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Not yet recruitingNCT07798622Updated Sep 1, 2026

Acute Effects of Randori and Yakusoku Geiko in Young Judokas

An interventional study of Randori and Yakusoku Geiko in Visual Performance, Heart Rate Response and Judo Performance, sponsored by Bogazici University. Not yet recruiting at 1 site in Turkey (Türkiye). Open to male participants aged 18 Years to 30 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-09-01.

Sponsored by Bogazici University · Not applicable, Interventional, and Basic science

Phase
Not applicable
Study type
Interventional
Enrollment
18
Allocation
Randomized
Ages
18 Years to 30 Years
Sex
Male
01

Study summary

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.

02

Conditions studied

  • Visual Performance
  • Heart Rate Response
  • Judo Performance
03

Who can participate

Ages eligible
18 Years to 30 Years
Sexes eligible
Male
Accepts healthy volunteers
Yes

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

Exclusion Criteria:

Any known history of disease. Regular medication use. Failure to meet the study inclusion criteria.

04

Study design

Phase
Not applicable
Primary purpose
Basic science
Allocation
Randomized
Intervention model
Crossover assignment
Masking
None (open label)
Enrollment
18 participants (estimated)

Study arms

  • Experimental
    Sequence 1: Randori → Yakusoku Geiko → Control

    Behavioral: Randori · Behavioral: Yakusoku Geiko

  • Experimental
    Sequence 2: Randori → Control → Yakusoku Geiko

    Behavioral: Randori · Behavioral: Yakusoku Geiko

  • Experimental
    Sequence 3: Yakusoku Geiko → Randori → Control

    Behavioral: Randori · Behavioral: Yakusoku Geiko

  • Experimental
    Sequence 4: Yakusoku Geiko → Control → Randori

    Behavioral: Randori · Behavioral: Yakusoku Geiko

  • Experimental
    Sequence 5: Control → Randori → Yakusoku Geiko

    Behavioral: Randori · Behavioral: Yakusoku Geiko

  • Experimental
    Sequence 6: Control → Yakusoku Geiko → Randori

    Behavioral: Randori · Behavioral: Yakusoku Geiko

Interventions

  • BehavioralRandori

    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.

  • BehavioralYakusoku Geiko

    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.

05

What researchers measure

Primary outcomes

  1. Change in King-Devick Test Completion Time

    Time frame: 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.

  2. Change in King-Devick Test Error Count

    Time frame: 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.

Secondary outcomes

  1. Change in Heart Rate

    Time frame: Immediately before and immediately after each study condition (randori, yakusoku geiko, and control) during three separate testing sessions.

06

Study locations

1 site
  • Boğaziçi University
    Istanbul, Türkiye 34342, Turkey (Türkiye)
    • Muhammed Sıddık Çemç, Dr. · Contact · mscemc@gmail.com · +90 537 016 29 25
    • Muhammed Sıddık Çemç, Dr. · Principal investigator
07

References and documents

Individual participant data

Plan to share: No — 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.

No publications or documents are linked to this record.

08

Registry details

Key details

Study ID
NCT07798622
Lead sponsor
Bogazici University
Responsible party
Muhammed Sıddık Çemç (Associate Professor, Bogazici University) — Principal investigator
First posted
Sep 1, 2026
Start date
Sep 15, 2026 (estimated)
Primary completion
Oct 15, 2026 (estimated)
Completion
Oct 30, 2026 (estimated)
Last update
Sep 1, 2026

Study contacts

Muhammed Sıddık Çemç, Dr.
Contact
mscemc@gmail.com
+90 537 016 29 25

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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