- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT04966260
Virtual Reality Therapy to Improve Physical and Psychological Symptoms and Quality of Life for End-of-life Patients on a Palliative Care Unit
Virtual Reality Therapy to Improve Physical and Psychological Symptoms and Quality of Life for End-of-life Patients on a Palliative Care Unit: a Randomized Controlled Study
People with advanced and life-threatening illnesses experience challenges across multiple domains of function including physical, psychological, social, and spiritual. The benefits of non-pharmacological interventions for palliative care patients are well recognized, but are relatively under-utilized. Virtual Reality (VR) therapy may help address these challenges and be a valuable addition to the current therapies used in palliative care.
VR is a computer generated, three-dimensional environment that individuals can explore and interact with using specialized equipment such as a head-mounted display with internal sensors. VR has been increasingly adapted for applications in healthcare, as a simulation for medical training and an intervention tool to impact pain management, stress and anxiety. VR has the potential to improve both physical and psychological symptoms in patients with terminal illnesses.
The current study is a small randomized controlled trial to understand the impact of VR on physical symptoms, psychological symptoms and quality of life in patients at the end of life. Participants will be randomized to a single comparator session, single session of standard VR, or single session of personalized VR. The comparator arm will consist of participants viewing an ordinary two-dimensional video on an iPad such as a peaceful nature scene. The standard VR arm will consist of participants viewing a "bucket list" experience self-selected from a VR library i.e. an experience the participant desires but has never experienced. The personalized VR arm will consist of participants viewing content that is personally meaningful to them. This content will be obtained through either a) family/friends creating a personalized video (e.g. video footage of their summer cottage) or b) the participant will select an experience from the VR library that is personally meaningful (e.g. visiting their honeymoon destination, exploring their childhood hometown, etc.) if option a) is not possible.
Participants will complete self-report questionnaires about their physical and psychological symptoms and quality of life before and after the intervention (two days and seven days post intervention). Participants will also complete a feedback survey to evaluate their satisfaction with the intervention. Surveys will be administered by the research assistant.
Studieoversikt
Status
Intervensjon / Behandling
Studietype
Registrering (Forventet)
Fase
- Ikke aktuelt
Kontakter og plasseringer
Studiekontakt
- Navn: Ginah Kim, MD
- Telefonnummer: 2854 4167852500
- E-post: gkim@baycrest.org
Studer Kontakt Backup
- Navn: Giulia Perri, MD
- Telefonnummer: 6073 4167852500
- E-post: gperri@baycrest.org
Studiesteder
-
-
Ontario
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Toronto, Ontario, Canada, M6A 2E1
- Rekruttering
- Baycrest Health Sciences
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Ta kontakt med:
- Ginah Kim, MD
- Telefonnummer: 2854 4167852500
- E-post: gkim@baycrest.org
-
-
Deltakelseskriterier
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
Tar imot friske frivillige
Kjønn som er kvalifisert for studier
Beskrivelse
Inclusion Criteria:
- Admitted to Baycrest PCU
- Capable to consent to the study
- Able to complete the outcome measures through a telephone interview with a research assistant
- Estimated prognosis ≥3 weeks
- At least 2 or more ESAS scores of 4 or greater within the week of the intervention
- English speaking
Exclusion Criteria:
- Intractable nausea/vomiting
- History of seizures or epilepsy
- Vision and/or hearing impairment that cannot be accommodated e.g. pocket talker
- Any abnormalities of the head preventing use of the headset
- Patients who are too unwell to participate based on the opinion of the clinical team
Studieplan
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Annen
- Tildeling: Randomisert
- Intervensjonsmodell: Parallell tildeling
- Masking: Ingen (Open Label)
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
---|---|
Eksperimentell: Standardized Virtual Reality
Participants in the standard virtual reality (VR) group will choose from the general library of VR experiences.
Participants will be asked to select an experience they desire but have never experienced in person.
The session will be facilitated by the therapeutic recreation staff on the unit.
|
This is a one session intervention, where participants will be asked to wear a VR headset and view a three-dimensional standard VR video.
The activity session will be approximately 15 minutes in length.
Prior to starting the intervention, the therapeutic recreation staff will explain the activity and familiarize participants with the VR headset.
|
Eksperimentell: Personalized Virtual Reality
There are two types of personalized VR: 1) Family/friends provide personalized content (e.g., life stories, photos, videos) that will be used during the VR session.
