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Baseline Neuromuscular Performance and Responses to a Simulated Match in Young Athletes (SIMMATCH-NM)

6 novembre 2026 aggiornato da: Assoc. Prof. Dr. Özgür EKEN, Inonu University

Predictive Power of Baseline Neuromuscular Performance Characteristics for Physiological and Perceptual Responses After a Simulated Match in Young Athletes

This study looks at whether the physical fitness of young judo athletes before a match can help predict how their bodies and effort perception respond after a match. Judo matches are short, intense and tiring. After a match, athletes show higher blood lactate (a marker of intense effort), weaker grip strength and lower jump height. Not much is known about whether baseline tests of core endurance, throwing power, speed, agility and force-velocity profile can predict these changes in young athletes. Male judo athletes aged 10-13 years will complete these baseline tests in one session and then take part in one 3-minute simulated judo match with a training partner of similar body mass. Blood lactate, vertical jump height and grip strength will be measured before and right after the match, and athletes will rate how hard the match felt. The study will examine how the changes after the match relate to the baseline test results. The findings may help coaches monitor training load and plan conditioning for young judo athletes.

Panoramica dello studio

Descrizione dettagliata

Judo is a high-intensity intermittent combat sport. Matches produce marked blood lactate accumulation, loss of handgrip strength, and reduced lower-body power. Baseline physical profiling is widely used to monitor athletic development, but its ability to predict individual physiological and perceptual responses to a judo match in young athletes is not well understood.

This is a single-group, pre-post study. Fifteen male judo athletes aged 10-13 years will be recruited in Malatya, Turkey. Written informed consent will be obtained from parents or legal guardians, and assent from participants. About one week before testing, participants are familiarized with the procedures and the Borg 6-20 rating of perceived exertion (RPE) scale. Participants avoid high-intensity training, caffeine and ergogenic supplements for 48 hours before testing. Testing takes place in a climate-controlled hall (20-22 °C).

Test day: After anthropometric measurements, baseline profiling is performed: McGill core endurance tests (trunk flexion, trunk extension, right and left lateral bridge), a 2-kg backward overhead medicine ball throw, a 20-m sprint, the pro-agility test, and a force-velocity profile using Samozino's field method (MyJump2 app, 240 fps video). After a standardized 10-minute warm-up (low-intensity jogging, dynamic stretching, breakfalls), pre-match measures are taken: blood lactate (finger-prick capillary sample, single-use lancet), countermovement jump height (contact mat) and handgrip strength (hand dynamometer).

Athletes then complete one 3-minute simulated judo match (randori) under International Judo Federation rules with a training partner of similar body mass (±5 kg), supervised by a coach. Immediately afterwards, blood lactate, jump height, grip strength and RPE are measured in this order within about 3 minutes.

Pre- and post-match values are compared with paired-samples t-tests (Cohen's d). Change scores (post minus pre) for lactate, jump height and grip strength, and RPE, are related to baseline variables using Pearson correlation and simple linear regression. The sample size (minimum 15) was calculated with G*Power for a paired t-test (d = 0.80, alpha = 0.05, power = 0.80).

Tipo di studio

Interventistico

Iscrizione (Stimato)

15

Fase

  • Non applicabile

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Contatto studio

Backup dei contatti dello studio

  • Nome: Özgür Eken, PhD, Associate Professor
  • Numero di telefono: +90 553 213 27 95
  • Email: ozgur.eken@inonu.edu.tr

Luoghi di studio

    • Malatya
      • Malatya, Malatya, Turchia (Türkiye), 44280
        • Department of Physical Education and Sport Teaching, Faculty of Sports Sciences, Inonu University,
        • Contatto:

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

Da 10 anni a 13 anni (Bambino)

Accetta volontari sani

Sì

Sessi ammissibili allo studio

Maschio

Descrizione

Inclusion Criteria:

  • Actively competing judo athlete in Malatya, Turkey
  • Male, aged 10-13 years
  • At least 2 years of regular judo training and competition experience
  • At least four structured technical-tactical training sessions per week
  • No limiting musculoskeletal injury in the last 6 months
  • No musculoskeletal, cardiometabolic, or neurological condition that could prevent testing
  • Willing to participate in all planned tests
  • Written informed consent signed by parent or legal guardian, and assent from the participant

Exclusion Criteria:

