Acute Effects of Randori and Yakusoku Geiko in Young Judokas
28 augustus 2026 bijgewerkt door: 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.
Studie Overzicht
Toestand
Nog niet aan het werven
Interventie / Behandeling
Studietype
Ingrijpend
Inschrijving (Geschat)
18
Fase
- Niet toepasbaar
Contacten en locaties
In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.
Studiecontact
- Naam: Muhammed Sıddık Çemç, Dr.
- Telefoonnummer: +90 537 016 29 25
- E-mail: mscemc@gmail.com
Studie Locaties
-
-
Türkiye
-
Istanbul, Türkiye, Turkije (Türkiye), 34342
- Boğaziçi University
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Contact:
- Muhammed Sıddık Çemç, Dr.
- Telefoonnummer: +90 537 016 29 25
- E-mail: mscemc@gmail.com
-
Hoofdonderzoeker:
- Muhammed Sıddık Çemç, Dr.
-
-
Deelname Criteria
Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
- Volwassen
Accepteert gezonde vrijwilligers
Ja
Beschrijving
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.
Studie plan
Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.
Hoe is de studie opgezet?
Ontwerpdetails
- Primair doel: Fundamentele wetenschap
- Toewijzing: Gerandomiseerd
- Interventioneel model: Crossover-opdracht
- Masker: Geen (open label)
Wapens en interventies
Deelnemersgroep / Arm |
Interventie / Behandeling |
|---|---|
|
Experimenteel: 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.
|
|
Experimenteel: 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.
|
|
Experimenteel: 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.
|
|
Experimenteel: 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.
|
|
Experimenteel: 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.
|
|
Experimenteel: 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.
|
Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Tijdsspanne |
|---|---|
|
Change in King-Devick Test Completion Time
Tijdsspanne: 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.
|
|
Change in King-Devick Test Error Count
Tijdsspanne: 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.
|
Secundaire uitkomstmaten
Uitkomstmaat |
Tijdsspanne |
|---|---|
|
Change in Heart Rate
Tijdsspanne: 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.
|
Medewerkers en onderzoekers
Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.
Sponsor
Studie record data
Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.
Bestudeer belangrijke data
Studie start (Geschat)
15 september 2026
Primaire voltooiing (Geschat)
15 oktober 2026
Studie voltooiing (Geschat)
30 oktober 2026
Studieregistratiedata
Eerst ingediend
28 augustus 2026
Eerst ingediend dat voldeed aan de QC-criteria
28 augustus 2026
Eerst geplaatst (Werkelijk)
1 september 2026
Updates van studierecords
Laatste update geplaatst (Werkelijk)
1 september 2026
Laatste update ingediend die voldeed aan QC-criteria
28 augustus 2026
Laatst geverifieerd
1 augustus 2026
Meer informatie
Termen gerelateerd aan deze studie
Andere studie-ID-nummers
- E-84391427-050.04-297822
Plan Individuele Deelnemersgegevens (IPD)
Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?
NEE
Beschrijving IPD-plan
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.
Informatie over medicijnen en apparaten, studiedocumenten
Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel
Nee
Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct
Nee
Deze informatie is zonder wijzigingen rechtstreeks van de website clinicaltrials.gov gehaald. Als u verzoeken heeft om uw onderzoeksgegevens te wijzigen, te verwijderen of bij te werken, neem dan contact op met register@clinicaltrials.gov. Zodra er een wijziging wordt doorgevoerd op clinicaltrials.gov, wordt deze ook automatisch bijgewerkt op onze website .