This Study Will Use Real-time Pressure Mapping Technology to Determine Which Positioning Strategies and Devices Exert the Least Amount of Pressure on Peri-operative Burn Patients

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorSunnybrook Health Sciences Centre

About this trial

Burn patients are especially vulnerable to developing hospital-acquired pressure sores. The goal of this study is to determine which positions and positioning devices exert the least amount of pressure on problem areas such as the heels, the tailbone, the elbow and the back of the head.

With the use of a pressure mapping device, it will allow the investigators to:

1. Identify patients at the highest risk of developing pressure injuries related to positioning/devices. 2. Use the findings to create positioning/device guidelines

By optimizing positioning strategies, the investigators aim to enhance patient comfort, prevent complications, and ultimately improve the overall quality of care for burn patients.

Eligibility criteria

Qualifiers

adult patients (18 years of age or greater)

burns of any size

pre and post-operative patients

Disqualifiers

pediatric burn patients

patients with pre-existing (pre-admission) pressure injuries

patients unable to provide informed consent or decline consent

patients with large burns that are not expected to survive past 72 hours

Trial design

Treatments tested in this trial

  • Positioning and positioning devices

Treatment groups

80 Participants
are divided into 1 treatment group

Locations

This trial has no locations