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Clinical Trials/NCT05472974
NCT05472974
Completed
Not Applicable

Prevention of Pressure Ulcers in Patients at Medium to High Risk of Developing Pressure Ulcers and Using the DOMUS 4 / AUTO Motorized Air Mattress: Non-interventional Study

Wellell France5 sites in 1 country86 target enrollmentSeptember 17, 2018
ConditionsPressure Injury

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Pressure Injury
Sponsor
Wellell France
Enrollment
86
Locations
5
Primary Endpoint
percentage of patients who developed at least one stage 2 pressure injury
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

The aim of the study is to determine the clinical value of using a powered alternating pressure air mattress (P-APAM) in the prevention of pressure injury (PI) in patients at medium to high risk.

This study is noncomparative, observational study.

Patients older than 18 years of age, with a medium to high risk of PI, without PI, up during the day, and lying more than 15 hours a day on a specific P-APAM were included. The study was conducted in nursing homes, and in long-stay geriatrics department.

Patients are followed up for 35 days. The use of the P-APAM is associated with the usual PI prevention measures. The primary outcome is the percentage of patients who developed between day 0 and day 35 at least one PI of at least stage 2 on the sacrum, spine, or heel. Secondary endpoints are patient assessments of comfort, caregiver satisfaction, mattress noise level, and mattress safety.

Registry
clinicaltrials.gov
Start Date
September 17, 2018
End Date
July 22, 2019
Last Updated
3 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Patient over 18 years old
  • Patient with a medium to high risk of developing pressure ulcers (clinical judgment and a score of \[10 to 14\] on the Braden scale (6 (maximum risk) to 23 (no risk))
  • Patient without pressure injury on the day of inclusion
  • Patient up during the day, lying between 3 p.m. and 8 p.m. a day on a Domus 4 / AUTO mattress
  • Patient with a weight \< 200 kg
  • Patient (or a trusted third party) having been informed of the study and agreeing to participate

Exclusion Criteria

  • Patient at end of life (estimated life expectancy less than 6 months)
  • Malnourished patient according to the french health authority (Haute Autorité de la santé) definition\*
  • \* For adults under 70:
  • weight loss ≥ 5% in one month or ≥ 10% in six months
  • or body mass index (BMI) ≤ 18.5 (excluding constitutional thinness)
  • for adults over 70:
  • weight loss ≥ 5% in one month or ≥ 10% in six months
  • or BMI ≤ 21
  • or Mini Nutritional Assessment (MNA) ≤ 17 (/30)
  • or albuminemia \< 35 g/L

Outcomes

Primary Outcomes

percentage of patients who developed at least one stage 2 pressure injury

Time Frame: 35 days after installation on the mattress (at day 35)

Percentage of patients who developed at least one stage 2 PI of the sacrum, backbone, or heel (areas of support when lying down)

Secondary Outcomes

  • Assessment of the degree of maceration(35 days after installation on the mattress (at day 35))
  • Percentage of patients who developed a o pressure injury (any stage), other than those of the sacrum, backbone, or heel between(35 days after installation on the mattress (at day 35))
  • Assessment by the nursing staff with the use of the mattress (implementation, cleaning maintenance turning, changing to a sitting position)(35 days after installation on the mattress (at day 35))
  • Assessment of mattress safety(At day 35)
  • Assessment by the patient (or family or staff in the case of incapacity) of the comfort of the mattress (general comfort, stability)(35 days after installation on the mattress (at day 35))

Study Sites (5)

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