Simple training may cut Babies' chemical exposure
NCT ID NCT07349927
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tests whether giving parents a short video and brochure about endocrine disruptors (chemicals in everyday products) can lower the levels of these chemicals in their babies' urine. About 90 newborns and their parents will be split into two groups: one gets the training, the other does not. Researchers will measure changes in urinary phthalate levels over one month to see if the training makes a difference.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Training video and brochure on reducing exposure to endocrine disruptors
- What this could lead to
- If successful, this could show that simple parental education can lower infants' exposure to harmful chemicals, informing future public health strategies.
- What could go wrong
- This is a small pilot study with only 90 participants, so results may not apply broadly. The intervention is brief, and actual exposure reduction may be minimal 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
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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 90 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Mar 2026
- Expected to finish
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Jun 2027
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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0 to 5 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: * Newborns born at the Bron hospital after 37 weeks of amenorrhea * Eutrophic * Affiliated to a social security scheme or beneficiary of a similar scheme * Consent signed by parents Exclusion Criteria: * Congenital anomaly diagnosed antenatally or postnatally * Parents who do not speak French
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Genom att skicka in godkänner du våra Användarvillkor
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
1 site. 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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Service de gynécologie obstétrique, Hôpital Femme-Mère-Enfant
RECRUITINGBron, 69677, France