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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT06403397
Other study ID # Remember Me Tool
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date June 15, 2024
Est. completion date December 15, 2024

Study information

Verified date May 2024
Source Istanbul Demiroglu Bilim University
Contact Serpil Topçu
Phone 05324676179
Email serpilakkustopcu@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Bedside monitors are frequently used in monitoring vital signs of critically ill patients. Nurses working in healthcare facilities, especially in intensive care units, are required to manage devices with different alarm threshold values, categories, and types of alerts, leading to alarm fatigue. In response to this serious threat to patient safety, the FDA and The Joint Commission worked to develop strategies to address alarm fatigue in 2011. Alarm monitoring, identification of the cause, and silencing are typically performed by nurses. When reviewing alarm control studies in the literature, the CEASE care package developed by Levis et al. in 2019 was encountered. The tool was developed for personalized clinical alarm monitoring for the patient.


Description:

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Study Design


Related Conditions & MeSH terms


Intervention

Other:
Experimental group: CEASE Care Package and Remember Me Tool
Before the intervention, the intervention group will first undergo the 'Nurse Identification Form' and the 'Alarm Fatigue Scale'. The current root cause analysis of monitor alarms in the clinical setting will be conducted through the 'CEASE Care Package' and the 'Current Situation Analysis Form'. Each patient monitor in the intensive care unit will be observed and recorded by two observers for a period of 24 hours.The Monitor Alarm Control Tool - "Remember Me" will be attached beneath each monitor to facilitate easier monitoring by nurses. Nurses are expected to use the tool for a period of 15 days. After intervention; Two observers will conduct a re-evaluation using the "CEASE Care Package" and the "Current Status Analysis Form". Monitor alarms will be continuously assessed and recorded for 24 hours. Following the completion of this stage, the "Alarm Fatigue Scale" will be reapplied to the intervention group.

Locations

Country Name City State
Turkey Demiroglu Bilim University Istanbul Sisli

Sponsors (1)

Lead Sponsor Collaborator
Istanbul Demiroglu Bilim University

Country where clinical trial is conducted

Turkey, 

References & Publications (12)

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Outcome

Type Measure Description Time frame Safety issue
Primary The use of the CEASE care package tool will result in a decrease in the number of alarms in the intensive care unit end of the 3 weeks. This outcome will measured by Current Situation Analysis Form and CEASE care package tool. 2 months
Primary The use of the CEASE care package tool will lead to a reduction in alarm fatigue levels end of the 3 weeks. This outcome will measured by alarm fatigue scale. 2 months
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