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Can hypnosis help new moms breastfeed better? study investigates

NCT ID NCT07461428

Knowledge-focused Sponsor: Ankara Yildirim Beyazıt University 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
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Sep 02, 2026 · Updated 2 times

Summary

This study tests a special education program for first-time mothers that combines hypnosis techniques with breastfeeding information. The goal is to see if it helps mothers feel more confident and motivated to breastfeed. About 80 healthy pregnant women will take part, and researchers will measure their knowledge, self-efficacy, and motivation before and after the program.

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.

Started

May 2025

Expected to finish

Aug 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: * • Aged 18 years or older, * At least primary school graduates, * Between 27 and 28 weeks of gestation, * Primiparous, * Without high-risk pregnancies (e.g., gestational diabetes, epilepsy, preeclampsia, multiple pregnancy, etc.), * Without pre-existing health conditions prior to pregnancy (e.g., diabetes mellitus, hypertension, renal failure, epilepsy, etc.), * Without diagnosed psychiatric disorders (e.g., anxiety, mood disorders, depression, bipolar disorder, etc.), * Willing to participate voluntarily in the prenatal education program, * Not previously enrolled in a structured breastfeeding education program, * Turkish-speaking and without any communication barriers (e.g., cognitive, hearing, or visual impairments), * Not a member of a health sciences profession, and * Having access to the internet, a computer, or a smartphone. Exclusion Criteria: * • Incomplete completion of data collection forms, * Withdrawal from participation in the study, * Failure of pregnant women in the intervention group to fully participate in the educational program, * Lack of internet access, * Prior participation in a structured breastfeeding education program, * Discontinuation of breastfeeding by the mother after delivery, and * Any circumstances that would prevent the breastfeeding process or require mother and infant to be separated.

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As listed by the trial registrant

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

Breastfeeding Breastfeeding education Breastfeeding motivation Breastfeeding self-efficacy Healthy Healthy controls Healthy subjects Hypno-breastfeeding education Hypnobreastfeeding Information motivation behavioral skills model Pregnancy

How to take part

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

  1. The places running it

    2 sites. 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

  • Ankara Yildirim Beyazit Üniversitesi Esenboğa Külliyesi

    Ankara, Esenboğa, 06010, Turkey (Türkiye)

  • Sivas Cumhuriyet Üniversitesi Sağlik Hizmetleri Uygulama Ve Araşturma Hastanesi

    Sivas, Merkez, 58140, Turkey (Türkiye)

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