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The Effects of Neuro-Athletic Training on Performance Parameters and Injury Risk in Taekwondo Athletes

8 luglio 2026 aggiornato da: Rabia Nur Ata Ozturk, Pamukkale University

Our study is a randomized controlled trial. The aim of the study is to investigate the effects of neuro-athletic training on balance, agility, jump performance parameters, and injury risk in Taekwondo athletes.

Hypotheses H0: Neuro-athletic training has no effects on balance, agility, jump performance parameters, and injury risk in Taekwondo athletes.

H1: Neuro-athletic training has effects on balance, agility, jump performance parameters, and injury risk in Taekwondo athletes.

Sample

A total of 26 participants will be included in the study. Randomization will be used to divide them into two groups:

Experimental group: 13 participants Control group: 13 participants Inclusion Criteria

  • Regular participation in Taekwondo training for at least 2 years
  • No musculoskeletal injury within the last 6 months
  • Participation in Taekwondo training at least 2 days per week during the past 2 years
  • Athletes with an anterior reach distance asymmetry of 4 cm or more after Y-Balance Test (YBT)
  • Voluntary participation in the study Exclusion criteria for participants;
  • Having had hip/pelvis, knee, or ankle surgery in the past year,
  • Having a neurological disease,
  • Using any medication that could affect balance, having a vestibular system disorder,
  • Having a diagnosis of attention deficit.

Panoramica dello studio

Stato

Attivo, non reclutante

Condizioni

Descrizione dettagliata

Our study is a randomized controlled trial. The aim of the study is to investigate the effects of neuro-athletic training on balance, agility, jump performance parameters, and injury risk in Taekwondo athletes.

The hypotheses are as follows:

H0: Neuro-athletic training has no effects on balance, agility, jump performance parameters, and injury risk in Taekwondo athletes.

H1: Neuro-athletic training has effects on balance, agility, jump performance parameters, and injury risk in Taekwondo athletes.

A total of 26 participants will be included in the study. Randomization will be used to divide them into two groups: 13 participants in the experimental group and 13 participants in the control group.

nclusion criteria for participants are: regular participation in Taekwondo training for at least two years, no musculoskeletal injury within the last six months, participation in Taekwondo training at least two days per week during the past two years, anterior reach distance asymmetry of 4 cm or more after the Y-Balance Test (YBT), and voluntary participation in the study.

Exclusion criteria are: hip/pelvis, knee, or ankle surgery within the last year, presence of a neurological disorder, use of any medication that may affect balance, vestibular system disorders, and diagnosis of attention deficit. Power analysis was conducted using G*Power 3.1 software to determine the sample size. For repeated measures ANOVA with two groups and two measurement points, the effect size reported in a previous study for the Taekwondo-Specific Agility Test (TSAT) variable (η²p = 0.26) was taken as reference. With α = 0.05 and power (1-β) = 0.95, a total of 26 participants was calculated to be sufficient.

Participants, both male and female athletes, will be randomized into two groups using the sealed envelope method. Each group will consist of 13 athletes. In the experimental group, athletes will perform a neuro-athletic exercise program in addition to their regular training program, while athletes in the control group will continue only with their regular training. he study is planned to last eight weeks. Athletes will continue their normal training routines, but those in the experimental group will perform neuro-athletic exercises twice a week during the warm-up phase of their training. The program consists of 15-20 minutes of neuro-athletic exercises, as described in Table 1, and will be implemented for eight weeks. Assessments will be conducted at baseline and at the end of the eighth week (pre-test and post-test).

All participants will be informed in detail about the purpose of the study, procedures, and forms used, and written informed consent will be obtained.

The methods of evaluation include anthropometric measurements, Y-Balance Test, Reactive Balance Test, vertical jump assessment, and the Taekwondo-Specific Agility Test.

The study is planned to be conducted at Konya Selçuklu Municipality Sports School.

The expected benefit of the study is that neuro-athletic training, which focuses on the training of the central and peripheral nervous system, will improve communication between the brain and the body, thereby enhancing movement quality and training quality. For Taekwondo athletes, balance, agility, and jump height are crucial for success in competitions. Although the literature suggests that neuro-athletic training improves these parameters, the number of clinical studies is limited. Therefore, the expected benefit of this study is to clinically demonstrate the effectiveness of neuro-athletic training, enhance athlete performance, and contribute to injury prevention.

Tipo di studio

Interventistico

Iscrizione (Stimato)

26

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.

