Effect of a Shortened FIFA11+ Warm-up Program and Sex-specific Footwear on Cutting in Youth Soccer Players

December 12, 2025 updated by: Karen Chen, McGill University

The Effect of Sex-specific Footwear and Tailored Injury Prevention Program on Cutting Performance

This research aims to look at how warm-up programs and types of footwear affect movement patterns that are associated with injury risk during change-of-direction tasks, also known as cutting, in youth soccer players. Specifically, this research is conducted in two parts with two different study designs: a quasi-randomized controlled trial and a crossover design. The main questions it aims to answer are:

  • [Part 1: Quasi-RCT] How does sex and a shortened FIFA11+ warm-up program, lasting 3 months, affect movement patterns during cutting compared to a standard warm-up program in youth soccer players?
  • [Part 2: Crossover design] How does female-specific footwear affect movement patterns during cutting, compared to unisex footwear, in youth female players? Secondarily, whether specific shoe properties (comfort, functional traction, pressure distribution) differ between the two types of footwear.

For part 1 of the research:

  • Researchers will compare a shortened FIFA11+ with a Brazilian warm-up program (standard) to see its effect on movement patterns during cutting.
  • Participants will perform their assigned warm-up program twice a week for 3 months (12-weeks).
  • To assess movement patterns, participants will perform an unplanned sidestep cutting task, captured with markerless cameras, before and after the training period.

For part 2, only female participants will be involved:

  • Researchers will compare the effects of female-specific soccer cleats (designed exclusively for female) with unisex soccer cleats on cutting patterns and certain shoe properties.
  • All participants will test both types of footwear and perform an unplanned sidestep task captured with markerless cameras, run through a slalom course (multiple acceleration and change of directions) to test for shoe traction, and complete an online survey on shoe comfort and perceived performance.
  • A subset of participants will perform a planned sidestep task with wireless insoles to test for pressure distribution.

Study Overview

Detailed Description

With the rise of soccer's global prominence, injury risks among players remain a concern. Deceleration and change of direction maneuvers are frequently employed as an evasive strategy during games. However, they often contribute to higher risk of non-contact anterior cruciate ligament (ACL) injuries. Sidestep cutting involves planting with one foot and pushing off in the opposite direction. Improper movement patterns may increase loads on the planted leg leading to injuries. Injury prevention initiatives such as the FIFA11+ have been introduced to reduce injury rates, but it is unclear whether these programs can correct movement patterns during cutting. Moreover, the length of these programs (often lasting 20 minutes) can reduce adherence and hinder their practical implementation in the real-world. This results in alternative programs like the Brazilian warm-up to be used instead.

In addition, females are significantly more at-risk of ACL injuries than males. This is often attributed to differences in movement pattern and anatomy. Variations in foot anatomy can affect how players interact with footwear, which may in turn, influence cutting patterns. Yet, soccer footwear is typically designed using a male foot template (i.e. last), resulting in a one-size for all approach for female athletes.

In order to address current limitations, this study aims to estimate the effect of a shortened FIFA11+ and sex-specific footwear on cutting kinematics in youth soccer players. This will be done in two parts, where part 1 examines two warm-up programs, and part 2 examines two types of footwear. Ethics approval and informed participants and parental consent as well as assent have been obtained.

For part 1 of the study, 64 healthy soccer players will be recruited from Soccer Montréal (formerly known as Association Régionale de Soccer Concordia (ARSC)) sport study program. Soccer Montréal provides soccer sport study programs to high schools for high performance soccer players. Soccer Montréal conducts soccer training with pre-established cohorts separated by sex and age. Two male and 2 female cohorts will be allocated to either the intervention or control group. Male cohorts of similar age groups will be selected, and the entire cohort will be randomly allocated using a computer. The female cohorts have different age groups, and thus allocation to intervention or control will be divided within each cohort following a quasi-randomized fashion. During the testing, participants are required to perform an unanticipated sidestep maneuver at 45 (±10) degrees on artificial turf. Data will be collected with markerless motion capture systems. A total of 7 trials will be captured in each direction, only 5 out of 7 will be analyzed.

