A Comparison Between Physical and Virtual Simulation: A Randomized Controlled Trial

April 1, 2020 updated by: Liaw Sok Ying, National University, Singapore

Nurse-Physician Communication Team Training in Virtual Reality Versus Live Simulations: Randomized Controlled Study

Nurse-physician communication skills can be improve through inter-professional team training. Simulation is often used to conduct these training. However, constraints to conduct these sessions such as scheduling and logistic arrangements have been widely reported. Thus with the advancement of technology in education, the use of virtual environment to conduct the team training is being explored and evaluated.

Study Overview

Detailed Description

All recruited participants underwent a 3-hour nurse-physician communication training prior to the simulation session. Team Strategies and Tools to Enhance Performance and Patient Safety (TeamSTEPPS) curriculum and pre-learning videos were introduced to the participants. Pre-test questionnaires were administered after the training. Participants were then randomized to the control (live simulation) or intervention group (virtual simulation).

Intervention group participants will undergo a virtual simulation session training via the multi-user virtual world by logging in into the 3D virtual environment while participants in the control group performed the simulations in a physical simulated ward setting. Each pair of 1 medical student and 1 nursing student participate in two role-playing simulation scenarios (15-20 minutes each) along with a facilitator who will provide a debrief (30-minutes). Prior to the simulation, participants were given a smart-watch to monitor their physiological parameters such as heart rate. Post-test questionnaires were administered after the simulation sessions.

After the simulation training, a 30-minutes team-based assessments were conducted based on a inter-professional bedside care scenario in pairs of one medical and one nursing student within their randomized group. The assessments were video recorded for evaluation by assessors who are blinded to the groupings. All participants were then invited to complete a follow-up questionnaire 2 months after the simulation training.

Study Type

Interventional

Enrollment (Actual)

120

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

      • Singapore, Singapore
        • National University of Singapore

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

18 years and older (ADULT, OLDER_ADULT)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

i) Full time students undertaking National University of Singapore's

  • Third or fourth year Bachelor of Science (Nursing)
  • Third or fourth year Bachelor of Medicine & Bachelor of Surgery

ii) Completed acute care management modules

Exclusion Criteria:

i) Does not voluntarily agree to join the study

ii) Does not want their performance to be video-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
  • Masking: SINGLE

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
EXPERIMENTAL: Virtual Reality
3D avatar in a virtual simulation environment
3D virtual hospital environment where participants can perform physical and social interaction and presence using avatars.
NO_INTERVENTION: Live Simulation
Live-based simulation in a simulation ward

