- ICH GCP
- Registro de ensaios clínicos dos EUA
- Ensaio Clínico 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
Visão geral do estudo
Status
Intervenção / Tratamento
Descrição detalhada
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.
Tipo de estudo
Inscrição (Real)
Estágio
- Não aplicável
Contactos e Locais
Locais de estudo
-
-
Trabzon, Ordu, Giresun, Rize, Artvin, Gümüşhane
-
Gümüşhane, Trabzon, Ordu, Giresun, Rize, Artvin, Gümüşhane, Turquia (Türkiye), 29600
- Gumushane Univetsity
-
-
Critérios de participação
Critérios de elegibilidade
Idades elegíveis para estudo
- Adulto
Aceita Voluntários Saudáveis
Descrição
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
Plano de estudo
Como o estudo é projetado?
Detalhes do projeto
- Finalidade Principal: Outro
- Alocação: Randomizado
- Modelo Intervencional: Atribuição Paralela
- Mascaramento: Nenhum (rótulo aberto)
Armas e Intervenções
Grupo de Participantes / Braço |
Intervenção / Tratamento |
|---|---|
|
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.
Outros nomes:
|
|
Sem intervenção: Control Group
Participants continued their regular football training without additional neuro-athletic training.
|
O que o estudo está medindo?
Medidas de resultados primários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
|
Dynamic Balance (Y Balance Test)
Prazo: 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)
Prazo: 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
|
Medidas de resultados secundários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
|
Vertical Jump (Countermovement Jump)
Prazo: 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
Prazo: 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
|
Colaboradores e Investigadores
Patrocinador
Datas de registro do estudo
Datas Principais do Estudo
Início do estudo (Real)
Conclusão Primária (Real)
Conclusão do estudo (Real)
Datas de inscrição no estudo
Enviado pela primeira vez
Enviado pela primeira vez que atendeu aos critérios de CQ
Primeira postagem (Real)
Atualizações de registro de estudo
Última Atualização Postada (Real)
Última atualização enviada que atendeu aos critérios de controle de qualidade
Última verificação
Mais Informações
Termos relacionados a este estudo
Palavras-chave
Termos MeSH relevantes adicionais
Outros números de identificação do estudo
- E-95674917-108.99-322122
Plano para dados de participantes individuais (IPD)
Planeja compartilhar dados de participantes individuais (IPD)?
Descrição do plano IPD
Informações sobre medicamentos e dispositivos, documentos de estudo
Estuda um medicamento regulamentado pela FDA dos EUA
Estuda um produto de dispositivo regulamentado pela FDA dos EUA
Essas informações foram obtidas diretamente do site clinicaltrials.gov sem nenhuma alteração. Se você tiver alguma solicitação para alterar, remover ou atualizar os detalhes do seu estudo, entre em contato com register@clinicaltrials.gov. Assim que uma alteração for implementada em clinicaltrials.gov, ela também será atualizada automaticamente em nosso site .