Interest of an Attentional Evaluation by a Computerized Battery in the Management of Concussion in Young Rugby Players

NCT ID: NCT05719844

Last Updated: 2023-07-21

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

90 participants

Study Classification

INTERVENTIONAL

Study Start Date

2023-03-09

Study Completion Date

2025-02-01

Brief Summary

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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.

Detailed Description

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The objective is to carry out a complete neuropsychological assessment, detailing the attentional and executive aspects using the TAP computerized battery. In addition, various paper-and-pencil tests, standardized in French, more commonly used in the context of neuropsychological data related to concussions in athletes, will also be administered. These assess processing speed, short-term memory and auditory-verbal working memory capacity, episodic memory and selective attention. This preliminary study would make it possible to shed light on the links that may exist between performance in the various tests proposed and the characteristics inherent in the symptomatology of concussion. Furthermore, it seems relevant to compare the results of computerized tests with other paper-and-pencil tests but also with the performance of individuals who have no history of concussion with the practice of a non-contact sport.

The results of this study would make it possible in practice to have a neuropsychological assessment more specific to cerebral concussion, with a potentially reduced consultation time due to the use of more sensitive tools, and therefore, an earlier rehabilitative intervention.

Conditions

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Concussion, Brain

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

DIAGNOSTIC

Blinding Strategy

NONE

Study Groups

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Neuropsychological tests

The neuropsychological tests are computerized (TAP battery) or paper-and-pencil tests. They assess processing speed, short-term memory and auditory-verbal working memory capacity, episodic memory and selective attention.

Group Type EXPERIMENTAL

Neuropsychological tests

Intervention Type DIAGNOSTIC_TEST

List of neuropsychological tests:

* Matrix reasoning
* D2-R
* Coding
* Symbol search
* Digit span
* Alertness (computerized TAP battery)
* Divided Attention (computerized TAP battery)
* Go / No go (computerized TAP battery)
* Incompatibility (computerized TAP battery)
* Working memory (computerized TAP battery)
* 16-item Free and Cued Recall or Stories subtest of the Children Memory Scale (CMS) for children only (\< 17 years old)
* complex figure of the memory efficiency battery 144 or Word pairs of the Children Memory Scale for children only (\< 17 years old)

Interventions

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Neuropsychological tests

List of neuropsychological tests:

* Matrix reasoning
* D2-R
* Coding
* Symbol search
* Digit span
* Alertness (computerized TAP battery)
* Divided Attention (computerized TAP battery)
* Go / No go (computerized TAP battery)
* Incompatibility (computerized TAP battery)
* Working memory (computerized TAP battery)
* 16-item Free and Cued Recall or Stories subtest of the Children Memory Scale (CMS) for children only (\< 17 years old)
* complex figure of the memory efficiency battery 144 or Word pairs of the Children Memory Scale for children only (\< 17 years old)

Intervention Type DIAGNOSTIC_TEST

Eligibility Criteria

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Inclusion Criteria

* Patients :
* concussion in the context of the practice of rugby
* French or reading French without help
* Controls :
* no concussion
* practicing a non-contact sport (athletics, rowing, badminton, capoeira, circus, running, crossfit, cycling, dancing, climbing, fencing, fitness, golf, gymnastics, bodybuilding, swimming, skating, Qi Gong, Taï chi, tennis, table tennis, shooting, trail running, volleyball, water polo) within a sports association
* age matched to patient (+/- 1 year)
* study level matched to patient (+/- 1 year)
* French or reading French without help

Exclusion Criteria

* Patients :
* Legal protection measure
* Other neurological or psychiatric pathologies prior to concussion episodes
* Diagnosis of a neurodevelopmental disorder in childhood
* Score less than or equal to 5/19 on the "Matrix" subtest (intellectual retardation)
* Addictive behaviors
* Current major depressive disorder or treated with antidepressants or benzodiazepines for less than 3 months
* Severe visual or motor problems that may interfere with the performance of the tests
* Controls :
* Legal protection measure
* History of proven concussion
* Other neurological or psychiatric pathologies
* Diagnosis of a neurodevelopmental disorder in childhood
* Score less than or equal to 5/19 on the "Matrix" subtest (intellectual retardation)
* Addictive behaviors
* Current major depressive episode or treated with antidepressants or benzodiazepines for less than 3 months
* Severe visual or motor problems that may interfere with the performance of the tests
Minimum Eligible Age

11 Years

Maximum Eligible Age

25 Years

Eligible Sex

MALE

Accepts Healthy Volunteers

Yes

Sponsors

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University Hospital, Clermont-Ferrand

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Tiphaine Vidal

Role: PRINCIPAL_INVESTIGATOR

University Hospital, Clermont-Ferrand

Locations

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CHU de Clermont-Ferrand

Clermont-Ferrand, , France

Site Status RECRUITING

Countries

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France

Central Contacts

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Lise LACLAUTRE

Role: CONTACT

+334.73.754.963

Facility Contacts

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Lise Laclautre

Role: primary

+33473754963

Other Identifiers

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AOI 2021 VIDAL

Identifier Type: -

Identifier Source: org_study_id

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