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Acute Effects of Randori and Yakusoku Geiko in Young Judokas

Comparison of the Acute Effects of Randori and Yakusoku Geiko on Visual-Motor Performance and Heart Rate in Young Judokas

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07798622
Enrollment
18
Registered
2026-09-01
Start date
2026-09-15
Completion date
2026-10-30
Last updated
2026-09-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Heart Rate Response, Judo Performance, Visual Performance

Brief 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.

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.

Sponsors

Bogazici University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
BASIC_SCIENCE
Masking
NONE

Eligibility

Sex/Gender
MALE
Age
18 Years to 30 Years
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

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

Design outcomes

Primary

MeasureTime frame
Change in King-Devick Test Completion TimeImmediately 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 CountImmediately 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

MeasureTime frame
Change in Heart RateImmediately before and immediately after each study condition (randori, yakusoku geiko, and control) during three separate testing sessions.

Countries

Turkey (Türkiye)

Contacts

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

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Sep 2, 2026