Parents take the syringe: a new way to feed premature babies
NCT ID NCT05313464
First seen Sep 10, 2026 · Last updated Sep 11, 2026 · Updated 1 time
Summary
Researchers are studying whether letting parents push their premature baby's tube feeding while holding the baby skin-to-skin improves the quality of early parent-child interactions. The trial enrolls 42 premature infants born before 30 weeks of pregnancy, along with their mothers and fathers. When the babies reach about 34 weeks of gestational age, researchers film 10-minute interactions and code behaviors like vocalizations, eye contact, and smiles. Parents also fill out questionnaires about their confidence and parenting skills.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- parent-pushed enteral feeding, where a parent gives their premature baby tube feeding while holding the baby skin-to-skin
- What this could lead to
- If it helps, hospitals could involve parents more directly in tube feeding their premature babies, which may support earlier bonding and more confident parenting.
- What could go wrong
- This is a small study of 42 babies in one hospital, so results may not apply everywhere. Filming early interactions cannot prove long-term effects on the parent-child relationship.
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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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42 people
The number who actually took part.
- Started
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Apr 2022
- Finished
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Aug 2026
- 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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30 to 32 weeks
- Sex
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Anyone
- Healthy volunteers
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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 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: Children born before 30 SA Age of child at start of study: 32 SA Exclusion Criteria: * Child with ongoing infection, neurological pathology More than one desaturation and/or bradycardia per hour within 12 last hours Balloon ventilation in last 12 hours * Medical contraindication to oral nutrition * Intubated child * Parents with a disabling mental illness * Parents not available * Minor parents * Parents under guardianship or protection of justice * Refusal to sign consent * Parents not affiliated with a social security system
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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.
Contacts and locations
Locations
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Centre Hospitalier Intercommunal Créteil
Créteil, Val-deMarne, 94000, France
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Other studies related to the condition(s) this trial covers.
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