Agility and Sprint Performance in Youth Soccer: A Comparison of FIFA 11+ and RAMP Protocols

November 17, 2025 updated by: Riphah International University

Comparative Effects of FIFA 11+ and RAMP Protocols on Agility and Sprint Performance Outcomes in Young Soccer Players

This randomized clinical trial investigates the comparative effects of the FIFA 11+ and RAMP (Raise, Activate, Mobilize, Potentiate) warm-up protocols on the agility and sprint performance of young soccer players. The study involves 34 male players aged 8 to 15, who will be randomly assigned to one of the two warm-up groups for a six-week intervention period. Key performance outcomes-agility, measured by the Illinois Agility Test, and sprint speed, measured by a 30-meter sprint test-will be assessed both before and after the intervention. The research aims to address a gap in sports science by directly comparing these two popular protocols in a youth population, with the goal of providing coaches with clear, evidence-based recommendations for optimizing athlete development and reducing injury risk. Data will be analyzed through SPSS version 27.00.

Study Overview

Status

Recruiting

Conditions

Detailed Description

This randomized clinical trial provides a detailed comparison of the FIFA 11+ and RAMP (Raise, Activate, Mobilize, Potentiate) warm-up protocols to determine their respective impacts on agility and sprint performance in young male soccer players. The study is grounded in the understanding that soccer requires exceptional speed and agility, and that well-structured warm-ups are critical for enhancing performance and preventing injuries, especially during the crucial developmental years of youth athletes. While both FIFA 11+ (a program focused on neuromuscular control and injury prevention) and RAMP (a systematic, four-phase preparation protocol) are widely used, there is a notable lack of research directly comparing their acute effectiveness in a youth soccer context. This study seeks to fill that gap by providing empirical evidence to guide coaches and practitioners in selecting the most effective warm-up strategy.

The study will recruit 34 male soccer players between the ages of 8 and 15, who will be randomly assigned to either the FIFA 11+ or the RAMP intervention group for a six-week period. Performance will be measured using standardized, valid, and reliable tests: the Illinois Agility Test (IAT) to assess agility and a 30-meter sprint test to measure speed. These assessments will be conducted at baseline before the intervention begins and again immediately following the six-week training period. The collected data will be analyzed to compare within-group improvements and between-group differences, with statistical adjustments for baseline values to ensure a robust comparison. The findings are expected to offer practical, evidence-based recommendations for optimizing warm-up routines to specifically enhance agility and sprint capabilities in young soccer players, thereby supporting superior athletic development. Data will be analyzed through SPSS version 27.00.

Study Type

Interventional

Enrollment (Estimated)

34

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 Contact

Study Contact Backup

Study Locations

    • Punjab Province
      • Lahore, Punjab Province, Pakistan, 54000
        • Recruiting
        • Model Town Football Club
        • Contact:

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

No

Description

Inclusion Criteria:

  • Male, aged 8-15 years.
  • Minimum one year of organized soccer experience.
  • Currently training at least three times per week.
  • Willingness to participate and provide informed consent.

Exclusion Criteria:

  • Cardiovascular, neurological, or musculoskeletal disorders.
  • Musculoskeletal injury in the past six months.
  • Participation in other structured injury prevention or strength programs.
  • Inability to complete baseline testing.

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: Other
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Active Comparator: FIFA 11+ Protocol Group
Participants in this group will perform the FIFA 11+ warm-up protocol at the beginning of each training session for six weeks. This comprehensive, 20-minute program consists of 15 exercises, 3 days a week. Participants with receive total 18 sessions.
The intervention for the first group is the FIFA 11+ warm-up protocol, a standardized 20-minute program developed by FIFA for injury prevention and performance enhancement. It consists of 15 exercises performed in a specific sequence at the start of each training session, divided into three parts: the first part (8 minutes) involves slow-speed running combined with active stretching and partner contacts to practice cutting, deceleration, and proper landing; the second part (10 minutes) focuses on strength, plyometrics, and balance exercises, including core stability, eccentric hamstring strengthening, and proprioceptive training, with three progressive difficulty levels; and the third part (2 minutes) consists of high-intensity running drills with planting and cutting movements to prepare for game-speed activities.
Active Comparator: RAMP Protocol Group
Participants in this group will perform the RAMP warm-up protocol at the beginning of each training session for six weeks. This protocol is a systematic, four-phase approach designed to progressively prepare athletes for high-intensity activity, 20 minutes session, 3 days a week. Participants with receive total 18 sessions.
The intervention for the second group is the RAMP (Raise, Activate, Mobilize, Potentiate) protocol, a systematic, four-phase warm-up designed to progressively prepare athletes for high-intensity performance. The first phase, Raise (5 minutes), uses light cardiovascular activities like jogging and skipping to elevate body temperature and heart rate. The second phase, Activate (5 minutes), involves dynamic mobility exercises such as leg swings, lunges, and bodyweight squats to activate key muscle groups. The third phase, Mobilize (5 minutes), focuses on enhancing joint range of motion and movement patterns through dynamic stretches and sport-specific drills. The final phase, Potentiate (5 minutes), includes high-intensity, explosive activities like sprint accelerations, box jumps, and change-of-direction drills to activate the nervous system and optimize neuromuscular readiness for peak performance.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Illinois Agility Test (IAT)
Time Frame: [Time Frame: Baseline, 1st week and 6th week]
The Illinois Agility Test is a field-based assessment designed to measure an athlete's ability to accelerate, decelerate, and change direction rapidly. The test involves sprinting and weaving through a set course marked by cones. The total time to complete the course is recorded using a stopwatch. The IAT is a highly valid and reliable tool for assessing agility. Recent studies report high content validity (Aiken's V = 0.93) and strong reliability (r = 0.81), confirming its effectiveness for evaluating agility in athletes. Additional research has shown the IAT to have excellent interrater reliability and moderate to good test-retest reliability, making it suitable for both research and applied sports settings.
[Time Frame: Baseline, 1st week and 6th week]
Stopwatch for Sprint Speed
Time Frame: [Time Frame: Baseline, 1st week and 6th week]
A standard handheld stopwatch is used to measure sprint speed over set distance 30m. The assessor starts and stops the watch as the participant crosses the start and finish lines. The best time from two trials is recorded for analysis. Manual timing with a stopwatch is a practical and cost-effective method for field-based sprint assessment. Research shows that hand-held stopwatches have strong concurrent validity compared to electronic timing systems (R² = 0.981-0.994) and excellent inter-rater reliability (ICC = 0.980-0.994) when used by experienced raters. The typical measurement error is small (about 1.6-2.5%), making this method acceptable for sports performance testing.
[Time Frame: Baseline, 1st week and 6th week]

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Adil Munir, MS-PT, Riphah International 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.

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)

October 22, 2025

Primary Completion (Estimated)

June 2, 2026

Study Completion (Estimated)

June 16, 2026

Study Registration Dates

First Submitted

November 17, 2025

First Submitted That Met QC Criteria

November 17, 2025

First Posted (Actual)

November 24, 2025

Study Record Updates

Last Update Posted (Actual)

November 24, 2025

Last Update Submitted That Met QC Criteria

November 17, 2025

Last Verified

November 1, 2025

More Information

Terms related to this study

Other Study ID Numbers

  • REC/RCR&AHS/ADILMUNIR

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

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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