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Clinical Trials/NCT05627050
NCT05627050UnknownNot Applicable

Online AR Training Platform for the Elderly and Persons With Chronic Diseases at Home

Chinese University of Hong Kong1 site in 1 country600 target enrollmentStarted: January 13, 2021Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Enrollment
600
Locations
1
Primary Endpoint
Fugl-Meyer Assessment

Study Overview

Brief Summary

Video Communications, like ZOOM, have been widely used in the time of this epidemic. But how about to design an AR / VR communication system with coaching from clinician to facilitate training at home in this time of epidemic. Vulnerable individuals at home can interact with the training platform and his/her clinician can provide online training progamme with guidance.

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •age >=65 years old or suffering from chronic disease;
  • •sufficient cognition to follow simple instructions as well as understand the content and purpose of the study MoCA> 21); and
  • •Home setting: TV with HDMI input, internet access, and a distance of 1.5m away from TV.

Exclusion Criteria

  • •Any additional medical or psychological condition that would affect their ability to comply with the study protocol, e.g., a significant orthopaedic or chronic pain condition, major post-stroke depression, epilepsy, artificial cardiac pacemaker / joint;
  • •Severe shoulder or arm contracture/pain;
  • •Severe knee or hip contracture/pain;
  • •Pregnant women

Arms & Interventions

AR Training System

Experimental

The subjects follow the daily rehabilitation training program designed by clinical and healthcare team. The system will monitor their movement and provide feedbacks to the users. The clinicians/healthcare workers can provide feedbacks and guidance to correct their movements and postures.

Intervention: An Online Augmented Reality (AR) Training Platform (Device)

Outcomes

Primary Outcomes

Fugl-Meyer Assessment

Time Frame: 6-month after the first training

Fugl-Meyer Assessment for Upper-Extremity the maximum score is 66, divided into 33 items in the form of a 3-point scale (0-2), 0 is cannot perform and 2 performs fully. Fugl-Meyer Assessment for Lower-Extremity consists of 34-level cumulative scoring system to examine lower-limb functions of hemiplegic stroke patients quantitatively through a set of lower-limb movement tasks in reflex, flexor/extensor synergy, volitional movement, coordination and speed (Fugl-Meyer, et al., 1975).

Secondary Outcomes

  • The 12-item Short Form Survey(6-month after the first training)
  • Modified Ashworth Scale(6-month after the first training)
  • Berg Balance Scale(6-month after the first training)
  • Functional Ambulation Category Test(6-month after the first training)
  • Barthel Index(6-month after the first training)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Raymond KY Tong

Professor and Chairman

Chinese University of Hong Kong

Study Sites (1)

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