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Home visits aim to boost healthy eating in at-risk kids

NCT ID NCT03003117

Prevention Sponsor: French Red Cross Source: ClinicalTrials.gov ↗

What the study statuses mean

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Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Sep 10, 2026 · Updated 2 times

Summary

This study tests a home-visit program for 800 pregnant women from disadvantaged backgrounds. The program teaches healthy eating, lifestyle, and feeding practices to help their children grow well. Researchers will measure how often kids eat vegetables at age 2 and track breastfeeding rates.

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

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

607 people

The number who actually took part.

Started

Apr 2017

Finished

Aug 2026

Lead sponsor

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

18 years and older

Sex

Female participants only

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

Show 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: * Pregnant woman at her 3rd term of pregnancy * Healthy * Aged ≥ 18 years * From a socially disadvantaged background * Living in Lille, Lomme, Loos, Faches-Thumesnil, Ronchin, Hellemmes, Haubourdin, La Madeleine, Lambersart, Mons-en-Baroeul, Saint-André-Lez-Lille, Wattignies, Villeneuve-d'Ascq, Marcq-en-Barœul or Wasquehal; or in the Valenciennes conurbation. * Willing and able to sign informed consent * Who, in the Investigator's judgement, is able to comply with the protocol or study procedures (including French speaking) * If twins are born from this pregnancy, only one will be randomly selected for inclusion Exclusion Criteria: * Pregnant woman under guardianship * Participation in any other interventional clinical trial that is not compatible with the participation into the ECAIL study * No permanent mailing address * Housed in emergency accommodation centres, hotels, movable dwellings or homeless * Planning to move outside the study area prior to the child's first birthday * Serious illness during pregnancy that could interfere with optimal participation in the ECAIL study * Hard drug consumption * Multiple pregnancy (≥3 foetuses).

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Conditions

The condition(s) this trial relates to.

Breast Feeding Motor Activity Sedentary Behavior

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

DIET GROWTH Infant Physical activity Sedentary behavior

Contacts and locations

Locations

  • University Hospital

    Lille, 59037, France

  • Valenciennes Hospital, Monaco Hospital maternity

    Valenciennes, 59300, France

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