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FIFA 11+ Warm-Up and Injury Risk Classification in Youth Amateur Soccer Players

17 luglio 2026 aggiornato da: Engin Güneş Atabaş, Pamukkale University

Effects of the FIFA 11+ Neuromuscular Warm-Up Program on Move2Perform Injury Risk Classification in Youth Amateur Soccer Players: A Randomized Controlled Trial

This randomized controlled trial evaluated whether an eight-week, supervised FIFA 11+ neuromuscular warm-up program improves multifactorial injury risk classification, functional performance, and time-loss injury incidence in youth amateur male soccer players aged 15 to 18 years.

Forty-four players from a regional amateur league were randomly allocated to either the FIFA 11+ group or a control group that continued its routine pre-training warm-up. Injury risk was classified using the Move2Perform algorithm, which integrates demographic data, injury history, the Functional Movement Screen (FMS), and the Lower Quarter Y-Balance Test (YBT-LQ). Jump performance and isometric lower extremity strength were also assessed at baseline and after eight weeks. Time-loss injuries were recorded prospectively throughout the intervention period.

This study was registered retrospectively.

Panoramica dello studio

Descrizione dettagliata

Background. Lower extremity injuries are a major burden in youth soccer. Isolated screening tools such as the Functional Movement Screen (FMS) and the Lower Quarter Y-Balance Test (YBT-LQ) have shown limited standalone predictive accuracy, whereas multifactorial classification frameworks may better identify at-risk athletes. The FIFA 11+ program is an established neuromuscular warm-up shown to reduce injury incidence, but its combined application with multifactorial risk classification has been studied mainly in collegiate and elite cohorts, leaving youth amateur players underrepresented.

Design. Parallel-group, single-blinded randomized controlled trial. Outcome assessments were performed at baseline and after eight weeks. All testing took place on the natural grass field where the athletes regularly trained, under standard training conditions. The study was conducted in accordance with the principles of the Declaration of Helsinki.

Randomization and blinding. After baseline assessment, participants were allocated 1:1 using computer-generated block randomization with a block size of four. The allocation sequence was prepared by an independent researcher not involved in data collection or analysis, and assignments were concealed from the recruiting investigator until after baseline testing. Investigators administering the FMS, YBT-LQ, jump tests, and strength assessments at both time points were blinded to group allocation. Participants and the supervising physiotherapist could not be blinded due to the nature of the intervention. Data were de-identified prior to statistical analysis.

Intervention. The experimental group performed the complete FIFA 11+ program three times per week for eight weeks before regular training, each session lasting approximately 20 minutes, supervised throughout by a certified physiotherapist who monitored technical execution, progressed exercise difficulty when criteria were met, and provided real-time correction to ensure intervention fidelity. The control group continued its routine pre-training warm-up over the same period.

Sample size. An a priori power analysis (G*Power 3.1; F-test, repeated measures within-between interaction) indicated a minimum total sample of 34 participants to detect a moderate effect (f = 0.25) for the Group x Time interaction with alpha = 0.05 and power = 0.80. Forty-four participants were enrolled.

Statistical analysis. A mixed-design (2x2) ANOVA assessed Group x Time interactions. Within-group changes were examined with paired t-tests following confirmation of normality using the Shapiro-Wilk test. Effect sizes were reported as Cohen's d and partial eta-squared. Bonferroni correction was applied to post hoc comparisons. Between-group injury incidence was compared using Fisher's exact test, with relative risk and 95% confidence intervals reported. Significance was set at p < 0.05.

Registration note. This trial was registered retrospectively.

Tipo di studio

Interventistico

Iscrizione (Effettivo)

44

Fase

  • Non applicabile

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Luoghi di studio

    • Pamukkale
      • Denizli, Pamukkale, Turchia (Türkiye), 20000
        • Pamukkale University, Sports Sciences and Technology Research and Application Center

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

  • Bambino
  • Adulto

Accetta volontari sani

Sì

Descrizione

Inclusion Criteria:

  • Male, aged 15 to 18 years
  • Minimum of one year of competitive experience in an amateur soccer league
  • Actively competing in the Mugla Regional Amateur League at the time of enrolment
  • No diagnosed systemic disease
  • Written informed consent from a parent or legal guardian and written assent from the participant

Exclusion Criteria:

  • Pain reported at the time of baseline assessment
  • Injury sustained within the six months preceding the study

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Prevenzione
  • Assegnazione: Randomizzato
  • Modello interventistico: Assegnazione parallela
  • Mascheramento: Separare

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: FIFA 11+ Group
Participants performed the complete FIFA 11+ neuromuscular warm-up program three times per week for eight weeks prior to regular training, each session lasting approximately 20 minutes, under the supervision of a certified physiotherapist.
The FIFA 11+ program comprises three sequential parts performed as a complete warm-up: (1) an initial running-based warm-up; (2) a central section of strength, plyometric, and balance exercises targeting neuromuscular control and core stability, progressed across three levels of difficulty; and (3) a final part of higher-speed running drills incorporating planting and cutting movements. Performed three times weekly for eight weeks, approximately 20 minutes per session, before regular training. All sessions were supervised by a certified physiotherapist who monitored technical execution, progressed exercise difficulty when criteria were met, and provided real-time correction to ensure intervention fidelity.
Comparatore attivo: Control Group
Participants continued their routine pre-training warm-up over the same eight-week period, with no additional structured neuromuscular component.
The team's usual pre-training warm-up routine, continued unchanged for eight weeks with no additional structured neuromuscular component.

