Ecological Test Standardization for Concussion Assessment in Football Players (COMOFOOT)

Concussion is a major concern in the sports world. It represents an immediate and transient alteration of neurological functions due to a direct or indirect trauma, with or without loss of consciousness. Concussions affect between 1.6 and 3.8 million people per year in the United States across all sports. The prevalence varies depending on the sport. In France, the incidence of sport-related concussions is estimated at 200,000 cases. According to the French Academy of Medicine (March 2025), concussions account for between 5% and 9% of all sports-related injuries. Among these cases, 30% involve individuals aged 5 to 19. Football (soccer) is one of the most affected sports, with its 2 million registered players. In French professional football (Ligue 1 and 2), during the 2023-2024 season, one concussion was recorded every 55 matches on average (declared concussion). During the 2018-2019 and 2019-2020 seasons, the rate of matches with concussion was approximately 2.5%. In professional rugby, it is estimated that one concussion occurs every three matches in France.

There are no precise statistics on the number or frequency of concussions in amateur football in France, due to a lack of reporting and insufficient diagnosis. Currently, practical recommendations exist for managing football players from the moment of impact on the field, implemented within the French Football Federation. The current concussion protocol includes a standardized tool for evaluating concussion intended for healthcare professionals, the SCAT6. However, this protocol is not always sufficient, and return-to-play sometimes occurs too early. Indeed, current assessments are too brief and do not evaluate all cognitive functions. They do not allow a clear understanding of the real on-field consequences. It is estimated that 50% of athletes return to play too early after a concussion, with risks of neurological complications or prolonged symptoms.

However, defining rest time and return-to-play criteria is not straightforward. In practice, return to play relies, among other things, on neuropsychological tests, whose interpretation is difficult in the absence of baseline data. The concussion protocol does not allow for an accurate determination of whether performance has normalized without this neuropsychological baseline.

Recent European and international recommendations advise conducting pre-season assessments to provide comparative values. Several studies have been published on the type of pre-season assessments to perform, most using paper-and-pencil or computerized neurocognitive tests.

The current concussion protocol relies mainly on paper-and-pencil tests. However, the literature shows dissociations between cognitive performance measured in ecological environments and performance measured through paper-and-pencil tests. Ecological tasks have the advantage of closely approximating the daily actions of a player and assessing cognitive functioning more precisely.

Thus, these ecological tasks, combined with a baseline assessment, would improve the evaluation of athletes following a concussion. These tasks would facilitate return-to-play decisions through more objective observations and normed data. Finally, ecological tasks would enhance player monitoring and allow a more accurate understanding of their health status.

For this reason, it seems necessary to develop a standardized ecological test performed in real-game situations. This would improve decision-making regarding return to play without medically endangering the player and would allow better understanding of the cognitive effects of concussion. These tasks will first be reviewed and tested by experts (players, football staff members, national concussion reference physician, and neuropsychologists) for feedback and refinement.

Study Overview

Study Type

Interventional

Enrollment (Estimated)

100

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

      • Ploemeur, France, 56270
        • Centre de Kerpape

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
  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

Professional football players:

  • Male professional football players from French clubs
  • Aged 18 years and older
  • Provided written informed consent to participate
  • Adequate understanding of written and spoken French

Youth football players from training centers:

  • Registered in a training center affiliated with a French football club
  • Aged 16 years and older
  • Provided written assent to participate, with parental or legal guardian consent for minors
  • Adequate understanding of written and spoken French

Exclusion Criteria:

All players:

  • History of concussion in the past 6 months (for inclusion, a statement from the club physician confirming no concussion in the past 6 months will be requested)
  • Physically unfit (if applicable, a medical certificate from the club physician will be required, e.g., incapacitating musculoskeletal injury)

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: Diagnostic
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Cognitive evaluation: paper-and-pencil tests and ecological tasks
Participants complete a dual-task on the football field combining a cognitive task of counting whistle signals and a motor task of dribbling through cones, identifying colored markers, performing juggling sequences, and shooting into a rebound board. Duration approximately 15 minutes for single tasks, 2 minutes for dual-task execution. Purpose is to evaluate and standardize cognitive performance in realistic game situations.
Participants navigate a defined space on the field, touching cones in a sequence demonstrated by the examiner with the ball at their feet. Tasks increase in difficulty and include reversing the sequence. Duration approximately 20 minutes. Purpose is to assess and norm visuospatial working memory performance in football-specific contexts.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Ecological Cognitive Performance Scores
Time Frame: Day 0 to 7 : time 1 assessment

The ecological task consists of two exercises :

  • The first exercise is the dual-task, which involves performing two tasks separately and then simultaneously. (count sequences of whistle blows and complete a slalom between cones while dribbling the ball, gathering information (the color of a card)
  • The second exercise is a visuospatial memory task. It consists of touching cones while moving within a delimited space, dribbling a ball.

The primary outcome measure is based on the results of the ecological tasks according to age categories:

For the dual-task: task score, number of ball losses, total cone score, number of successful shots on goal, number of correct color-information responses, and percentage of correct responses to the whistle blows.

For the visuospatial working-memory task: forward and backward span, total score, and number of ball losses during the course.

Day 0 to 7 : time 1 assessment

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Reliability of the Ecological Tests - Intra-rater reliability
Time Frame: Day 30 to 45 : Time 2 assessment

The scores will be assigned by the same evaluator during two identical testing sessions carried out at different times and performed by 32 players.

Thirty-two players will be selected from the 100 participants to complete the ecological tasks for a second time

Day 30 to 45 : Time 2 assessment
Reliability of the Ecological Tests - Inter-rater reliability
Time Frame: Day 0 to 7 : Time 1 assessment

Correlation of results rated by two different evaluators for the same tests performed by the same 32 players.

Thirty-two players will be selected from the 100 participants to repeat the ecological tasks a second time.

Day 0 to 7 : Time 1 assessment
Correlation with Standardized Paper-and-Pencil Tests
Time Frame: Day 0 : Time 1 assessment

Correlation between scores obtained on paper-and-pencil tests and ecological tests.

Visuospatial working memory, using the Corsi Block-Tapping Test Short- and long-term visual memory, using the Clinical Memory Scale (MEM-IV, Visual Reproduction I and II) Mental flexibility, using the Trail Making Test (TMT) Planning abilities, using the Tower of London test (TOL) Dual-task performance and divided attention, using Baddeley's Dual-Task Test Sustained and selective attention, using the Battery for Attention and Memory Screening - Test (BAMS-T) Affective aspects, through an anxiety questionnaire (T-FAI2) and a self-esteem questionnaire,Rosenberg Self-Esteem Scale (RSE)

Day 0 : Time 1 assessment

Collaborators and Investigators

This is where you will find people and organizations involved with this 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 (Estimated)

April 1, 2026

Primary Completion (Estimated)

April 1, 2028

Study Completion (Estimated)

April 1, 2028

Study Registration Dates

First Submitted

February 18, 2026

First Submitted That Met QC Criteria

February 18, 2026

First Posted (Actual)

February 24, 2026

Study Record Updates

Last Update Posted (Actual)

February 24, 2026

Last Update Submitted That Met QC Criteria

February 18, 2026

Last Verified

February 1, 2026

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

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.

Clinical Trials on Concussion, Brain

Clinical Trials on Ecological Dual-Task Cognitive Assessment

Subscribe