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Optimal Patient Turning for Reducing Hospital Acquired Pressure Ulcers

Not Applicable
Completed
Conditions
Pressure Ulcer
Interventions
Other: Optimal Turning
Other: Standard Care Practices
Other: Patient Sensor
Registration Number
NCT02533726
Lead Sponsor
Stanford University
Brief Summary

The purpose of this study is to test whether optimal patient turning, strictly every 2 hours with at least 15 minutes of tissue decompression, reduces the occurrence of hospital acquired pressure ulcers.

Detailed Description

This single site, open label, two arm randomized control trial aims to evaluate whether optimal patient turning, strictly every 2 hours with at least 15 minutes of tissue decompression, reduces the occurrence of hospital acquired pressure ulcers. Optimal turning procedures will be obtained with the use of a patient monitoring system (Leaf Healthcare, Inc.) and compared to standard preventative care practices.

Sensors were placed on all participants as they were admitted to ICU. A nurse's user dashboard was turned on for participants in the Optimal Turning Group, but was not turned on for participants in the Standard Care group.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
1312
Inclusion Criteria
  • Adults (>18 years of age)
  • Admission to Intensive Care Unit
Read More
Exclusion Criteria
  • Children (<18 years of age)
  • Adhesive allergy
  • Physical limitation for sensor application
Read More

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Treatment - Optimal TurningOptimal TurningAll patients will have a sensor applied. Patients within this arm will receive care from nurses who have access to a User Dashboard that provides visual advisories for patient turning, based on data obtained from a wearable patient sensor (Leaf Healthcare, Inc.).
Treatment - Optimal TurningPatient SensorAll patients will have a sensor applied. Patients within this arm will receive care from nurses who have access to a User Dashboard that provides visual advisories for patient turning, based on data obtained from a wearable patient sensor (Leaf Healthcare, Inc.).
Control - Standard CarePatient SensorAll patients will have a sensor applied. Patients within this arm will receive care from nurses who DO NOT have access to a User Dashboard that provides visual advisories for patient turning. Instead, these patients will receive standard care practices, patient turning initiated by nurses as necessary.
Control - Standard CareStandard Care PracticesAll patients will have a sensor applied. Patients within this arm will receive care from nurses who DO NOT have access to a User Dashboard that provides visual advisories for patient turning. Instead, these patients will receive standard care practices, patient turning initiated by nurses as necessary.
Primary Outcome Measures
NameTimeMethod
Count of Participants With Pressure Ulcer According to the National Pressure Ulcer Advisory Panel (NPUAP) Criteria for Pressure UlcersDuration of ICU admission (average 1 week)

NPUAP criteria include 4 stages and 2 unstaged criteria. The count of patients with pressure ulcer according to any of the criteria are reported.

* Stage 1: Non-blanchable erythema of intact skin

* Stage 2: Partial-thickness skin loss with exposed dermis

* Stage 3: Full-thickness skin loss

* Stage 4: Full-thickness skin and tissue loss

* Unstageable: Obscured full-thickness skin and tissue loss

* Suspected deep tissue injury: Persistent non-blanchable deep red, maroon or purple discoloration

Secondary Outcome Measures
NameTimeMethod
Compliance With Patient Turning ProceduresDuration of ICU admission (average 1 week)

Compliance is reported as the percentage of time during ICU admission that patients received turning every two hours.

Trial Locations

Locations (1)

Stanford Health Care

🇺🇸

Stanford, California, United States

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