For part 2 of the study, female participants from part 1 (32 females) will test two types of footwear: Female-specific and unisex soccer cleats. Testing will be done at one time point. Female-specific cleats are provided from IDA sports, specifically the IDA centra FG/AG model. Unisex cleats are the Nike Tiempo Legend 10 Academy. Proper fit of shoe sizes will be examined manually by the research team prior to testing. Kinematic data will be collected using the same unanticipated sidestep task as part 1. Additional testing will include a slalom course to examine functional traction of the shoes. Participants will complete an online comfort survey, following the slalom course, once for each shoe. A subset of female participants will also complete a sidestep cutting task with wireless insoles to measure pressure data.

Findings of this study will advance knowledge of ACL injury mechanism during cutting tasks, aid in the design of more practical injury prevention programs and guide the development of female-specific footwear.

Study Type

Interventional

Enrollment (Actual)

64

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Quebec
      • Montreal, Quebec, Canada, H4A 1J6
        • McGill University

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Soccer players
  • Enrolled in Association Régionale de Soccer Concordia (ARSC), now known as Soccer Montréal, soccer sport study program.
  • Age between 13-17 years old.

Exclusion Criteria:

  • Any history of major lower limb or back injuries (e.g., torn ACL, herniated vertebrae)
  • History of any lower extremity surgery
  • Current medical/neurological condition preventing cutting maneuver or training.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Basic Science
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: [Part 1 of study]: Shortened FIFA 11+ Intervention Group
The intervention group will complete a shortened FIFA11+ pre-activation training, incorporating 5 exercises from FIFA11+. The program will be performed twice a week for 12 weeks. The program lasts approximately 7 minutes.

The shortened FIFA11+ incorporates 5 exercises from the original FIFA11+ part 2 and 3: Sideways bench, single-leg stance, squats, jumping and plant and cut (refer to FIFA 11+ manual). All exercises, except plant and cut, have three levels of difficulty. Difficulty progression will follow FIFA11+ guideline option C where all players progress to the next level of all exercises after 3 or 4 weeks. This program is done on artificial turf.

Coaches will be trained on FIFA guidelines by the primary investigator and provided with explanatory placards and the FIFA 11+ manual. The primary investigator will conduct checks twice a week with the coaches to address any questions and review the program. Only the shortened FIFA11+ group will receive verbal feedback as per FIFA11+ guidelines.

Active Comparator: [Part 1 study]: Control Group (Standard warm-up)
The control group will engage in a Brazilian warm-up, lasting approximately 7 minutes, 2 times a week for 3 months. Brazilian warm-ups are typically performed the usual warm-up routine at Soccer Montréal. A standardized version of the warm-up will be given so that all participants in the control group will undergo the same program.

The control group engages in a Brazilian warm-up. The warm-up consists of exercises performed in standing and while running including the following:

  • Performed in standing: Circular Arms (20-30 sec total), Opening and closing of the hips (20-30 sec total).
  • Performed while running back and forth on the field: Jogging (2 times), high kicks (2 times), glute kicks (2 times)
  • Performed while running forward (exercise), then small jog back without performing the exercise: hand-to-heel touches (2 times), knee and heel touches (2 times each side), side leg swings (2 times) and progressive sprint 80-90% speed (2 times).

Coaches will supervise the session but will not be allowed to give verbal feedback. This program is done on artificial turf.

Other Names:
  • Usual soccer warm-up
  • Standard warm-up
  • Typical warm-up

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
[Study Part 1: Warm-up programs]: Joint kinematics of lower extremity and trunk
Time Frame: At baseline

Kinematic data will be captured for both intervention and control group using markerless motion capture system. Joint angles will be assessed throughout the cutting phase from pre-contact (100ms prior to foot strike) to foot-off of the planted leg. Specifically, joint kinematics will include: hip flexion/extension, hip abduction/adduction, hip internal/external rotation, knee flexion/extension, knee abduction/adduction, ankle dorsiflexion/plantarflexion, ankle inversion/eversion, trunk flexion/extension, trunk side flexion and trunk rotation.

Principal component analysis will be used to analyze the whole angle waveform throughout cutting. Therefore, each kinematic outcome measure will be expressed as angle PC-scores which measures the degree of correspondence between angle waveform and principal components (PCs). PCs will captures variability features of angle waveform data such as amplitude, angle differences, etc.

At baseline
[Study Part 2: Footwear]: Joint kinematics of lower extremity and trunk
Time Frame: Baseline (one time point)

Kinematic data will be collected for female-specific footwear and unisex footwear using markerless motion capture system. Joint angles will be assessed throughout the cutting phase from pre-contact (100ms prior to foot strike) to foot-off of the planted leg. Specifically, joint kinematics will include: hip flexion/extension, hip abduction/adduction, hip internal/external rotation, knee flexion/extension, knee abduction/adduction, ankle dorsiflexion/plantarflexion, ankle inversion/eversion, trunk flexion/extension, trunk side flexion and trunk rotation.

