- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07589816
Effects of Neuro-Athletic Training on Goalkeeper Performance
From Neural Input to Athletic Output: Effects of Neuro-Athletic Training on Dynamic Balance, Strength, and Agility in Elite Soccer Goalkeepers
Study Overview
Status
Intervention / Treatment
Detailed Description
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.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Trabzon, Ordu, Giresun, Rize, Artvin, Gümüşhane
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Gümüşhane, Trabzon, Ordu, Giresun, Rize, Artvin, Gümüşhane, Turkey (Türkiye), 29600
- Gumushane Univetsity
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
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
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
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.
Other Names:
|
|
No Intervention: Control Group
Participants continued their regular football training without additional neuro-athletic training.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Dynamic Balance (Y Balance Test)
Time Frame: 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.
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8 week
|
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Agility (T-Test)
Time Frame: 8 week
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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
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Vertical Jump (Countermovement Jump)
Time Frame: 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).
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8 Week
|
|
Handgrip Strength
Time Frame: 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
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- E-95674917-108.99-322122
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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