AR training helps med students deliver better simulated births
NCT ID NCT07391085
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested whether an augmented reality (AR) training module helps medical and midwifery students perform better in simulated vaginal births. 389 students from Chile and Colombia were randomly assigned to either standard text/video preparation or the same plus an AR module. After training, all students completed a simulated birth, and their skills were scored by blinded evaluators. The goal was to see if AR could improve early competency in this critical skill.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Augmented reality training module
- What this could lead to
- If successful, this could point toward a scalable, low-cost way to improve hands-on training for medical students learning vaginal birth procedures.
- What could go wrong
- This is an educational study, not a clinical treatment trial. Results may not translate to real-world birth outcomes or apply to all training settings.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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389 people
The number who actually took part.
- Started
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Mar 2023
- Finished
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Dec 2024
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 65 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Undergraduate medical students or midwifery students enrolled in obstetrics and gynecology or women's health courses at the participating universities. * Enrollment in the corresponding academic cohort during the study period. * Age 18 years or older. * Willingness to participate and provision of informed consent. Exclusion Criteria: * Declined participation or withdrawal of consent. * Incomplete participation in the simulation session. * Incomplete or missing performance assessment data.
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As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Pontificia Universidad Católica de Chile
Santiago, Santiago Metropolitan, Chile