Virtual Reality Training for Obstetric and Neonatal Care Quality
What You Need to Know Before You Apply
What is the purpose of this trial?
This study will test a new virtual reality (VR) Indigenous cultural safety training designed for hospital nurses attending births and caring for sick babies. The training (study Arm #1) includes two one-hour sessions that each include a VR encounter with a virtual Indigenous patient. This will compared to two one hour sessions of unrelated online clinical training (study Arm #2). Participant nurses will be randomly put into one of these two study arms. The study team will then assess whether or not the training improved Indigenous patient care outcomes using live Indigenous actors performing as patients. Participating nurses will be scheduled to assess these mock patients 10-12 weeks after their training. The quality of care they provide during these mock patient encounters will be rated using standard scales. They study hypothesis is that nurses who take the virtual reality Indigenous patient encounter training will have better relational engagement and provide higher quality clinical care during the Indigenous standardized patient encounter compared to nurses who were randomized to the unrelated clinical online training.
Who Is on the Research Team?
Janet Smylie, MD MPH
Principal Investigator
Unity Health Toronto, University of Toronto
Are You a Good Fit for This Trial?
This trial is for hospital nurses who work with mothers giving birth or care for sick newborns. Nurses must be able to participate in two one-hour training sessions and follow-up assessments. There are no other specific inclusion or exclusion criteria listed.Inclusion Criteria
Exclusion Criteria
What Are the Treatments Tested in This Trial?
Interventions
- Virtual Reality Indigenous Cultural Safety Training
Trial Overview
The study compares a new virtual reality Indigenous cultural safety training (with VR patient encounters) to standard online clinical education on unrelated topics. Nurses are randomly assigned to either group, and their skills are assessed about 10-12 weeks later using mock patient scenarios.
How Is the Trial Designed?
2
Treatment groups
Experimental Treatment
Placebo Group
Participants randomized into Arm #1 will receive virtual reality Indigenous cultural safety education. The intervention consists of two sessions over a two-week period. Each session will take approximately one hour and will each include an orientation to the VR technology, a 15-minute interactive virtual reality patient care scenario, and a facilitated debrief. The timing and repetition of the sessions is consistent with adult learning pedagogies and VR re-enforcement psychology.
Participants randomized into Arm #2 will complete a time-matched online clinical education session on a topic unrelated to Indigenous cultural safety (ICS). These sessions will be hosted concomitantly with VR training sessions. Facilitators will be present during these sessions to support set-up. Similar to the intervention, two sessions will be held one week a part (time matched to intervention). The content will be on a subject matter relevant to participant nurses that is unrelated to ICS. We will provide a range of online control training materials for participants to choose from that will appeal to nurse participants across clinical units (labour \& delivery, postpartum, and neonatal intensive care nursing).
Find a Clinic Near You
Who Is Running the Clinical Trial?
Unity Health Toronto
Lead Sponsor
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