A Mother's lullaby and touch may soothe newborns during blood tests
NCT ID NCT07747649
First seen Aug 05, 2026 · Last updated Aug 06, 2026 · Updated 1 time
Summary
This trial tests whether combining breastfeeding, gentle stroking, a mother's singing, and eye contact can reduce pain in healthy newborns during a routine heel blood sample. About 72 newborns will be randomly assigned to receive this multisensory stimulation or to be held in their mother's arms as usual. Researchers will compare pain scores, crying time, heart rate, and oxygen levels between the two groups to see if this comforting approach makes the procedure less distressing.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Multisensory stimulation (breastfeeding, gentle stroking, maternal singing, and eye contact)
- What this could lead to
- If effective, this simple, drug-free approach could become a standard way to comfort newborns during routine blood tests, reducing pain and stress without medication.
- What could go wrong
- The trial is small and early, so results may not apply to all newborns or settings. The effect may vary with each baby's temperament and the mother's comfort with the technique.
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 72 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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Aug 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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1 day to 28 days
- Sex
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Anyone
- 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: * Healthy newborns aged 0-28 days * Newborns receiving routine monitoring and care with their mothers in the hospital's newborn care unit * Written informed consent provided by the newborn's parent or legal representative Exclusion Criteria: * Presence of any lower-extremity anomaly * Ongoing monitoring or treatment in the neonatal intensive care unit * Presence of a congenital disease
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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
2 sites. 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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Bitlis State Hospita
RECRUITINGBitlis, Bitlis, 60300, Turkey (Türkiye)
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Tatvan State Hospital
RECRUITINGAnkara, Beşevler, 60300, Turkey (Türkiye)