Clinical Trials Directory

Trials / Completed

CompletedNCT04994600

Design and Validation of a German Language Questionnaire for Measuring Alarm Fatigue in Intensive Care Units

Design and Validation of a German Language Questionnaire for Measuring Alarm Fatigue in Nurses and Medical Doctors in Intensive Care Units

Status
Completed
Phase
Study type
Observational
Enrollment
700 (actual)
Sponsor
Charite University, Berlin, Germany · Academic / Other
Sex
All
Age
Healthy volunteers
Not accepted

Summary

False-positive and non-actionable alarms can lead to staff desensitization ("alarm fatigue") and thus patient endangerment. With this study the investigators create a basic tool to survey alarm fatigue of intensive care staff: the first German language alarm fatigue questionnaire.

Detailed description

In intensive care units (ICUs), patients' vital signs are monitored automatically. As soon as one of the parameters indicates a critical or potentially critical condition, an alarm is triggered on the ward. However, if there are too many alarms, even most of which are false or require no treatment, ward staff may develop alarm fatigue and become desensitized to alarms. This puts patients at risk, especially by overhearing critical alarms. Overburdening staff with alarms is part of everyday life in most ICUs. Considering the demographic development as well as the COVID-19 pandemic, it is to be expected that the number of intensive care patients and thus also the alarm burden in intensive care units will increase. This will also be exacerbated by the increasing digitization of the ICU. Evidence-based and data-driven alarm management enables clinicians to trust alarms again. With this study the investigators create a basic tool to survey alarm fatigue of intensive care staff: the first German language alarm fatigue questionnaire. The questionnaire will be collected in two phases. With the data from the first phase (N ≈ 300), the investigators aim to uncover any structure that may be latent in the questionnaire data (by exploratory factor analysis) and reduce the number of questions from 27 to \~15. The reduced questionnaire will be collected in the second phase (N ≈ 300 - 400). With the data obtained, the investigators intend to test the structure postulated in the first survey in a confirmatory factor analysis.

Conditions

Interventions

TypeNameDescription
OTHERReduces number of question itemsThe number of alarm fatigue questions are reduced to about 15 in the CFA\_2nd\_phase group.

Timeline

Start date
2021-03-19
Primary completion
2023-09-01
Completion
2023-09-01
First posted
2021-08-06
Last updated
2023-09-08

Locations

1 site across 1 country: Germany

Source: ClinicalTrials.gov record NCT04994600. Inclusion in this directory is not an endorsement.