Navigator support may boost health for hospitalized children

NCT ID NCT07687238

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Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting This study
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
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Paused for now. It may or may not start again.
Ongoing
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 Results may not be published yet.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

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Status unknown
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First seen Jul 07, 2026 · Last updated Jul 08, 2026 · Updated 1 time

Summary

This study compares two methods of helping families of hospitalized children connect with social and economic resources. One group receives a list of local services (passive referral), while the other also gets help from trained navigators who assist with applications and follow-up. The goal is to see whether active navigator support leads to better child health and quality of life. Families of children aged 0–17 hospitalized on general pediatric units are eligible.

What this could mean

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

Active substance
social needs assistance (navigator support vs. passive referral)
What this could lead to
If navigator support proves more effective, hospitals may adopt this approach to help families address social and economic needs, potentially improving children's overall health.
What could go wrong
The trial is relatively small and focused on one hospital system, so results may not apply everywhere. The benefit of navigator support over simple referrals may be modest 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

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 1,880 people

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

Expected to start

Sep 2026

An estimate. Start dates often move.

Expected to finish

Sep 2030

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

Children (under 18), adults (18 to 64) and older adults (65 and over)

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

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: Aim 1 - Caregiver-Child Dyads Sample Caregiver-child dyads will be eligible to participate in the study if they meet the following criteria assessed during the recruitment and enrollment process: 1. children are hospitalized on the general pediatric/pediatric hospital medicine (PHM) team/service 2. the child is between the ages of 0-17 3. the child's caregiver is \>17 years-old 4. the caregiver speaks English or Spanish 5. the family lives in the same county as the hospital or in a neighboring county to the hospital 6. the child is not in Child Protective Services custody 7. the family has not previously been enrolled in the study 8. the caregiver screens positive for \>=1 of the following social risks: food insecurity, housing instability, housing quality concerns, transportation needs, utilities needs, child care needs, or financial strain 9. the family is not enrolled in another social needs assistance-related research study (e.g., another social needs navigation study) Aim 2 - Caregiver and Community-based Organization (CBO) Qualitative Interviews Sample Caregivers of children enrolled in Aim 1 will be eligible for study interviews. CBO staff will be eligible to participate if they are: 1. \> 17 years old 2. speak English or Spanish 3. work at a CBO serving the area in which patients at the study sites live EXCLUSION CRITERIA: Aim 1 - Caregiver-Child Dyads Sample Participants will be excluded from participation if they are: 1. not hospitalized or hospitalized outside of general/PHM SERVICE 2. children are 18 years of age or older 3. caregiver/guardians are under the age of 18 years of age 4. caregivers are do not speak English or Spanish 5. the family does not live in the same or neighboring county of the recruitment hospital 6. the child is under the care of Child Protective Services custody 7. the family has already been previously enrolled in the study 8. the caregiver does not screen positive for any of the following social risks: food insecurity, housing instability, housing quality concerns, transportation needs, utilities needs, child care needs, or financial strain 9. the family is already enrolled in a social needs assistance-related research study (e.g., another social needs navigation study) Aim 2 - Caregiver and CBO qualitative interviews Caregivers of children not enrolled in Aim 1 will not be eligible to participate study interviews. CBO staff will not be eligible to participate if they are: 1. under 18 years of age 2. do not speak English or Spanish 3. do not work at a CBO serving the recruitment site areas

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As listed by the trial registrant

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How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    6 sites. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. A doctor treating you

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Contacts and locations

Locations

  • Children's Hospital of Philadelphia

    Philadelphia, Pennsylvania, 19104, United States

  • Children's Memorial Hermann Hospital

    Houston, Texas, 77030, United States

  • Texas Children's Hospital - West Campus

    Houston, Texas, 77094, United States

  • UCSF Benioff Children's Hospital - Oakland

    Oakland, California, 94609, United States

  • UCSF Benioff Children's Hospital - San Francisco

    San Francisco, California, 49158, United States

  • Zuckerberg San Francisco General Hospital and Trauma Center

    San Francisco, California, 94110, United States

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