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Mindfulness boosts breast milk and reduces stress for NICU moms

NCT ID NCT07346339

Symptom relief Sponsor: Cukurova 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
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 This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Jul 01, 2026 · Updated 2 times

Summary

This study tested whether a sensory mindfulness technique could help mothers of babies in the neonatal intensive care unit (NICU) produce more breast milk and feel better. 60 mothers who were pumping milk for their hospitalized infants took part. The approach involved mindfulness training and using a hat worn by the baby to enhance connection. The goal was to reduce stress and improve milk production and overall well-being.

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

60 people

The number who actually took part.

Started

Sep 2025

Finished

Dec 2025

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 65 years

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

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 * Having an infant hospitalized in the neonatal intensive care unit * Expressing breast milk for the infant * Having a term newborn * Not having twins * Having no health condition that would prevent participation in the study * Being able to speak Turkish * Volunteering to participate in the research. Exclusion criteria * Missing two or more intervention sessions * Leaving more than 5% of the questionnaire's incomplete * The newborn having a high risk of morbidity or mortality * The presence of a congenital malformation in the newborn * Undergoing a surgical procedure during the study period * Having a history of a physical or mental condition that could hinder participation or receiving psychological treatment before or during the intervention. Termination criteria * The participant expressing a wish to withdraw from the study at any stage * Inability to complete the data collection protocol due to the end of the newborn's NICU hospitalization (discharge, transfer etc.) * Failure to maintain adherence to the research protocol (e.g., inability to complete planned milk expression records or scale administrations) * The development of a clinical condition during the study that prevented participation in the intervention or assessments (e.g., an acute health problem, treatment requiring sedation, or the need for intensive medical intervention) * A determination by the research team that continuation was not appropriate in terms of safety or data integrity.

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Conditions

The condition(s) this trial relates to.

Breast Milk Expression perinatal disease

As listed by the trial registrant

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

Breast milk collection Mi̇ndfulness Newborn diseases Well being

Contacts and locations

Locations

  • Balcalı Hastanesi

    Adana, Sarıçam, 01331, Turkey (Türkiye)

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