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NCT05163340 Clinical Trial

Views of Nurses on Alarm Fatigue in ICUs

Nurse's Role Clinical Trial

Official title:
Nurses' Views on Alarm Fatigue and Its Reduction in Adult Intensive Care Units: Convergent Parallel Design

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT05163340
Other study ID # KAEK-271
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 6, 2022
Est. completion date June 30, 2022

Study information
Verified date July 2022
Source Akdeniz University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This study focused on determining the views of nurses on alarm fatigue and its reduction in adult intensive care units.

Description:

Backround: Physiological monitoring of critically ill patients in ICU is a complex nursing task, and nurses are key professionals managing multiple monitoring devices. Aim: The aim of this study is to determine the views of nurses on alarm fatigue and its prevention in adult intensive care units. Study Design: In the study, the minimum sample size was calculated as 67 for a population size of 106 and a 95% confidence interval, taking into account the alarm fatigue standard deviation (σ=6.82) found in the Turkish validity study of the "Nurses' Alarm Fatigue Scale" (t=1.96; d=1) . Considering that there may be losses, 74 nurses will be included in the study by taking 10% more. In the qualitative phase of the research, intensive care nurses who agreed to be interviewed during the collection of quantitative data will be included. Method: In this study, parallel data type will be used in convergent parallel mixed design. The quantitative phase of the study is a descriptive study to determine alarm fatigue levels in nurses working in adult intensive care units. In the qualitative phase of the research; A case study will be conducted at the same time in order to examine the findings revealed with quantitative data in more depth and to determine the views of nurses on reducing alarm fatigue. Individual in-depth interviews will be held in a suitable room using the "Semi-Structured Interview Form" created by the researchers with those who agree to participate in the qualitative study.

Recruitment information / eligibility
Status Completed
Enrollment 67
Est. completion date June 30, 2022
Est. primary completion date June 30, 2022
Accepts healthy volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - 18 years and older - Who volunteered to participate in the research - Working in adult intensive care units Exclusion Criteria: - Under the age of 18 - Not working in adult intensive care unit

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
Turkey Akdeniz University Hospital Antalya

Sponsors (1)
Lead Sponsor Collaborator
Akdeniz University

Country where clinical trial is conducted

Turkey, 

Outcome
Type Measure Description Time frame Safety issue
Primary Nurses' Alarm Fatigue Scale The scale consists of 9 items and the score range is between 0-36. High scores indicate the effects of alarm fatigue on nurses' performance. Each item in the questionnaire is scored between 0 and 4. 30 May 2022
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