このページは自動翻訳されたものであり、翻訳の正確性は保証されていません。を参照してください。 英語版 ソーステキスト用。

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

2026年7月17日 更新者: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.

調査の概要

詳細な説明

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.

研究の種類

介入

入学 (実際)

44

段階

  • 適用できない

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究場所

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

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

  • 子
  • 大人

健康ボランティアの受け入れ

はい

説明

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

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

  • 主な目的:防止
  • 割り当て:ランダム化
  • 介入モデル:並列代入
  • マスキング:独身

武器と介入

参加者グループ / アーム
介入・治療
実験的: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.
アクティブコンパレータ: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.

この研究は何を測定していますか?

主要な結果の測定

結果測定
メジャーの説明
時間枠
Change in Move2Perform Injury Risk Category
時間枠: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
時間枠: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

二次結果の測定

結果測定
メジャーの説明
時間枠
Change in Lower Quarter Y-Balance Test Composite Score
時間枠: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
時間枠: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
時間枠: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
時間枠: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
時間枠: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
時間枠: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
時間枠: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

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

スポンサー

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (実際)

2024年8月20日

一次修了 (実際)

2024年10月22日

研究の完了 (実際)

2024年10月22日

試験登録日

最初に提出

2026年7月13日

QC基準を満たした最初の提出物

2026年7月17日

最初の投稿 (実際)

2026年7月20日

学習記録の更新

投稿された最後の更新 (実際)

2026年7月20日

QC基準を満たした最後の更新が送信されました

2026年7月17日

最終確認日

2026年7月1日

詳しくは

本研究に関する用語

個々の参加者データ (IPD) の計画

個々の参加者データ (IPD) を共有する予定はありますか?

いいえ

医薬品およびデバイス情報、研究文書

米国FDA規制医薬品の研究

いいえ

米国FDA規制機器製品の研究

いいえ

この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。

購読する