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Personalized diet and exercise program aims to stop childhood obesity before it starts

NCT ID NCT05121090

Prevention Sponsor: University Hospital, Lille Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

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 This study
Running, but no longer taking on new participants.
Completed
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Jun 27, 2026

Summary

This study tests a 2-year personalized program for overweight children aged 6-7 that includes diet advice, physical activity, psychology, and relaxation techniques. The goal is to reduce their body mass index (BMI) and prevent obesity. Researchers will compare results to a historical group of similar children who did not receive the program.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
educational program (diet, physical activity, psychology, and sophrology)
What this could lead to
If it works, this could provide an effective, personalized approach to prevent obesity in at-risk children, reducing long-term health problems.
What could go wrong
This is a single study with a historical control group, not a randomized trial. The program is intensive and may not be scalable or effective for all children.

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.

Participants

About 460 people

The number the study aims to enrol. It can still change while the study runs.

Started

Jan 2022

Expected to finish

Apr 2027

An estimate. End dates often move.

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.

Who is studied

Children from the first year of primary school in Lille City

Ages

5 to 6 years

Sex

Anyone

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: * Children from the first year of primary school in Lille City * Overweight or obese children as defined by the IOTF and/or with at least one of the following risk factors: 1) early adiposity rebound (before 6 years old), 2) an upward crossing of major percentiles on the BMI curve (after 6 years old). * Children whose legal tutor(s) is(are) able to understand the enlightened information. * Children whose legal tutor(s) has(ve) signed the free and informed consent. Exclusion Criteria: * Refusal from children or their tutors to participate in the study. * Impossibility to participate in the study in its totality. * Pathology known to impact the BMI: follow-up care for eating behaviour problems, endocrine disorders (hypercorticism, hypothyroidism, growth factor deficiency, hypothalamic-hypophysis lesions), genetic disorders (Prader Willi syndrome, Bardet-Biedl syndrome), drugs that affect body weight (antidepressant, neuroleptics, corticoids). * Previous participation in a similar educational program.

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Conditions

The condition(s) this trial relates to.

Obesity obesity disorder Overweight Pediatric Obesity

As listed by the trial registrant

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

Overweight and obesity Overweight, childhood Overweight, infant

Contacts and locations

Locations

  • Association PrevSanté MEL

    Lille, 59000, France

More trials for these conditions

Other studies related to the condition(s) this trial covers.