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The Effectiveness of a Chatbot-facilitated High Alert Medication Education for 2-year Post Graduate Nurses

The Effectiveness of a Chatbot-facilitated High Alert Medication Education for 2-year Post Graduate Nurses

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05985005
Enrollment
124
Registered
2023-08-09
Start date
2023-01-01
Completion date
2023-12-31
Last updated
2023-09-11

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

Conditions

Education, Nursing

Brief summary

This study involves three stages. In the first stage, qualitative research design is used to understand clinical nurses' learning needs on high alert medication. In the second stage, high alert medication knowledge inventory and high alert medication safety inventory will be developed based on the literature and results from qualitative study in the stage one. In the third stage, randomized control trail study design will be used. The nursing staffs in the experimental group receive online simulation of high alert medication safety training , the staffs from the control group receive classroom teaching regarding high alert medication. A total of 124 nurses will be invited to participate in this study, 62 subjects will be assigned in each group . After the intervention, we will examine the learning effectiveness.

Interventions

OTHERonline simulation of high alert medication safety training

online simulation of high alert medication safety training

Sponsors

National Taipei University of Nursing and Health Sciences
CollaboratorOTHER
Shin Kong Wu Ho-Su Memorial Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

1. Nursing staff who are licensed and have passed the Medication Safety Course for Newcomers to independently perform drug delivery techniques. 2. Nursing staff who are willing to participate in this research and complete the research consent form.

Exclusion criteria

1. Not fully involved in the study 2. Nursing staff not involved in dispensing medicine

Design outcomes

Primary

MeasureTime frameDescription
high alert medication knowledge inventoryChange from Baseline high alert medication knowledge inventory at 1 monthsNurse ' medication knowledge
high alert medication safety inventoryChange from high alert medication safety inventory at 1 monthsNurse ' medication safety
Learning Engagement ScaleChange from high alert medication safety inventory at 1 monthsNurse ' Learning Engagement Scale

Secondary

MeasureTime frameDescription
Learning satisfactionthrough study completion, an average of 1 WeekLearning satisfaction

Countries

Taiwan

Contacts

Primary ContactHE ting-I
skys1012@gmail.com0976335848

Outcome results

None listed

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