aux critères de contrôle qualité
30 juillet 2026
Dernière vérification
1 juillet 2026
Plus d'information
Termes liés à cette étude
Autres numéros d'identification d'étude
- ETurkmen0226
Informations sur les médicaments et les dispositifs, documents d'étude
Étudie un produit pharmaceutique réglementé par la FDA américaine
Non
Étudie un produit d'appareil réglementé par la FDA américaine
Non
Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .