AR Training Platform at Home

NCT ID: NCT05627050

Last Updated: 2022-11-25

Basic Information

• Recruitment Status: UNKNOWN
• Clinical Phase: NA
• Total Enrollment: 600 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2021-01-13
• Study Completion Date: 2024-12-31

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.

Conditions

Stroke; Chronic Disease

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

AR Training System

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.

Group Type: EXPERIMENTAL

An Online Augmented Reality (AR) Training Platform

Intervention Type: DEVICE

The hardware system is based on camera depth sensor and combined with 3D human tracking technology and intelligent technology, to monitor, correct and record the user's whole body movements in real-time, and the users can follow the training program.

Interventions

An Online Augmented Reality (AR) Training Platform

The hardware system is based on camera depth sensor and combined with 3D human tracking technology and intelligent technology, to monitor, correct and record the user's whole body movements in real-time, and the users can follow the training program.

Intervention Type: DEVICE

Eligibility Criteria

Inclusion Criteria

1. age >=65 years old or suffering from chronic disease;

2. sufficient cognition to follow simple instructions as well as understand the content and purpose of the study MoCA> 21); and

3. Home setting: TV with HDMI input, internet access, and a distance of 1.5m away from TV.

Exclusion Criteria

1. 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;

2. Severe shoulder or arm contracture/pain;

3. Severe knee or hip contracture/pain;

4. Pregnant women

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Chinese University of Hong Kong

OTHER

Sponsor Role: lead

Responsible Party

Raymond KY Tong

Professor and Chairman

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Raymond Kai-yu Tong, PhD

Role: PRINCIPAL_INVESTIGATOR

Department of Biomedical Engineering, The Chinese University of Hong Kong

Locations

Department of Biomedical Engineering, The Chinese University of Hong Kong

Hong Kong, , Hong Kong

Site Status: RECRUITING

Countries

Hong Kong

Central Contacts

Raymond Kai-yu Tong, PhD

Role: CONTACT

kytong@cuhk.edu.hk

+85239438454

Facility Contacts

Raymond Tong, PhD

Role: primary

kytong@cuhk.edu.hk

+852 3943 8454

Other Identifiers

2020.538

Identifier Type: -

Identifier Source: org_study_id