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The Effects of a Simulation-based Clinical Decision-Making Program for High-Alert Medication on the Near Miss Experience in Intensive Care Units Nurses

Not Applicable
Completed
Conditions
Not Applicable
Registration Number
KCT0009692
Lead Sponsor
Yonsei University, Wonju Severance Christian Hospital
Brief Summary

As a result of linear mixed model (LMM) analysis using clinical experience, which showed a significant difference in the preliminary homogeneity test results of the experimental and control groups (Z=-2.12, p=.034) as a control variable, the experimental group that received the clinical decision-making program Compared to the control group, clinical decision-making ability (F=3.94, p=.026), medication safety competency (F=4.97, p=.011), and safety motivation (F=5.20, p=.004) improved over time. found to be high. In addition, the experimental group that received the clinical decision-making program showed a lower number of medication administration errors experienced over time (F=14.28, p<.001) than the control group.

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
All
Target Recruitment
18
Inclusion Criteria

The target population of this study was nurses in the adult intensive care unit at a tertiary general hospital in Gangwon-do. The study subjects were a convenience sample of nurses who met the selection and exclusion criteria at a tertiary general hospital in Gangwon-do. The criteria for selecting subjects are nurses working in an intensive care unit related to adult patients at the advanced beginner level with a total clinical experience of more than 12 months but less than 36 months (Yuna Kim, 2021).

Exclusion Criteria

? Those participating in patient safety education programs other than this research program
? Those who have experienced a department change within the last 2 months
*In the case of mobile nurses, a period of adaptation to the department was required, so nurses whose department transfer period was less than 8 weeks were excluded (Jang Mi-ae, 2011).

Study & Design

Study Type
Interventional Study
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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