- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg 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.
Studieoversigt
Status
Intervention / Behandling
Undersøgelsestype
Tilmelding (Anslået)
Fase
- Ikke anvendelig
Kontakter og lokationer
Studiesteder
-
-
Türkiye
-
Istanbul, Türkiye, Tyrkiet (Türkiye), 34342
- Boğaziçi University
-
Kontakt:
- Muhammed Sıddık Çemç, Dr.
- Telefonnummer: +90 537 016 29 25
- E-mail: mscemc@gmail.com
-
Kontakt:
- E-mail: mscemc@gmail.com
-
Ledende efterforsker:
- Muhammed Sıddık Çemç, Dr.
-
-
Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
- Voksen
Tager imod sunde frivillige
Beskrivelse
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.
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Andet
- Tildeling: Ikke-randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Ingen (Åben etiket)
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
|
Eksperimentel: 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.
|
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.
|
|
Ingen indgriben: 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.
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Change in Flanker Task Correct Responses
Tidsramme: Approximately 1 minute before and 1 minute after the intervention
|
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.
|
Approximately 1 minute before and 1 minute after the intervention
|
|
Change in Flanker Task Reaction Time
Tidsramme: Approximately 1 minute before and 1 minute after the intervention
|
Reaction time will be assessed for congruent and incongruent trials using a computerized Flanker Task.
Lower reaction times indicate faster cognitive responses.
|
Approximately 1 minute before and 1 minute after the intervention
|
Samarbejdspartnere og efterforskere
Sponsor
Datoer for undersøgelser
Studer store datoer
Studiestart (Anslået)
Primær færdiggørelse (Anslået)
Studieafslutning (Anslået)
Datoer for studieregistrering
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først opslået (Faktiske)
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Andre undersøgelses-id-numre
- E-84391427-050.04-297820
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
IPD-planbeskrivelse
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
Studerer et amerikansk FDA-reguleret lægemiddelprodukt
Studerer et amerikansk FDA-reguleret enhedsprodukt
Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .