Clinical
outcome report
Evidence from a seven-day, in-home adjustable bed and mattress trial, documented for funding and clinical justification.
Report Date
November 2025
Trial Period
7 Days
Location
Melbourne Metro
01 · Overview
Executive summary
"Across seven nights in the client's home, every measured outcome moved in the expected direction. The equipment configuration is clinically appropriate and ready for funding submission."
02 · Outcomes
Clinical measurements
Baseline versus follow-up across the seven-day trial.
| Measurement | Day 1 | Day 7 | Change |
|---|---|---|---|
| Comfort Score | 4/10 | 8/10 | +4 |
| Pain Score | 7/10 | 3/10 | −4 |
| Sleep Quality | Poor | Good | Improved |
| Night Waking | 4–5 times | 1–2 times | Reduced |
| Morning Stiffness | Severe | Mild | Improved |
| Transfer Confidence | Low | High | Improved |
03 · Configuration
Equipment trialled
Bed
Icare IC333 Homecare HiLo Bed
Mattress
ICON Medium Foam Mattress
Accessories
Quarter-length bed rails (both sides)
Settings Used
Bed height 40–80cm, head elevation nightly
04 · Notes
Clinical observations
- 01Client demonstrated improved independent transfers at 55cm bed height
- 02Pressure redistribution adequate for low to medium risk level
- 03Head elevation of 30° reduced nocturnal reflux symptoms
- 04Rails provided psychological reassurance during repositioning
- 05Carer reported reduced manual handling strain
05 · Outcome
Recommendation
Trial Outcome
Recommend purchase
Clinical justification
Based on documented improvements in comfort, pain management, and transfer safety, this equipment configuration is clinically appropriate for the client's ongoing needs. The trial evidence supports funding application under NDIS, Support at Home or CHSP programs.