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Video lessons may ease breastfeeding anxiety in new moms

NCT ID NCT07705932

Symptom relief Sponsor: Bilecik Seyh Edebali Universitesi Source: ClinicalTrials.gov ↗

What the study statuses mean

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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 Results may not be published yet.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

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This status has not been confirmed recently, so it may be out of date.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 Jul 15, 2026 · Last updated Jul 24, 2026 · Updated 3 times

Summary

This study tests whether video-based education can reduce anxiety, correct myths, and boost motivation in first-time mothers. Pregnant women between 32 and 36 weeks will receive three educational video modules via WhatsApp alongside routine care. The goal is to see if this technology-supported approach improves their breastfeeding experience.

What this could mean

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

Active substance
Video-Assisted Breastfeeding Education
What this could lead to
If effective, this approach could offer a simple, scalable way to support first-time mothers and improve breastfeeding outcomes.
What could go wrong
This is a small, single-site trial, so results may not apply broadly. The intervention relies on self-directed video watching, which may not suit all participants.

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 80 people

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

Expected to start

Aug 2026

An estimate. Start dates often move.

Expected to finish

Dec 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 years and older

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: * Women aged 18 years or older. * Primiparous pregnant women. * Gestational age between 32 and 36 weeks. * Planning to breastfeed after delivery. * Singleton pregnancy. * Able to read and write in Turkish. * Using WhatsApp. * Willing to participate and provide written informed consent. Exclusion Criteria: * High-risk pregnancy or serious obstetric complications. * Newborns with serious congenital anomalies or medical conditions requiring treatment and separation from the mother (e.g., dysphagia). * Mothers with severe nipple abnormalities that may prevent breastfeeding. * Withdrawal of informed consent at any stage of the study.

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Conditions

The condition(s) this trial relates to.

anxiety anxiety disorder Breast Feeding

As listed by the trial registrant

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

Anxiety Breast feeding

How to take part

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  1. 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.

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