Can virtual reality help new mothers master breastfeeding?

NCT ID NCT07768527

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Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting This study
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
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 Results may not be published yet.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

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This status has not been confirmed recently, so it may be out of date.

First seen Aug 17, 2026 · Last updated Aug 18, 2026 · Updated 1 time

Summary

This study tests whether teaching new mothers about breastfeeding using virtual reality or hands-on simulation with mannequins can improve their breastfeeding skills and confidence. The trial will include first-time mothers who are experiencing breastfeeding problems shortly after giving birth. Participants will be randomly assigned to receive one of three types of education: virtual reality, simulation, or standard hospital care, and their breastfeeding success and continuation will be compared.

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 glasses or simulation with mannequins for breastfeeding education
What this could lead to
If effective, these training methods could offer new ways to support new mothers struggling with breastfeeding, potentially improving success rates and duration.
What could go wrong
The trial is relatively small and results may not apply to all mothers. The effectiveness of VR or simulation may vary, and it's unclear if benefits will last beyond the immediate postpartum period.

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

About 159 people

The number the study aims to enrol. It can still change while the study runs.

Expected to start

Sep 2026

An estimate. Start dates often move.

Expected to finish

Apr 2027

An estimate. End dates often move.

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 49 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: * Primiparous * Infant in the neonatal period * Over 18 years of age * Term delivery * Healthy baby and individual * No communication barriers * Willing to participate in the study * Able to read and write Turkish Exclusion Criteria: * Multiparous * Infant not in the neonatal period * Under 18 years of age * Premature delivery * Unhealthy baby and individual * No communication barriers * Unwilling to participate in the study * Unable to read and write Turkish

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As listed by the trial registrant

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How to take part

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