AI-Based Hamstring Injury Risk Analysis and Effects of the FUNBALL Program
10 juin 2026 mis à jour par: Yeditepe University
AI-Based Hamstring Injury Risk Analysis and the Effects of the FUNBALL Program on Physical Performance and Cognitive Function in Professional Football Players
This study investigates hamstring injury risk in football players using artificial intelligence-based motion analysis (OpenPose) and evaluates the effects of a targeted exercise intervention (FUNBALL).
Hamstring risk is assessed during a 30-m sprint using sagittal-plane video analysis, and players classified as medium or high risk receive a four-month FUNBALL program.
A pre-post intervention design is employed, with sprint performance, agility, balance, jumping ability, kicking power, and cognitive function assessed using standardized field and cognitive tests.
Aperçu de l'étude
Statut
Complété
Les conditions
Intervention / Traitement
Description détaillée
Before the implementation of the FUNBALL program, artificial intelligence (OpenPose) based hamstring risk analysis and 30-meter sprint test, 505 agility and direction change test, modified star balance test, 5-point jump test, maximum shot distance test and cognition tests will be applied as pre-tests (18,19).
AI risk analysis will be done by examining video (30 frame rate) captured with a phone camera (iPhone 14 Pro) from the sagittal (side) plane during the 240 m sprint test.
The camera will be positioned 15 meters from the level of the middle of the 30-meter sprint test with the help of a tripod.
It will follow the participant's run for 30 meters in motion.
The football player will be asked to do a 30 m sprint with 3 repetitions and the average of 3 repetitions will be taken as a basis.
According to the artificial intelligence risk analysis, the FUNBALL program will be applied to medium and high risk groups for 4 months.
At the end of the Middle Program, the same parameters will be re-evaluated.
Hamstring risk analysis and speed parameter will be evaluated with 30 meter sprint test, agility parameter 505 with direction change and agility test, cognition parameter with color word stroop test, n-back test and digit span test, balance and proprioception parameter with modified star balance test, jump parameter with 5-point jump test, and power parameter with maximum shot distance test.
Type d'étude
Interventionnel
Inscription (Réel)
30
Phase
- N'est pas applicable
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.
Lieux d'étude
-
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Büyükçekmece
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Istanbul, Büyükçekmece, Turquie (Türkiye), 34537
- Istanbulspor Ömer Sarıalioglu Football Team Facilitu
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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
La description
Inclusion Criteria:
- To be a professional football player between the ages of 18-35.
- Not having a history of ligament, joint, bone, muscle or tendon injury that requires at least 2 months away from the field in the last 6 months.
- Not having an active disability.
- To have verbal and written communication skills who accept to participate in the study voluntarily and to perform exercise applications.
Exclusion Criteria:
- Presence of an active disability
- Having a history of ligament, joint, bone, muscle or tendon injury that requires at least 2 months away from the field in the last 6 months.
- Vestibular or disconnected vision problems
- History of cancer
- Illiteracy
- Mental and cognitive disorders that may affect 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
- Objectif principal: La prévention
- Répartition: N / A
- Modèle interventionnel: Affectation à un seul groupe
- Masquage: Aucun (étiquette ouverte)
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
|---|---|
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Expérimental: FUNBALL Intervention Arm
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The FUNBALL Prevention Program is an evidence-based injury prevention exercise program described in the literature.
The program was developed by Obertinca et al. and has been shown to reduce thigh muscle injury incidence by approximately 38% in football players.
In the present study, the FUNBALL program is implemented as a structured training intervention aimed at reducing hamstring injury risk.
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Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
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Number of Participants Classified as High Hamstring Injury Risk by OpenPose-Based Biomechanical Analysis
Délai: Baseline (Day 0) and post-intervention (Week 12)
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Outcome measure: Number of participants classified as high hamstring injury risk.
Assessment tool: OpenPose-based biomechanical motion analysis of a 30-meter sprint.
Classification is based on hip flexion angle, knee extension angle, and terminal swing phase mechanics.
Unit of measure: Number of participants classified as high risk.
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Baseline (Day 0) and post-intervention (Week 12)
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Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
505 COD Agility Test
Délai: Baseline (Day 0) and post-intervention (Week 12)
|
The 505 Change of Direction (COD) test is a widely used field-based assessment designed to evaluate an athlete's ability to decelerate, rapidly change direction, and re-accelerate over a short distance.
The players are going to sprint forward 10 m, perform a 180-degree turn off a designated foot at the 5-m mark, and sprint back as quickly as possible, with total time is going to record using electronic timing gates or a stopwatch.
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Baseline (Day 0) and post-intervention (Week 12)
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Number of Players With Elevated Hamstring Injury Risk During Sprint Testing
Délai: Baseline (Day 0) and post-intervention (Week 12)
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The primary outcome will be the number of players identified with elevated hamstring injury risk during a 30-m sprint test, assessed using an artificial intelligence-based movement analysis.
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Baseline (Day 0) and post-intervention (Week 12)
|
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N-Back Task Accuracy (%)
Délai: Baseline (Day 0) and Post-Intervention (Week 12)
|
Working memory performance assessed using a computerized N-Back task and reported as percentage accuracy (%).
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Baseline (Day 0) and Post-Intervention (Week 12)
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Digit Span Total Score
Délai: Baseline (Day 0) and Post Intervention (Week 12)
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Total number of correctly recalled digits during a computerized Digit Span task.
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Baseline (Day 0) and Post Intervention (Week 12)
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Composite Reach Distance in Modified Star Excursion Balance Test
Délai: Baseline ( Day 0) and Post-Intervention (Week 12)
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Composite normalized reach distance during the Modified Star Excursion Balance Test.
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Baseline ( Day 0) and Post-Intervention (Week 12)
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Horizontal Distance in Multiple Five Bounds Test
Délai: Baseline (Day 0) and Post-Intervention (Week 12)
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Horizontal distance achieved during the Multiple Five Bounds Test assessing horizontal power.
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Baseline (Day 0) and Post-Intervention (Week 12)
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Maximal Soccer Ball Kicking Distance
Délai: Baseline (Day 0) and Post-Intervention (Week 12)
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Maximum horizontal distance of a soccer ball following a maximal instep kick.
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Baseline (Day 0) and Post-Intervention (Week 12)
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Stroop Reaction Time
Délai: Baseline (Day 0) and Week 12
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Mean reaction time during incongruent trials of a computerized Stroop task.
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Baseline (Day 0) and Week 12
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Collaborateurs et enquêteurs
C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.
Parrainer
Les enquêteurs
- Chercheur principal: Elif Tuğçe t Çil Sertöz, Asst. Prof. Dr., Yeditepe University
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)
1 février 2026
Achèvement primaire (Réel)
25 avril 2026
Achèvement de l'étude (Réel)
25 avril 2026
Dates d'inscription aux études
Première soumission
29 décembre 2025
Première soumission répondant aux critères de contrôle qualité
10 juin 2026
Première publication (Réel)
16 juin 2026
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
16 juin 2026
Dernière mise à jour soumise répondant aux critères de contrôle qualité
10 juin 2026
Dernière vérification
1 juin 2026
Plus d'information
Termes liés à cette étude
Mots clés
Autres numéros d'identification d'étude
- Yeditepe U1
Plan pour les données individuelles des participants (IPD)
Prévoyez-vous de partager les données individuelles des participants (DPI) ?
OUI
Délai de partage IPD
January 2026-January 2027
Type d'informations de prise en charge du partage d'IPD
- PROTOCOLE D'ÉTUDE
- SÈVE
- CIF
- ANALYTIC_CODE
- RSE
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 .