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Hypnobreastfeeding: a new way to calm High-Risk pregnancies?

NCT ID NCT07281339

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now This study
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
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 25, 2026 · Last updated Jun 27, 2026 · Updated 2 times

Summary

This study tests whether hypnobreastfeeding education can reduce anxiety and improve breastfeeding in high-risk pregnant women. Researchers will compare 34 women who receive the training with 34 who do not, measuring anxiety, breastfeeding intentions, and how well they adapt to breastfeeding after birth. The goal is to see if this simple, non-drug approach can make a difference for mothers and babies.

What this could mean

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

Active substance
Hypnobreastfeeding education
What this could lead to
If it works, this could offer a simple, drug-free way to lower anxiety and support breastfeeding for high-risk pregnant women.
What could go wrong
This is a small, early-stage study with only 68 participants. Results may not apply to all women, and the effect may be small or not statistically significant.

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 68 people

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

Started

Oct 2025

Expected to finish

Jun 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

Children (under 18), adults (18 to 64) and older adults (65 and over)

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: * High-risk primiparous pregnant women * Those with 28-34 weeks of pregnancy * Those who volunteered to participate in the study * Those who can read and write Turkish Exclusion Criteria: * Those with communication disabilities * Those with psychiatric and mental illnesses * Those who have an obstacle to breastfeeding * Those who have previously attended a birth preparation class * Those who receive breastfeeding-related training and consultancy * Those who gave birth prematurely * Those with anomalies in their babies

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Conditions

The condition(s) this trial relates to.

anxiety disorder Breast Feeding

As listed by the trial registrant

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

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

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

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. A doctor treating you

    A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.

Contacts and locations

Locations

  • Amasya University

    RECRUITING

    Amasya, 05000, Turkey (Türkiye)

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