DRIVing Simulator and People With NeuroCognitive Disorders

NCT06320639 | Recruiting

• 1 other identifier: UGustaveEiffel
• Study Type: observational
• Target: 150
• Locations: 1 country
• Sites: 1

Brief Summary

The ageing of the population is leading to an increasing number of older drivers on the roads. At the same time, the proportion of older people with pathological ageing and neurocognitive disorders (NCD) is increasing. In terms of road safety, this raises the question of whether these drivers should continue to drive or not. People with NCDs may not be aware of the presence, extent and progression of their cognitive impairment and the impact it can have on daily life, including driving. Despite their loss of autonomy and medical advice, 22% of people with major NCD continue to drive. In addition, the presence of minor NCD also puts people at a higher risk of road accidents. However, several studies demonstrated that an NCD does not lead to a systematic and immediate impairment of driving ability and abruptly stopping driving leads to health problems, such as the risk of depression and greatly reduces quality of life. It is therefore relevant to focus research on driving with people with NCD in order to have a reliable indicator of the person's abilities and the impact of their cognitive impairment on driving activity. The proposed study seeks to meet this need by studying the performance of people with NCD on a driving station (mini-simulator) while assessing their ability to evaluate their performance. To achieve this goal, people with NCDs will perform tasks on a driving simulator. In addition, after each task on the driving simulator, they will answer questions about how they evaluate their own driving. Two assessors will observe the participants' driving and will estimate their driving performance. By comparing the driver's self-assessment with the assessors' assessment, an "awareness score of driving ability" will be calculated to determine whether the driver correctly assessed his or her performance. Another project already underway aims to collect similar data from people without a diagnosis of NCDs (control group). The principal objective of the present study is to compare the driving performance in a simulator and the awareness of driving ability of people with NCDs with those of a control group. Secondary objectives are :

• The driving performance and awareness of driving skills of people with NCDs are poorer compared to those of older, control individuals.
• Individuals' driving performance and awareness of driving ability are lower in the presence of major NCDs compared to minor NCDs.

Conditions

Neurocognitive Disorders

Keywords

Alzheimer's Disease; Vascular encephalopathy; Parkinson's Disease

Outcome Measures

Primary Outcomes (2)

• Awareness score of driving ability

  After each task on the driving simulator, participants answer questions about what they think of their driving performance. Two experimenters write their observations about the participant's performance. Answers are coded in a way that a greater driving performance lead to a greater score. The Awareness score is computed by subtracting the score given by the participant to the average of the scores given by the experimenters. The further away from zero the score is, the less aware the participants will be of their abilities. Zero will indicate a perfect assessment of one's abilities.

  Up to 2 hours, from the inclusion until the end of the experiment (2 hours later)

• Driving performance variables measured by the driving simulator

  For each driving task, the driving variables of interest from the driving simulator will be collected: total braking response time, average speed and lateral lane position for the keeping lane task; distance between vehicles for the car-tracking task; reaction time to unexpected events for the rural and urban driving tasks.

  Up to 2 hours, from the inclusion until the end of the experiment (2 hours later)

Eligibility Criteria

• Age: 50 Years - 95 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)
• Sampling Method: Non-Probability Sample

Study Population

Diagnosed with minor or major Neurocognitive Disorders according to the Diagnostic and Statistical Manual of Mental Disorders-V (DSM-V) and recruited from the daycare hospital

You may qualify if:

• Diagnosed with Neurocognitive Disorders according to the Diagnostic and Statistical Manual of Mental Disorders-V (DSM-V)
• Normal or corrected vision
• B licence holder with 3+ years driving experience
• Active drivers or drivers who stopped driving less than 2 months ago (time between the medical consultation and the day in the day care hospital)
• For participants able to give consent:
• Written informed consent to participate in the study
• Informed consent of the participant in the presence of his/her curator.
• For participants who are not able to receive information and to give consent:
• Written informed consent of the legal representative (tutor) for participants under tutelage.
• Signature of a relative (family member and/or trusted person) of the participant
• The participant has to be affiliated to a social security scheme.

You may not qualify if:

• History of epilepsy
• People with vestibular disorders, motion sickness or migraines
• Psychiatric history (e.g. schizophrenia)
• Non-stabilized use of antidepressants and/or anxiolytics (started or modified within the last 3 months)
• History of alcoholism
• Use of anti-epileptics
• Osteo-articular pathologies compromising walking

Sponsors & Collaborators

• University Gustave Eiffel: lead
• Hospices Civils de Lyon: collaborator

Study Sites (1)

Hôpital des Charpennes

Villeurbanne, 69100, France

RECRUITING

Related Publications (1)

• Delphin-Combe F, Coste MH, Bachelet R, Llorens M, Gentil C, Giroux M, Paire-Ficout L, Ranchet M, Krolak-Salmon P. An innovative therapeutic educational program to support older drivers with cognitive disorders: Description of a randomized controlled trial study protocol. Front Neurol. 2022 Jul 18;13:901100. doi: 10.3389/fneur.2022.901100. eCollection 2022.

  PMID: 35923824 RESULT

MeSH Terms

Conditions

Neurocognitive Disorders; Alzheimer Disease; Parkinson Disease

Condition Hierarchy (Ancestors)

Mental Disorders; Dementia; Brain Diseases; Central Nervous System Diseases; Nervous System Diseases; Tauopathies; Neurodegenerative Diseases; Parkinsonian Disorders; Basal Ganglia Diseases; Movement Disorders; Synucleinopathies

Central Study Contacts

Maud Ranchet, PhD

CONTACT

0472142599; maud.ranchet@univ-eiffel.fr

Marion Giroux, PhD

CONTACT

0472432372; marion.giroux@chu-lyon.fr

Study Design

• Study Type: observational
• Observational Model: COHORT
• Time Perspective: CROSS SECTIONAL
• Sponsor Type: OTHER
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: February 19, 2024
• First Posted: March 20, 2024
• Study Start: October 3, 2023
• Primary Completion (Estimated): October 10, 2026
• Study Completion (Estimated): October 10, 2026
• Last Updated: March 20, 2024

Record last verified: 2024-03

Data Sharing

• IPD Sharing: Will not share

Locations

FR (1)