Can parenting coaching stop childhood overweight before it starts?
NCT ID NCT07823582
First seen Sep 16, 2026 · Last updated Sep 17, 2026 · Updated 1 time
Summary
Researchers are testing whether a telehealth parenting program can help prevent early childhood overweight in rural, low-income families. The study enrolls 328 first-time mothers and their infants who receive WIC services in Pennsylvania. Families are randomly assigned to different combinations of coaching on sleep, soothing, play, infant signing, and mindfulness. The goal is to learn which combination works best for healthy growth through age 2.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- A telehealth parenting program that coaches parents on infant sleep, soothing, play, signing, and mindfulness
- What this could lead to
- If it works, this could give WIC and similar programs a practical, low-cost way to help families prevent early childhood overweight.
- What could go wrong
- The trial tests several parenting strategies at once, so it may not show which parts matter most. Overweight risk depends on many factors beyond parenting, and results in this group may not apply to everyone.
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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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About 328 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Jan 2027
An estimate. Start dates often move.
- Expected to finish
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Dec 2032
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 years and older
- 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.
Infant inclusion criteria: * Singleton * Born at ≥37 weeks gestation. * Birthweight at or above the 50th percentile for gestational age and sex. Mother inclusion criteria: * Age 18 years or older * Pregnant in the third trimester (at recruitment)/≤1 month postpartum (at enrollment) * Participating in the Pennsylvania Special Supplemental Nutrition Program for Women, Infants, and Children (WIC) at a participating site * First-time mother (primiparous) * English-speaking * Willing and able to provide informed consent and participate in study procedures through the child's age of 24 months. Infant exclusion criteria: * Multiple gestation (e.g., twins, triplets) * Born \<37 weeks gestation * Birthweight below the 50th percentile for gestational age and sex * Medical conditions, congenital anomalies, genetic disorders, or chronic health conditions that may substantially affect growth, feeding, development, or participation in study activities. * Participation in another study that, in the opinion of the investigators, could interfere with study outcomes or participation. Mother exclusion criteria: * Age less than 18 years * Unable to communicate in English * Medical, psychiatric, cognitive, or developmental conditions that, in the opinion of the investigators, would interfere with participation in the intervention or completion of study procedures. * Plans to relocate outside the service area of participating WIC clinics during the 24-month study period. * Inability or unwillingness to provide informed consent. * Participation in another study that, in the opinion of the investigators, could interfere with study outcomes or participation.
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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 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.
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