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Effects of Scenario-based Education Initiative and OSCE for Recognition and Management of Delirium

Evaluating the Effects of Implementing a Scenario-based Education Initiative and OSCE for Recognition and Management of Delirium: a Cluster Randomized Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05623475
Enrollment
100
Registered
2022-11-21
Start date
2021-10-25
Completion date
2023-02-21
Last updated
2024-10-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Delirium

Keywords

Intensive Care Unit Syndrome, Delirium, OSCE

Brief summary

Delirium is a disturbance in consciousness with reduced ability to focus, sustain, or shift attention that occurs over a short period of time and tends to fluctuate over the course of the day. 50% to 81.7% had delirium during their ICU hospitalization. Delirium is associated with increased physical restraint, ventilation use, length of ICU stay, and mortality. However, there is no established delirium care pathway in target hospital. Chen et al. (2014) demonstrated that structured assessment stations with immediate feedback may improve overall learning efficiency over an EBP workshop alone. However, no published delirium care education study has used OSCEs as an intervention for healthcare professionals. The aim is to evaluate the effects of implementing a Scenario- based education intervention, including objective structured clinical examinations (OSCEs) on delirium care among healthcare professionals. This is a knowledge translation research, builds on eight years of delirium care research in University of Wollongong, Australia. The research will be undertaken at ICUs in a medical center in northern of Taiwan. There are two phases: (1) systematic review to identify delirium screen tool, and (2) a randomized controlled trial was conducted to determine the effects of implementing a Scenario-based education intervention, including OSCE (experimental group), and on-line education only (control group) focused on recognition and management of delirium. The hypothesis is: Scenario-based education intervention, including OSCE can increase the competence and self-efficacy among healthcare professionals in delirium care.

Detailed description

OSCEs are an integral aspect of all levels of medical education but limited to undergraduate nursing and allied health education. OSCEs are rarely used in the workplace as learning activities with nursing and allied health clinicians. This is the reason why this education initiative was innovative. OSCEs are simulated 'real life' clinical scenarios presented to clinicians who are required to demonstrate to an assessor the clinical tasks which form an OSCE scenario.

Interventions

BEHAVIORALOSCEs

Scenario-based education intervention, including objective structured clinical examinations (OSCEs)

BEHAVIORALLecture

Face-to-face Education using Delirium Care Flip Chart

BEHAVIORALE-learning

Delirium care video

Sponsors

Taipei Medical University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
20 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

1. Registered nurse worked in acute care unit and care with critical patients 2. Licensed physician which undertake the post graduate year program worked in acute care unit and care with critical patients

Exclusion criteria

1.Unwilling to involved the research

Design outcomes

Primary

MeasureTime frameDescription
Delirium KnowledgeT0(Baseline), T1(Immediately after the intervention), T2(Six weeks after the intervention)1. The ICU Delirium Care Knowledge Quiz (Traditional Chinese version ) developed by Ho et al. (2021) was used in this study. 2. The ICU Delirium Care Knowledge Quiz (Traditional Chinese version ) consists of 16 multiple-choice questions, with 1 point awarded for each correct answer, and a maximum score of 16 points. The total score of the participants is analyzed as a continuous variable. The total range from 0 to 16 (minimum score: 0 point; and maximum score 16 points). Higher points represent better ICU Delirium Care Knowledge. 3. The overall KR-20 coefficient of the questionnaire is 0.85, the intra-class correlation coefficient over a 30-day interval is 0.97, the content validity index (CVI) is 83%, and the exploratory factor analysis (EFA) demonstrates appropriate structural validity, with four factors explaining 60.87% of the total variance, indicating good reliability and validity.

Countries

Taiwan

Participant flow

Participants by arm

ArmCount
Experimental Group
1. face-to-face delirium care session (30 minutes in duration); 2. online learning delirium care activities (20 minutes in duration); and 3. delirium care OSCE and reflective activity (30 minutes in duration). OSCEs: Scenario-based education intervention, including objective structured clinical examinations (OSCEs) Lecture: Face-to-face Education using Delirium Care Flip Chart E-learning: Delirium care video
59
Control Group
1. face-to-face delirium care session (30 minutes in duration); 2. online learning delirium care activities (20 minutes in duration) Lecture: Face-to-face Education using Delirium Care Flip Chart E-learning: Delirium care video
38
Total97

Baseline characteristics

CharacteristicExperimental GroupControl GroupTotal
Age, Customized
20-24 year-old
16 Participants9 Participants25 Participants
Age, Customized
25-34 year-old
39 Participants25 Participants64 Participants
Age, Customized
35-44 year-old
3 Participants2 Participants5 Participants
Age, Customized
45-54 year-old
1 Participants2 Participants3 Participants
Education
Associate Degree
9 Participants5 Participants14 Participants
Education
Bachelor Degree
49 Participants32 Participants81 Participants
Education
Master Degree
1 Participants1 Participants2 Participants
ICU training
No
8 Participants4 Participants12 Participants
ICU training
Yes
51 Participants34 Participants85 Participants
Race (NIH/OMB)
American Indian or Alaska Native
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Asian
59 Participants38 Participants97 Participants
Race (NIH/OMB)
Black or African American
0 Participants0 Participants0 Participants
Race (NIH/OMB)
More than one race
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Unknown or Not Reported
0 Participants0 Participants0 Participants
Race (NIH/OMB)
White
0 Participants0 Participants0 Participants
Sex: Female, Male
Female
55 Participants37 Participants92 Participants
Sex: Female, Male
Male
4 Participants1 Participants5 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
0 / 590 / 38
other
Total, other adverse events
0 / 590 / 38
serious
Total, serious adverse events
0 / 590 / 38

Outcome results

Primary

Delirium Knowledge

1. The ICU Delirium Care Knowledge Quiz (Traditional Chinese version ) developed by Ho et al. (2021) was used in this study. 2. The ICU Delirium Care Knowledge Quiz (Traditional Chinese version ) consists of 16 multiple-choice questions, with 1 point awarded for each correct answer, and a maximum score of 16 points. The total score of the participants is analyzed as a continuous variable. The total range from 0 to 16 (minimum score: 0 point; and maximum score 16 points). Higher points represent better ICU Delirium Care Knowledge. 3. The overall KR-20 coefficient of the questionnaire is 0.85, the intra-class correlation coefficient over a 30-day interval is 0.97, the content validity index (CVI) is 83%, and the exploratory factor analysis (EFA) demonstrates appropriate structural validity, with four factors explaining 60.87% of the total variance, indicating good reliability and validity.

Time frame: T0(Baseline), T1(Immediately after the intervention), T2(Six weeks after the intervention)

ArmMeasureGroupValue (MEAN)Dispersion
Experimental GroupDelirium KnowledgeT012.40 pointStandard Deviation 1.72
Experimental GroupDelirium KnowledgeT113.08 pointStandard Deviation 1.69
Experimental GroupDelirium KnowledgeT213.10 pointStandard Deviation 1.81
Control GroupDelirium KnowledgeT112.71 pointStandard Deviation 2.02
Control GroupDelirium KnowledgeT213.78 pointStandard Deviation 1.33
Control GroupDelirium KnowledgeT013.26 pointStandard Deviation 1.5

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026