Acute Effects of Randori and Yakusoku Geiko in Young Judokas
28. august 2026 oppdatert av: 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.
Studieoversikt
Status
Har ikke rekruttert ennå
Intervensjon / Behandling
Studietype
Intervensjonell
Registrering (Antatt)
18
Fase
- Ikke aktuelt
Kontakter og plasseringer
Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.
Studiekontakt
- Navn: Muhammed Sıddık Çemç, Dr.
- Telefonnummer: +90 537 016 29 25
- E-post: mscemc@gmail.com
Studiesteder
-
-
Türkiye
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Istanbul, Türkiye, Tyrkia (Türkiye), 34342
- Boğaziçi University
-
Ta kontakt med:
- Muhammed Sıddık Çemç, Dr.
- Telefonnummer: +90 537 016 29 25
- E-post: mscemc@gmail.com
-
Hovedetterforsker:
- Muhammed Sıddık Çemç, Dr.
-
-
Deltakelseskriterier
Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
- Voksen
Tar imot friske frivillige
Ja
Beskrivelse
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.
Studieplan
Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Grunnvitenskap
- Tildeling: Randomisert
- Intervensjonsmodell: Crossover-oppdrag
- Masking: Ingen (Open Label)
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
|---|---|
|
Eksperimentell: 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.
|
|
Eksperimentell: 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.
|
|
Eksperimentell: 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.
|
|
Eksperimentell: 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.
|
|
Eksperimentell: 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.
|
|
Eksperimentell: 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.
|
Hva måler studien?
Primære resultatmål
Resultatmål |
Tidsramme |
|---|---|
|
Change in King-Devick Test Completion Time
Tidsramme: 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
Tidsramme: 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.
|
Sekundære resultatmål
Resultatmål |
Tidsramme |
|---|---|
|
Change in Heart Rate
Tidsramme: 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.
|
Samarbeidspartnere og etterforskere
Det er her du vil finne personer og organisasjoner som er involvert i denne studien.
Sponsor
Studierekorddatoer
Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.
Studer hoveddatoer
Studiestart (Antatt)
15. september 2026
Primær fullføring (Antatt)
15. oktober 2026
Studiet fullført (Antatt)
30. oktober 2026
Datoer for studieregistrering
Først innsendt
28. august 2026
Først innsendt som oppfylte QC-kriteriene
28. august 2026
Først lagt ut (Faktiske)
1. september 2026
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
1. september 2026
Siste oppdatering sendt inn som oppfylte QC-kriteriene
28. august 2026
Sist bekreftet
1. august 2026
Mer informasjon
Begreper knyttet til denne studien
Andre studie-ID-numre
- E-84391427-050.04-297822
Plan for individuelle deltakerdata (IPD)
Planlegger du å dele individuelle deltakerdata (IPD)?
NEI
IPD-planbeskrivelse
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.
Legemiddel- og utstyrsinformasjon, studiedokumenter
Studerer et amerikansk FDA-regulert medikamentprodukt
Nei
Studerer et amerikansk FDA-regulert enhetsprodukt
Nei
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