Texts boost breast milk production in NICU moms
NCT ID NCT04097860
First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tested whether personalized text messages, including real-time breast milk sodium levels, could help mothers of critically ill infants pump more milk. 122 mothers participated. The goal was to see if this mobile health approach is feasible and increases milk volume.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- personalized text messages with breast milk sodium biomarker feedback
- What this could lead to
- If successful, this approach could help mothers of hospitalized infants produce more breast milk, supporting infant health.
- What could go wrong
- This was a small feasibility study with 122 participants, so results may not apply broadly. The intervention relies on daily text messaging, which may not suit all mothers.
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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122 people
The number who actually took part.
- Started
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Dec 2020
- Finished
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Sep 2025
- 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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18 years and older
- Sex
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Female participants only
- 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: * stated intent to provide BM to the infant * infant not expected to be stable enough to bottle/breastfeed for \> 14 days * owns a mobile phone with unrestricted SMS capability. * English speaking Exclusion Criteria: * known illicit drug use * breast reduction or augmentation * positive HIV status * does not anticipate being able to bring BM to the NICU at least 4X/week * infant not expected to live \> 7 days following delivery * COVID-19 positive
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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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UF Health Children's Hospital
Gainesville, Florida, 32610, United States
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