Can mapping a Coalition's connections boost child health?

NCT ID NCT07804550

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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.
Paused
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 Results may not be published yet.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

Details not published
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Status unknown
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First seen Sep 04, 2026 · Last updated Sep 04, 2026

Summary

Community coalitions bring together residents and organizations to improve child health, but they often need support to put research-backed strategies into practice. This pilot study tests whether a program called FICAS, which uses information about relationships within a coalition to guide decision-making, can be delivered successfully and is useful to members. Three coalitions will participate, with one receiving Catalyzing Communities alone, one receiving Catalyzing Communities plus FICAS, and one starting later. The study will help determine whether FICAS and the study procedures should be refined and tested in a larger trial.

What this could mean

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

Active substance
FICAS implementation intervention and Catalyzing Communities platform
What this could lead to
If FICAS proves useful, it could help community coalitions more effectively adopt evidence-based strategies to improve child health and prevent obesity.
What could go wrong
This is a small pilot study with only three coalitions, so results may not apply broadly. The intervention is complex and may not be acceptable or feasible in other settings.

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 3,300 people

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

Expected to start

Jan 2027

An estimate. Start dates often move.

Expected to finish

Jun 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

18 years and older

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 Coalition-level criteria * Coalition focuses on child health, childhood obesity prevention, healthy eating, active living, nutrition security, policy, systems, or environmental change, or related community health priorities. * Coalition works in or serves a community experiencing socioeconomic disadvantage. * Coalition has multisector participation. * Coalition has identifiable leadership or backbone capacity to participate in the study. * Coalition is willing to participate in study procedures and data collection and accept randomized coalition-level assignment. * Coalition has a feasible membership roster or is able to work with the study team to construct one and has an identifiable leadership contact. * Coalition can support participant recruitment and scheduling without coercing individual participation. Individual-level criteria * Age 18 years or older. * Coalition member, leader, staff member, partner, changemaker, committee or core-group participant, named network connection, survey-only participant, invited guest, or other adult with relevant community, organizational, policy, professional, or implementation expertise or connections. * Able to provide informed consent. * Able to participate in English. * For direct committee or core-group participants, able to participate through the internet, telephone, or another study-supported mode. * Willing to complete the study activities applicable to the participant's role, which may include meetings, surveys, network assessments, or interviews. Exclusion Criteria Coalition-level criteria * Coalition is unable to participate in required study activities. * Coalition lacks a feasible membership roster or the ability to construct one with study-team assistance, or lacks an identifiable leadership contact. * Coalition is unwilling to accept randomized coalition-level assignment. * Coalition is participating in a comparable formal coalition intervention that would prevent interpretation of the study findings. Individual-level criteria * Younger than 18 years. * Unable to provide informed consent. * Unable to participate in English. * Does not have an eligible coalition, professional, community, organizational, policy, or implementation role, expertise, or connection. * For direct committee or core-group participants, unable to participate through an available study-supported mode. * Participation would create an unmanaged conflict or undue pressure that cannot be resolved.

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Conditions

The condition(s) this trial relates to.

Pediatric Obesity

As listed by the trial registrant

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

How to take part

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  1. The places running it

    1 site. 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

  • University of Pittsburgh

    Pittsburgh, Pennsylvania, 15216, United States

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