Neuro-Athletic Training in Football
Optimizing Elite Football Performance Through Neuro-Athletic Training: A Parallel-Group Randomized Controlled Trial
1 other identifier
interventional
56
1 country
1
Brief Summary
This randomized controlled trial evaluates the effectiveness of an 8-week neuro-athletic training (NAT) program in enhancing sport-specific skills and physical capacities in elite male football players aged 18-23 years. Participants were randomly assigned to a NAT intervention group or a control group that maintained standard training. The NAT program involved oculomotor, vestibular, and proprioceptive drills. Primary outcomes include passing and shooting accuracy; secondary outcomes include flexibility and isokinetic knee strength.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Jun 2024
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
June 12, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 12, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
August 12, 2024
CompletedFirst Submitted
Initial submission to the registry
July 9, 2025
CompletedFirst Posted
Study publicly available on registry
July 30, 2025
CompletedJuly 30, 2025
July 1, 2025
1 month
July 9, 2025
July 22, 2025
Conditions
Outcome Measures
Primary Outcomes (2)
Passing Accuracy (Mor-Christian Passing Test)
Measured as a score (max 120) based on 12 passes from 7, 8.5, and 10 meters toward a mini-goal. Assessed pre- and post-intervention.
Pre-intervention (baseline) and post-intervention (after 8 weeks).
Shooting Accuracy (Mor-Christian Shooting Test)
Measured as a score (max 80) based on 16 shots from 14.5 meters toward four 45 cm targets. Assessed pre- and post-intervention.
Pre-intervention (baseline) and post-intervention (after 8 weeks).
Secondary Outcomes (2)
Flexibility (Sit-and-Reach Test)
Pre-intervention (baseline) and post-intervention (after 8 weeks)
Isokinetic Knee Strength (ISOMED 2000 Dynamometer)
Pre-intervention (baseline) and post-intervention (after 8 weeks).
Study Arms (2)
Neuro-Athletic Training (NAT) Group
EXPERIMENTALParticipants receive a structured 8-week NAT program including oculomotor, vestibular, and proprioceptive drills, 3 sessions/week (35-45 minutes each).
Standard Training Group
ACTIVE COMPARATORParticipants continue their standard in-season football training program without any NAT components.
Interventions
Participants receive a structured 8-week NAT program including oculomotor, vestibular, and proprioceptive drills, 3 sessions/week (35-45 minutes each).
Participants continue their standard in-season football training program without any NAT components.
Eligibility Criteria
You may qualify if:
- Male football players aged 18-23 years
- Active in the Turkish Regional Amateur League (2023-2024 season)
- Minimum of 5 years of uninterrupted football training experience
- No known neuromuscular or visual impairments
- Participation in at least four football training sessions per week
- Willingness and ability to participate in all assessments and training sessions
- Provision of written informed consent
You may not qualify if:
- History of orthopedic or neurological surgery within the past year
- Acute or chronic musculoskeletal injuries preventing full participation
- Uncorrected visual impairment
- Use of medications affecting neuromuscular performance or coordination
- Previous or concurrent involvement in structured neuromuscular or neuro-athletic training programs
- Irregular attendance to training sessions (\>20% missed)
- Any condition precluding safe participation, as determined by medical staff
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Balikesir University
Balıkesir, Turkey (Türkiye)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Masking Details
- Outcome assessments were performed by an independent physiotherapist who was blinded to group allocation to reduce measurement bias. Additionally, the researcher conducting the statistical analysis was also blinded to group assignments to ensure data objectivity. Participants and intervention providers were not blinded due to the nature of the behavioral intervention.
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
July 9, 2025
First Posted
July 30, 2025
Study Start
June 12, 2024
Primary Completion
July 12, 2024
Study Completion
August 12, 2024
Last Updated
July 30, 2025
Record last verified: 2025-07
Data Sharing
- IPD Sharing
- Will not share
Individual participant data (IPD) will not be shared due to privacy concerns and institutional data protection policies.