← Eichor
Study identifier: NCT06653270 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Virtual Reality Birth Simulator

Condition: Medical Education · Normal Vaginal Delivery · Simulation Training  ·  Sponsor: National University Hospital, Singapore

PhaseNA
Planned participants300
Who can joinAll sexes, 18 Years to 50 Years
Healthy volunteersYes

About this study

The investigators compared an in-house developed virtual reality simulator for normal vaginal deliveries with a legacy mannequin-based simulation in a cluster randomised study involving Year 4 medical students undergoing their Ob/Gyn clerkship with aims to compare pre- and post-simulation knowledge questionnaire score. As part of a cross-over component, the investigators will also compare feedback scores for each modality and the preferred modality. Ethical approval and waiver of consent has been obtained from the National University of Singapore Institutional Review Board, Reference Number 2020-606.

This description comes directly from the study's public registry record.

Talk to the study team

Arundhati Gosavi, MBBS, DGO, MRCOG  ·  656-772-5555  ·  arundhati_gosavi@nuhs.edu.sg

Always discuss trial participation with your own doctor first.

Locations (1)

Yong Loo Lin School of Medicine, National University of SingaporeSingapore, SingaporeRecruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT06653270