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CompletedNCT05461677SAIREUpdated Apr 4, 2025

Walking With the SAIRE Smart Walker

An interventional study of SAIRE smart walker and Standard 4-wheeled walker in Gait Disorders in Old Age, Gait Disorders, Neurologic and Walking, Difficulty, sponsored by Vrije Universiteit Brussel. Completed at 1 site in Belgium. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2025-04-04.

Sponsored by Vrije Universiteit Brussel · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
14
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

The current study aims to investigate the effect of walking with the SAIRE smart walker on spatiotemporal parameters and gait kinematics in a population who suffer from difficulties during gait, and compare this to walking with a standard walker or no walking aid.

Read the detailed description

This study is an experimental single group study investigating the effect of walking with a smart walker compared to walking with a standard walker or no walking aid in persons who suffer from gait difficulties. Participants will perform one session of walking in three different conditions, (1) walking with the SAIRE smart walker, (2) walking with a standard walker and (3) if the participants are able to walk without the use of an assistive device, walking without a walker. During this session, gait parameters will be compared between the three conditions.

Experimental session: During the experimental session, participants will walk along the 10-meter walkway (5 times for every condition) After every 5 trials, a rest period of minimum 5 minutes will be held to avoid fatigue. Three different walking conditions will be measured: (1) walking with the SAIRE smart walker, (2) walking with a standard walker and if possible (3) walking with no walking aid. Each walking condition will be measured five consecutive times in a randomized order. The order of the conditions will be randomized using closed envelopes containing notes that say what order of conditions will be used. This randomization is done to avoid fatigue effects that might occur when a strict order is used.

Before the start of the experimental session, participants will practice using the SAIRE smart walker for maximum 10 minutes to familiarize with the feedback given by the walker. After this familiarization session, the surface electrodes and reflective markers will be placed on the participants and the experimental session will start.

Analysis: This study will investigate the difference in gait biomechanics of adults with gait difficulties while using different walking aids.

Descriptive statistics of the baseline characteristics of all participants will be performed. The effect of gait with a smart walker on spatiotemporal gait parameters, kinematics and muscle activity will be compared to gait with a standard 2-wheeled walker and gait without a walking aid. Data will be visualized using LO(W)ESS smoothing (locally weighted scatterplot smoothing) to explore the effect (per condition and outcome). Values will be compared between conditions in a one-way repeated measures analysis of variance. For the analysis of the USE questionnaire, percentage distribution of every item and mean scores for every subscale will be calculated using Microsoft Excel (Microsoft, Washington, DC).

02

Conditions studied

  • Gait Disorders in Old Age
  • Gait Disorders, Neurologic
  • Walking, Difficulty
03

In context

Nervous System Diseases

974 studies on the registry are indexed under Nervous System Diseases; 252 are open to participants now.

This study's enrollment of 14 is below the median of 48 across 623 interventional studies indexed under Nervous System Diseases.

Browse Nervous System Diseases studies →

Lead sponsor

Vrije Universiteit Brussel is the lead sponsor of 154 studies on the registry; 43 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • Ability to walk along a 10-meter walkway multiple times over a period of 120 minutes
  • Ambulation with any sort of assistive device (e.g. cane, crutches, walker, etc.)
  • Sufficient arm/hand function to walk with a walker
  • Capable of understanding and carrying out instructions
  • Capable of giving informed consent

Exclusion criteria

Exclusion Criteria:

  • Presence of cognitive impairement (MoCA score \<23)
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Single group
Masking
None (open label)
Enrollment
14 participants (actual)

Study arms

  • Experimental
    SAIRE smart walker

    The investigational device used in this clinical investigation is called the SAIRE smart walker. This first prototype version is equipped with a depth camera and two cheaper cameras. The depth camera is used to acquire high-quality data to train artificial intelligence (AI) models which then can run on the cheaper camera modules. Additionally, two ultrasonic sensors are applied to estimate the distance. A touch monitor is used to provide audiovisual feedback and display the user interface. Two LED strips are also attached to the walker to provide additional visual feedback to the patient. The SAIRE smart walker gives feedback to the patient in terms of cadence using a metronome, and foot placement using the LED strips and the video stream presented on the monitor. Additionally, the walker will give information about step length and step width through AI-models.

