Highlights
- •Identifying impaired driving capacity in ALS is difficult.
- •No difference in simulated driving task was observed despite mild to moderate functional and cognitive decline.
- •Results do not imply these are “safe” drivers.
- •Cost-effective and reliable clinical assessments, to determine medical fitness to drive in individuals with ALS are needed.
Abstract
Objective
Compare driving capacity of individuals with Amyotrophic Lateral Sclerosis (ALS) and
healthy controls (HC) using a driving simulation program.
Methods
A prospective study was performed on individuals with ALS who reported they were still
driving, and a group of HCs. Demographic data included age and gender. Assessment
included cognitive assessments (Montreal cognitive assessment [MoCA] and ALS Cognitive
Behavioral Scale [ALS-CBS]); gait speed (m/s); ALS Functional Rating Scale-revised
total score (ALSFRS-R); and simulated driving assessment (Lane Change Task [LCT]).
The LCT is a simple assessment tool which simulates the visual, cognitive, and motor
demands of driving to detect at-risk drivers and uses distractions (secondary tasks)
to quantify the performance loss on the primary task (lane changes).
Results
Twenty-eight individuals with ALS (22 males, mean age 64 years) and 20 HCs (7 males,
mean age 59 years) were studied. Individuals with mild to moderate ALS (ALSFRS-R mean
36.2) were older, had mild cognitive difficulty (MoCA 24 vs 27; ALS-CBS 14.19 [SD
3.85]) and mobility decline (gait speed 1.1 vs 1.4 m/s) compared to HC. Driving assessment
using the LCT found no differences in baseline scores or during motor, cognitive,
or visually distracting conditions.
Conclusions
Individuals with ALS with mild to moderate disease progression, with cognitive and
motor weakness still demonstrate similar driving capacity to HCs using a driving simulation
task. Driving assessment needs to be expanded longitudinally and perhaps with more
robust measures to more precisely identify types of driving challenges that lead to
cessation of driving in individuals with ALS.
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Article info
Publication history
Published online: February 19, 2020
Accepted:
February 15,
2020
Received in revised form:
January 23,
2020
Received:
November 27,
2019
Identification
Copyright
© 2020 Elsevier B.V. All rights reserved.