VR&R: Providing Caregiver Respite by Managing BPSDs and Improving QoL in People with Dementia Using Immersive VR-Therapy

Recruiting now · Not applicable

Conditions studied: Dementia

In brief

The goal of this interventional trial is to learn about how immersive Virtual Reality (VR) therapy can be used at home by individuals with dementia, with assistance from their informal (e.g., friend/family) caregivers. The main question it aims to answer are: 1. Can caregivers receive quality respite time by using VR-therapy at home with their loved ones with dementia? Does this intervention reduce feelings of burden and improve well-being and resilience for caregivers? 2. Does VR-therapy help to manage behavioural and psychological symptoms (e.g., mood, apathy, agitation) and improve quality of life for individuals with dementia? 3. What types of VR "medium" (passive or cooperative) are most effective for achieving the above objectives? Participant pairs will be asked to: * Take part in an initial at-home VR technology training session and complete a series of brief questionnaires (e.g., health history/technology use, well-being/quality of life, symptoms of dementia) * Use "VR\&R" (VR Rest \& Relaxation Therapy) for a period of 4 weeks (30 minute sessions, desired frequency), and answer a brief set of questions after each VR\&R session * Provide feedback on the VR\&R intervention in semi-structured interview with the researcher and answer additional questionnaires at a 2-week follow-up During VR\&R sessions, participants with dementia will have the opportunity to choose to watch (1) immersive 360-degree videos (e.g., of a live performance, or beach) on their own and (2) experience the same VR videos together with a researcher. Caregivers will be asked to assist their loved one with dementia to use VR\&R by helping to put on the VR headset, selecting a VR experience through a user-friendly application, and remaining nearby to supervise and provide assistance as needed. During VR\&R sessions, caregivers may use this time to take a personal break or complete short tasks (e.g., make a cup of coffee, have an uninterrupted phone call).

Key facts

Study ID

NCT05867641

Run by

University Health Network, Toronto

People needed

50

Starts

2025-02-12

Expected to finish

2027-02-01

Last updated by the study team

2025-03-28

Who can join

Age: 65 and older. Sex: any. Healthy volunteers: not accepted.

You may not qualify if…

• Individuals with open wounds on face (sutured lacerations exempted)
• Individuals with a history of seizures or epilepsy
• Individuals with a pacemaker
• Individuals with head trauma or stroke leading to their current admission
• Individuals with cervical conditions or injuries that would make it unsafe for them to use the VR headset
• Individuals who identify as being legally blind
• Individuals with alcohol related dementia/ Korsakoff syndrome.
• Individuals who have a Public Guardian and Trustee (PGT) as Substitute Decision Maker (SDM)
• Individuals who cannot speak and understand English
• Caregiver inclusion criteria:
• Individuals who identify as a primary caregiver for the PwD
• Individuals who have access to the internet through a device (computer, tablet, or mobile phone) that can be used during the study
• Caregiver exclusion criteria:
• Individuals who cannot speak and understand English
• Individuals who are cognitively unable to provide informed consent for themselves
• Identify as legally blind

Where it is running

• Toronto Grace Hospital - Specialized Care Centre — Toronto, Ontario, Canada (enrolling)
• Chester Village — Toronto, Ontario, Canada (enrolling)
• Circle of Care — Toronto, Ontario, Canada (enrolling)
• Acclaim Health — Oakville, Ontario, Canada (enrolling)
• Toronto Grace Hospital - Remote Care Monitoring — Toronto, Ontario, Canada (enrolling)
• Toronto Grace Hospital - Main Site — Toronto, Ontario, Canada
• McGill Dementia Education Centre — Montreal, Quebec, Canada

Full record on ClinicalTrials.gov

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