Lullaby bath time: a simple song to soothe postpartum blues?

NCT ID NCT07370025

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Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting This study
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
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Paused for now. It may or may not start again.
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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 Results may not be published yet.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)

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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

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First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study tests whether mothers singing lullabies while bathing their newborns can strengthen bonding, reduce postpartum depression symptoms, and boost parenting confidence. About 98 healthy mothers and their full-term babies will take part. Half will bathe their baby three times a week for two weeks while singing a lullaby; the other half will follow standard care. Researchers will measure bonding, mood, and confidence before and after the two weeks.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
maternal lullaby singing during infant bathing
What this could lead to
If it works, this could offer a simple, low-cost way to help new mothers bond with their babies, feel less depressed, and gain confidence in parenting.
What could go wrong
This is a small, early-stage trial with only 98 participants and a short two-week intervention. Results may not apply to all mothers, and the effect may be small or hard to measure.

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 98 people

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

Expected to start

May 2026

An estimate. Start dates often move.

Expected to finish

Jan 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 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: * Mothers who have had an uncomplicated pregnancy and delivery * Mothers who are healthy enough to care for their baby * Mothers who have suitable conditions at home to bathe their baby * Babies born at term (≥ 37 weeks of gestation) and with stable general health after birth Exclusion Criteria: * Mothers with a history of serious postpartum complications (such as postpartum hemorrhage) * Mothers diagnosed with psychiatric illness * Mothers who are unable to participate directly in the care of their baby (due to severe disability, mandatory bed rest, etc.) * Mothers who cannot participate in the lullaby program due to hearing impairment * Infants who experience serious respiratory, cardiac, or neurological problems at birth or thereafter, who have a skin disease or dermatological condition that limits bathing, who have a history of admission to the neonatal intensive care unit, or who have a chronic disease or congenital anomaly

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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

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  1. The places running it

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  2. The official record

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Contacts and locations

Locations

  • Istanbul University - Cerrahpasa

    Istanbul, Turkey (Türkiye)

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