Actively Recruiting
Interest of an Attentional Evaluation by a Computerized Battery in the Management of Concussion in Young Rugby Players
Led by University Hospital, Clermont-Ferrand · Updated on 2026-04-30
90
Participants Needed
1
Research Sites
208 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The goal of this study is to test the ability of a computerized neuropsychological battery to identify attentional disorders resulting from a concussion occurring during the practice of rugby. Thirty young people with a concussion (11-25 years old) will take several neuropsychological tests. Researchers will compare their results with those of young athletes without concussion to see the effect of concussion.
CONDITIONS
Official Title
Interest of an Attentional Evaluation by a Computerized Battery in the Management of Concussion in Young Rugby Players
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Participants with a concussion sustained during rugby practice
- Participants who can read French without assistance
- Control participants with no history of concussion
- Control participants practicing a non-contact sport within a sports association
- Control participants matched by age (+/- 1 year) to concussed participants
- Control participants matched by study level (+/- 1 year) to concussed participants
- Participants aged between 11 and 25 years
You will not qualify if you...
- Participants under legal protection measures
- Participants with other neurological or psychiatric disorders before concussion
- Participants diagnosed with neurodevelopmental disorders in childhood
- Participants scoring 5 or below on the "Matrix" subtest indicating intellectual disability
- Participants with addictive behaviors
- Participants with current major depressive disorder or treated with antidepressants or benzodiazepines for less than 3 months
- Participants with severe visual or motor impairments affecting test performance
- Control participants with a history of proven concussion
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
CHU de Clermont-Ferrand
Clermont-Ferrand, France, 63000
Actively Recruiting
Research Team
L
Lise LACLAUTRE
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
DIAGNOSTIC
Number of Arms
1
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