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Scan to bond: could QR codes boost confidence in new moms?

NCT ID NCT07763041

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
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 Results may not be published yet.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
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This status has not been confirmed recently, so it may be out of date.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 Aug 13, 2026 · Last updated Aug 14, 2026 · Updated 1 time

Summary

This trial tests whether a special infant care training program, supported by QR codes and a mobile app, can help first-time mothers feel more confident and attached to their babies after a NICU stay. Mothers in the intervention group receive face-to-face training, a guide with QR codes linking to videos, and app access, while others get standard care. The study measures maternal confidence, attachment, and infant health at discharge and at one and three months after.

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-supported infant care education, including face-to-face training, a printed guide with QR codes to videos, and a mobile app
What this could lead to
If effective, this approach could improve maternal confidence and attachment, and potentially enhance infant health outcomes after NICU discharge.
What could go wrong
This is a small, early-stage trial, and results may not apply broadly. The intervention depends on digital literacy and smartphone access, which could limit its use.

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

84 people

The number who actually took part.

Started

Jun 2025

Finished

Feb 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 years and older

Sex

Female participants only

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

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 mothers with a singleton birth, * Aged 18 years or older, * Able to read and communicate in Turkish, * Owning a smartphone with internet access and having sufficient digital literacy to use QR code applications, * No diagnosed psychiatric disorder, * Mothers whose infants had been hospitalized in the neonatal intensive care unit for at least one month, * Willing to participate and providing written informed consent, * Infants with a gestational age of ≥34 weeks, * Infants without life-threatening congenital, neurological, gastrointestinal, or genetic disorders requiring surgical intervention or expected to affect long-term prognosis. Exclusion Criteria: * Mothers who did not continue in the post-discharge follow-up period, * Participants whose mother or infant died (exitus) during the study period.

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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

  • Lokman Hekim University Ankara Hospital

    Ankara, Turkey (Türkiye)