Alarm Fatigue
Conditions
Interventions
Group 1: The intervention in this study includes several steps: First, the results from the analysis of the alarm data and the alarm fatigue questionnaire are presented to key stakeholders of the uni
Sponsors
Charité Campus Charité Mitte
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Working in the investigated intensive care unit during the investigated period of time. Medical staff (physicians, nurses)
Exclusion criteria
Exclusion criteria: Not working in the investigated intensive care unit (ICU) during the investigated time period No medical staff (physicians, nurses) Refusal to participate
Design outcomes
Secondary
| Measure | Time frame |
|---|---|
| Alarm fatigue among staff; Questionnaire | — |
Primary
| Measure | Time frame |
|---|---|
| Number of alarms in an intensive care unit (ICU); Collection through data analysis | — |
Countries
Germany
Contacts
Public ContactFelix Balzer
Institut für Medizinische Informatikder Charité – Universitätsmedizin Berlin
Outcome results
None listed