Anxiety, Appetite Loss, Depression, Dyspnea, End of Life, Fatigue, Nausea, Pain, Well-Being, Psychological
Conditions
Keywords
Hospice, Serious Illness, Virtual reality, End-of-life
Brief summary
The purpose of this research is to determine the effect that repeated, personalized virtual reality experiences have on symptom severity, comparing self-reported symptom severity both pre and post each session, and overtime across sessions. Researchers will also determine if this intervention results in a high rating of presence in VR, and if presence is related to the magnitude of the change in symptoms.
Detailed description
The purpose of this research is to determine the effect that repeated, personalized virtual reality experiences have on symptom severity, comparing self-reported symptom severity both pre and post each session, and overtime across sessions. The researchers will also determine if this intervention results in a high rating of presence in VR, and if presence is related to the magnitude of the change in symptoms. H1: Symptom severity will decrease from pre-intervention to post-intervention. H2: The change in symptom severity will be greater in session two than it was in session one. H3: Presence score will be higher in session two than session one. To recruit 30-40 participants, the researchers will have the clinical team working to help the research team identify eligible participants from existing caseloads. Researchers will include all hospice eligible patients, this includes people who are enrolled in hospice care but also a subset of those who are enrolled in palliative care who qualify for hospice but have refused to or haven't yet transitioned to hospice care. The site serves about 670 (as of May 2023) patients a month. Therefore, it is the researcher's intent to recruit about 3 patents per month, or a total of 30-40 patients (about 5% of the monthly population) over the course of one year. The intervention that participants will be experiencing is personalized virtual reality experiences. The content of this experience will be determined at the initial visit during which the participant will complete a preference questionnaire which identifies the location they want to go to. These experiences will be filmed on the insta360 One R camera by the research coordinator. Each experience will be approximately 20 minutes. To view the videos participants will wear the Oculus Quest 2 virtual reality headset.
Interventions
BEHAVIORALPersonalized virtual reality experience
The intervention that participants will be experiencing is personalized virtual reality experiences. The content of this experience will be determined at the initial visit during which the participant will complete a preference questionnaire which identifies the location they want to go to. These experiences will be filmed on the insta360 One R camera by the research coordinator. Each experience will be approximately 20 minutes. To view the videos participants will wear the Oculus Quest 2 virtual reality headset.
Sponsors
State University of New York - Upstate Medical University
State University of New York at Buffalo
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
SUPPORTIVE_CARE
Masking
NONE
Intervention model description
Single group open pilot, pre- post-intervention study
Eligibility
Sex/Gender
ALL
Healthy volunteers
No
Inclusion criteria
Healthy volunteers are not applicable to this study as they study focuses on pain and symptom management at end-of-life through the virtual reality experience. Inclusion Criteria: * Patients who are hospice care eligible as defined by the Medicare Hospice benefit and receive hospice or palliative care from Hospice and Palliative Care Buffalo.
Exclusion criteria
* Their Palliative Performance Score (PPS) is below 30. * They are not cognitively intact (display symptoms of delirium or senility, or have a cognitive diagnosis such as Alzheimer's or Dementia) as measured by the Confusion Assessment Method (CAM) (Inouye et al., 1990) * They have hearing, vision, or speech impairments that are uncorrected. * They have current symptoms of or a history of dizziness, nausea, headaches, migraines, seizures, or motion sickness. * They do not speak English. * They are not 18 years old.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Edmonton Symptom Assessment System - Revised (ESAS) | Two weeks | End-of-life symptom assessment |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| igroup presence questionnaire (IPQ) | Two weeks | Presence during virtual reality experience |
Countries
United States
Outcome results
None listed