    Device: SAIRE smart walker

  • Active comparator
    Standard walker

    The comparator device consist of a standard 4-wheeled walker

    Device: Standard 4-wheeled walker

  • Active comparator
    No walking aid

    Other: No walking aid

Interventions

  • DeviceSAIRE smart walker

    Participants will walk along the 10-meter walkway 5 times using the SAIRE smart walker

  • DeviceStandard 4-wheeled walker

    Participants will walk along the 10-meter walkway 5 times using a standard 4-wheeled walker

  • OtherNo walking aid

    Participants will walk along the 10-meter walkway 5 times without using a walking aid

06

What researchers measure

Primary outcomes

  1. 3D kinematic measurements of the lower limb

    Kinematic data (i.e., movement amplitudes of the bilateral hip, knee and ankle joint) of the lower limbs during walking will be recorded continuously with the use of a 14-camera Vicon Vero 1.3 system at 100 Hz.

    Time frame: At the end of the experimental session, Day 1

  2. Walking speed

    Walking speed will be recorded continuously with the use of a 14-camera Vicon Vero 1.3 system at 100 Hz.

    Time frame: At the end of the experimental session, Day 1

  3. Cadence

    Cadence will be recorded continuously with the use of a 14-camera Vicon Vero 1.3 system at 100 Hz.

    Time frame: At the end of the experimental session, Day 1

  4. Step length

    Step length will be recorded continuously with the use of a 14-camera Vicon Vero 1.3 system at 100 Hz.

    Time frame: At the end of the experimental session, Day 1

  5. Step time

    Step time will be recorded continuously with the use of a 14-camera Vicon Vero 1.3 system at 100 Hz.

    Time frame: At the end of the experimental session, Day 1

  6. Swing time of the lower limbs

    Swing time of the lower limbs during walking will be recorded continuously with the use of a 14-camera Vicon Vero 1.3 system at 100 Hz.

    Time frame: At the end of the experimental session, Day 1

  7. Stance time

    Stance time of the lower limbs during walking will be recorded continuously with the use of a 14-camera Vicon Vero 1.3 system at 100 Hz.

    Time frame: At the end of the experimental session, Day 1

  8. Single limb support period

    Single limb support period will be recorded continuously with the use of a 14-camera Vicon Vero 1.3 system at 100 Hz.

    Time frame: At the end of the experimental session, Day 1

  9. Double limb support period

    Double limb support period will be recorded continuously with the use of a 14-camera Vicon Vero 1.3 system at 100 Hz.

    Time frame: At the end of the experimental session, Day 1

  10. Electromyography

    Muscle activity of the lower limb muscles (bilateral: M. rectus femoris, M. vastus lateralis, M. biceps femoris, M. tibialis anterior, M. gastrocnemius medialis) will be recorded continuously during treadmill walking with the use of surface electrodes. Signals will be recorded with the wireless Cometa Wave Plus EMG system (16 channels).

    Time frame: At the end of the experimental session, Day 1

Secondary outcomes

  1. User experience with a modified version of the USE questionnaire

    User experience will be assessed using a translated version of the self-administered Usefulness, Satisfaction and Ease of use (USE) questionnaire. This scale ranges from 30 to 210, with a higher score translating to higher satisfaction. Additionally, open questions were added to the questionnaire to uncover possible barriers and facilitators in the use of the smart walker.

    Time frame: At the end of the experimental session, Day 1

07

Study locations

1 site
  • Brubotics Rehabilitation Research center
    Jette, Brussels Hoofdstedelijk Gewest 1090, Belgium
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 4, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05461677
Lead sponsor
Vrije Universiteit Brussel
Collaborators
Erasmus University Rotterdam, Odisee University College
Responsible party
Ruben Debeuf (Principal investigator, Vrije Universiteit Brussel) — Principal investigator
First posted
Jul 18, 2022
Start date
Sep 1, 2022
Primary completion
Dec 31, 2023
Completion
Dec 31, 2023
Last update
Apr 4, 2025

Study contacts

Eva Swinnen, Prof. Ph.D
principal investigator · Vrije Universiteit Brussel

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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