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Clinical Trials/NCT04467216
NCT04467216CompletedNot Applicable

Virtual Reality Motor-cognitive Training for Older People With Cognitive Frailty: A Pilot Trial

The Hong Kong Polytechnic University1 site in 1 country17 target enrollmentStarted: July 15, 2020Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
17
Locations
1
Primary Endpoint
Global cognitive function

Study Overview

Brief Summary

Cognitive frailty is a clinical syndrome in which cognitive impairment (e.g., poor memory, visuospatial function) and physical frailty (e.g., slowness, poor muscle strength, physical inactivity) co-exist. It is prevalent in community-dwelling older people. The progressive decline of cognitive and physical functions restricts older people from participating in activities (e.g., social get-togethers). Reduced participation further jeopardizes their life-space mobility (e.g., ability to travel to areas far away from home). Therefore, those with cognitive frailty are at risk of developing dementia and becoming dependent.

Simultaneous motor-cognitive training is more effective at promoting optimal functioning in older people than motor or cognitive training alone. Gaming is effective at promoting the motivation to participate. The contents of games in the market are unrelated to the context or daily living of the elderly. Currently, available training is non-simultaneous. This makes the training less transferable to the daily life of the elderly and reduces its effects.

Virtual reality (VR) technology can provide a virtual space that mimics the real environment. This allows clients to participate in daily activities in a virtual space. Older people can be trained to improve their cognitive and physical skills in a painless, fun way. However, the effect and feasibility of employing simultaneous motor-cognitive training launching on a VR platform mimicking the daily living environment in older people with cognitive frailty is poorly known. This pilot trial aims to examine the preliminary effects on cognitive function and frailty syndrome, as well as examine the feasibility.

Detailed Description

In the intervention, VR will be employed to simulate a daily living environment familiar to older people. Participants will wear a commercially available head-mounted VR system with hand-held controllers to experience the participation of daily activities in a virtual environment. Simultaneous physical and cognitive training will be embedded in the training system to promote optimal function. Participants will attend physical training in a sitting position through cycling on an ergometer and moving the hand-held controllers. Motion sensors built into the VR system and ergometer will track these movements to control everyday tasks in the virtual environment (e.g., moving around the city). Simultaneously, participants will undergo cognitive training by participating in various tasks demanding cognitive functions, such as visual-spatial (e.g., wayfinding) and problem-solving (e.g., wallet loss) functions. Gamification will be employed to promote the motivation to participate. All training activities will be gamified by blending in fun elements, such as difficulty-levelling, competition, and e-tokens. Co-participation is allowed to promote interpersonal interactions. The prototype enables real-time co-viewing among participants. Other elderly centre members and the activity facilitators can share the view of the participants in the game on either a large-screen monitor or a tablet computer. They can simultaneously talk about and share their gaming experiences.

Study Design

Study Type
Interventional
Allocation
Non Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Single (Outcomes Assessor)

Masking Description

Outcome assessors at both pre- and post-observations will be blinded to the group label

Eligibility Criteria

Ages
60 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Age ≥ 60 years,
  • •Community dwelling, as defined by living at home without staying in long-term care facilities (e.g., nursing home) in the last 12 months, and
  • •Cognitive frailty, as defined by co-existence of mild cognitive impairment and physical frailty,
  • •Mild cognitive impairment, measured by Montreal Cognitive Assessment (MoCA) ≤ 25 and Clinical Dementia Rating (CDR) = 0.5, and
  • •Frailty status from pre-frail to frail, measured by Fried Frailty Phenotype score ≥ 1.

Exclusion Criteria

  • •Diagnosed dementia, according to subjects' medical record, or
  • •Probable dementia, as defined by MoCA ≤ 18, or
  • •Mobility restriction, as defined by Modified Functional Ambulatory Classification (MFAC) < Category 7 (i.e., Outdoor walker), or

Arms & Interventions

Intervention group

Experimental

This arm will undertake VR simultaneous motor-cognitive training in 30 minutes session, twice a week for 8 weeks

Intervention: Computerised cognitive training using virtual reality (Device)

Control Group

No Intervention

This arm will be doing existing forms of motor-cognitive training in 30 minutes session, twice a week for 8 weeks

Outcomes

Primary Outcomes

Global cognitive function

Time Frame: Change is being assessed: "baseline" and "immediately after the completion" (2 months)

Montreal Cognitive Assessment (score), scores on the MoCA range from zero to 30. With a score of 26 and higher generally considered normal, with 25 to 18 are considered Mild Cognitive Impairment and with score lower then 18 are defined as Alzheimer's disease.

Selective attention

Time Frame: Change is being assessed: "baseline" and "immediately after the completion" (2 months)

Stroop test (score)

Visual-spatial perception

Time Frame: Change is being assessed: "baseline" and "immediately after the completion" (2 months)

Visual Object Space Perception test (score)

Secondary Outcomes

  • Walking(Change is being assessed: "baseline" and "immediately after the completion" (2 months))
  • Frailty(Change is being assessed: "baseline" and "immediately after the completion" (2 months))
  • Strength(Change is being assessed: "baseline" and "immediately after the completion" (2 months))

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Dr Rick Kwan

Assistant Professor

The Hong Kong Polytechnic University

Study Sites (1)

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