A prototype support surface has been designed which aims to successfully redistributes the pressures exerted and provides sufficient support to human soft tissue We want to prove the effectiveness of the prototype support surface by enlisting patients in a clinical trial, where we will assess the presence of pressure ulcers, and the ability of the patients to tolerate the support surface, and also measure the pressure over time and compare them to when the patients are using standard mattresses.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Enrollment
10
This is a magnetorheological elastomer that can dynamically redistribute the pressure over a bony prominence to be lower than the critical closing pressure while at the same time providing sufficient support.
Tan Tock Seng Hospital Rehabilitation Centre
Singapore, Singapore
PTAUC
pressure-time area under curve
Time frame: For a maximum of 14 days (duration of trial)
Pressure sores - NPUAP (National Pressure Ulcer Advisory Panel) grade
If pressure sores are present, they will be graded based on the NPUAP grade from 1-4. Location will also be recorded.
Time frame: For a maximum of 14 days (duration of trial)
Patient's comfort
Patient comfort measured on a visual analogue scale (1- 10)
Time frame: For a maximum of 14 days (duration of trial)
Discomfort or pain
Presence of discomfort or pain at high risk pressure points. This will be asked of patients, and will be scored as yes or no.
Time frame: For a maximum of 14 days (duration of trial)
Suggestions
This will be a qualitative open-ended question for patient's verbatim report or suggestions
Time frame: For a maximum of 14 days (duration of trial)
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