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Demographics
Time Frame: Baseline
Collection of participant demographic data.
Baseline
Communication skill performance
Time Frame: Post-test (immediately after simulation assessment)
Participants nurse-doctor communication skill was measured using a validated team communication scale that was self-developed. It is a 7-item checklist with a 5-point scale. The score ranges from 5 to 35 with higher score indicating better nurse-doctor communication performance.
Post-test (immediately after simulation assessment)
Baseline (Attitudes Toward Interprofessional Health Care Team)
Time Frame: Pre-test
Measurement of participants' attitudes towards working in interprofessional care team using the 14-item Attitudes Toward Interprofessional Health Care Team questionnaire using a 5-point scale. The scores ranges from 14 to 70 with higher score indicating more positive attitudes.
Pre-test
Post-test (Change of Attitudes Toward Interprofessional Health Care Team from baseline)
Time Frame: Post-test (immediately after simulation training)
Measurement of participants' attitudes towards working in interprofessional care team using the 14-item Attitudes Toward Interprofessional Health Care Team questionnaire using a 5-point scale. The scores ranges from 14 to 70 with higher score indicating more positive attitudes.
Post-test (immediately after simulation training)
Follow-up (Change of Attitudes Toward Interprofessional Health Care Team from baseline and post-test)
Time Frame: Follow-up (2-months after simulation training)
Measurement of participants attitudes towards working in interprofessional care team using the 14-item Attitudes Toward Interprofessional Health Care Team questionnaire using a 5-point scale. The scores ranges from 14 to 70 with higher score indicating more positive attitudes.
Follow-up (2-months after simulation training)
Baseline (Interprofessional Socialization and Valuing Scale)
Time Frame: Pre-test
Measurement of participants behaviors, beliefs and attitudes in interprofessional socialization using the 24-item Interprofessional Socialization and Valuing Scale questionnaire using a 7-point scale (1= not at all ; 7= to a very great extent; "not applicable" response is also available). The score ranges from 24 to 168 with higher score indicating greater presence of the attributes measured.
Pre-test
Post-test (Change of Interprofessional Socialization and Valuing Scale from baseline)
Time Frame: Post-test (immediately after simulation training)
Measurement of participants behaviors, beliefs and attitudes in interprofessional socialization using the 24-item Interprofessional Socialization and Valuing Scale questionnaire using a 7-point scale (1= not at all ; 7= to a very great extent; "not applicable" response is also available). The score ranges from 24 to 168 with higher score indicating greater presence of the attributes measured.
Post-test (immediately after simulation training)
Follow-up (Change of Interprofessional Socialization and Valuing Scale from baseline and post-test)
Time Frame: Follow-up (2-months after simulation training)
Measurement of participants behaviors, beliefs and attitudes in interprofessional socialization using the 24-item Interprofessional Socialization and Valuing Scale questionnaire using a 7-point scale (1= not at all ; 7= to a very great extent; "not applicable" response is also available). The score ranges from 24 to 168 with higher score indicating greater presence of the attributes measured.
Follow-up (2-months after simulation training)
Pulse rate
Time Frame: Pre-test
Stress measurement parameter using a continuous monitoring smart watch
Pre-test
Pulse rate (Change of parameter from baseline)
Time Frame: Post-test (immediately after simulation training)
Stress measurement parameter using a continuous monitoring smart watch
Post-test (immediately after simulation training)
Blood pressure (diastolic & systolic)
Time Frame: Pre-test
Stress measurement parameter using a sphygmomanometer
Pre-test
Blood pressure (diastolic & systolic) (Change of parameter from baseline)
Time Frame: Post-test (immediately after simulation training)
Stress measurement parameter using a sphygmomanometer
Post-test (immediately after simulation training)
Baseline (State-Trait Anxiety Inventory)
Time Frame: Pre-test
Measurement of participants state anxiety were measured using the 20-items State-Trait Anxiety Inventory questionnaire using a 4 point likert scale (almost never-almost always). The score ranges from 20 to 80 with higher score indicating higher sense of anxiety.
Pre-test
Post-test (Change of State-Trait Anxiety Inventory from baseline)
Time Frame: Post-test (immediately after simulation training)
Measurement of participants state anxiety were measured using the 20-items State-Trait Anxiety Inventory questionnaire using a 4 point likert scale (almost never-almost always). The score ranges from 20 to 80 with higher score indicating higher sense of anxiety.
Post-test (immediately after simulation training)
Baseline (Confidence and self-efficacy)
Time Frame: Pre-test
Measurement of participants confidence and self-efficacy was measured using a 5-items self-efficacy questionnaire through a 10-point likert scale ranging from scores ranging from 5 to 50 with higher score indicating better self-efficacy in their ability in contributing to patient-centered care in a multidisciplinary team.
Pre-test
Post-test (Change of Confidence and self-efficacy from baseline)
Time Frame: Post-test (immediately after simulation training)
Measurement of participants confidence and self-efficacy was measured using a 5-items self-efficacy questionnaire through a 10-point likert scale ranging from scores ranging from 5 to 50 with higher score indicating better self-efficacy in their ability in contributing to patient-centered care in a multidisciplinary team.
Post-test (immediately after simulation training)
Baseline (Student Stereotype Rating)
Time Frame: Pre-test

Measurement of participants stereotype towards other health disciplines was measured using the 9-items Student Stereotype Rating Questionnaire through a 5-point Likert scale (1=very low to 5= very high).

The score ranges from 9 to 45 with higher scores indicating higher perceived ability of the particular healthcare discipline by the other discipline.

Pre-test
Post test (Change of Student Stereotype Rating from baseline)
Time Frame: Post-test (immediately after simulation training)
Measurement of participants stereotype towards other health disciplines was measured using the 9-items Student Stereotype Rating Questionnaire through a 5-point Likert scale (1=very low to 5= very high). The score ranges from 9 to 45 with higher scores indicating higher perceived ability of the particular healthcare discipline by the other discipline.
Post-test (immediately after simulation training)
Follow up (Change of Student Stereotype Rating from baseline and post test)
Time Frame: Follow-up (2-months after simulation training)
Measurement of participants stereotype towards other health disciplines was measured using the 9-items Student Stereotype Rating Questionnaire through a 5-point Likert scale (1=very low to 5= very high). The score ranges from 9 to 45 with higher scores indicating higher perceived ability of the particular healthcare discipline by the other discipline.
Follow-up (2-months after simulation training)

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

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)

July 1, 2018

Primary Completion (ACTUAL)

December 31, 2019

Study Completion (ACTUAL)

December 31, 2019

Study Registration Dates

First Submitted

March 26, 2020

First Submitted That Met QC Criteria

March 30, 2020

First Posted (ACTUAL)

April 2, 2020

Study Record Updates

Last Update Posted (ACTUAL)

April 3, 2020

Last Update Submitted That Met QC Criteria

April 1, 2020

Last Verified

April 1, 2020

More Information

Terms related to this study

Other Study ID Numbers

  • S-17-107

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

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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