- ICH GCP
- Register voor klinische proeven in de VS.
- Klinische proef NCT07798635
SJFT Performance, Inhibitory Control, and Attention in Young Judokas
The Relationship Between Special Judo Fitness Test (SJFT) Performance and Inhibitory Control and Selective Attention in Young Judokas
This study will examine the relationship between judo-specific physical fitness and cognitive performance in young male judo athletes and will evaluate the immediate effects of the Special Judo Fitness Test (SJFT) on attention and inhibitory control. Licensed male judo athletes who train regularly at least three days per week will be compared with male participants who do not actively participate in sports.
Judo athletes will complete a standardized warm-up followed by the SJFT, a judo-specific high-intensity fitness test involving repeated throws performed over three short exercise periods separated by brief rest intervals. Heart rate will be measured immediately after the SJFT and again one minute later.
Cognitive performance will be assessed using a computerized Flanker Task, which will measure reaction time and response accuracy while participants respond to relevant visual information and ignore distracting information. Judo athletes will complete the Flanker Task approximately one minute before and one minute after the SJFT. Participants in the control group will complete the same cognitive assessment twice over a similar time interval without performing the physical exercise.
The study will aim to determine whether judo-specific physical fitness and judo experience are associated with attention and inhibitory control and whether a single high-intensity judo-specific exercise session will produce an immediate change in cognitive performance.
Studie Overzicht
Toestand
Interventie / Behandeling
Studietype
Inschrijving (Geschat)
Fase
- Niet toepasbaar
Contacten en locaties
Studie Locaties
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Türkiye
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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
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Contact:
- E-mail: mscemc@gmail.com
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Hoofdonderzoeker:
- Muhammed Sıddık Çemç, Dr.
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Deelname Criteria
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
- Volwassen
Accepteert gezonde vrijwilligers
Beschrijving
Inclusion Criteria:
Male participants residing in Istanbul. For the judo group: licensed judo athletes who regularly participate in judo training at least three days per week.
For the control group: individuals who are not actively involved in any sports branch.
Right-handed participants, as determined using the Edinburgh Handedness Inventory.
Participants who provide informed consent to participate in the study.
Exclusion Criteria:
History of visual impairment. History of neurological disorders. History of psychiatric disorders. History of cardiovascular disease. Current medication use.
Studie plan
Hoe is de studie opgezet?
Ontwerpdetails
- Primair doel: Ander
- Toewijzing: Niet-gerandomiseerd
- Interventioneel model: Parallelle opdracht
- Masker: Geen (open label)
Wapens en interventies
Deelnemersgroep / Arm |
Interventie / Behandeling |
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Experimenteel: Judo Group
Participants in the judo group will complete a standardized warm-up followed by the Special Judo Fitness Test (SJFT).
Cognitive performance will be assessed using the Flanker Task approximately one minute before and one minute after the SJFT.
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The Special Judo Fitness Test is a judo-specific high-intensity exercise test consisting of three exercise periods: 15 seconds, 30 seconds, and 30 seconds, with 10-second rest intervals between periods.
During the test, the participant will perform as many ippon-seoi-nage throws as possible using two partners positioned six meters apart.
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Geen tussenkomst: Control Group
Participants in the control group will not perform the SJFT or any other exercise intervention.
They will complete the Flanker Task twice over a similar time interval while remaining at rest.
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Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
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Change in Flanker Task Correct Responses
Tijdsspanne: Approximately 1 minute before and 1 minute after the intervention
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Response accuracy will be assessed using a computerized Flanker Task.
The number of correct responses will be recorded separately for congruent and incongruent trials.
Higher numbers of correct responses indicate greater response accuracy.
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Approximately 1 minute before and 1 minute after the intervention
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Change in Flanker Task Reaction Time
Tijdsspanne: Approximately 1 minute before and 1 minute after the intervention
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Reaction time will be assessed for congruent and incongruent trials using a computerized Flanker Task.
Lower reaction times indicate faster cognitive responses.
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Approximately 1 minute before and 1 minute after the intervention
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Medewerkers en onderzoekers
Sponsor
Studie record data
Bestudeer belangrijke data
Studie start (Geschat)
Primaire voltooiing (Geschat)
Studie voltooiing (Geschat)
Studieregistratiedata
Eerst ingediend
Eerst ingediend dat voldeed aan de QC-criteria
Eerst geplaatst (Werkelijk)
Updates van studierecords
Laatste update geplaatst (Werkelijk)
Laatste update ingediend die voldeed aan QC-criteria
Laatst geverifieerd
Meer informatie
Termen gerelateerd aan deze studie
Trefwoorden
Andere studie-ID-nummers
- E-84391427-050.04-297820
Plan Individuele Deelnemersgegevens (IPD)
Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?
Beschrijving IPD-plan
Informatie over medicijnen en apparaten, studiedocumenten
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