Effectiveness of Delirium Simulation Education of Nurses in Intensive Care Unit
Self Efficacy, Nursing Caries, Intensive Care Unit Delirium
About this trial
This is an interventional prevention trial for Self Efficacy focused on measuring intensive care unit,nurses,delirium,simulation
Eligibility Criteria
Inclusion Criteria:
- Nurses who have worked in the intensive care unit for more than 3 months,
- No physical or mental illness or recent major family events,
- Never received delirium simulation training.
Exclusion Criteria:
- Those who are not working in the intensive care unit for less than 3 months,
- Those who have recently suffered from physical and mental illness or a major family event recently,
- Those who have received delirium simulation training,
- Those who are currently working as nursing supervisors.
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Experimental
No Intervention
Experimental(simulation education group)
Control(traditional group)
The experimental group (simulation teaching group), the content of simulation teaching is based on the simulation model, and includes five important elements: Instructor, student, educational practice, simulation situation design and characteristics, and result that design covering the four stages of learning, concrete experience, reflective observation, abstract conceptualization and action experience, and design lesson plans, which include delirium assessment and delirium risk factor detection. Delirium prevention and management (PADIS guidelines). The main objectives of the teaching plan design of the experimental group are: to be able to confirm delirium by assessment of the Delirium Assessment Scale; to confirm the risk factors by the history taking; to propose treatment and measures according to the assessment results. Secondary goals: Be able to perform handovers.
Nurses in the control group did not receive simulated situational teaching, but received classroom teaching 3 times (once every other week) (delirium assessment, risk factor assessment; PADIS treatment), each session of about 2 hours. In order to avoid inconsistent teaching content, the control group and the experimental group are not to be together in classroom.