Acute Effects of Randori and Yakusoku Geiko in Young Judokas
28 août 2026 mis à jour par: Muhammed Sıddık Çemç, Bogazici University
Comparison of the Acute Effects of Randori and Yakusoku Geiko on Visual-Motor Performance and Heart Rate in Young Judokas
This study will compare the immediate effects of two common judo practice methods, randori and yakusoku geiko, on visual-motor performance and heart rate in young male judokas. Randori is a free-practice form of judo that involves active resistance and unpredictable interaction with an opponent, whereas yakusoku geiko is a more controlled practice method in which techniques are performed with less resistance.
The study will use a randomized, counterbalanced crossover design. The same participants will complete three conditions on separate days: randori, yakusoku geiko, and a seated rest control condition. The order of these conditions will be randomized, and there will be at least 48 hours between sessions.
Before and immediately after each condition, visual-motor performance will be assessed using the King-Devick Test, a rapid number-naming task that measures visual scanning, attention, and eye movement-related performance. Heart rate will also be measured before and immediately after each condition using a Polar H10 chest strap.
Randori and yakusoku geiko will each be performed for 4 minutes after a standardized warm-up. During the control condition, participants will rest for 4 minutes without performing physical activity. The study will examine whether these different judo practice conditions produce different immediate changes in King-Devick Test completion time, error count, and heart rate.
Aperçu de l'étude
Statut
Pas encore de recrutement
Intervention / Traitement
Type d'étude
Interventionnel
Inscription (Estimé)
18
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.
Coordonnées de l'étude
- Nom: Muhammed Sıddık Çemç, Dr.
- Numéro de téléphone: +90 537 016 29 25
- E-mail: mscemc@gmail.com
Lieux d'étude
-
-
Türkiye
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Istanbul, Türkiye, Turquie (Türkiye), 34342
- Boğaziçi University
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Contact:
- Muhammed Sıddık Çemç, Dr.
- Numéro de téléphone: +90 537 016 29 25
- E-mail: mscemc@gmail.com
-
Chercheur principal:
- Muhammed Sıddık Çemç, Dr.
-
-
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:
Male participants. Licensed judo athletes residing in Istanbul. Regular participation in judo training at least three days per week. Willingness to provide informed consent. Willingness to avoid high-intensity exercise during the 24 hours before each testing session.
Exclusion Criteria:
Any known history of disease. Regular medication use. Failure to meet the study inclusion criteria.
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: Science basique
- Répartition: Randomisé
- Modèle interventionnel: Affectation croisée
- Masquage: Aucun (étiquette ouverte)
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
|---|---|
|
Expérimental: Sequence 1: Randori → Yakusoku Geiko → Control
|
Participants will complete a 4-minute randori session following an approximately 15-minute standardized warm-up.
Randori will involve free judo practice with active resistance and unpredictable interaction between matched training partners.
Participants will be paired with consideration of weight category and belt level.
Participants will complete a 4-minute yakusoku geiko session following an approximately 15-minute standardized warm-up.
Yakusoku geiko will involve controlled and repetitive judo technique practice with little or no active resistance from the training partner.
Participants will be paired with consideration of weight category and belt level.
|
|
Expérimental: Sequence 2: Randori → Control → Yakusoku Geiko
|
Participants will complete a 4-minute randori session following an approximately 15-minute standardized warm-up.
Randori will involve free judo practice with active resistance and unpredictable interaction between matched training partners.
Participants will be paired with consideration of weight category and belt level.
Participants will complete a 4-minute yakusoku geiko session following an approximately 15-minute standardized warm-up.
Yakusoku geiko will involve controlled and repetitive judo technique practice with little or no active resistance from the training partner.
Participants will be paired with consideration of weight category and belt level.
|
|
Expérimental: Sequence 3: Yakusoku Geiko → Randori → Control
|
Participants will complete a 4-minute randori session following an approximately 15-minute standardized warm-up.
Randori will involve free judo practice with active resistance and unpredictable interaction between matched training partners.
