In-bed sensor system Mobility Monitor - Patient-Project
Not Applicable
- Conditions
- L89Decubitus ulcer and pressure area
- Registration Number
- DRKS00015492
- Lead Sponsor
- niversitätsklinikum Freiburg, Pflegedirektion,
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 808
Inclusion Criteria
Patients receiving in-patient treatment at the Neurosurgical or Neurological Intensive Care Unit at the Medical Center – University of Freiburg and lying in a bed with a Mobility Monitor installed.
Exclusion Criteria
Patients coming to the Intensive Care Unit with an external bed and/or Patients with a need of special beds that can not be used with the Mobility Monitor (for example beds with fixed mattresses, special beds, bariatric beds, etc.).
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The patients’ inactive time in bed exceeding two hours without pressure relieving movements in proportion to the time the MoMo was in bed. <br><br>The data basis for this are the measured values of the Mobility Monitors. These continously cover the in-bed motion data (micro-movements and pressure-relieving repositioning) of the incuded patients.<br>
- Secondary Outcome Measures
Name Time Method (1) Pressure Ulcer Incidence: The occurrence of new pressure ulcers while a MoMo was in bed. <br>(2) The rate of relevant repositionings: This is a measure that indicates how many of the repositionings done or supported by the health care staff were recognised by the MoMo as a pressure-relieving repositioning. <br>