Parkinson Disease Clinical Trial
Official title:
Using Advanced Driver Assistance Systems (ADAS) as an Intervention Strategy for Drivers With Parkinson's Disease
NCT number | NCT03195608 |
Other study ID # | 109272 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | April 15, 2019 |
Est. completion date | December 31, 2022 |
Verified date | February 2024 |
Source | Western University, Canada |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Parkinson's disease (PD) impacts an individual's fitness to drive in a number of ways that increase the crash risk in this population. Current vehicle automation technologies are available, that although designed for the general public, may help drivers with PD stay on the roads longer and safer than currently possible. Using a driving simulator (a safe and cost-effective alternative with no impact on licensing for participants), this study will investigate the feasibility and preliminary efficacy of utilizing in-vehicle technology (i.e., a simulated lane change assistance system) to address critical driving errors in individuals with mild to moderate Parkinson's disease.
Status | Completed |
Enrollment | 22 |
Est. completion date | December 31, 2022 |
Est. primary completion date | December 30, 2022 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 21 Years and older |
Eligibility | Inclusion Criteria: - Participants must be 21 years of age or older (as a feasibility study, this study will provide the opportunity to participate to those diagnosed with early onset PD) - Have been diagnosed with Parkinson's disease by a neurologist or movement disorder specialist - Currently hold a valid G driver's license - Meet provincial visual acuity (20/50 binocular) and visual field (120 continuous along the horizontal meridian with both eyes examined together) requirements for driving - Be proficient in English reading and speaking (self-reported). Exclusion Criteria: - Have any other neurological or psychiatric conditions that would interfere with full participation in the study - Be taking psychotropic medication(s) that affect their mental and/or physical functioning |
Country | Name | City | State |
---|---|---|---|
Canada | University of Western Ontario | London | Ontario |
Lead Sponsor | Collaborator |
---|---|
Western University, Canada |
Canada,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change in number of lane maintenance errors from baseline to post-test 1(4 weeks) and post-test 2 (6 weeks) | Refers to the lateral position of the vehicle in the lane. | Baseline, 4 weeks, and 6 weeks | |
Primary | Change in number of visual scanning errors from baseline to post-test 1(4 weeks) and post-test 2 (6 weeks) | Visual scanning is defined as eye movement and turning of the neck and head (e.g. glances, look sideways at an intersection, look at mirrors) to detect oncoming objects | Baseline, 4 weeks, and 6 weeks | |
Primary | Change in number of signalling errors from baseline to post-test 1(4 weeks) and post-test 2 (6 weeks) | Refers to the proper use of turning signals during lane changes | Baseline, 4 weeks, and 6 weeks |
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