Enhancing Clinical and Cultural Virtual Encounter in Health Professional Students: 3 Is (Internationalization, Innovation, Interdisciplinary) in Action (3I in action)

March 27, 2025 updated by: Chan Siu Ling, The University of Hong Kong
This is a cross-over randomized control study with 3 time-points' measurement. This study is mainly to evaluate if the online pedagogic innovative learning modules could benefit students through their interprofessional and intercultural virtual encounters, with a focus on assessing their cultural awareness, interprofessional attitude and online learning engagement.

Study Overview

Status

Completed

Intervention / Treatment

Detailed Description

This study aims to promote and implement internationalization, innovative and intedisciplinary teaching and learning strategies through the set up of online modules of selected topics of interest. The specific objectives are: :

To enhance the educational outcomes of students from respective health disciplines in interdisciplinary learning via case-based clinical scenarios adopted in the online modules; To develop internationalization experience among students of different countries in terms of intercultural learning through the cultural exchange; To assess level of students' empowerment in active learning via 'student-as-partner' initiatives in the cultural exchange; To evaluate the effectiveness of online learning engagement among students through participating in the online modules.

Based on the Phase of Engagement Framework, two online orthopaedic modules focusing on interprofessional and intercultural educations on low back pain (LBP) and adolescent idiopathic scoliosis (AIS) are developed. The students (n=104) are randomized into two groups using SNOSE. In the first module, one group receives a virtual reality (VR)-enhanced LBP education (intervention group), while the other group engages with a case study on LBP (control group). After a 3-week washout period, the groups cross over: the intervention group receives the VR-enhanced education on AIS, and the control group focuses on an AIS case study. Interprofessional learning experience, cultural awareness, and online learning engagement are measured using validated tools at three time points (baseline, after first and second modules).

Study Type

Interventional

Enrollment (Actual)

104

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

      • Hong Kong, Hong Kong, 852
        • 5/F, Academic Building, 3 Sassoon Road

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

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • undergraduate healthcare students

Exclusion Criteria:

  • cannot communicate in English

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: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Virtual Reality Group
Based on the Phase of Engagement Framework, two online orthopaedic modules focusing on interprofessional and intercultural educations on low back pain (LBP) and adolescent idiopathic scoliosis (AIS) were developed. The students (n=104) were randomized into two groups. In the first module, the Virtual Reality Group as the intervention group received a virtual reality (VR)-enhanced LBP education, while the Case-based Learning Group as the control group engaged with a case study on LBP. After a 3-week washout period, the groups crossed over: the the Virtual Reality Group as the intervention group received the VR-enhanced education on AIS, and the Case-based Learning Group as the control group focused on an AIS case study.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Students' Perceptions of Interprofessional Clinical education - Revised
Time Frame: 2 months
Using Students' Perceptions of Interprofessional Clinical Education-Revised (SPICE-R) as the tool to measure the increased level of interprofessional learning experiences. The SPICE-R instrument includes ten items, and is divided into three factors: interprofessional teamwork and team-based practice (items 1, 5, 6, 8, 9 and 10), roles/responsibilities for collaborative practice (items 2 and 7), and patient outcomes from collaborative practice (items 3 and 4). It is a 5-point Likert scales (1 = 'strongly disagree' and 5 = 'strongly agree') with score ranging from 10-50. SPICE-R was chosen for its strong psychometric properties including reliability and construct validity (Dominguez et al., 2016; Lockeman et al., 2017). The instrument has high composite reliability at 0.84, indicating strong validity based on established criteria. Higher score on SPICE-R reflect more positive interprofessional experiences.
2 months

Collaborators and Investigators

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

September 1, 2022

Primary Completion (Actual)

August 31, 2023

Study Completion (Actual)

August 31, 2023

Study Registration Dates

First Submitted

March 20, 2025

First Submitted That Met QC Criteria

March 27, 2025

First Posted (Actual)

April 4, 2025

Study Record Updates

Last Update Posted (Actual)

April 4, 2025

Last Update Submitted That Met QC Criteria

March 27, 2025

Last Verified

March 1, 2025

More Information

Terms related to this study

Other Study ID Numbers

  • HKWC-2022-389
  • 899 (Other Grant/Funding Number: HKU)

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

product manufactured in and exported from the U.S.

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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