Effects of simulation education for improving critical care nurses' knowledge and clinical skills for recognition and management of delirium

Not Applicable

• Conditions: delirium; Public Health - Health promotion/education; Neurological - Other neurological disorders

• Registration Number: ACTRN12619001696189
• Lead Sponsor: Professor Shu-Tai Shen Hsiao

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2019-12-02
• Last Update Posted: 10 December 2019

Recruitment & Eligibility

• Status: ot yet recruiting
• Sex: All
• Target Recruitment: 80

Inclusion Criteria

Registered nurse worked in acute care unit and care with critical patients.

Exclusion Criteria

Unwilling to involve in this study.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Delirium Knowledge will be assessed by a 10 items questionnaire designed by research and has been examined by five experts to confirm the content validity and face validity. This questionnaire will be distributed to participants at all timepoints measurement. <br>[Measures will be assessed at three timepoints: T0 (Baseline), T1 (Immediately after the intervention), T2 (Six weeks after the intervention). ];Delirium skills will be assessed by a 10 items questionnaire designed by research and has been examined by five experts to confirm the content validity and face validity. This questionnaire will be distributed to participants at all timepoints measurement. [Measures will be assessed at three timepoints: T0 (Baseline), T1 (Immediately after the intervention), T2 (Six weeks after the intervention).]

Secondary Outcome Measures

Name	Time	Method
A specific self-efficacy scale which modified from General Self-Efficacy Scale (GSE) for assessing delirium care self-efficacy will be used and it has been examined by five experts to confirm the content validity and face validity will be adopted. [Measures will be assessed at three timepoints: T0 (Baseline), T1 (Immediately after the intervention), T2 (Six weeks after the intervention). ]