Parkinson Disease(PD)
Conditions
Keywords
DANU, Wearable Electronic Devices, Gait Analysis, Validity and Reliability, Mobility Assessment, Smart Socks
Brief summary
The main objective of this observational trial is to explore the validity and reliability of DANU smart socks when used for mobility assessments in people with Parkinson's. Using a series of laboratory gold standard equipment, this project aims to compare the metrics observed by DANU to the reference standards. No intervention is included. Specifically, this study will explore metrics relating to walking (gait) and balance of a Parkinson's cohort through a series of motor tasks. Moreover, this study seeks to investigate the clinical validity of DANU outcome metrics exploring relationships with clinical scales, fall history and prospective falls.
Detailed description
Background: Mobility impairments are common in Parkinson's disease (PD) and increase the risk of falling. Data derived from wearable inertial measurement units can provide useful information regarding gait in different situations and environments, which may help to identify those at risk of falling. However, rigorous testing is required to evaluate whether new devices are fit for purpose. DANU Smart Socks are a multi-modal system for movement analysis, containing 15 silicone based capacitive pressure sensors and an IMU pod, with tri-axal accelerometers, gyroscope and magnetometers, currently at use within a sporting context. Potential has been highlighted for clinical use in people with Parkinson's (PwP). This study aims to evaluate the validity, reliability and usability of the DANU Sport System in PwP for balance and gait assessment. The V3+ framework for determining fit-for-purpose biometric monitoring devices will be employed, evaluating verification, usability, analytical and clinical validation. Methods: Institutional ethics have been obtained (Project ID: 8543). Utilising a a repeated measures observational design, participants will be asked to attend two visits to Northumbria University, Newcastle Upon Tyne. Visit 1: Participants will complete a series of clinical and cognitive measures including the Movement Disorders Society's-Unified Parkinson's Disease Rating Scale, Montreal Cognitive Assessment, Freezing of Gait Questionnaire and Falls Efficacy Scale. Following this, concurrent data collection will occur throughout a battery of motor tasks to observe gait/balance metrics. Laboratory references employed include Axivity AX6, Vicon 3D Motion Capture, APDM Mobility Lab, GAITRite and AMTI Force Plates. Mobility assessments include a 2-Minute Walk Test, 3 walkway trials, a Timed Up and Go and a series of 2-Minute Balance tasks. Visit 2: Participants attend a second visit to repeat the mobility assessment previously detailed utilizing DANU Smart Socks and APDM Mobility Lab systems to explore test-retest reliability. Wearable device (DANU) validity and reliability will be examined using intra-class correlation coefficients and Bland-Altman plots to compare to laboratory reference standards. Moreover time series plots will be employed to evaluate the raw data agreement.
Interventions
None listed
Sponsors
Study design
Eligibility
Inclusion criteria
* Clinical diagnosis of Parkinson's by a movement disorder specialist according to UK brain bank criteria. * Hoehn \& Yahr stages I-III * Able to attend Northumbria University, Newcastle Upon Tyne for study visits * Able to walk and stand unassisted for a minimum of 2-minutes
Exclusion criteria
* History of neurological disorders other than PD (e.g., Huntington's disease, stroke, traumatic brain injury, multiple sclerosis, Alzheimer's disease etc.) * Montreal Cognitive Assessment (MoCA) score \< 21 * Injury to the lower extremities within the past 6-weeks.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Stride Length | Outcomes will be obtained on Visit 1 (Day 1) and Visit 2 (Day 8). | (m, mean ± standard deviation) |
| Step Time | Outcomes will be obtained on Visit 1 (Day 1) and Visit 2 (Day 8). | (s, mean ± standard deviation) |
| Stride Time | Outcomes will be obtained on Visit 1 (Day 1) and Visit 2 (Day 8). | (s, mean ± standard deviation) |
| Cadence | Outcomes will be obtained on Visit 1 (Day 1) and Visit 2 (Day 8). | (steps per minute, mean ± standard deviation) |
| Ground Contact Time | Outcomes will be obtained on Visit 1 (Day 1) and Visit 2 (Day 8). | (s, mean ± standard deviation) |
| Swing Time | Outcomes will be obtained on Visit 1 (Day 1) and Visit 2 (Day 8). | (s, mean ± standard deviation) |
| Stride Velocity | Outcomes will be obtained on Visit 1 (Day 1) and Visit 2 (Day 8). | (m/s, mean ± standard deviation) |
| Gait Velocity | Outcomes will be obtained on Visit 1 (Day 1) and Visit 2 (Day 8). | (m/s, mean ± standard deviation) |
| Area of Ellipse | Outcomes will be obtained on Visit 1 (Day 1) and Visit 2 (Day 8). | (mm², mean ± standard deviation) |
| Length of Ellipse | Outcomes will be obtained on Visit 1 (Day 1) and Visit 2 (Day 8). | (mm, mean ± standard deviation) |
| Width of Ellipse | Outcomes will be obtained on Visit 1 (Day 1) and Visit 2 (Day 8). | (mm, mean ± standard deviation) |
| Total Displacement | Outcomes will be obtained on Visit 1 (Day 1) and Visit 2 (Day 8). | (mm, mean ± standard deviation) |
| Medio-Lateral Range | Outcomes will be obtained on Visit 1 (Day 1) and Visit 2 (Day 8). | (mm, mean ± standard deviation) |
| Anterior-Posterior Range | Outcomes will be obtained on Visit 1 (Day 1) and Visit 2 (Day 8). | (mm, mean ± standard deviation) |
Countries
United Kingdom
Contacts
Northumbria University