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Neuro-Athletic Training on Goalkeeper Performance (NAT)

28. august 2026 oppdatert av: Coşkun YILMAZ

Effects of an 8-Week Progressive Neuro-Athletic Training Program on Goalkeeper Movement Performance: A Randomized Controlled Trial

This randomized controlled trial investigated the effects of an 8-week neuro-athletic training (NAT) program on dynamic balance, explosive strength, grip strength, and agility in elite soccer goalkeepers. Participants were randomly assigned to either an experimental group receiving NAT in addition to regular training or a control group continuing standard training. Pre- and post-intervention performance assessments were conducted to determine the effectiveness of the intervention.

Studieoversikt

Detaljert beskrivelse

This study was designed as a parallel-group randomized controlled trial with a pretest-posttest structure to examine the neuromuscular and performance adaptations induced by neuro-athletic training (NAT) in elite soccer goalkeepers. A total of 16 athletes competing in the TFF 3rd League and Regional Amateur League were randomly assigned to either an experimental group (n=8) or a control group (n=8).

The experimental group completed an 8-week NAT intervention in addition to their regular football training, while the control group continued standard training routines. The NAT program was conducted twice weekly and incorporated visual, vestibular, and proprioceptive exercises using specialized tools such as Brock strings, pinhole glasses, and Marsden balls. The intervention followed a progressive structure across four phases, targeting visual clarity, coordination, peripheral awareness, and dynamic integration.

Primary performance outcomes included dynamic balance (Y Balance Test), agility (T-test), vertical jump (CMJ), and handgrip strength. Measurements were obtained under standardized conditions before and after the intervention. The study aimed to determine whether integrating neuro-athletic components into training enhances both neuromuscular efficiency and sport-specific performance in goalkeepers.

Studietype

Intervensjonell

Registrering (Faktiske)

16

Fase

  • Ikke aktuelt

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiesteder

    • Trabzon, Ordu, Giresun, Rize, Artvin, Gümüşhane
      • Gümüşhane, Trabzon, Ordu, Giresun, Rize, Artvin, Gümüşhane, Tyrkia (Türkiye), 29600
        • Gumushane Univetsity

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

  • Voksen

Tar imot friske frivillige

Nei

Beskrivelse

Inclusion Criteria:

  • Elite male soccer goalkeepers Minimum 5 years of structured training experience Participation in ≥80% of team training sessions No injury in the last 6 months

Exclusion Criteria:

  • Musculoskeletal or neurological disorders Incomplete participation Additional external training interventions

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Annen
  • Tildeling: Randomisert
  • Intervensjonsmodell: Parallell tildeling
  • Masking: Ingen (Open Label)

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Eksperimentell: Neuro-Athletic Training Group
Participants completed an 8-week neuro-athletic training program in addition to regular football training. The program was performed twice weekly (~20 minutes/session) and included visual, vestibular, and proprioceptive exercises (Brock string, pinhole glasses, Marsden ball). Training intensity and complexity were progressively increased across four phases.
Participants completed an 8-week neuro-athletic training program in addition to regular football training. The program was performed twice weekly (~20 minutes/session) and included visual, vestibular, and proprioceptive exercises (Brock string, pinhole glasses, Marsden ball). Training intensity and complexity were progressively increased across four phases.
Participants continued their regular football training without additional neuro-athletic training.
Andre navn:
  • Ingen inngripen
Ingen inngripen: Control Group
Participants continued their regular football training without additional neuro-athletic training.

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Dynamic Balance (Y Balance Test)
Tidsramme: 8 week
The Y-Balance Test (YBT) assesses dynamic balance by measuring the distances (cm) a participant can reach anteriorly, posteromedially, and posterolaterally while standing on one leg. The composite score is obtained by dividing the sum of the three directions by the leg length and calculating it as a percentage (%), with a higher score indicating better balance.
8 week
Agility (T-Test)
Tidsramme: 8 week
The 505 Agility Test measures the speed of dynamic changes of direction in seconds (s) using electronic timing gates or a stopwatch, consisting of a 10-meter sprint, a 180-degree turn, and a 5-meter reverse sprint. The fastest time of three trials is recorded, with lower times indicating better agility.
8 week

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Vertical Jump (Countermovement Jump)
Tidsramme: 8 Week
Vertical jump (CMJ) height is a secondary outcome measure measured in centimeters (cm) using a force platform (Hawkin Dynamics) device, performed with maximum effort with hands on hips. The measurement is recorded based on a baseline and the best of three trials over a specified time interval (8 weeks).
8 Week
Handgrip Strength
Tidsramme: 8 week
Maximal isometric hand grip strength measured in kilograms (kg) using a standardized Jamar hydraulic hand dynamometer. Measurements will be performed in a standardized sitting position with 90-degree elbow flexion. Three trials will be recorded for each hand, and the highest value (or mean) will be used for analysis
8 week

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Sponsor

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart (Faktiske)

10. mai 2026

Primær fullføring (Faktiske)

15. juli 2026

Studiet fullført (Faktiske)

20. juli 2026

Datoer for studieregistrering

Først innsendt

6. mai 2026

Først innsendt som oppfylte QC-kriteriene

13. mai 2026

Først lagt ut (Faktiske)

15. mai 2026

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

1. september 2026

Siste oppdatering sendt inn som oppfylte QC-kriteriene

28. august 2026

Sist bekreftet

1. august 2026

Mer informasjon

Begreper knyttet til denne studien

Plan for individuelle deltakerdata (IPD)

Planlegger du å dele individuelle deltakerdata (IPD)?

NEI

IPD-planbeskrivelse

Individual participant data will not be shared publicly.

Legemiddel- og utstyrsinformasjon, studiedokumenter

Studerer et amerikansk FDA-regulert medikamentprodukt

Nei

Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .

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