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CompletedNCT05163340Updated Jul 8, 2022

Views of Nurses on Alarm Fatigue in ICUs

An observational study in Nurse's Role, sponsored by Akdeniz University. Completed at 1 site in Turkey. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2022-07-08.

Sponsored by Akdeniz University · Observational

Study type
Observational
Model
Other
Time perspective
Cross-sectional
Enrollment
67
Ages
18 Years and older
Sex
All
01

Study summary

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

Read the detailed 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.

02

Conditions studied

  • Nurse's Role

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Keywords

  • Alarm fatigue
  • Intensive care
  • Nursing
  • Mixed method
03

In context

Fatigue

1,860 studies on the registry are indexed under Fatigue; 376 are open to participants now.

This study's enrollment of 67 is below the median of 100 across 367 observational studies indexed under Fatigue.

Browse Fatigue studies →

Lead sponsor

Akdeniz University is the lead sponsor of 289 studies on the registry; 60 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Sampling method
Probability sample

Study population

The research populations consists of nurses working in adult ICU a University Hospital. The sample number was calculated with the formula known population and the cases average of the event in the study. In this study, considering the alarm fatigue standard deviation (σ=6.82) found in the Turkish validity study of the scale, the minimum sample size was calculated as 67 for a population size of 106 and a 95% confidence interval (t=1.96; d=1). Considering that there may be losses 10% more (74 nurses) will be taken.

The qualitative phase of the research will be with nurses who agreed to be interview and will be terminated when the data reach the saturation point and no new information emerge.

Inclusion criteria

  • 18 years and older
  • Who volunteered to participate in the research
  • Working in adult intensive care units

Exclusion criteria

Exclusion Criteria:

  • Under the age of 18
  • Not working in adult intensive care unit
05

Study design

Observational model
Other
Time perspective
Cross-sectional
Enrollment
67 participants (actual)
Patient registry
No
06

What researchers measure

Primary outcomes

  1. 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.

    Time frame: 30 May 2022

07

Study locations

1 site
  • Akdeniz University Hospital
    Antalya, 07058, Turkey
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 8, 2022, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT05163340
Lead sponsor
Akdeniz University
Responsible party
Fatma CEBECİ (Fatma CEBECİ, Akdeniz University) — Principal investigator
First posted
Dec 20, 2021
Start date
Jan 6, 2022
Primary completion
Jun 30, 2022
Completion
Jun 30, 2022
Last update
Jul 8, 2022

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jul 2022. You cannot join it, but the record below documents what was studied.

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