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Change in Move2Perform Injury Risk Category
Lasso di tempo: Baseline and immediately after completion of the 8-week intervention
Injury risk is assessed using the Move2Perform injury risk classification system (Move2Perform LLC, Evansville, IN, USA). Each participant is assigned to one of four ordinal risk categories: Slight Risk, Moderate Risk, Substantial Risk, or High Risk. The outcome is the change in the assigned risk category from baseline to week 8. A shift toward a lower-risk category indicates improvement. The unit of measure is the ordinal risk category.
Baseline and immediately after completion of the 8-week intervention
Number of Time-Loss Injuries
Lasso di tempo: From the first intervention session through completion of week 8
The total number of time-loss injury events sustained during training or match play is recorded prospectively. A time-loss injury is defined as any physical complaint that prevents the participant from taking full part in a subsequent training session or match for at least 24 hours. The unit of measure is the number of injuries. Fewer injuries indicate a better outcome.
From the first intervention session through completion of week 8

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Change in Lower Quarter Y-Balance Test Composite Score
Lasso di tempo: Baseline and immediately after completion of the 8-week intervention
Dynamic balance is assessed using the Lower Quarter Y-Balance Test. The composite score is calculated from the maximal anterior, posteromedial, and posterolateral reach distances normalized to limb length and expressed as a percentage. Change is calculated as the week 8 score minus the baseline score. The unit of measure is percentage of limb length (%). Higher positive change values indicate greater improvement in dynamic balance.
Baseline and immediately after completion of the 8-week intervention
Change in Functional Movement Screen Total Score
Lasso di tempo: Baseline and immediately after completion of the 8-week intervention
Functional movement quality is assessed using the seven-item Functional Movement Screen. Each item is scored from 0 to 3, producing a total score ranging from 0 to 21 points. Change is calculated as the week 8 total score minus the baseline total score. The unit of measure is points. Higher positive change values indicate greater improvement in functional movement quality.
Baseline and immediately after completion of the 8-week intervention
Change in Three-Consecutive Double-Leg Horizontal Jump Distance
Lasso di tempo: Baseline and immediately after completion of the 8-week intervention
Horizontal jump performance is assessed using three consecutive double-leg horizontal jumps. The total distance covered across the three jumps is recorded in centimeters. Change is calculated as the week 8 distance minus the baseline distance. The unit of measure is centimeters (cm). Higher positive change values indicate greater improvement in jump performance.
Baseline and immediately after completion of the 8-week intervention
Change in Three-Consecutive Right Single-Leg Horizontal Jump Distance
Lasso di tempo: Baseline and immediately after completion of the 8-week intervention
Right single-leg horizontal jump performance is assessed using three consecutive horizontal jumps performed on the right leg. The total distance covered across the three jumps is recorded in centimeters. Change is calculated as the week 8 distance minus the baseline distance. The unit of measure is centimeters (cm). Higher positive change values indicate greater improvement in right single-leg jump performance.
Baseline and immediately after completion of the 8-week intervention
Change in Three-Consecutive Left Single-Leg Horizontal Jump Distance
Lasso di tempo: Baseline and immediately after completion of the 8-week intervention
Left single-leg horizontal jump performance is assessed using three consecutive horizontal jumps performed on the left leg. The total distance covered across the three jumps is recorded in centimeters. Change is calculated as the week 8 distance minus the baseline distance. The unit of measure is centimeters (cm). Higher positive change values indicate greater improvement in left single-leg jump performance.
Baseline and immediately after completion of the 8-week intervention
Change in Isometric Quadriceps Strength
Lasso di tempo: Baseline and immediately after completion of the 8-week intervention
Maximal isometric quadriceps strength is assessed using a Powertrak handheld dynamometer (JTech Medical, Utah, USA). The highest recorded value across the maximal voluntary contraction trials is used for analysis. Change is calculated as the week 8 value minus the baseline value. The unit of measure is newtons (N). Higher positive change values indicate greater improvement in quadriceps strength.
Baseline and immediately after completion of the 8-week intervention
Change in Isometric Hamstring Strength
Lasso di tempo: Baseline and immediately after completion of the 8-week intervention
Maximal isometric hamstring strength is assessed using a Powertrak handheld dynamometer (JTech Medical, Utah, USA). The highest recorded value across the maximal voluntary contraction trials is used for analysis. Change is calculated as the week 8 value minus the baseline value. The unit of measure is newtons (N). Higher positive change values indicate greater improvement in hamstring strength.
Baseline and immediately after completion of the 8-week intervention

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Effettivo)

20 agosto 2024

Completamento primario (Effettivo)

22 ottobre 2024

Completamento dello studio (Effettivo)

22 ottobre 2024

Date di iscrizione allo studio

Primo inviato

13 luglio 2026

Primo inviato che soddisfa i criteri di controllo qualità

17 luglio 2026

Primo Inserito (Effettivo)

20 luglio 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

20 luglio 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

17 luglio 2026

Ultimo verificato

1 luglio 2026

Maggiori informazioni

Termini relativi a questo studio

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

NO

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

No

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

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