Virtual reality peek at your baby during labor: a new way to ease childbirth?

NCT ID NCT07793136

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Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
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Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Aug 28, 2026 · Last updated Aug 28, 2026

Summary

This trial tests whether first-time mothers who view their own fetal ultrasound images through a virtual reality headset during labor feel more comfortable and less traumatized by childbirth. The study will include 114 pregnant women at 28-32 weeks of gestation. Half will watch their personalized fetal images with fetal heart sounds for at least four minutes during early labor, while the other half receives standard care. Researchers will measure childbirth comfort, maternal attachment, and perceived traumatic childbirth to see if this simple intervention makes a difference.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
Virtual reality viewing of personalized fetal ultrasound images with fetal heart sounds during labor
What this could lead to
If it works, this could offer a simple, drug-free way to improve childbirth comfort and mother-baby bonding, and reduce the emotional trauma of labor.
What could go wrong
This is a small, early-stage trial, so results may not apply to all women. The effect may be modest, and some women might find the VR headset uncomfortable during labor.

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

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

114 people

The number who actually took part.

Started

Jan 2026

Finished

Apr 2026

Lead sponsor

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

18 to 35 years

Sex

Female participants only

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

Show 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: * Pregnant women aged 18 years or older * Primiparous women * Gestational age of 28-32 weeks at the time of eligibility assessment * Singleton pregnancy * Able to communicate in Turkish * Willing to participate in the study * Able to provide written informed consent for study participation and recording of personalized fetal ultrasound images. Exclusion Criteria: * Indication for elective cesarean delivery * Visual or hearing impairment that could interfere with the intervention * Maternal or fetal medical complications * Pregnancy conceived through assisted reproductive techniques

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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

  • Selcuk University

    Konya, Turkey (Türkiye)

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