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Immersive Virtual Reality (IVR) Procedure (IVR-P)

N

National University of Singapore

Status

Completed

Conditions

Procedure

Treatments

Procedure: IVR-Procedure
Procedure: Nursing Clinical Laboratory practice

Study type

Interventional

Funder types

Other

Identifiers

NCT06396572
IVR-Procedure

Details and patient eligibility

About

A pilot randomised controlled trial to assess the nursing students' learning outcomes of the urinary catheterisation procedure by comparing the immersive virtual reality (IVR) to traditional lab sessions.

Full description

Design: A pilot randomised controlled trial was employed to assess the learning outcomes of the urinary catheterisation procedure by comparing the immersive virtual reality (IVR) intervention to traditional lab sessions.

Eligibility: Second-year undergraduate nursing students (n = 200) enrolled into the module NUR2125 (Pathophysiology, Pharmacology and Nursing Practice II) were invited to participate in the study.

Setting: The study was conducted at a university in Singapore from January to April 2023.

Procedure: Ten lab groups of second-year undergraduate nursing students were invited to participate in the study. They received the standard blended learning activities, which included clinical lab sessions and videos on the urinary catheterisation procedure. Out of the ten groups, four groups were randomly allocated to the IVR intervention group, and another four groups were randomly assigned to the waitlist control group (traditional lab sessions).

  1. For the intervention group (IVR), the students used the IVR device for practice in class under the supervision of their tutor. They then loaned the IVR device for two weeks for home practice.
  2. For the waitlist control group (traditional lab sessions), they learned and practiced the urinary catheterisation procedure in class. Students received the additional intervention (using the IVR device for home practice) after the collection of post-test data.

Data collection: Prior to lab practice, each participant completed a demographic survey and a set of pre-test questionnaires on personality inventory, cognitive load, and representation of VR in education. Only students who voluntarily joined the programme were recruited into the study.

The participants completed the post-test questionnaires in March 2023 prior to their formative clinical assessment.

Enrollment

93 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Year 2 Nursing students enrolled in the PPNP2 module

Exclusion criteria

  • Students who declined to participate

Trial design

Primary purpose

Health Services Research

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

93 participants in 2 patient groups

Immersive Virtual Reality
Experimental group
Description:
The Participants used Immersive Virtual Reality for learning and practice urinary catheterisation procedure
Treatment:
Procedure: IVR-Procedure
Nursing clinical laboratory
Active Comparator group
Description:
The Participants used a traditional nursing clinical laboratory for face to face learning and practice urinary catheterisation procedure
Treatment:
Procedure: Nursing Clinical Laboratory practice

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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