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Completed
NCT07364097
A Study of Silent Alarm Delivery Versus Standard Audible Alarm Delivery in Intensive Care and High Dependency Units
Conditions: Delirium in the Intensive Care Unit, Burnout, Healthcare Workers, Noise in the ICU, Alarm Fatigue, Alarm Fatigue in Intensive Care Unit Nurses, Alarms, Nursing Workload
Sex: All
Ages: 18 Years – N/A
Healthy volunteers: No
Phase: NA
Enrollment: 311
Sponsor: MindWave Medical Inc
Location: Udayananda Multispecialty Hospital Nandyāl Andrah Pradesh
Summary
The goal of the trial is to learn if a strategy to eliminate audible alarm noise in intensive care and high dependency units can reduce overall noise levels, patient delirium, staff alarm fatigue, and staff burnout. Researchers will implement a silent alarm strategy in specific care units for four weeks and compare this to a separate 4 weeks where a silent strategy is not implemented. Noise, burnout, delirium levels, and staff alarm response times will be compared between the silent and non-silent units.
Eligibility Criteria
Inclusion Criteria:
* Admission to Intensive or high dependency care unit.
Exclusion Criteria:
* Pre-existing diagnosis of dementia
* Endotracheally intubated (may enroll when extubated)
* CNS injury, infection, or malignancy as reason for admission.
Source: ClinicalTrials.gov (NCT07364097). StuddyBuddy aggregates publicly available trial information.