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Convalida di indumenti intelligenti per la classificazione dell'andatura

5 ottobre 2026 aggiornato da: Myant Medical Corp.

Convalida di indumenti intelligenti per la valutazione dell'andatura e dell'equilibrio

The aim of this study is therefore to validate Myant SKIIN garments for the purpose of gait and balance assessment. To achieve this, we recruit young healthy adults from the University of Waterloo to wear Skiin products (see Fig. 1). Participants will be asked to perform a number of scripted gait and balance tasks.

Panoramica dello studio

Stato

Completato

Condizioni

Intervento / Trattamento

Descrizione dettagliata

Specific objectives of this study are:

  1. To validate Skiin gait characterization algorithm (based on single garment solutions - already developed based on a literature and a previous study conducted at the University of Waterloo);
  2. To develop algorithms for multi-garments solutions that aim to extract additional kinematic parameters such as joint angles.

Gait metrics from Skiin garments will be compared to metrics from a gold standard measurement (Vicon motion capture) to indicate accuracy, precision and reliability.

Tipo di studio

Osservativo

Iscrizione (Effettivo)

20

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Luoghi di studio

    • Ontario
      • Waterloo, Ontario, Canada, N2L3G1
        • University of Waterloo - Engineering 7

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

Da 18 anni a 64 anni (Adulto)

Accetta volontari sani

Sì

Sessi ammissibili allo studio

Tutto

Metodo di campionamento

Campione non probabilistico

Popolazione di studio

A convenience-sample of 20 healthy individuals will be recruited for this study.

Descrizione

Inclusion Criteria:

- Healthy male and female adults aged 18y - 64y old

Exclusion Criteria:

- Self-reported lower limb conditions, neurological disorders, history of concussion/brain trauma, and/or condition limiting exercise is to mitigate additional risk for injury and/or adverse reactions associated with exercise.

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Modelli osservazionali: COHORT
  • Prospettive temporali: PROSPECTIVE

Coorti e interventi

Gruppo / Coorte
Intervento / Trattamento
Healthy individuals

Gait study protocol

Participants will be asked to wear a Skiin smart garment over their own clothes.

Small motion capture markers will be placed on their body and pressure-sensitive insoles placed into their shoes to measure the pressure underneath their feet during the study tasks.

Once the sensors are ready for collection, participants will be asked to complete 5 tasks associated with their daily activities: 1. Locomotion; 2. Lower limb strength - repeated sit-to-stand-to-sit transitions; 3. Lower limb strength and locomotion - Timed Up and Go; 4. Free walking during a 2min walk; 5. Standing balance, postural control.

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Error in step length metric
Lasso di tempo: Collection during the single study session of 1.5 hours.

The difference between step lengths calculated from Skiin data and from Vicon data for each scripted gait tasks.

Collection during the single study session of 1.5 hours.
Error in stride length metric
Lasso di tempo: Collection during the single study session of 1.5 hours.

The difference between stride length calculated from Skiin data and from Vicon data for each scripted gait tasks.

Collection during the single study session of 1.5 hours.
Error in cadence metric
Lasso di tempo: Collection during the single study session of 1.5 hours.

The difference between cadence calculated from Skiin data and from Vicon data for each scripted gait tasks.

Collection during the single study session of 1.5 hours.
Error in step duration (s) metric, and its asymmetry
Lasso di tempo: Collection during the single study session of 1.5 hours.

The difference between step duration (s), and its asymmetry calculated from Skiin data and from Vicon data for each scripted gait tasks.

Collection during the single study session of 1.5 hours.
Error in stride duration (s) metric, and its asymmetry
Lasso di tempo: Collection during the single study session of 1.5 hours.

The difference between stride duration (s), and its asymmetry calculated from Skiin data for each scripted gait tasks.

Collection during the single study session of 1.5 hours.
Error in stance duration (s) metric, and its asymmetry
Lasso di tempo: Collection during the single study session of 1.5 hours.

The difference between stance duration (s), and its asymmetry calculated from Skiin data and from Vicon data for each scripted gait tasks.

Collection during the single study session of 1.5 hours.
Error in swing duration (s) metric, and its asymmetry
Lasso di tempo: Collection during the single study session of 1.5 hours.

The difference between swing duration(s), and its asymmetry calculated from Skiin data and from Vicon data for each scripted gait tasks.

Collection during the single study session of 1.5 hours.
Error in initial double support (s) metric, and its asymmetry
Lasso di tempo: Collection during the single study session of 1.5 hours.

The difference between double support (s), and its asymmetry calculated from Skiin data and from Vicon data for each scripted gait tasks.

Collection during the single study session of 1.5 hours.
Error in terminal double support (s) metric, and its asymmetry
Lasso di tempo: Collection during the single study session of 1.5 hours.

The difference between terminal double support (s), and its asymmetry calculated from Skiin data and from Vicon data for each scripted gait tasks.

Collection during the single study session of 1.5 hours.
Error in double support (s) metric, and its asymmetry
Lasso di tempo: Collection during the single study session of 1.5 hours.

The difference between double support (s), and its asymmetry calculated from Skiin data and from Vicon data for each scripted gait tasks.

Collection during the single study session of 1.5 hours.
Error in single limb support (s) metric, and its asymmetry
Lasso di tempo: Collection during the single study session of 1.5 hours.

The difference between single limb support (s), and its asymmetry calculated from Skiin data and from Vicon data for each scripted gait tasks.

Collection during the single study session of 1.5 hours.
Error in gait speed metric
Lasso di tempo: Collection during the single study session of 1.5 hours.

The difference between gait speed calculated from Skiin data and from Vicon data for each scripted gait tasks.

Collection during the single study session of 1.5 hours.
Error in stride speed metric
Lasso di tempo: Collection during the single study session of 1.5 hours.

The difference between stride speed calculated from Skiin data and from Vicon data for each scripted gait tasks.

Collection during the single study session of 1.5 hours.
Error in mean CoM sway distance
Lasso di tempo: Collection during the single study session of 1.5 hours.

The difference between sway distance of the Center of mass calculated from Skiin data and from Vicon data for each scripted balance tasks.

Collection during the single study session of 1.5 hours.
Error in mean CoM sway velocity
Lasso di tempo: Collection during the single study session of 1.5 hours.

The difference between sway velocity of the Center of mass calculated from Skiin data and from Vicon data for each scripted balance tasks.

Collection during the single study session of 1.5 hours.
Error in CoM sway area
Lasso di tempo: Collection during the single study session of 1.5 hours.

The difference between sway area of the Center of mass calculated from Skiin data and from Vicon data for each scripted balance tasks.

Collection during the single study session of 1.5 hours.
Error in CoM sway frequency
Lasso di tempo: Collection during the single study session of 1.5 hours.

The difference between sway frequency of the Center of mass calculated from Skiin data and from Vicon data for each scripted balance tasks.

Collection during the single study session of 1.5 hours.

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Collaboratori

Investigatori

  • Investigatore principale: James Tung, PhD, University of Waterloo

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Effettivo)

26 maggio 2023

Completamento primario (Effettivo)

18 settembre 2023

Completamento dello studio (Effettivo)

14 marzo 2024

Date di iscrizione allo studio

Primo inviato

1 giugno 2023

Primo inviato che soddisfa i criteri di controllo qualità

1 giugno 2023

Primo Inserito (Effettivo)

12 giugno 2023

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

6 ottobre 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

5 ottobre 2026

Ultimo verificato

1 marzo 2024

Maggiori informazioni

Termini relativi a questo studio

Altri numeri di identificazione dello studio

  • Myant/Waterloo/42689

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

INDECISO

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

No

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

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