NCT07092735

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

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
56

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Jun 2024

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

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

Completed
1 month until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 12, 2024

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

August 12, 2024

Completed
11 months until next milestone

First Submitted

Initial submission to the registry

July 9, 2025

Completed
21 days until next milestone

First Posted

Study publicly available on registry

July 30, 2025

Completed
Last Updated

July 30, 2025

Status Verified

July 1, 2025

Enrollment Period

1 month

First QC Date

July 9, 2025

Last Update Submit

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

EXPERIMENTAL

Participants receive a structured 8-week NAT program including oculomotor, vestibular, and proprioceptive drills, 3 sessions/week (35-45 minutes each).

Behavioral: Neuro-Athletic Training

Standard Training Group

ACTIVE COMPARATOR

Participants continue their standard in-season football training program without any NAT components.

Other: Standard Training

Interventions

Participants receive a structured 8-week NAT program including oculomotor, vestibular, and proprioceptive drills, 3 sessions/week (35-45 minutes each).

Neuro-Athletic Training (NAT) Group

Participants continue their standard in-season football training program without any NAT components.

Standard Training Group

Eligibility Criteria

Age18 Years - 23 Years
Sexmale(Gender-based eligibility)
Gender Eligibility DetailsOnly individuals who self-identify as male are eligible to participate in this study. The study targets elite male football players to ensure homogeneity in performance characteristics and to align with league-specific demographics during the 2023-2024 season.
Healthy VolunteersYes
Age GroupsAdult (18-64)

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)

Location

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
Model Details: This study used a parallel-group randomized controlled trial design with pre- and post-intervention assessments. Participants were randomly assigned to either a Neuro-Athletic Training (NAT) group or a control group. The NAT group received an 8-week structured program targeting sensorimotor integration through oculomotor, vestibular, and proprioceptive drills, while the control group continued standard football training without additional interventions. Outcome assessors and statistical analysts were blinded to group allocations. The study was conducted under standardized conditions to ensure methodological rigor and group comparability.
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.

Locations