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Can virtual reality help reduce pain during wound care? A pilot study at the Maimonides Geriatric Centre

The pain reduction using immersive virtual reality during wound care evaluation study at Maimonides (PRISM) – pilot study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN56831265
Enrollment
20
Registered
2025-11-11
Start date
2025-11-17
Completion date
Unknown
Last updated
2025-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pain, depression, agitation/aggression Other

Interventions

Data will be collected to understand the overall feasibility, acceptability, and efficacy of using iVR during wound care episodes at Donald Berman Maimonides Geriatric Centre. We will obtain informed

Sponsors

The Integrated Health and Social Services University Network for West-Central Montreal (CIUSSS West-Central Montreal)
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 110 Years

Inclusion criteria

Inclusion criteria: 1. Living in the long-term care centre for at least 2 months prior to the start of the study 2. Receiving regular wound care for PUs, as per the recommendation of the wound care nurse, and reflected in the resident’s nursing care plan 3. Able to tolerate iVR, based on consultations with the Recreation Technology team and the research team’s preliminary study visit with the resident

Exclusion criteria

Exclusion criteria: 1. Diagnosis of blindness, severe cataracts or glaucoma 2. Having allergies to synthetic plastic 3. Having skin conditions or wounds on both wrists, or on the head/ears, which impact the wearability of the headset 4. Diagnosis of neuropathy 5. Exhibiting behavior within the past 30 days that has endangered or posed a significant safety risk to regular care staff during routine care activities (e.g., wound care or personal hygiene assistance) 6. Must be able to understand English or French

Design outcomes

Primary

MeasureTime frame
Pain measured using the Pain Assessment Checklist for Seniors with Limited Ability to Communicate (PACSLAC-II) at three points in time: Time Point 1: 1 hour before the commencement of a wound care episode Time Point 2: During the care episode Time Point 3: 1 hour after the wound care episode has been completed

Secondary

MeasureTime frame
Pain measured using the Pain Assessment in Advanced Dementia (PAINAD) validated pain scales at three points in time: Time Point 1: 1 hour before the commencement of a wound care episode Time Point 2: During the care episode Time Point 3: 1 hour after the wound care episode has been completed

Countries

Canada

Contacts

Public ContactStephanie Ballard
stephanie.ballard@ssss.gouv.qc.ca+1 (0)5144832121

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026