NMT: Neuromuscular Training in Female Youth Soccer

Sponsor
The Methodist Hospital Research Institute (Other)
Overall Status
Completed
CT.gov ID
NCT06136299
Collaborator
(none)
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Study Details

Study Description

Brief Summary

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.

Condition or Disease Intervention/Treatment Phase
  • Other: Neuromuscular Training
N/A

Detailed Description

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.

Study Design

Study Type:
Interventional
Actual Enrollment :
93 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
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.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.
Masking:
Single (Outcomes Assessor)
Masking Description:
All staff members measuring performance at the pre- and post-intervention testing sessions were unaware of which group the subject was randomized to.
Primary Purpose:
Prevention
Official Title:
Effect of Neuromuscular Training on Physical Performance and Injury Rate in Elite Female Youth Soccer Players
Actual Study Start Date :
Dec 7, 2022
Actual Primary Completion Date :
May 20, 2023
Actual Study Completion Date :
May 20, 2023

Arms and Interventions

Arm Intervention/Treatment
No Intervention: Control - Standard warm-up

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

Experimental: Intervention - NMT

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

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

Outcome Measures

Primary Outcome Measures

  1. Dynamic balance assessment [Dynamic balance will be measured at two separate timepoints: pre-intervention (baseline) and post-intervention (within 5-months after baseline measures).]

    The Y-balance test is a standardized protocol consisting of lower extremity reach in the anterior, posteromedial and posterolateral directions.

  2. Strength assessment [Strength will be measured at two separate timepoints: pre-intervention (baseline) and post-intervention (within 5-months after baseline measures).]

    Hamstring and quadriceps strength will be measured using a handheld dynamometer. Each strength measure will be taken 3 times with the average calculated.

  3. Agility assessment [Agility will be measured at two separate timepoints: pre-intervention (baseline) and post-intervention (within 5-months after baseline measures).]

    The Pro-Agility Test utilizes three cones. The farthest cone is sprinted to, the ground is touched with one hand and direction changed back to the starting cone (9.1m sprint). The ground is touched at the starting cone, direction is changed to the 'middle cone' into a 4.6m sprint. Passing the 'middle cone' is the finish line for the test. Each strength measure will be taken 3 times with the average calculated.

  4. Hop testing assessment [Hop performance will be measured at two separate timepoints: pre-intervention (baseline) and post-intervention (within 5-months after baseline measures).]

    Participants will complete a single leg hop, triple hop and a timed 6 meter hop

  5. Kinetic jump testing assessment [Kinetic jump performance will be measured at two separate timepoints: pre-intervention (baseline) and post-intervention (within 5-months after baseline measures).]

    A countermovement jump and a single leg vertical jump on a force plate platform system.

Secondary Outcome Measures

  1. Injury rates [Duration of spring soccer season, January - May (5 months).]

    Injury information provided by coaches and/or parents throughout the spring soccer season.

Eligibility Criteria

Criteria

Ages Eligible for Study:
8 Years to 11 Years
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
Yes
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.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Houston Methodist Hospital Houston Texas United States 77030

Sponsors and Collaborators

  • The Methodist Hospital Research Institute

Investigators

  • Principal Investigator: Shari Liberman, MD, The Methodist Hospital Research Institute

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Shari Liberman, Principal Investigator, The Methodist Hospital Research Institute
ClinicalTrials.gov Identifier:
NCT06136299
Other Study ID Numbers:
  • Pro00036803
First Posted:
Nov 18, 2023
Last Update Posted:
Nov 18, 2023
Last Verified:
Nov 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Nov 18, 2023