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NCT03969927Completed

User-friendliness of a Portable Driving Simulator

User-friendliness of a Portable Driving Simulator to Retrain Impaired Driving Skills in Stroke Survivors and in Individuals With Parkinson's Disease and Multiple Sclerosis

Source: ClinicalTrials.gov · Last updated 7 Aug 2026

Brief summary (registry, in English)

The use of simulators to retrain driving skills of patients with stroke, Parkinson's disease (PD), or multiple sclerosis (MS) is very limited because of cost, space required, and incidence of simulator sickness in high fidelity simulators. The Principal investigator recently developed a low cost low fidelity portable driving simulator (PDS). In this pilot study, the study team will (1) determine the ease of use and occurrence of simulator sickness while operating the low fidelity PDS in a clinic setting and (2) the efficacy of the low fidelity PDS to reproduce the benefits from retraining impaired driving skills of stroke survivors in a high-fidelity simulator. Participants: 30 participants, separated according to neurological condition including stroke, PD, or MS, will be randomly allocated to either the PDS or fixed-base high-fidelity simulator training. Each participant will undergo a pre-training evaluation, five hours of designated training and a post-training assessment, similar to the pre-training evaluation. Data will be analyzed according to study aims. The investigators hypothesize that the simple set up of the PDS will make it easier to use and better decrease the incidence of simulator sickness that typically leads to stopping therapy than the high-fidelity simulator. The investigators hypothesize that improvements in lane maintenance, adherence to speed limits, reaction to traffic lights, and overall reaction time after training using the PDS will not be significantly different from improvements observed after training using the high-fidelity driving simulator.

Status (registry)
Completed
Study type
Interventional
Enrollment
21 (actual)
First submitted
25 May 2019
Start date
28 Aug 2019
Primary completion date
1 Jun 2025
Lead sponsor
University of Kansas Medical Center
NCT number
NCT03969927

What you commit to

  • Study type: Interventional
  • Participants enrolled: 21
  • From 28 Aug 2019 to the primary completion date, 1 Jun 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • \- Diagnosis of traumatic brain injury or any other neurological condition apart from stroke, PD, and MS.

Who the study is looking for

  • Diagnosis of a first ever stroke, PD, or MS
  • Valid driver's licenses, ≥ 3 years driving experience,
  • Mini-mental State Examination score ≥24, and
  • Binocular acuity of at least 20/60 in compliance with state of Kansas driving laws

Age in the registry: 25 years to 75 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Abiodun Akinwuntan
Coordinator of this site? Confirm its status
Kansas CityUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.