- ICH GCP
- US-Register für klinische Studien
- Klinische Studie NCT07589816
Neuro-Athletic Training on Goalkeeper Performance (NAT)
Effects of an 8-Week Progressive Neuro-Athletic Training Program on Goalkeeper Movement Performance: A Randomized Controlled Trial
Studienübersicht
Status
Intervention / Behandlung
Detaillierte Beschreibung
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.
Studientyp
Einschreibung (Tatsächlich)
Phase
- Unzutreffend
Kontakte und Standorte
Studienorte
-
-
Trabzon, Ordu, Giresun, Rize, Artvin, Gümüşhane
-
Gümüşhane, Trabzon, Ordu, Giresun, Rize, Artvin, Gümüşhane, Türkei (türkiye), 29600
- Gumushane Univetsity
-
-
Teilnahmekriterien
Zulassungskriterien
Studienberechtigtes Alter
- Erwachsene
Akzeptiert gesunde Freiwillige
Beschreibung
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
Studienplan
Wie ist die Studie aufgebaut?
Designdetails
- Hauptzweck: Sonstiges
- Zuteilung: Zufällig
- Interventionsmodell: Parallele Zuordnung
- Maskierung: Keine (Offenes Etikett)
Waffen und Interventionen
Teilnehmergruppe / Arm |
Intervention / Behandlung |
|---|---|
|
Experimental: 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.
Andere Namen:
|
|
Kein Eingriff: Control Group
Participants continued their regular football training without additional neuro-athletic training.
|
Was misst die Studie?
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
Dynamic Balance (Y Balance Test)
Zeitfenster: 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)
Zeitfenster: 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
|
Sekundäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
Vertical Jump (Countermovement Jump)
Zeitfenster: 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
Zeitfenster: 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
|
Mitarbeiter und Ermittler
Sponsor
Studienaufzeichnungsdaten
Haupttermine studieren
Studienbeginn (Tatsächlich)
Primärer Abschluss (Tatsächlich)
Studienabschluss (Tatsächlich)
Studienanmeldedaten
Zuerst eingereicht
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
Zuerst gepostet (Tatsächlich)
Studienaufzeichnungsaktualisierungen
Letztes Update gepostet (Tatsächlich)
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
Zuletzt verifiziert
Mehr Informationen
Begriffe im Zusammenhang mit dieser Studie
Schlüsselwörter
Zusätzliche relevante MeSH-Bedingungen
Andere Studien-ID-Nummern
- E-95674917-108.99-322122
Plan für individuelle Teilnehmerdaten (IPD)
Planen Sie, individuelle Teilnehmerdaten (IPD) zu teilen?
Beschreibung des IPD-Plans
Arzneimittel- und Geräteinformationen, Studienunterlagen
Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt
Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt
Diese Informationen wurden ohne Änderungen direkt von der Website clinicaltrials.gov abgerufen. Wenn Sie Ihre Studiendaten ändern, entfernen oder aktualisieren möchten, wenden Sie sich bitte an register@clinicaltrials.gov. Sobald eine Änderung auf clinicaltrials.gov implementiert wird, wird diese automatisch auch auf unserer Website aktualisiert .