Luoghi di studio

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

  • Bambino
  • Adulto
  • Adulto più anziano

Accetta volontari sani

Descrizione

Inclusion criteria:

  • Attending taekwondo training regularly for at least 2 years
  • Not having had any muscle or skeletal injuries in the last 6 months
  • Training in taekwondo at least 2 days a week in the past 2 years
  • Athletes with anterior reach distance asymmetry of 4 cm or more after YDT
  • Being willing to participate in the study

Exclusion criteria:

  • Having had hip/pelvis, knee, or ankle surgery in the past year
  • Having a neurological disease
  • Using any medication that could affect balance, having a vestibular system disorder
  • Being diagnosed with attention deficit

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: Terapia di supporto
  • Assegnazione: Randomizzato
  • Modello interventistico: Assegnazione parallela
  • Mascheramento: Nessuno (etichetta aperta)

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Comparatore attivo: study group
In addition to their regular workouts, the athletes will follow a neuroathletic training program for 8 weeks.
Neuroathletic training is a treatment approach that, in addition to regular training, provides athletes with more sensory input to the central nervous system and trains them neurologically.
It is a regular training program prepared for athletes specific to the sport field.
Comparatore attivo: Control group
Athletes in this group will continue their regular training prepared by their sport-specific coaches for 8 weeks.
It is a regular training program prepared for athletes specific to the sport field.

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Risk of injury
Lasso di tempo: start and 8 weeks
The risk of injury will be assessed with the Y Balance Test. There are no specific upper or lower limits in the Y Balance Test; however, clinically accepted threshold values exist. The most critical threshold is an asymmetry greater than 4 cm between legs in the anterior direction and a composite score of less than 94%, which significantly increases the risk of injury.
start and 8 weeks

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Reactive Balance Test
Lasso di tempo: start and 8 weeks
The Reactive Balance Test (RBT) assesses an individual's ability to maintain balance when exposed to unexpected external stimuli. It evaluates neuromotor adaptability through measures such as response time, accuracy, and time to stability. While there are no fixed upper or lower limits, clinically meaningful thresholds-like prolonged response times or reduced accuracy-are used to identify impaired performance and increased injury risk. In the Reactive Balance Test, there are no fixed upper or lower limits; instead, clinically meaningful thresholds (e.g., response time >0.6 s, low accuracy) are considered indicators of risk.
start and 8 weeks
Vertical Jump Assessment
Lasso di tempo: start and 8 week
The Vertical Jump Assessment (Vertical Jump Test) is a widely used method to measure an athlete's explosive lower-body power by recording how high they can jump vertically. It does not have fixed "upper or lower limits," but jump height values are interpreted against normative data for age, gender, and sport.
start and 8 week
TSAT (Taekwondo-Specific Agility Test)
Lasso di tempo: Start and 8 week

TSAT (Taekwondo-Specific Agility Test): It is an agility test that includes rapid changes of direction, sprinting, and kicking combinations specific to taekwondo athletes.

Purpose: To measure sport-specific agility, anaerobic capacity, and movement control.

Application: The athlete performs rapid changes of direction over set distances and executes taekwondo techniques (e.g., roundhouse kick).

There are no fixed upper or lower limits; performance is evaluated based on time and movement accuracy, and normative values are interpreted according to the athlete's level."

Start and 8 week
Athlete Injury Anxiety Scale
Lasso di tempo: start and 8 week

SIAS (Sport Injury Anxiety Scale): Developed by Rex & Metzler (2016), it measures the tendency of athletes to perceive injury situations as threatening.

Purpose: To evaluate the psychological impact of injury risk on athletes, including fear of reinjury, loss of performance, and social consequences.

Format: 21 items, 5-point Likert scale (1 = strongly disagree, 5 = strongly agree).

It does not have fixed upper or lower limits; instead, it uses subscales to capture different dimensions of injury-related anxiety.

start and 8 week

Collaboratori e investigatori

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

Investigatori

  • Direttore dello studio: FATMA ÜNVER, PROFESÖR, Pamukkale Üniversitesi

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 (Effettivo)

1 ottobre 2025

Completamento primario (Stimato)

1 settembre 2026

Completamento dello studio (Stimato)

1 ottobre 2027

Date di iscrizione allo studio

Primo inviato

20 giugno 2026

Primo inviato che soddisfa i criteri di controllo qualità

8 luglio 2026

Primo Inserito (Effettivo)

14 luglio 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

14 luglio 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

8 luglio 2026

Ultimo verificato

1 ottobre 2025

Maggiori informazioni

Termini relativi a questo studio

Altri numeri di identificazione dello studio

  • PamukkaleU-FTR-RA-01

Piano per i dati dei singoli partecipanti (IPD)

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

NO

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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