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Clinical Trials/NCT07711873
NCT07711873CompletedNot Applicable

Virtual Reality-based Training for Safe Medication Administration Among Nursing Students: a Randomized Wait-list Crossover Trial

University of Medicine and Pharmacy at Ho Chi Minh City1 site in 1 country60 target enrollmentStarted: November 25, 2024Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
60
Locations
1
Primary Endpoint
Confidence in medication administration

Study Overview

Brief Summary

This study evaluated a virtual reality-based training programme designed to support safe medication administration among undergraduate nursing students. Medication administration is a core nursing competency, but students often have limited opportunities to practise medication safety scenarios repeatedly before entering clinical settings. Virtual reality provides an immersive and repeatable simulated environment for practising routine, high-alert, and semi-emergency medication administration scenarios without risk to patients.

Third- and fourth-year undergraduate nursing students at a healthcare university in Ho Chi Minh City, Vietnam, were randomly allocated to two groups. Group A received the VR training first, while Group B served as a wait-list comparison group and received the same training later, after crossover. The intervention consisted of three 90-minute sessions, each including pre-briefing, immersive VR simulation, and PEARLS-informed debriefing. Outcomes included confidence in medication administration, self-reported safe medication practice, system usability, and cybersickness symptoms.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Crossover
Primary Purpose
Health Services Research
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Enrolled as a third- or fourth-year undergraduate nursing student during the study period
  • Aged 18 years or older

Exclusion Criteria

  • Health condition contraindicating virtual reality use
  • On academic leave during the study period
  • Unable to attend the scheduled study sessions

Outcomes

Primary Outcomes

Confidence in medication administration

Time Frame: Baseline (before any training); approximately 5 weeks after baseline (about 1 week after Group A completed VR training, while Group B remained on the wait-list); approximately 3 months after baseline (about 1 week after Group B completed VR training).

Confidence in medication administration was measured using a 6-item self-report scale. Each item was rated from 1 (not at all confident) to 5 (extremely confident). Total scores range from 6 to 30, with higher scores indicating greater confidence.

Secondary Outcomes

  • Self-reported safe medication practice(Baseline (before any training); approximately 5 weeks after baseline (about 1 week after Group A completed VR training, while Group B remained on the wait-list); approximately 3 months after baseline (about 1 week after Group B completed VR training).)
  • System usability(Approximately 1 week after each group completed VR training (approximately 5 weeks after baseline for Group A and approximately 3 months after baseline for Group B).)
  • Cybersickness symptoms(Approximately 1 week after each group completed VR training (approximately 5 weeks after baseline for Group A and approximately 3 months after baseline for Group B).)

Investigators

Sponsor
University of Medicine and Pharmacy at Ho Chi Minh City
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Thi Phuong Lan Nguyen

Senior lecturer, School of Nursing and Medical Technology

University of Medicine and Pharmacy at Ho Chi Minh City

Study Sites (1)

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