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New program aims to heal war trauma passed down in refugee families

NCT ID NCT06176638

Symptom relief Sponsor: Washington University School of Medicine 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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 program that combines family group sessions with a virtual peer mentoring program for US-born teens (ages 14-17) whose parents resettled as refugees. The goal is to reduce symptoms of PTSD, depression, anxiety, and behavior problems caused by intergenerational trauma. About 308 teens and their parents will take part, with half receiving the program and half getting usual care.

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 308 people

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

Started

Jun 2024

Expected to finish

Dec 2026

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

14 to 17 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 for Children: * Child born in the US * Ages 14-17 years * In the 9th - 12th grades * Enrolled in one of the schools in Omaha and Lincoln, NE area Schools Inclusion Criteria for Peer Mentors: * Peer mentors must be students in upper class (11th or 12th grade) and * Willing and able to serve as good role models * Peer mentors must be nominated by community leaders Inclusion Criteria for Parents: * Parents must be someone resettled in the U.S. as refugee and be a biological parent of a child between the ages 14-17 years * Parents must be ≥30 years of age Exclusion Criteria for All Participants: * Can understand the study procedures and/or participant rights during the informed consent process * Unwilling or unable to commit to completing the study; 2) * Present with emergency needs (e.g., hospitalization), needed care will be secured, rather than study participation.

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Conditions

The condition(s) this trial relates to.

Aggression antisocial personality disorder anxiety anxiety disorder Depression depressive disorder post-traumatic stress disorder

As listed by the trial registrant

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

Aggressive behavior Antisocial personality disorder Anxiety Depression Stress disorders, post-traumatic

Contacts and locations

Locations

  • Nile Lutheran Church

    Omaha, Nebraska, 68111, United States

More trials for these conditions

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