Acupressure lessons may boost breastfeeding success
NCT ID NCT07410949
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests whether teaching new mothers how to do acupressure on themselves can help them breastfeed exclusively for longer. 360 mothers will either get standard care or also learn acupressure within 48 hours after giving birth. Researchers will track breastfeeding rates at 6 and 12 months.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- acupressure education program
- What this could lead to
- If it works, this could offer a simple, drug-free way to help more mothers breastfeed exclusively for longer.
- What could go wrong
- This is a small, early-stage study. Acupressure is self-administered, so results depend on how consistently participants follow the routine at home.
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 360 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Apr 2026
- Expected to finish
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Feb 2027
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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18 to 45 years
- 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: * Age 18 to 45 years * Term singleton birth (≥37 weeks of gestation) * ≤48 hours postpartum at the time of enrollment * Intention to breastfeed * Ability to communicate in Turkish * Access to a smartphone for educational materials and follow-up reminders * Willingness to provide written informed consent Exclusion Criteria: * Contraindications to breastfeeding (e.g., infant galactosemia) * Severe neonatal condition preventing breastfeeding * Severe maternal medical or psychiatric condition interfering with breastfeeding * Current opioid, alcohol, or substance dependence * Multiple gestation pregnancy * Severe breast injury or condition within the first 72 hours postpartum preventing breastfeeding
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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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Niğde Ömer Halisdemir University Hospital
RECRUITINGNiğde, Merkez, 51240, Turkey (Türkiye)
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