Outcomes and User Acceptance of the IntelliVue Alarm Advisor Software (Europe)
- Conditions
- Clinical Alarms
- Interventions
- Other: Alarm Advisor
- Registration Number
- NCT03182452
- Lead Sponsor
- Philips Healthcare
- Brief Summary
This Clinical Study will be conducted as a comparative study focusing on usability and efficiency by comparing alarm burden pre- and post-implementation of an "Alarm Advisor software".
- Detailed Description
In a first phase of data collection (pre-implementation) all alarms of an intensive care unit population are recorded.
In an interim period an Alarm Advisor software will be introduced to the unit.
In a second phase (post-implementation) the same set of alarm data will be recorded.
The "Alarm Advisor" Software can identify alarms based on criteria set by the medical staff and provide hints to reduce alarms and alarm nuisance (e.g. by proposing adjustments of alarm limits).
The effect of reduction of recurring nuisance alarms through the implementation of the Alarm Advisor shall be evaluated.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 1487
- Patients admitted to the intensive care unit during the study period
- none
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Arm && Interventions
Group Intervention Description Post Phase (Alarm Advisor installed) Alarm Advisor Software implemented and staff trained (Interventional Phase)
- Primary Outcome Measures
Name Time Method Clinical Alarms six to eight months Number of Different Alarms on Intensive Care
- Secondary Outcome Measures
Name Time Method
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Trial Locations
- Locations (1)
Klinikum Konstanz
🇩🇪Konstanz, Baden-Württemberg, Germany
Klinikum Konstanz🇩🇪Konstanz, Baden-Württemberg, Germany