Multiple Sclerosis (MS) Clinical Trials

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Early Detection of Selected Neuropathologies in Motor Vehicle Drivers

Status: Recruiting
Study Type: Observational
SUMMARY

This study aims to develop accessible methods for the early detection of selected neuropathologies in drivers, focusing on multiple sclerosis and Parkinson's disease. The primary objective is to identify clinical tests that correlate with outcomes from the Vienna Test System (VTS), thereby enabling early diagnosis without the need for complex neurological or neuropsychological assessments. Findings could improve the effectiveness of routine driver medical check-ups and inform future modifications to Czech traffic law to enhance road safety.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 85
Healthy Volunteers: f
View:

• Person after signing informed consent.

• After meeting the valid diagnostic criteria for the given neurological diagnosis.

• Possession of a valid driver's license and proof of active driving.

• Age limit 18 - 85 years.

Contact Information
Primary
Dalibor Zimek, M.D.
Dalibor.Zimek@fnol.cz
+420 702 048 036
Backup
Ladislav Stanke, Ph.D.
Ladislav.Stanke@fnol.cz
+420 588 443 713
Time Frame
Start Date: 2025-11-01
Estimated Completion Date: 2028-12-31
Participants
Target number of participants: 200
Treatments
Parkinson disease cohort
PD patients cohort will consist of 100 patients with parkinson disease aged between 18-85 years, with, with a balanced sex distribution to ensure representativeness and reduce gender bias. The target sample size (N = 100) has been chosen to provide adequate statistical power to detect moderate to strong correlations between clinical and paraclinical measures , we also want to distribute patients regularly across all those ages. Participants with premorbid cognitive impairment or those not clinically stable during the study period will be excluded, also participants with a Hoehn and Yahr stage greater than 4 will be excluded.
Multiple sclerosis cohort
Multiple sclerosis patient cohort will consist of 100 patients with multiple sclerosis. aged between 18-85 years, with, with a balanced sex distribution to ensure representativeness and reduce gender bias. The target sample size (N = 100) has been chosen to provide adequate statistical power to detect moderate to strong correlations between clinical and paraclinical measures , we also want to distribute patients regularly across all those ages. Participants with premorbid cognitive impairment or those not clinically stable during the study period will be excluded also an Expanded Disability Status Scale (EDSS) score above 6.5 will serve as an exclusion criterion.
Sponsors
Collaborators: Palacky University
Leads: University Hospital Olomouc

This content was sourced from clinicaltrials.gov