The Pain Reduction Using Immersive Virtual Reality During Wound Care Evaluation Study at Maimonides (PRISM) - Pilot Study

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
AgeNot listed
SponsorMcGill University

About this trial

This study will test whether immersive virtual reality (iVR) can reduce pain and discomfort during wound care for residents living in long-term care (LTC). Pressure ulcers are common and painful among older adults, and dressing changes often cause additional distress.

Up to 20 residents at the Donald Berman Maimonides Geriatric Centre will use virtual reality headsets during routine wound care. The headsets display calm, low-stimulus scenes (e.g., puppies in a meadow) designed to distract and comfort participants.

Each participant will take part for six weeks in three phases:

* Two weeks of usual wound care (baseline) * Two weeks using virtual reality during wound care (intervention) * Two weeks of usual care again (washout)

Pain will be assessed using validated tools, and the research team will also observe agitation, mood, and other behavioral indicators. Nursing staff will provide feedback on feasibility and acceptability of iVR use in LTC settings.

Eligibility criteria

Qualifiers

Resident of LTC for ≥2 weeks

Receiving regular wound care for pressure ulcers

Able to tolerate iVR headset use

(If cognitively apt) able to understand English or French

Disqualifiers

Blindness, severe cataracts, or glaucoma

Allergies to synthetic plastics or headset materials

Head or ear wounds preventing headset placement

Peripheral neuropathy

Trial design

Treatments tested in this trial

  • Rendever Immersive Virtual Reality Platform

Treatment groups

25 Participants
are divided into 2 treatment groups

Sponsors and collaborators

McGill University

Lead sponsor

Lady Davis Institute

Collaborator