Neuromuscular Training in Female Youth Soccer

NCT ID: NCT06136299

Last Updated: 2023-11-18

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

93 participants

Study Classification

INTERVENTIONAL

Study Start Date

2022-12-07

Study Completion Date

2023-05-20

Brief Summary

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The goal of this clinical trial is to analyze the effectiveness of an NMT-based, injury prevention training program ('FIFA 11+ for Kids') in pre-adolescent (Ages 8 to 11) elite female soccer players by measuring neuromuscular control and motor coordination through pre-intervention and post-intervention testing. As well as monitoring the incidence of injury throughout a soccer season.

Detailed Description

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This study will recruit females aged between 8-11 from several teams within a large, competitive elite soccer club. Whole teams will be assigned to either the intervention group or an age-matched control group. Participants will be informed which group they will be placed in prior to participation in the research study. As directed by their respective coaches, the intervention group will receive neuromuscular training (NMT) through an already established, validated protocol (FIFA 11+ Kids); whilst the control group will perform their standard warm-up during soccer practice sessions. The program will last for the duration of the spring soccer season (January - May 2023; 5 months). All study participants will be required to attend two evaluation sessions (pre-intervention and post-intervention) in order to measure performance in speed, agility, hop testing, dynamic balance and strength.

Conditions

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Injury;Sports

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

There are two groups for this study. The control group performs their standard warm-up during soccer practice sessions and the experimental group performs neuromuscular training (NMT) in the form of the FIFA 11+ Kids program as their warm up.
Primary Study Purpose

PREVENTION

Blinding Strategy

SINGLE

Outcome Assessors
All staff members measuring performance at the pre- and post-intervention testing sessions were unaware of which group the subject was randomized to.

Study Groups

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Control - Standard warm-up

This group performed a standard warm-up protocol during their soccer practice sessions.

Group Type NO_INTERVENTION

No interventions assigned to this group

Intervention - NMT

This group performed a specific Neuromuscular Training (NMT) warm-up program known as FIFA 11+ Kids during their soccer practice sessions

Group Type EXPERIMENTAL

Neuromuscular Training

Intervention Type OTHER

This intervention uses the FIFA 11+ Kids program as a warm-up during soccer practice sessions.

Interventions

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Neuromuscular Training

This intervention uses the FIFA 11+ Kids program as a warm-up during soccer practice sessions.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Elite female soccer players aged 8-11.
* Member of an elite youth soccer club.

Exclusion Criteria

* Female not aged 8-11 years old.
* Not a member of a youth soccer club.
* Unable to attend the pre-intervention or post-intervention evaluation, for reasons other than injury.
* Unable to attend 80% or more of scheduled training sessions.
* If a participant discontinues playing soccer they will be excluded.
* Declines to participate in study.
Minimum Eligible Age

8 Years

Maximum Eligible Age

11 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes

Sponsors

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The Methodist Hospital Research Institute

OTHER

Sponsor Role lead

Responsible Party

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Shari Liberman

Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Shari Liberman, MD

Role: PRINCIPAL_INVESTIGATOR

The Methodist Hospital Research Institute

Locations

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Houston Methodist Hospital

Houston, Texas, United States

Site Status

Countries

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United States

Other Identifiers

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Pro00036803

Identifier Type: -

Identifier Source: org_study_id

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