Exploratory study to evaluate the acceptability of a wearable accelerometer to assess motor progression in motor neuron disease

• Published in: Journal of neurology 2024-08, Vol.271 (8), p.5083-5101
• Main Authors: Beswick, Emily, Christides, Alexander, Symonds, Alexander, Johnson, Micheaela, Fawcett, Thomas, Newton, Judith, Lyle, Dawn, Weaver, Christine, Chandran, Siddharthan, Pal, Suvankar
• Format: Article
• Language: English
• Subjects: Accelerometry - instrumentation; Aged; Amyotrophic lateral sclerosis; Ankle; Disease Progression; Female; Humans; Male; Medicine; Medicine & Public Health; Middle Aged; Motor Neuron Disease - diagnosis; Motor Neuron Disease - physiopathology; Motor neuron diseases; Motor neurone disease; Neurology; Neuroradiology; Neurosciences; Original Communication; Patient Acceptance of Health Care; Physical activity; Surveys and Questionnaires - standards; Wearable computers; Wearable Electronic Devices; Wrist
• ISSN: 0340-5354; 1432-1459; 1432-1459
• DOI: 10.1007/s00415-024-12449-3

Motor neuron disease (MND) is a rapidly progressive condition traditionally assessed using a questionnaire to evaluate physical function, the revised amyotrophic lateral sclerosis functional rating scale (ALSFRS-R). Its use can be associated with poor sensitivity in detecting subtle changes over time and there is an urgent need for more sensitive and specific outcome measures. The ActiGraph GT9X is a wearable device containing multiple sensors that can be used to provide metrics that represent physical activity. The primary aim of this study was to investigate the initial suitability and acceptability of limb-worn wearable devices to group of people with MND in Scotland. A secondary aim was to explore the preliminary associations between the accelerometer sensor data within the ActiGraph GT9X and established measures of physical function. 10 participants with MND completed a 12-week schedule of assessments including fortnightly study visits, both in-person and over videoconferencing software. Participants wore the device on their right wrist and right ankle for a series of movements, during a 6-min walking test and for a period of 24-h wear, including overnight. Participants also completed an ALSFRS-R and questionnaires on their experience with the devices. 80% of the participants found wearing these devices to be a positive experience and no one reported interference with daily living or added burden. However, 30% of the participants experienced technical issues with their devices. Data from the wearable devices correlated with established measures of physical function.