Family/friends of participants in the personalized VR group will have the opportunity to upload custom photos, videos, life stories or capture their own 360° footage of family events using a GoPro camera that will be loaned to them for the study.
This content will be uploaded to a cloud-based portal.
2) If the family/friends of those in the personalized VR arm are unavailable/unable/unwilling to provide personalized content the participant will select a video from the VR library of an experience that is personally memorable to them, such as their childhood hometown, a favourite vacation destination.
The session will be facilitated by the therapeutic recreation staff on the unit.
|
This is a one session intervention, where participants will be asked to wear a VR headset and view a three-dimensional personalized VR video.
The activity session will be approximately 15 minutes in length.
Prior to starting the intervention, the therapeutic recreation staff will explain the activity and familiarize participants with the VR headset.
|
Aktiv komparator: Two-Dimensional Video
Participants in the active comparator group will choose a two-dimensional video such as a mountain view, ocean view or safari.
Participants will view the two-dimensional video on an iPad and the session will be facilitated by the therapeutic recreation staff on the unit.
|
This is a one session intervention, where participants will be asked to view a two-dimensional video on an iPad.
The activity session will be approximately 15 minutes in length.
Prior to starting the activity session, the therapeutic recreation staff will explain the activity.
|
Hva måler studien?
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
---|---|---|
Change in Edmonton Symptom Assessment Scale (ESAS) Score
Tidsramme: Pre-intervention, post-intervention, 2 day follow up, 7 day follow up
|
The ESAS is a self-report measure used to assist in the assessment of pain, tiredness, nausea, depression, anxiety, drowsiness, appetite, wellbeing, and shortness of breath (Bruera, Kuehn, Miller, Selmser, & Macmillan, 1991). The severity of the symptom at the time of the assessment is rated from zero to ten, with zero meaning the symptom is absent and ten meaning worst possible severity. For the purpose of the study the ESAS was modified to include two additional items, headache and dizziness. Analysis of the ESAS scores across the different time points will help determine whether VR effects are transient (within 24 hours) or sustained (after 2 and 7 days). |
Pre-intervention, post-intervention, 2 day follow up, 7 day follow up
|
Change in Missoula-VITAS Quality of Life Index (MVQOLI)
Tidsramme: Pre-intervention, post-intervention, 2 day follow up, 7 day follow up
|
The MVQOLI evaluates subjective quality of life among people living with advanced, life-threatening illness by assessing the domains of symptoms, function, interpersonal, wellbeing, and transcendence (Schwartz, Merriman, Reed, & Byock, 2005). Each domain includes three Likert-scale evaluation questions. Analysis of the MVQOLI scores across the different time points will help determine whether VR effects are transient (within 24 hours) or sustained (after 2 and 7 days). |
Pre-intervention, post-intervention, 2 day follow up, 7 day follow up
|
Samarbeidspartnere og etterforskere
Sponsor
Etterforskere
- Hovedetterforsker: Ginah Kim, MD, Baycrest
Publikasjoner og nyttige lenker
Generelle publikasjoner
- Anderson F, Downing GM, Hill J, Casorso L, Lerch N. Palliative performance scale (PPS): a new tool. J Palliat Care. 1996 Spring;12(1):5-11.
- Hui D, Shamieh O, Paiva CE, Perez-Cruz PE, Kwon JH, Muckaden MA, Park M, Yennu S, Kang JH, Bruera E. Minimal clinically important differences in the Edmonton Symptom Assessment Scale in cancer patients: A prospective, multicenter study. Cancer. 2015 Sep 1;121(17):3027-35. doi: 10.1002/cncr.29437. Epub 2015 Jun 8.
- Schwartz CE, Merriman MP, Reed G, Byock I. Evaluation of the Missoula-VITAS Quality of Life Index--revised: research tool or clinical tool? J Palliat Med. 2005 Feb;8(1):121-35. doi: 10.1089/jpm.2005.8.121.
Studierekorddatoer
Studer hoveddatoer
Studiestart (Faktiske)
Primær fullføring (Forventet)
Studiet fullført (Forventet)
Datoer for studieregistrering
Først innsendt
Først innsendt som oppfylte QC-kriteriene
Først lagt ut (Faktiske)
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
Siste oppdatering sendt inn som oppfylte QC-kriteriene
Sist bekreftet
Mer informasjon
Begreper knyttet til denne studien
Ytterligere relevante MeSH-vilkår
Andre studie-ID-numre
- 21-15
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