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Neuroathletic Training in Adolescent Basketball Players

6. maj 2026 opdateret af: Gizem Gül, Pamukkale University

Effects of Neuroathletic Training on Dynamic Visual Acuity, Endurance, Balance, Kinesiophobia, and Injury Risk in Adolescent Basketball Players: A Randomized Controlled Trial

This randomized controlled study aims to investigate the effects of neuroathletic training on dynamic visual acuity, endurance, balance, and injury risk in adolescent basketball players. Licensed basketball players aged 14-17 years will be randomly assigned to either a neuroathletic training group or a control group. The training group will receive sport-specific progressive neuroathletic exercises in addition to their regular basketball training for one week, while the control group will continue their usual training routine. Before and after the intervention, participants will be assessed for dynamic visual acuity, core muscle endurance, balance, functional movement, pain, and kinesiophobia. The findings of this study may help clarify whether neuroathletic training can improve performance-related outcomes and reduce injury risk in adolescent basketball players.

Studieoversigt

Status

Afsluttet

Betingelser

Intervention / Behandling

Undersøgelsestype

Interventionel

Tilmelding (Faktiske)

30

Fase

  • Ikke anvendelig

Kontakter og lokationer

Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.

Studiesteder

  • Tyrkiet (Türkiye)
    • Pamukkale/Kınıklı
      • Denizli, Pamukkale/Kınıklı, Tyrkiet (Türkiye), 20070
        • Pamukkale University

Deltagelseskriterier

Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.

Berettigelseskriterier

Aldre berettiget til at studere

  • Barn

Tager imod sunde frivillige

Ja

Beskrivelse

Inclusion Criteria:

Aged between 14 and 17 years, Being a professional or amateur basketball player, Participating in sports for at least five hours per week and having engaged in the sport for a minimum of two years, Having no cognitive or motor dysfunction, Providing written informed consent signed by the parents/legal guardians.

Exclusion Criteria:

Reporting a back or lower extremity injury within the previous six months, Having any relevant medical history or current condition that could affect the balance system or perception-action system (e.g., neurological disorders, inner ear disorders, or color blindness), Using medications or substances that could affect balance and visual-motor reaction time performance.

Studieplan

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Primært formål: Forebyggelse
  • Tildeling: Randomiseret
  • Interventionel model: Parallel tildeling
  • Maskning: Enkelt

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Ingen indgriben: Kontrolgruppe
Eksperimentel: Neuroatletisk Træningsgruppe
Andet: neuroathletic training
This intervention is a progressive neuroathletic training program developed by the research team to improve motor skills, balance, eye coordination, and vestibular function in adolescent basketball players. The program is performed for approximately 20 minutes per day over 6 days and includes visual relaxation exercises, eye massage, unilateral vertical jumping, Brock string training, shoulder/wrist/ankle circular movements, sacculus activation, cerebellar activation, and antisaccade exercises. The content is progressively advanced across days by integrating balance challenges and visual-vestibular tasks.

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Functional Movement Screen (FMS) total score
Tidsramme: Baseline and immediately following the 1-week intervention
Assessment of injury risk and movement quality using the Functional Movement Screen total score. The test consists of 7 movement patterns scored from 0 to 3, with higher scores indicating better functional movement quality and lower injury risk.
Baseline and immediately following the 1-week intervention

Sekundære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Dynamic Visual Acuity (DVA)
Tidsramme: Baseline and immediately following the 1-week intervention
Dynamic visual acuity assessed using a visual chart while the participant performs active horizontal head movements. The lowest clearly read line will be recorded.
Baseline and immediately following the 1-week intervention
Balance Error Scoring System (BESS) / Denge Hata Puanlama Sistemi
Tidsramme: Baseline and immediately following the 1-week intervention
Postural stability assessed by the number of balance errors performed in double-leg, single-leg, and tandem stance conditions. Lower scores indicate better balance performance.
Baseline and immediately following the 1-week intervention
Core muscle endurance (Prone plank test)
Tidsramme: Baseline and immediately following the 1-week intervention
Core endurance assessed by the duration the participant maintains the correct prone plank position. Longer duration indicates better core endurance.
Baseline and immediately following the 1-week intervention
Tampa Scale for Kinesiophobia (TSK)
Tidsramme: Baseline and immediately following the 1-week intervention
Kinesiophobia assessed using the Tampa Scale for Kinesiophobia. Higher scores indicate greater fear of movement.
Baseline and immediately following the 1-week intervention
Visual Analog Scale (VAS) for pain
Tidsramme: Baseline and immediately following the 1-week intervention
Pain intensity assessed using a 100-mm visual analog scale, with higher scores indicating greater pain intensity.
Baseline and immediately following the 1-week intervention

Samarbejdspartnere og efterforskere

Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.

Sponsor

Pamukkale University

Datoer for undersøgelser

Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.

Studer store datoer

Studiestart (Faktiske)

15. februar 2025

Primær færdiggørelse (Faktiske)

26. oktober 2025

Studieafslutning (Faktiske)

12. januar 2026

Datoer for studieregistrering

Først indsendt

29. april 2026

Først indsendt, der opfyldte QC-kriterier

6. maj 2026

Først opslået (Faktiske)

13. maj 2026

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

13. maj 2026

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

6. maj 2026

Sidst verificeret

1. maj 2026

Mere information

Begreber relateret til denne undersøgelse

Andre undersøgelses-id-numre

  • PAU-FTR-GG-01

Plan for individuelle deltagerdata (IPD)

Planlægger du at dele individuelle deltagerdata (IPD)?

INGEN

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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 .

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