Comparative Measurements of Interface Pressures Between Two Pressure-ulcer Prevention Mattresses: Softform Premier and Airsoft Duo

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

60 participants

Study Classification

INTERVENTIONAL

Study Start Date

2015-06-30

Study Completion Date

2016-03-31

Brief Summary

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The main objective of this study is to compare the Softform Premier mattress (in static mode) and AIRSOFT DUO mattresses in terms of skin pressures measured at the sacral area.

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Detailed Description

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The secondary objectives of the study are to compare the two devices in terms of:

A. contact surface. B. heel pressure. C. On the occurrence of pressure ulcers anywhere on the body at month 1. D. patient comfort after 1 month (visual analog scale ranging from 1 to 10).

Conditions

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Pressure Ulcer

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

CROSSOVER

Primary Study Purpose

PREVENTION

Blinding Strategy

NONE

Study Groups

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AirsoftDuo first

Patients randomized to this arm will be placed on the Airsoft Duo mattress, and the investigator will proceed with 2 series (for reproductibility) of measures for 30 minutes with the bed headboard at 0°. A pause, consisting of ten minutes of sitting and 1 minute of verticalization is then carried out. The bed is then positioned at 30°, and the 2 series of measures over 30 minutes are repeated. The next day, all of the above are repeated with the Softform Premium mattress (in static mode). The patient will then continue his/her stay with the Softform Premium mattress (in static mode) for 1 month.

Intervention: Airsoft Duo mattress Intervention: Softform Premier mattress (in static mode)

Group Type EXPERIMENTAL

Airsoft Duo mattress

Intervention Type DEVICE

A multi-layer mattress for pressure sore prevention. Made by NAUER FOAMPARTNER AG et OBA AG (Germany).

Softform Premier mattress (in static mode)

Intervention Type DEVICE

A multi-layer mattress for pressure sore prevention. Made by INVACARE MSS (United Kingdom).

Softform Premium first

Patients randomized to this arm will be placed on the Softform Premium mattress (in static mode), and the investigator will proceed with 2 series (for reproductibility) of measures for 30 minutes with the bed headboard at 0°. A pause, consisting of ten minutes of sitting and 1 minute of verticalization is then carried out. The bed is then positioned at 30°, and the 2 series of measures over 30 minutes are repeated. The next day, all of the above are repeated with the Airsoft Duo mattress. The patient will then continue his/her stay with the Airsoft Duo mattress for 1 month.

Intervention: Softform Premier mattress (in static mode) Intervention: Airsoft Duo mattress

Group Type EXPERIMENTAL

Airsoft Duo mattress

Intervention Type DEVICE

A multi-layer mattress for pressure sore prevention. Made by NAUER FOAMPARTNER AG et OBA AG (Germany).

Softform Premier mattress (in static mode)

Intervention Type DEVICE

A multi-layer mattress for pressure sore prevention. Made by INVACARE MSS (United Kingdom).

Interventions

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Airsoft Duo mattress

A multi-layer mattress for pressure sore prevention. Made by NAUER FOAMPARTNER AG et OBA AG (Germany).

Intervention Type DEVICE

Softform Premier mattress (in static mode)

A multi-layer mattress for pressure sore prevention. Made by INVACARE MSS (United Kingdom).

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

* The patient must have given his/her informed and signed consent
* The patient must be insured or beneficiary of a health insurance plan
* The patient spends more than 12 hours in bed with a possible verticalization and a predictable length of stay of at least 1 month.
* The patient has a stable medical condition (no complications in the last 10 days) without pressure ulcers
* The patient is at risk of pressure ulcers assessed a score ≤ 14 on the Norton scale
* The patient's weight is less than 120 Kg

Exclusion Criteria

* The patient is in an exclusion period determined by a previous study
* The patient is under judicial protection, under tutorship or curatorship
* The patient refuses to sign the consent
* It is impossible to correctly inform the patient
* Contra-indication for strict decubitus dorsal position
* The patient has a rotation of the pelvis, asymmetric deformations of the hips in the frontal plane.
* The patient has bedsores, a recent scar in a pressure area.
* The patient has a knee flexion deformity\> 10 °
* The patient is agitated or uncooperative
* The patient's weight is greater than 120 Kg

Minimum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No