Clinical Trials Directory

Trials / Active Not Recruiting

Active Not RecruitingNCT07364097

A Study of Silent Alarm Delivery Versus Standard Audible Alarm Delivery in Intensive Care and High Dependency Units

Does Eliminating Alarm Noise Cacophony for Intensive Care Staff and Patients Improve Burnout and Encephalopathy Levels

Status
Active Not Recruiting
Phase
N/A
Study type
Interventional
Enrollment
200 (estimated)
Sponsor
MindWave Medical Inc · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

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.

Conditions

Interventions

TypeNameDescription
OTHERSilent alarm strategyThe intervention consists of the implementation of a silent alarm system in the clinical environment. The silent alarm system consists of a self-locating interface device, which is interposed between an alarm-generating device and its audio output. This device contains communication, locating, motion, logic, and relay chips, which enable the interface device to identify its location and staff responsible for that location, as well as to detect audio output from the alarm-generating device, and to control the audible state of that output. The Interface device can communicate with separate bone conduction headsets worn by staff, which contain sensors that confirm staff presence at the headset, and buttons for response to an alarm announcement. The interface device then delivers alarms silently to those staff specifically responsible for its location when a responsible staff member can be identified, confirmed to be present, and accepts responsibility for the alarm through button action.

Timeline

Start date
2026-02-03
Primary completion
2026-04-28
Completion
2026-04-28
First posted
2026-01-23
Last updated
2026-02-06

Locations

1 site across 1 country: India

Source: ClinicalTrials.gov record NCT07364097. Inclusion in this directory is not an endorsement.