Principal component analysis will be used to analyze the whole angle waveform throughout cutting. Therefore, each kinematic outcome measure will be expressed as angle PC-scores which measures the degree of correspondence between angle waveform and principal components (PCs). PCs will capture variability features of angle waveform data such as amplitude, angle differences, etc.

Baseline (one time point)
[Study Part 1: Warm-up programs]: Joint kinematics of lower extremity and trunk
Time Frame: After the 12-week intervention

Kinematic data will be captured for both intervention and control group using markerless motion capture system. Joint angles will be assessed throughout the cutting phase from pre-contact (100ms prior to foot strike) to foot-off of the planted leg. Specifically, joint kinematics will include: hip flexion/extension, hip abduction/adduction, hip internal/external rotation, knee flexion/extension, knee abduction/adduction, ankle dorsiflexion/plantarflexion, ankle inversion/eversion, trunk flexion/extension, trunk side flexion and trunk rotation.

Principal component analysis will be used to analyze the whole angle waveform throughout cutting. Therefore, each kinematic outcome measure will be expressed as angle PC-scores which measures the degree of correspondence between angle waveform and principal components (PCs). PCs will captures variability features of angle waveform data such as amplitude, angle differences, etc.

After the 12-week intervention

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
[Study Part 2: Footwear]: Slalom course running time
Time Frame: Baseline (one time point)
Completion times will be captured with timing gates for both female-specific and unisex cleats. Faster completion times will reflect better functional traction properties. The average of three trials will be taken for each shoe.
Baseline (one time point)
[Study Part 2: Footwear]: Hindfoot mediolateral plantar pressure ratios
Time Frame: Baseline (one time point)

Higher ratios will indicate greater relative pressure on the medial borders, while lower ratios will indicate greater pressures on the lateral border.

Data will be determined for both for both female-specific and unisex cleats from the pressure data obtained with wireless insoles.

Baseline (one time point)
[Study Part 2: Footwear]: Forefoot mediolateral plantar pressure ratios
Time Frame: Baseline (one time point)

Higher ratios will indicate greater relative pressure on the medial borders, while lower ratios will indicate greater pressures on the lateral border.

Data will be determined for both for both female-specific and unisex cleats from the pressure data obtained with wireless insoles.

Baseline (one time point)
[Study Part 2: Footwear]: Peak plantar pressure
Time Frame: Baseline (one time point)

The plantar surface of the foot will be divided into regions. Peak pressure will represent the highest recorded pressure in each of the regions.

Data will be determined for both for both female-specific and unisex cleats from the pressure data obtained with wireless insoles.

Baseline (one time point)
[Study Part 2: Footwear]: Mean plantar pressure
Time Frame: Baseline (one time point)

The plantar surface of the foot will be divided into regions. Mean pressure will be the average pressure in each of the regions.

Data will be determined for both for both female-specific and unisex cleats from the pressure data obtained with wireless insoles.

Baseline (one time point)
[Study Part 2: Footwear]: Impulse plantar pressure
Time Frame: Baseline (one time point)

Impulse (pressure-time integral) will be derived by multiplying the pressure amplitude by the duration of application (i.e. contact phase of interest).

Data will be determined for both for both female-specific and unisex cleats from the pressure data obtained with wireless insoles.

Baseline (one time point)
[Study Part 2: Footwear]: Performance rating: Perceived traction suitability
Time Frame: Baseline (one time point)

Perceived ratings will be completed using an online survey, following the slalom course, once for each shoe (female-specific and unisex cleats). Traction suitability rating ranges from 0 (Worse suitability) to 15 (Best suitability) using a visual analogue scale.

Traction suitability refers to ability of the shoe to maintain its grip with the playing surface to minimize slip and falls. Worse suitability indicates greater slips and falls. Best suitability rating indicates a greater ability to maintain stability and less risk of slips and falls.

Baseline (one time point)
[Study Part 2: Footwear]: Performance rating: Overall performance
Time Frame: Baseline (one time point)

Perceived ratings will be completed using an online survey, following the slalom course, once for each shoe (female-specific and unisex cleats). Overall performance rating ranges from 0 (Worse performance) to 15 (Best performance) using a visual analogue scale.

