Optimal Patient Turning for Reducing Hospital Acquired Pressure Ulcers
- Conditions
- Pressure Ulcer
- Interventions
- Other: Optimal TurningOther: Standard Care PracticesOther: 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
- Adults (>18 years of age)
- Admission to Intensive Care Unit
- Children (<18 years of age)
- Adhesive allergy
- Physical limitation for sensor application
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Treatment - Optimal Turning Optimal Turning All 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 Turning Patient Sensor All 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 Care Patient Sensor All 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 Care Standard Care Practices All 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
Name Time Method Count of Participants With Pressure Ulcer According to the National Pressure Ulcer Advisory Panel (NPUAP) Criteria for Pressure Ulcers Duration 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
Name Time Method Compliance With Patient Turning Procedures Duration 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