Alzheimer Disease, Depression
Conditions
Keywords
virtual reality
Brief summary
Behavioural and psychological symptoms of dementia (BPSD), such as depression affect up to 90% patients with dementia. Non-pharmacological treatment of BPSD, can be difficult to access, require caregiver support, travel, and often have long waiting lists. Virtual reality (VR) is an innovative, portable, immersive, and accessible technology which can be used in-home. More information is required on the feasibility of using VR in-home with older adults with dementia. Our study will offer a 4-week program of 15-minutes sessions, twice per week nature-based VR program for BPSD delivered in-home by virtual reality (VR). Additionally, caregivers will have the option of taking part in the study and provide feedback regarding the VR intervention. If successful, this project has the potential to prolong aging in place for individuals with BPSD, as BPSD is a significant factor in institutionalization.
Detailed description
The burden of dementia is rapidly growing, affecting nearly 50 million individuals globally and costing $818 billion dollars yearly. Alzheimer's disease (AD) is the most common form of dementia. AD includes changes in mood and behavior, referred to as the behavioral and psychological symptoms of dementia (BPSD). Depression is among the most common BPSD, impacting 50% of older adults with AD. Existing pharmacological treatment for depressive symptoms in AD (AD-D) lack evidence for efficacy and have many potential side effects (e.g. cognitive impairments, falls, mortality), Non-pharmacological interventions have been recommended but are associated with significant challenges such as travel, cost and the difficulty in accessing specialized therapists. Virtual reality (VR), an immersive audiovisual technology, can address these challenges as it is an accessible and cost-effective intervention which can be delivered in a variety of settings. VR can easily be delivered in-home, and therefore address many of the limitations of traditionally delivered non-pharmacological interventions, such as accessibility, intervention non-adherence and difficulties with maintaining intervention frequency. Additional technology will be utilized to collect physiological data such as movement using the Fitbit Charge 6 and a Muse headband will measure electroencephalogram (EEG). Previous literature on VR based intervention for older adults is limited, with very few randomized control trials, rather it is primarily case studies, cross-sectional studies, and non-immersive VR. However, there are no studies assessing in-home VR for individuals with AD or for AD-D. We propose a pilot randomized controlled trial (RCT) to assess nature-based VR intervention (N-VR) for AD-D. We will randomize (1:1) 50 participants with AD-D to N-VR vs. an active control intervention of various nature-based videos (N-CI). All participants will receive the intervention as 15-min sessions delivered twice a week, assessor-blinded, for 4 weeks. Assessments will be conducted at baseline, within 7 days of starting the intervention, at follow-up, within 7 days of completing the 4-week course, and after each 15-min session.
Interventions
OTHERnature-based virtual reality applications and videos
Participants will receive nature-based applications available on the Oculus platform, as well as nature-based 360 videos with the same content as the control group however in a 360 format.
OTHERnature-based videos
Participants will receive YouTube links to watch nature-based videos on a device (e.g., a tablet).
Sponsors
St. Mary's Research Center, Canada
Centre for Addiction and Mental Health
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)
Eligibility
Sex/Gender
ALL
Age
50 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Clinical diagnosis of mild to early-moderate stage AD (including mixed dementia with AD) using the Diagnostic and Statistical Manual of Mental Disorders, 5th Ed. Criteria * Age of 50 years or older * Medical stability to participate in the trial * Patient Health Questionnaire score 5-14 * Investigator judgement on whether the participant is comfortable with technology * Access to WiFi and a smart device for connecting on WebEx and downloading the Fitbit and Muse applications * Have someone available to be present during all sessions
Exclusion criteria
* Unstable medical or psychiatric condition, including substance use based on an investigator opinion * Visual or hearing impairments that would impair participation * Patient Health Questionnaire score 15-27 and/or score of 1 or 2 in section E question 1 of the Cornell Scale for Depression in Dementia * Any other reason, which will make the study participation intolerable for the participant in the opinion of the study investigator
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Tolerability of nature-based virtual reality | 4 weeks | Hypothesis 1a (Tolerability): Using the Simulator Sickness Questionnaire (SSQ) at the end of the last session, the mean SSQ score for N-VR group will be less than 10 (with 10 or more being the cut-off for clinically significant cybersickness) |
| Feasibility of nature-based virtual reality | 4 weeks | The number of sessions completed and major/minor technical issues during the session. |
| Acceptability of nature-based virtual reality | 4 weeks | The Personal Involvement Inventory (PII) score mean after the last N-VR completed session. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Depression in AD-D | 4 weeks | The Cornell Scale for Depression in Dementia (CSDD) score improvement over 4 weeks for the N-VR versus control group. |
Other
| Measure | Time frame | Description |
|---|---|---|
| AD-D participant exploratory outcome - pleasure | 4 weeks | The preliminary efficacy of N-VR in improving pleasure in individuals with AD-D using the Snaith-Hamilton Pleasure Scale (SHAPS). |
| AD-D participant exploratory outcome - sleep | 4 weeks | The preliminary efficacy of N-VR in improving sleep in individuals with AD-D determined by the number of hours the participant slept, collected by the Fitbit Charge 6. |
| AD-D exploratory outcome - calmness | 4 weeks | The preliminary efficacy of N-VR in improving calmness in individuals with AD-D using data from the Muse headband. |
| AD-D exploratory outcome - loneliness | 4 weeks | The preliminary efficacy of N-VR in decreasing loneliness in individuals with AD-D using the UCLA loneliness scale. |
| Caregiver participant exploratory outcome | 4 weeks | The experiences of AD-D participants' caregivers with the VR intervention, VR usability with AD-D, what they liked/had challenges with, and feedback for future VR use with this population (qualitative-focus group). |
| AD-D participants exploratory outcome - activity | 4 weeks | The preliminary efficacy of N-VR in increasing activity in individuals with AD-D, determined by baseline vs post-assessment average over 5 days using Fitbit. |
| AD-D participant exploratory outcome - presence | 4 weeks | The preliminary efficacy of N-VR in improving presence in individuals with AD-D using the Slater-Usoh-Steed Presence Questionnaire (SUS). |
| AD-D participant exploratory outcome - immersion | 4 weeks | The preliminary efficacy of N-VR in improving immersion using the Immersive Tendencies Questionnaire (ITQ). |
| AD-D exploratory outcome - nature relatedness | 4 weeks | The preliminary efficacy of N-VR in improving nature relatedness in individuals with AD-D using the Nature-Relatedness Scale short version (NR-6). |
| AD-D participant exploratory outcome - quality of life | 4 weeks | The preliminary efficacy of N-VR in improving quality of life in individuals with AD-D using the Quality of Life in Alzheimer's Disease (QOL-AD). |
| AD-D participant exploratory outcome - perceived stress | 4 weeks | The preliminary efficacy of N-VR in improving stress in individuals with AD-D using the Perceived Stress Scale (PSS) and data from the Fitbit Charge 6. |
| AD-D participant exploratory outcome - attention | 4 weeks | The preliminary efficacy of N-VR in improving attention in individuals with AD-D using the Montreal Cognitive Assessment (MoCA) attention task. |
Countries
Canada
Contacts
Primary ContactAshnie Sukhu, BSc
Outcome results
None listed