  • Younger than 10 or older than 13 years
  • Musculoskeletal injury or surgery within the last 6 months
  • Musculoskeletal, cardiometabolic, or neurological condition that could prevent testing
  • Open wound, varicose veins, acute inflammation, or history of thrombosis
  • Regular use of analgesic or anti-inflammatory medication or ergogenic supplements in the last 3 months
  • Unable to attend all planned testing sessions
  • Unwilling to follow the pre-test rules (no high-intensity training, caffeine or ergogenic supplements for 48 hours; usual diet, hydration and rest)
  • Withdrawal during the study due to non-compliance, incomplete sessions, acute injury during the simulated match, serious illness, or participant request

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Scienza basilare
  • Assegnazione: N / A
  • Modello interventistico: Assegnazione di gruppo singolo
  • Mascheramento: Nessuno (etichetta aperta)

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: Young Judo Athletes

Male judo athletes aged 10-13 years complete baseline physical profiling, followed by one standardized 3-minute simulated judo match. Blood lactate, jump height, grip strength and perceived exertion are measured before and immediately after the match.

One 3-minute simulated judo match (randori) performed under International Judo Federation rules against a training partner of similar body mass (±5 kg), supervised by a coach. Athletes are instructed to fight at maximal competitive intensity.

Altri nomi:
  • Randori

McGill core endurance tests, 2-kg backward overhead medicine ball throw, 20-m sprint, pro-agility test and force-velocity profile (Samozino's field method). Followed by pre- and post-match measures of blood lactate, countermovement jump height, handgrip strength and rating of perceived exertion.

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Change in Blood Lactate Concentration After a Simulated Judo Match
Lasso di tempo: Immediately before and within 3 minutes after the simulated match (single test session)

Change (post-match minus pre-match) in capillary blood lactate concentration (mmol/L), measured from a finger-prick sample with a portable lactate analyzer. The relationship of this change with baseline physical performance variables is also analyzed.

Immediately before and within 3 minutes after the simulated match (single test session)
Change in Countermovement Jump Height After a Simulated Judo Match
Lasso di tempo: Immediately before and within 3 minutes after the simulated match (single test session)

Change (post-match minus pre-match) in maximal isometric handgrip strength (kg) of the dominant hand, measured with a hand dynamometer (best of two trials).

Immediately before and within 3 minutes after the simulated match (single test session)

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Rating of Perceived Exertion (RPE) After a Simulated Judo Match
Lasso di tempo: Within 30 seconds after the simulated match (single test session)

Perceived effort of the simulated match rated on the Borg 6-20 RPE scale (6 = no exertion, 20 = maximal exertion).

Within 30 seconds after the simulated match (single test session)
Change in Handgrip Strength After a Simulated Judo Match
Lasso di tempo: Immediately before and within 3 minutes after the simulated match (single test session)

Change (post-match minus pre-match) in maximal isometric handgrip strength (kg) of the dominant hand, measured with a hand dynamometer (best of two trials).

Immediately before and within 3 minutes after the simulated match (single test session)

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Investigatori

  • Investigatore principale: Özgür Eken, PhD, Assoc. Prof., Inonu University, Faculty of Sport Sciences
  • Direttore dello studio: Denizhan Caliskan, Eskisehir Provincial Directorate of Youth and Sports, Eskisehir, Türkiye

Pubblicazioni e link utili

La persona responsabile dell'inserimento delle informazioni sullo studio fornisce volontariamente queste pubblicazioni. Questi possono riguardare qualsiasi cosa relativa allo studio.

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Stimato)

11 gennaio 2027

Completamento primario (Stimato)

11 febbraio 2027

Completamento dello studio (Stimato)

11 febbraio 2027

Date di iscrizione allo studio

Primo inviato

2 novembre 2026

Primo inviato che soddisfa i criteri di controllo qualità

6 novembre 2026

Primo Inserito (Effettivo)

12 novembre 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

12 novembre 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

6 novembre 2026

Ultimo verificato

1 novembre 2026

Maggiori informazioni

Termini relativi a questo studio

Altri numeri di identificazione dello studio

  • INONU-SIMMATCH-2026-02
  • SIMMATCH-2026 (Altro identificatore: Inonu University)

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

NO

Descrizione del piano IPD

Individual participant data will not be shared, because participants are minors and the consent forms state that data will be used only for the purposes of this research and kept confidential. Aggregate results will be published.

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

No

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

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