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QR code tour of delivery room aims to ease childbirth fears in First-Time mothers

NCT ID NCT07496879

Symptom relief Sponsor: Ataturk University Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

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 This study
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 Results may not be published yet.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

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study tests whether giving first-time mothers a virtual tour of the delivery room through QR codes can reduce their fear of childbirth, increase readiness, and improve vaginal birth rates and breastfeeding confidence. One hundred pregnant women between 28-32 weeks will watch three short videos about admission, the labor room, and postpartum care. Researchers will measure fear, readiness, and self-efficacy using standard questionnaires before and after the intervention.

What this could mean

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

Active substance
QR code-based virtual tour videos of the delivery room
What this could lead to
If it works, this could offer a simple, low-cost way to help first-time mothers feel less afraid and more prepared for childbirth.
What could go wrong
This is a small, early-stage study with only 100 participants, so results may not apply to all women. The intervention is just videos, so it may not reduce fear for everyone.

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 100 people

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

Started

Jan 2026

Expected to finish

May 2026

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 45 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: * Being literate * Being 18 years of age or older * Being primigravida * Being between 28-32 weeks of gestation * Owning a smartphone * Having internet access * Being able to speak and understand Turkish Exclusion Criteria: * Multiparity * High-risk pregnancy * Having a diagnosed psychiatric disorder Failure to complete the questionnaires during the study period Preterm birth or pregnancy loss before completion of the study

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As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Childbirth readiness Fear of childbirth Primiparous women Vaginal birth rate

How to take part

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  1. The places running it

    1 site. The list below names each one and where it is.

  2. The official record

    The full official record for this study. This one lists no contact details, but it is the first place any would appear.

    Open the record ↗

  3. A doctor treating you

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Contacts and locations

Locations

  • Atatürk University - Faculty of Health Sciences, Department of Midwifery

    Erzurum, Yakutiye, 25030, Turkey (Türkiye)

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