Participants will be paired with consideration of weight category and belt level.
Participants will complete a 4-minute yakusoku geiko session following an approximately 15-minute standardized warm-up.
Yakusoku geiko will involve controlled and repetitive judo technique practice with little or no active resistance from the training partner.
Participants will be paired with consideration of weight category and belt level.
|
|
Expérimental: Sequence 4: Yakusoku Geiko → Control → Randori
|
Participants will complete a 4-minute randori session following an approximately 15-minute standardized warm-up.
Randori will involve free judo practice with active resistance and unpredictable interaction between matched training partners.
Participants will be paired with consideration of weight category and belt level.
Participants will complete a 4-minute yakusoku geiko session following an approximately 15-minute standardized warm-up.
Yakusoku geiko will involve controlled and repetitive judo technique practice with little or no active resistance from the training partner.
Participants will be paired with consideration of weight category and belt level.
|
|
Expérimental: Sequence 5: Control → Randori → Yakusoku Geiko
|
Participants will complete a 4-minute randori session following an approximately 15-minute standardized warm-up.
Randori will involve free judo practice with active resistance and unpredictable interaction between matched training partners.
Participants will be paired with consideration of weight category and belt level.
Participants will complete a 4-minute yakusoku geiko session following an approximately 15-minute standardized warm-up.
Yakusoku geiko will involve controlled and repetitive judo technique practice with little or no active resistance from the training partner.
Participants will be paired with consideration of weight category and belt level.
|
|
Expérimental: Sequence 6: Control → Yakusoku Geiko → Randori
|
Participants will complete a 4-minute randori session following an approximately 15-minute standardized warm-up.
Randori will involve free judo practice with active resistance and unpredictable interaction between matched training partners.
Participants will be paired with consideration of weight category and belt level.
Participants will complete a 4-minute yakusoku geiko session following an approximately 15-minute standardized warm-up.
Yakusoku geiko will involve controlled and repetitive judo technique practice with little or no active resistance from the training partner.
Participants will be paired with consideration of weight category and belt level.
|
Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Délai |
|---|---|
|
Change in King-Devick Test Completion Time
Délai: Immediately before and immediately after each study condition (randori, yakusoku geiko, and control) during three separate testing sessions, with 48 hours to 7 days between sessions.
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Immediately before and immediately after each study condition (randori, yakusoku geiko, and control) during three separate testing sessions, with 48 hours to 7 days between sessions.
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|
Change in King-Devick Test Error Count
Délai: Immediately before and immediately after each study condition (randori, yakusoku geiko, and control) during three separate testing sessions, with 48 hours to 7 days between sessions.
|
Immediately before and immediately after each study condition (randori, yakusoku geiko, and control) during three separate testing sessions, with 48 hours to 7 days between sessions.
|
Mesures de résultats secondaires
Mesure des résultats |
Délai |
|---|---|
|
Change in Heart Rate
Délai: Immediately before and immediately after each study condition (randori, yakusoku geiko, and control) during three separate testing sessions.
|
Immediately before and immediately after each study condition (randori, yakusoku geiko, and control) during three separate testing sessions.
|
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 (Estimé)
15 septembre 2026
Achèvement primaire (Estimé)
15 octobre 2026
Achèvement de l'étude (Estimé)
30 octobre 2026
Dates d'inscription aux études
Première soumission
28 août 2026
Première soumission répondant aux critères de contrôle qualité
28 août 2026
Première publication (Réel)
1 septembre 2026
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
1 septembre 2026
Dernière mise à jour soumise répondant aux critères de contrôle qualité
28 août 2026
Dernière vérification
1 août 2026
Plus d'information
Termes liés à cette étude
Autres numéros d'identification d'étude
- E-84391427-050.04-297822
Plan pour les données individuelles des participants (IPD)
Prévoyez-vous de partager les données individuelles des participants (DPI) ?
NON
Description du régime IPD
Individual participant data will not be shared because no formal data-sharing plan has been established for this study.
Study findings will be reported in aggregate form in scientific publications and presentations.
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 .