Overall performance refers to how well you feel you did during the dynamic tasks in terms of overall speed, turn and satisfaction. Worse performance means that you did not perform well in this shoe. Best performance means that this shoe allowed you to give your best performance.

Baseline (one time point)
[Study Part 2: Footwear]: Comfort rating: Overall comfort
Time Frame: Baseline (one time point)

Perceived ratings will be completed using an online survey, following the slalom course, once for each shoe (female-specific and unisex cleats). Overall comfort rating ranges from 0 (Not comfortable at all) to 15 (Most comfortable condition imaginable) using a visual analogue scale.

Overall comfort refers to your overall impression of the shoe in terms of how comfortable. Not comfortable at all means that the shoe is overall not comfortable. Most comfortable condition imaginable, means that the shoe comfort is perfect for your needs.

Baseline (one time point)
[Study Part 2: Footwear]: Comfort rating: Overall shoe fit
Time Frame: Baseline (one time point)

Perceived ratings will be completed using an online survey, following the slalom course, once for each shoe (female-specific and unisex cleats). Overall shoe fit rating ranges from 0 (Not comfortable at all) to 15 (Most comfortable condition imaginable) using a visual analogue scale.

Shoe fit refers to the overall fit and size of the shoe. Not comfortable at all means the fit of the shoe is not comfortable either too tight or too loose at some parts of the foot. Most comfortable condition imaginable, means that the size and the fit of the shoe is perfect for your foot.

Baseline (one time point)
[Study Part 2: Footwear]: Comfort rating: Overall cushioning
Time Frame: Baseline (one time point)

Perceived ratings will be completed using an online survey, following the slalom course, once for each shoe (female-specific and unisex cleats). Overall comfort rating ranges from 0 (Not comfortable at all) to 15 (Most comfortable condition imaginable) using a visual analogue scale.

Overall cushioning refers to the softness/hardness of the insole at the forefoot or heel region. Not comfortable means the cushioning at the front or back of your foot is too hard or too soft, making it uncomfortable during use. Most comfortable means that the cushioning is perfectly fitted for your foot and needs.

Baseline (one time point)
[Study Part 2: Footwear]: Comfort rating: Overall shoe weight
Time Frame: Baseline (one time point)

Perceived ratings will be completed using an online survey, following the slalom course, once for each shoe (female-specific and unisex cleats). Overall shoe weight rating ranges from 0 (Not comfortable at all) to 15 (Most comfortable condition imaginable) using a visual analogue scale.

Shoe weight refers to the weight/heaviness of the shoe. Not comfortable at all means that the weight is too heavy or too light for your comfort. Most comfortable means that the shoe weight is perfect for your foot and tasks.

Baseline (one time point)

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Study Director: Shawn Robbins, Associate Professor, PhD, McGill University
  • Principal Investigator: Karen Chen, PhD Candidate, McGill University

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Helpful Links

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

January 29, 2024

Primary Completion (Actual)

May 22, 2024

Study Completion (Actual)

May 22, 2024

Study Registration Dates

First Submitted

October 5, 2024

First Submitted That Met QC Criteria

October 9, 2024

First Posted (Actual)

October 15, 2024

Study Record Updates

Last Update Posted (Actual)

December 19, 2025

Last Update Submitted That Met QC Criteria

December 12, 2025

Last Verified

December 1, 2025

More Information

Terms related to this study

Other Study ID Numbers

  • A12-M61-23B (23-10-088)
  • RGPIN-2018-06525 (Other Grant/Funding Number: Natural Sciences and Engineering Research Council of Canada)

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

IPD Plan Description

The open-access content, encompass only de-identified biomechanical and demographic data. This will include metrics such as joint waveforms, plantar pressure, performance metrics, and anonymized demographic information including age, sex, height, weight, BMI, years of soccer experience, shoe size, and leg dominance.

IPD Sharing Time Frame

Available following publication. No end date

IPD Sharing Access Criteria

Our study data will be published in an open-access format (available to anyone who wishes to access the information), while protecting participant anonymity. It will encompass only de-identified biomechanical and demographic data, which will be shared via a dedicated repository on the McGill IHRG (Ice Hockey Research Group) server.

IPD Sharing Supporting Information Type

  • STUDY_PROTOCOL
  • SAP
  • ICF

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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