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New web tool aims to help states pick best mental health programs for kids

NCT ID NCT06375551

Knowledge-focused Sponsor: Chestnut Health Systems Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now This study
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
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 is testing a web-based tool called ORCA-A that helps state decision-makers choose the best evidence-based programs to support parent and child mental health. Researchers will work with 80 adults involved in state-level decisions under the Family First Prevention Services Act. The goal is to see if the tool improves decision quality, commitment, and program fit.

What this could mean

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

Active substance
ORCA-A (Optimizing Responses with Collaborative Assessments-Automated) behavioral decision-support tool
What this could lead to
If successful, this tool could help state leaders make better, more informed decisions about which mental health programs to fund, potentially improving outcomes for families.
What could go wrong
This is a small pilot study (80 people) testing a tool, not a treatment. It measures decision quality, not health outcomes, so real-world impact is uncertain.

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 80 people

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

Expected to start

Dec 2026

An estimate. Start dates often move.

Expected to finish

Jul 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.

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: * Non-institutionalized * Adults (18 years or older). * English-Speaking Aim 1: * Involved in initial state decision-making related to Family First Prevention Services Act. * Willing to participate in two data collection occasions. Aim 2: * Non-institutionalized * Adults (18 years or older). English-Speaking. * Involved in ongoing state decision-making related to Family First Prevention Services Act. * Willing to participate in three measurement occasions. Aim 3: -Willing to participate in multiple (bi-weekly up to two years) measurement occasions. Exclusion Criteria: -Not involved in or potentially influencing child welfare intervention decisions

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Conditions

The condition(s) this trial relates to.

Psychological Well-Being Social Facilitation

As listed by the trial registrant

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

Child abuse Child welfare Consensus Decision making Decision making, shared Decision support technique FAMILY Implementation science Mental health Organizations POLICY Social facilitation

How to take part

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

  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

    A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.

Contacts and locations

Locations

  • Chestnut Health Systems

    RECRUITING

    Eugene, Oregon, 97401, United States

More trials for these conditions

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