- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05953441
Artificial Intelligence Versus Human-controlled Doctor in Virtual Reality Simulation for Sepsis Team Training
July 17, 2023 updated by: Liaw Sok Ying, National University of Singapore
Artificial Intelligence Versus Human-controlled Doctor in Virtual Reality Simulation for Sepsis Team Training: Randomized Controlled Trial
The purpose of the study is to compare the effectiveness of Artificial Intelligence virtual doctor with human-controlled virtual doctor avatars on nursing students' sepsis care and interprofessional communication.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
65
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
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Singapore, Singapore, 117597
- Alice Lee Centre for Nursing Studies
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- All Year 3 NUS nursing students in Academic Year 2022
- Individuals 20 years old and above; and
- Consent to be video and/or audio-recorded
Exclusion Criteria:
- Year 1, 2 and 4 NUS nursing students;
- Incapable of giving informed consent;
- Unable to understand and/or speak in English language;
- Have visual, speech, and/or hearing impairment; and
- Do not agree to be video and/or audio-recorded.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: AI-powered group
Participants participated in a 2-hour Virtual Reality Simulation (VRS), which consisted of 2 simulation scenarios.
Participants had to perform nursing assessment and management of virtual patient, followed by communicating with an AI virtual doctor.
|
AI-powered virtual doctor
|
|
Active Comparator: Human-controlled group
Participants participated in a 2-hour Virtual Reality Simulation (VRS), which consisted of 2 simulation scenarios.
Participants had to perform nursing assessment and management of virtual patient, followed by communicating with a doctor avatar controlled by the medical student.
|
Virtual doctor avatar controlled by the medical student.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change from Baseline in Sepsis Knowledge on the 18-item sepsis knowledge test immediately after interventions.
Time Frame: Baseline and immediately after 2-hour VRS
|
The 8-item communication knowledge and 18-item sepsis knowledge tests were developed and content validated by a multidisciplinary team comprising a medical doctor, an advanced practice nurse, and nursing academics.
|
Baseline and immediately after 2-hour VRS
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change from Baseline in Team Communication Knowledge on the 8-item communication knowledge test immediately after interventions.
Time Frame: Baseline and immediately after 2-hour VRS
|
The 8-item communication knowledge and 18-item sepsis knowledge tests were developed and content validated by a multidisciplinary team comprising a medical doctor, an advanced practice nurse, and nursing academics.
|
Baseline and immediately after 2-hour VRS
|
|
Change from Baseline in Team Communication Self-Efficacy on the 6-item Patient Clinical Information Exchange and Interprofessional Communication Self-Efficacy Scale immediately after interventions.
Time Frame: Baseline and immediately after 2-hour VRS
|
The Patient Clinical Information Exchange and Interprofessional Communication Self-Efficacy Scale is a validated and self-reported instrument using a 0-100 Likert scale, which measures participants' perceptions of self-efficacy in team communication based on the ISBAR communication strategy.
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Baseline and immediately after 2-hour VRS
|
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Sepsis Care Performance through a 15-minute video-recorded simulation-based assessment within 2 weeks of postintervention.
Time Frame: Within 2 weeks of postintervention.
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2 independent raters used the validated RAPIDS (Rescuing A Patient In Deteriorating Situation) tool to measure nurses' simulation performance in assessing and managing a deteriorating patient.
|
Within 2 weeks of postintervention.
|
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Team Communication Performance through a 15-minute video-recorded simulation-based assessment within 2 weeks of postintervention.
Time Frame: Within 2 weeks of postintervention.
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2 independent raters used a validated 9-item team communication scale to assess nurses' simulation performance in communicating with doctor using the TeamSTEPPS communication strategies.
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Within 2 weeks of postintervention.
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Principal Investigator: Sok Ying Liaw, National University of Singapore
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
August 8, 2022
Primary Completion (Actual)
October 26, 2022
Study Completion (Actual)
November 13, 2022
Study Registration Dates
First Submitted
July 10, 2023
First Submitted That Met QC Criteria
July 17, 2023
First Posted (Actual)
July 20, 2023
Study Record Updates
Last Update Posted (Actual)
July 20, 2023
Last Update Submitted That Met QC Criteria
July 17, 2023
Last Verified
July 1, 2023
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- NUS-IRB-2022-202
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
IPD Plan Description
The data sets collected or analyzed during the study are available from the corresponding author on reasonable request.
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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