Abstract

Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disorder causing a progressive motor weakness of all voluntary muscles, whose progression challenges communication modalities such as handwriting or speech. The current study investigated whether ALS subjects can use Eye-On-Line (EOL), a novel eye-operated communication device allowing, after training, to voluntarily control smooth-pursuit eye-movements (SPEM) so as to eye-write in cursive. To that aim, ALS participants (n = 12) with preserved eye-movements but impaired handwriting were trained during six on-site visits. The primary outcome of the study was the recognition of eye-written digits (0–9) from ALS and healthy control subjects by naïve “readers.” Changes in oculomotor performance and the safety of EOL were also evaluated. At the end of the program, 69.4% of the eye-written digits from 11 ALS subjects were recognized by naïve readers, similar to the 67.3% found for eye-written digits from controls participants, with however, large inter-individual differences in both groups of “writers.” Training with EOL was associated with a transient fatigue leading one ALS subject to drop out the study at the fifth visit. Otherwise, itching eyes was the most common adverse event (3 subjects). This study shows that, despite the impact of ALS on the motor system, most ALS participants could improve their mastering of eye-movements, so as to produce recognizable eye-written digits, although the eye-traces sometimes needed smoothing to ease digit legibility from both ALS subjects and control participants. The capability to endogenously and voluntarily generate eye-traces using EOL brings a novel way to communicate for disabled individuals, allowing creative personal and emotional expression.

Highlights

  • Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disorder causing a progressive motor weakness of all voluntary muscles, with notable exceptions such as extra-ocular muscles that remain durably spared (Brockington et al, 2013; Gorges et al, 2015; Nijssen et al, 2017)

  • This study evaluates whether ALS subjects can use a new eye-operated system (Eye-On-Line, EOL)1 that relies on the voluntarily control over smooth-pursuit eyemovements (SPEM) (Krauzlis, 2005; Lorenceau, 2012)

  • We focus on the mean duration of endogenously generated smooth-pursuit, and the longest pursuit realized during the different sessions

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Summary

INTRODUCTION

Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disorder causing a progressive motor weakness of all voluntary muscles, with notable exceptions such as extra-ocular muscles that remain durably spared (Brockington et al, 2013; Gorges et al, 2015; Nijssen et al, 2017). As a matter of facts, classical eye-controlled ACD are based on the triad “saccade, fixation, selection” of predefined items (e.g., letters of the alphabet) displayed on a computer screen These items constrain the choices of the user, who cannot generate figures or symbols of its own, limiting its creativity. Using EOL, subjects face a temporally modulated visual display eliciting an illusory perception of motion that provides a positive visual feedback to the oculomotor system Relying on this feedback, individuals can gain volitional control over SPEM. EOL was first tested on 20 healthy participants to establish a stepwise training program designed to: (1) optimize the EOL display parameters that elicit a perception of illusory motion induced by eye-movements, detailed thereafter; (2) train participants to initiate and maintain SPEM for long durations; (3) execute imposed motor plans of increasing complexity (lines, figures, digits, letters, and words). Using the outcomes of this preliminary study, we evaluated the feasibility and safety of EOL with ALS subjects

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