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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06255275
Other study ID # 2023/787
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date April 8, 2024
Est. completion date December 2024

Study information

Verified date April 2024
Source Centre Hospitalier Universitaire de Besancon
Contact Karine Charrière, PhD
Phone +333 81 21 89 99
Email kcharriere@chu-besancon.fr
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The VASIS project aims to assess the impact of perceptual, executive and emotional factors on decision-making in the context of pedestrian crossing in an industrial environment involving autonomous vehicle traffic (forklift).


Recruitment information / eligibility

Status Recruiting
Enrollment 100
Est. completion date December 2024
Est. primary completion date August 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 45 Years
Eligibility Inclusion Criteria: - subjects aged 18 to 45 - no objection following submission of a non-objection form indicating that the subject has understood the purpose and procedures of the study and agrees to participate in the study and to comply with the requirements and restrictions inherent in the study Exclusion Criteria: - legal incapacity or limited legal capacity - subject unlikely to cooperate with the study and/or poor cooperation anticipated by the investigator - pregnant or breast-feeding women - color-blind subject - history of cardiovascular disease - current psychiatric or neurological disorders (including self-reported diagnoses of epilepsy) - known vestibular disorders (prone to frequent dizziness or vertigo) - headaches or migraines - deafness - subjects under the influence of psychotropic substances (alcohol, drugs) - motor disorders likely to prevent crossing

Study Design


Related Conditions & MeSH terms


Intervention

Other:
neurocognitifs tests + pedestrian crossign whith virtual reality
Neurocognitive tests (attention, executive functions, reaction to difficulty). Assessment of anxiety and impulsivity + pedestrian crossign with virtual reality + post-crossing questionnaire

Locations

Country Name City State
France Besançon University Hospital Besançon

Sponsors (2)

Lead Sponsor Collaborator
Centre Hospitalier Universitaire de Besancon University of Franche-Comté

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Evaluation of the impact of the attention of participants on decision-making in the context of pedestrian crossing (virtual reality), particularly on the time required to cross safely, in an industrial environment involving autonomous vehicle traffic. Quantication of the time required for a pedestrian to cross safely, according to the attention of participants Day 0
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