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NCT Number: NCT07281755

Objective Mobility Assessment Using Wearable Technology for Clinical Application in Parkinson's Disease: From Validation to Fall Prediction

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.

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Key information

Age range

50 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Northumbria University

Newcastle upon Tyne, United Kingdom

Location status: Recruiting

Location contact

Alan Godfrey, PhD

SUB_INVESTIGATOR

Gabriella R Gatti, BSc

CONTACT

[email protected]

01912273343

Gabriella R Gatti, Bsc

SUB_INVESTIGATOR

Rodrigo Vitorio, PhD

CONTACT

[email protected]

01912273343

Rodrigo Vitorio, PhD

PRINCIPAL_INVESTIGATOR

Rosie Morris, PhD

SUB_INVESTIGATOR

Samuel Stuart, PhD

SUB_INVESTIGATOR

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

Primary outcomes

  1. Stride Length

    Time frame: Outcomes will be obtained on Visit 1 (Day 1) and Visit 2 (Day 8).

    (m, mean ± standard deviation)

  2. Step Time

    Time frame: Outcomes will be obtained on Visit 1 (Day 1) and Visit 2 (Day 8).

    (s, mean ± standard deviation)

  3. Stride Time

    Time frame: Outcomes will be obtained on Visit 1 (Day 1) and Visit 2 (Day 8).

    (s, mean ± standard deviation)

  4. Cadence

    Time frame: Outcomes will be obtained on Visit 1 (Day 1) and Visit 2 (Day 8).

    (steps per minute, mean ± standard deviation)

  5. Ground Contact Time

    Time frame: Outcomes will be obtained on Visit 1 (Day 1) and Visit 2 (Day 8).

    (s, mean ± standard deviation)

  6. Swing Time

    Time frame: Outcomes will be obtained on Visit 1 (Day 1) and Visit 2 (Day 8).

    (s, mean ± standard deviation)

  7. Stride Velocity

    Time frame: Outcomes will be obtained on Visit 1 (Day 1) and Visit 2 (Day 8).

    (m/s, mean ± standard deviation)

  8. Gait Velocity

    Time frame: Outcomes will be obtained on Visit 1 (Day 1) and Visit 2 (Day 8).

    (m/s, mean ± standard deviation)

  9. Area of Ellipse

    Time frame: Outcomes will be obtained on Visit 1 (Day 1) and Visit 2 (Day 8).

    (mm², mean ± standard deviation)

  10. Length of Ellipse

    Time frame: Outcomes will be obtained on Visit 1 (Day 1) and Visit 2 (Day 8).

    (mm, mean ± standard deviation)

  11. Width of Ellipse

    Time frame: Outcomes will be obtained on Visit 1 (Day 1) and Visit 2 (Day 8).

    (mm, mean ± standard deviation)

  12. Total Displacement

    Time frame: Outcomes will be obtained on Visit 1 (Day 1) and Visit 2 (Day 8).

    (mm, mean ± standard deviation)

  13. Medio-Lateral Range

    Time frame: Outcomes will be obtained on Visit 1 (Day 1) and Visit 2 (Day 8).

    (mm, mean ± standard deviation)

  14. Anterior-Posterior Range

    Time frame: Outcomes will be obtained on Visit 1 (Day 1) and Visit 2 (Day 8).

    (mm, mean ± standard deviation)

Other outcomes

  1. Double Support Time

    Time frame: Outcomes will be obtained on Visit 1 (Day 1) and Visit 2 (Day 8).

    (s, mean ± standard deviation)

  2. Single Support Time

    Time frame: Outcomes will be obtained on Visit 1 (Day 1) and Visit 2 (Day 8).

    (s, mean ± standard deviation)

Study contacts

Contact information is provided by the study sponsor or research team.

Gabriella R Gatti, BSc

CONTACT

[email protected]

01912273343

Rodrigo Vitorio, PhD

CONTACT

[email protected]

01912273343

Sponsors and collaborators

Lead sponsor

Northumbria University

Other

Collaborators

  • DANU Sports Ltd

Registry information

Important dates

Study start
2025
Primary completion
2027
Study completion
2027
First posted
Dec 15, 2025
Registry last updated
Feb 12, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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