Hypnobreastfeeding: a new way to calm High-Risk pregnancies?
NCT ID NCT07281339
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
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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
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About 68 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Oct 2025
- Expected to finish
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Jun 2026
An estimate. End dates often move.
- Lead sponsor
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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
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Children (under 18), adults (18 to 64) and older adults (65 and over)
- Sex
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Female participants only
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide 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.
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.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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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
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Amasya University
RECRUITINGAmasya, 05000, Turkey (Türkiye)
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Other studies related to the condition(s) this trial covers.
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