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Can parent education shape healthier kids? new study investigates

NCT ID NCT05258656

Knowledge-focused Sponsor: Northwestern University 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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 aims to understand how common childhood conditions develop and whether providing parents with health education and resources can promote healthy development. It will enroll 1,800 infants and their caregivers, who will be randomly assigned to receive either the extra guidance or standard care. The study focuses on sleep, nutrition, bonding, and screen time, with follow-up visits at ages 1 and 2.

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

About 1,800 people

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

Started

Mar 2022

Expected to finish

Jan 2029

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.

Ages

Up to 26 weeks

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: * Parent/guardian(s) must understand and provide informed consent * Infant \<26 weeks of age at enrollment * Willing to be randomized to either intervention or control * In good general health as evidenced by medical history * Stated willingness to comply with all study procedures and availability for the duration of the study * Child assigned male or female sex at birth Exclusion Criteria: * Infant completed less than 28 weeks gestation * Co-morbid medical diagnoses that would prevent caregivers from initiating solid foods per protocol, such as dysphagia, chronic aspiration, malformations, etc. * Co-morbid medical diagnoses that would require specialized diet/nutritional needs, such as congenital heart disease, genetic/metabolic disorders, malignancy, etc. * Caregivers who express unwillingness to introduce peanut, milk, egg, or cashew * Caregivers who cannot provide informed consent in English or Spanish * Parents planning to move away from study sites before child is 12 months of age * Investigator or designee considers that the participant or parent/guardian would be unsuitable for inclusion in the study * Infant with a sibling enrolled in the study

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As listed by the trial registrant

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

Environmental exposure

Contacts and locations

Locations

  • Ann & Robert H Lurie Children's Hospital of Chicago

    Chicago, Illinois, 60611, United States

  • Rush University Medical Center

    Chicago, Illinois, 60612, United States

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