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Virtual Reality Training Simulator for Cesarean Section

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Seoul National University

Status

Completed

Conditions

Virtual Reality

Treatments

Other: virtual reality training for cesarean section

Study type

Interventional

Funder types

Other

Identifiers

NCT05604924
B-2205-759-303

Details and patient eligibility

About

The goal of this is to determine the effectiveness of virtual reality training simulator for cesarean section.

Evaluate the effect of using VR surgery on the self-confidence and knowledge of cesarean section procedures.

Full description

A single center randomized controlled trial (RCT) was performed. The participants were obstetrics residents, fellows and residents in other majors with limited experience in performing cesarean section. The primary outcome measures were the self-assessment scores of trainee confidence using a virtual reality training and an objective assessment of the cognitive skills. The participants were randomly divided into a study group of VR training group and a control group. Participants in the study group used the VR application. The control group participants used similar content in a standard PowerPoint presentation on a laptop.

Enrollment

150 patients

Sex

All

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Residents and fellows receiving training at Seoul National University Bundang Hospital and who wish to participate in this study

Exclusion criteria

  • If trainee refuse to participate in this study

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

150 participants in 2 patient groups, including a placebo group

Participants who received virtual reality training
Experimental group
Treatment:
Other: virtual reality training for cesarean section
Participants who received similar contents in a standard PowerPoint presentation on a laptop
Placebo Comparator group
Treatment:
Other: virtual reality training for cesarean section

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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