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Acupressure lessons may boost breastfeeding success

NCT ID NCT07410949

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 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

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 360 people

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

Started

Apr 2026

Expected to finish

Feb 2027

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 to 45 years

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: * 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.

Breast Feeding lactation disease

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

  • Niğde Ömer Halisdemir University Hospital

    RECRUITING

    Niğde, Merkez, 51240, Turkey (Türkiye)

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