ECCOREV: Assessment of the Cognitive Load of the Landed Combatant in Virtual Reality.

Sponsor
Direction Centrale du Service de Santé des Armées (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05676424
Collaborator
(none)
40
1
12
3.3

Study Details

Study Description

Brief Summary

To support the landed soldier during operational missions in hostile environment, equipment must be designed to enable soldiers to cope with strong visual, auditory and informational demands. Technological solutions proposed by manufacturers are embodied in increasingly sophisticated systems.

These systems take too little account of the characteristics of the perceptive and cognitive skills of human beings in an action situation.

Cognitive load results from the interaction between, on the one hand, the characteristics of the task and the constraints it imposes, and on the other hand, the resources available to the individual, in terms of skills, motivation, physiological state and social support. The phenomenon of cognitive overload occurs when the individual no longer has sufficient resources to meet the demands of the task, which leads to a deterioration in his performance which, in high-risk situations, jeopardizes his safety.

Tasks are treated differently depending on their level of difficulty. We will base ourselves on Rasmussen's SRK (Skill Rule Knowledge) model, which describes three levels of information processing: level S refers to the (automatic) processing of sensory-motor and cognitive skills, level R refers to the execution of rules and procedures embedded in mental models, and level K refers to the mental activities of elaborating procedures, based on high-level cognitive mechanisms, such as anticipation, evaluation or planning. Multitasking situations are therefore generally composed of tasks of various levels of difficulty which lead to a higher or lower cost of cognitive control.

Thus, this study is aimed at identifying variations in the subjective level of cognitive load of landed combatants (group leaders) as a function of the level of difficulty of primary tasks.

Condition or Disease Intervention/Treatment Phase

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    40 participants
    Observational Model:
    Other
    Time Perspective:
    Prospective
    Official Title:
    Assessment of the Cognitive Load of the Landed Combatant in Virtual Reality.
    Anticipated Study Start Date :
    May 1, 2023
    Anticipated Primary Completion Date :
    May 1, 2024
    Anticipated Study Completion Date :
    May 1, 2024

    Outcome Measures

    Primary Outcome Measures

    1. Subjective level of cognitive load, measured with the National Aeronautics and Space AdministrationTask Load Index (NASA-TLX) [Through study completion (12 months)]

      The National Aeronautics and Space AdministrationTask Load Index (NASA-TLX) is a widely used, subjective, multidimensional assessment tool that rates perceived workload in order to assess a task, system, or team's effectiveness or other aspects of performance. The NASA-TLX score is comprised between 0 and 100 with higher score meaning high level of cognitive load.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • to be a soldier in an infantry regiment,

    • to be a group leader.

    Exclusion Criteria:
    • to be in a situation of motor disability,

    • to have a cardiac pathology,

    • to have a visual pathology not corrected by glasses or contact lenses,

    • to have a hearing impairment,

    • to have a psychiatric disorder; a progressive neurological or organic pathology requiring drug treatment,

    • to take psychotropic drugs,

    • to take more than 28 units of alcohol per week,

    • to be epileptic.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Institut de Recherche Biomédicale des Armées Brétigny-sur-Orge France 91223

    Sponsors and Collaborators

    • Direction Centrale du Service de Santé des Armées

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Direction Centrale du Service de Santé des Armées
    ClinicalTrials.gov Identifier:
    NCT05676424
    Other Study ID Numbers:
    • 2021PBMD07
    • 2022-A01311-42
    First Posted:
    Jan 9, 2023
    Last Update Posted:
    Jan 9, 2023
    Last Verified:
    Dec 1, 2022
    Individual Participant Data (IPD) Sharing Statement:
    Undecided
    Plan to Share IPD:
    Undecided
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Direction Centrale du Service de Santé des Armées
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jan 9, 2023