Analysis of New Materials and Artificial Turf Products: Influence and Impact on Athlete Performance and Perception
ANMATT
1 other identifier
interventional
30
0 countries
N/A
Brief Summary
This request pertains to a series of related projects on a common theme. Specifically, this set of projects aims to analyze the impact of new alternatives in materials and structures of artificial turf on athlete performance and perception, within the context of the elimination of microplastics as per Commission Regulation (EU) 2023/2055 of September 25, 2023. Third-generation sports artificial turf is notable for including performance infill (granules) that provide the necessary functionality and safety for sports practice. The vast majority of fields worldwide use materials that do not comply with the new European regulation, which has granted an eight-year moratorium. Therefore, there is little time to find new alternatives. The challenge lies not only in developing new structural solutions but also in understanding their impact on athletes. This issue is of high severity, as these sports facilities are the largest in terms of space and host the highest number of Physical Activity and Sports practitioners in Europe (mainly Football, Rugby, Hockey, and Padel). For this reason, over the past year, the IGOID Group has requested various projects to cover all the necessary phases and nuances to address this issue. The activities included in these projects are divided into two phases: Phase 1: Evaluation of Sports Surfaces in the Laboratory (durability and surface-player and surface-ball interaction). Tests will be conducted on artificial turf samples constructed with SBR rubber (the main material to be replaced under the EU regulation), natural-origin infills, polymeric infills larger than 5 mm, and other infills. Initially, a market analysis and classification will be carried out, followed by laboratory tests. Across all projects, a minimum of 30 alternatives are expected to be analyzed. Phase 2: Field Study. Tests will be conducted on a sample of athletes on constructed surfaces representing the different alternatives evaluated in Phase 1. Performance tests and a battery of assessments will be carried out to understand athlete perception. A sample of 30 athletes will be randomly divided into groups to perform different repetitions of the test batteries, covering a minimum of six different sports facilities.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Sep 2025
Shorter than P25 for not_applicable
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
April 4, 2025
CompletedFirst Posted
Study publicly available on registry
April 22, 2025
CompletedStudy Start
First participant enrolled
September 1, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 30, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
June 30, 2026
ExpectedApril 22, 2025
April 1, 2025
4 months
April 4, 2025
April 14, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
Performance Metrics on Different Surfaces
Sprint times (seconds): The time taken to complete a 20-meter sprint will be measured in seconds. Jump heights (meters): The height achieved during a vertical jump will be measured in meters. Agility (seconds): The time taken to complete an agility course will be measured in seconds.
Sprint times: Measured at Baseline (Day 1) and Week 12. Jump heights: Measured at Baseline (Day 1) and Week 12. Agility: Measured at Baseline (Day 1) and Week 12.
Perception of Comfort and Performance
Participants' subjective ratings of comfort and performance on each surface using a Visual Analogue Scale (VAS).Scale Details: The VAS will range from 0 to 100 mm, where: 0 mm represents the lowest possible rating (e.g., "No comfort" or "Poor performance"). 100 mm represents the highest possible rating (e.g., "Maximum comfort" or "Excellent performance"). Interpretation of Scores: Higher scores on the VAS indicate better outcomes, meaning higher comfort and better performance.
Immediately after each testing session on each surface
Secondary Outcomes (7)
Impact Absorption
Measured at Baseline (Day 1) during the initial evaluation of each surface.
Rotational Resistance
Measured at Baseline (Day 1) during the initial evaluation of each surface.
Ball Rebound
Measured at Baseline (Day 1) during the initial evaluation of each surface.
Ball Roll
Measured at Baseline (Day 1) during the initial evaluation of each surface.
Critical Fall Height
Measured at Baseline (Day 1) during the initial evaluation of each surface.
- +2 more secondary outcomes
Study Arms (6)
Standard Turf
EXPERIMENTALarticipants test the standard turf surface first, followed by the other surfaces in a randomized order.
Ecolastene Turf
EXPERIMENTALParticipants test the Ecolastene turf surface, followed by the other surfaces in a randomized order.
Natural Turf
EXPERIMENTALParticipants test the natural turf surface, followed by the other surfaces in a randomized order.
No Performance Infill Turf
EXPERIMENTALParticipants test the turf surface without performance infill, followed by the other surfaces in a randomized order.
Natural Grass
EXPERIMENTALParticipants test the hybrid turf surface, followed by the other surfaces in a randomized order.
Hybrid Turf
EXPERIMENTALParticipants test the hybrid turf surface, followed by the other surfaces in a randomized order.
Interventions
Participants perform a vertical jump starting from a standing position, bending their knees to 90 degrees, and then jumping as high as possible. The height of the jump is measured using a laser measurement tool (OptoJump-Microgate, Optojump, Bolzano, Italy).
Participants perform repeated vertical jumps for 20 seconds, with the height of each jump measured using a laser measurement tool (OptoJump-Microgate, Optojump, Bolzano, Italy).
articipants perform six 30-meter sprints with 20 seconds of rest between each sprint. Sprint times are measured using photocell timing gates (RaceTime, Microgate, Bolzano, Italy).
Participants perform three maximum effort sprints over 40 meters. Sprint times and speeds are measured using 1080 motion analysis
Participants perform a sprint with a change of direction, running 5 meters in one direction and then 5 meters at a 90-degree angle. The time to complete the test is measured.
Participants perform a shooting test, aiming to hit a target with maximum speed. The speed of the shot is measured using radar.
Participants engage in a 5v5 small-sided game on a 600 m² field to simulate match conditions and assess performance in a game-like scenario.
Participants complete a questionnaire to assess their perception of performance and comfort on the surface, using a Visual Analogue Scale (VAS).
Participants complete a questionnaire to assess their perceived exertion during the tests, using the Borg scale
Eligibility Criteria
You may qualify if:
- Playing Level: Players who have played at the base or amateur level for at least 6 years.
- Health Status: Players who do not have active or chronic injuries that could affect their ability to perform performance tests.
- Willingness to Participate: Players who are willing to undergo performance tests and complete perception questionnaires.
- Recent Injury History: Players who have not experienced significant injuries in the three months prior to the start of the study.
- Medical Conditions: Players who do not have pre-existing medical conditions that could affect their ability to perform performance tests or endanger their health during the tests.
- Medication: Players who are not taking medications that could affect their ability to perform performance tests.
- Consent: Players who have signed an informed consent form to participate in the study and are willing to consistently follow the study protocols.
- Age: Players between 20 and 30 years old (to obtain a more homogeneous sample). -
You may not qualify if:
- Chronic Illness: Players who have a chronic illness that could affect their ability to perform performance tests.
- Medication: Players who are taking medications that could affect their ability to perform performance tests or could affect their understanding of the questionnaires and perception tools.
- Medical History: Players who have a history of cardiovascular, pulmonary, or neurological disease.
- Recent Surgery: Players who have had major surgery in the last six months that could affect their ability to perform performance tests.
- Protocol Compliance: Players who are not willing or able to consistently follow the study protocols.
- Disability: Players who have a physical or cognitive disability that could affect their ability to perform performance tests.
- Consent: Players who have not signed an informed consent form to participate in the study.
- Age: Players who do not meet the minimum and maximum age requirements to be included in the study.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
MeSH Terms
Interventions
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- PARTICIPANT
- Purpose
- BASIC SCIENCE
- Intervention Model
- CROSSOVER
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Senior Lecturer
Study Record Dates
First Submitted
April 4, 2025
First Posted
April 22, 2025
Study Start
September 1, 2025
Primary Completion
December 30, 2025
Study Completion (Estimated)
June 30, 2026
Last Updated
April 22, 2025
Record last verified: 2025-04