- ICH GCP
- Registre américain des essais cliniques
- Essai clinique NCT07840781
Development of a Performance Model for Amputee Football Players
Development and Evaluation of the Effectiveness of a Performance Model for Amputee Football Players
This study aims to investigate the effects of a cognitive game-based exercise program on cognitive and physical performance in amputee football players. Participants will complete a structured exercise program incorporating cognitive game activities designed to simultaneously stimulate cognitive and motor functions. Cognitive and physical performance outcomes will be assessed before and after the intervention. The findings are expected to provide evidence regarding the potential benefits of integrating cognitive game-based activities into exercise and rehabilitation programs for amputee football players.
Aperçu de l'étude
Statut
Les conditions
Intervention / Traitement
Description détaillée
Amputee football is a physically and cognitively demanding sport that requires rapid decision-making, attention, visuospatial processing, balance, coordination, and sport-specific motor performance. Therefore, training approaches that simultaneously target cognitive and physical functions may contribute to the performance of amputee football players.
This study aims to investigate the effects of a cognitive game-based exercise program on cognitive and physical performance in amputee football players. The intervention will incorporate structured cognitive game activities into an exercise program to provide simultaneous cognitive and motor stimulation. The activities will involve cognitive demands such as attention, concentration, planning, problem solving, decision-making, and visuospatial processing together with physical tasks.
Participants will undergo baseline assessments of cognitive and physical performance before the intervention. Following completion of the intervention program, the same outcome measures will be repeated to determine changes in cognitive and physical performance. The study will examine whether a structured cognitive game-based exercise approach can improve selected cognitive and physical performance outcomes in amputee football players.
The results may contribute to the development of multidimensional training approaches that integrate cognitive and motor components in amputee football and may provide a basis for future exercise and rehabilitation programs for athletes with lower-limb amputation.
Type d'étude
Inscription (Estimé)
Phase
- N'est pas applicable
Contacts et emplacements
Coordonnées de l'étude
- Nom: Ayşenur Gökşen
- Numéro de téléphone: 03246274804
- E-mail: aysenurgoksen@tarsus.edu.tr
Lieux d'étude
-
-
-
Adana, Turquie (Türkiye)
- Recrutement
- Cukurova Unıversty
-
Contact:
- Gonca İnce, Prof
- Numéro de téléphone: 0(322) 338 70 0(322) 338 70 01
- E-mail: gince@cu.edu.tr
-
Contact:
- Veysel Alcan, PhD
- Numéro de téléphone: 0(322) 338 70 01
-
-
Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
- Enfant
- Adulte
- Adulte plus âgé
Accepte les volontaires sains
Sexes éligibles pour l'étude
La description
Inclusion Criteria:
Individuals with lower-limb amputation who actively participate in amputee football Regular participation in amputee football training Ability to understand and follow the study instructions Voluntary agreement to participate in the study
Exclusion Criteria:
Presence of an acute musculoskeletal injury that prevents participation in training or performance tests Presence of a medical condition that prevents safe participation in exercise or performance testing Inability to complete the cognitive or physical performance assessments Withdrawal from the study or failure to complete the intervention program
Plan d'étude
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: Traitement
- Répartition: Randomisé
- Modèle interventionnel: Affectation parallèle
- Masquage: Seul
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
|---|---|
|
Expérimental: Experimental Arm - Gince Cognitive Game-Based Exercise Group
Participants in this group will receive the Gince cognitive game-based exercise program in addition to their usual amputee football training. The program is designed to improve cognitive and physical performance through structured game-based activities. |
The intervention consists of a 10-session cognitive game-based exercise program using the Gince Intelligence Game. The program is administered in addition to routine amputee football training and is designed to stimulate cognitive and physical performance through game-based activities. |
|
Expérimental: Control Arm - Usual Training Group:
Participants in this group will continue their usual amputee football training without receiving the Gince cognitive game-based exercise program during the intervention period. |
Participants will continue their usual amputee football training program throughout the study period without receiving the additional Gince Intelligence Game-based exercise intervention.
Autres noms:
|
Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Stroop Test Performance
Délai: Baseline and immediately after completion of the intervention
|
Cognitive inhibitory control and selective attention will be assessed using the Stroop Test. Completion time will be recorded in seconds, and the number of errors will also be recorded. Changes from baseline to post-intervention will be evaluated |
Baseline and immediately after completion of the intervention
|
Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Secondary Outcome Measure - Illinois Agility Test Performance
Délai: Baseline and immediately after completion of the intervention
|
Agility performance will be assessed using the Illinois Agility Test. Completion time will be recorded in seconds. The best performance and mean performance will be recorded. Time Frame: Baseline and immediately after completion of the intervention |
Baseline and immediately after completion of the intervention
|
Collaborateurs et enquêteurs
Parrainer
Collaborateurs
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude (Réel)
Achèvement primaire (Estimé)
Achèvement de l'étude (Estimé)
Dates d'inscription aux études
Première soumission
Première soumission répondant aux critères de contrôle qualité
Première publication (Réel)
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière vérification
Plus d'information
Termes liés à cette étude
Autres numéros d'identification d'étude
- 125C306
- 125C306 (Autre subvention/numéro de financement: The Scientific and technological research council of Türkiye)
Plan pour les données individuelles des participants (IPD)
Prévoyez-vous de partager les données individuelles des participants (DPI) ?
Description du régime IPD
Individual participant data are not planned to be shared due to participant confidentiality and data protection considerations.
Informations sur les médicaments et les dispositifs, documents d'étude
Étudie un produit pharmaceutique réglementé par la FDA américaine
Étudie un produit d'appareil réglementé par la FDA américaine
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 .