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NCT06176638 · ClinicalTrials.gov registry record · NA

Resettled Refugee Families for Healing

A NA study of Depression and Anxiety, sponsored by Washington University School of Medicine.

Active
Registry status
NA
Development phase
308
Enrollment target
1
Study location

NCT06176638: Active NA study of Depression and Anxiety, sponsored by Washington University School of Medicine.

NCT06176638 is a NA study of Depression and Anxiety that is active but no longer recruiting, run by Washington University School of Medicine. The registered enrollment target is 308 participants, below the 786-participant average among 679 other Depression trials with a reported enrollment target (61% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT06176638, a NA study of Depression and Anxiety, is active but no longer recruiting, sponsored by Washington University School of Medicine.

ACTIVE NOT RECRUITING
Registry status
NA
Development phase
308 participants
Enrollment target
1
Study location

Study Summary

The goal of this type I hybrid effectiveness-implementation trial is to test a family strengthening (FS) model delivered through multiple family groups (MFG) combined with a virtual peer mentoring program called TeenAge Health Consultants (Virtual TAHC) aimed at addressing emotional and behavioral problems among youth born in the U.S. to parents resettled as refugees. The specific aims of the study are: Aim 1: To systematically adapt an evidence-based family strengthening (FS) model delivered through multiple family groups (MFG) combined with a peer mentoring program (Virtual TAHC) (Goal 1). Aim 2: To assess preliminary short- and long-term impact of the combination intervention (MFG + Virtual TAHC) on behavioral emotional disorders (aggressive behavior, antisocial behaviors, anxiety, depression, and Posttraumatic Stress Disorder \[PTSD\]) related to intergenerational trauma among SGRC in the trial (Goal 2). Aim 3: Utilizing mixed methods and applying the Exploration, Preparation, Implementation, Sustainment (EPIS) framework, examine implementation strategies, facilitators, and barriers of the RRF4H intervention (Goal 3). Participants will receive: 1. Family strengthening intervention delivered through multiple family groups (MFG) where children and one of their biological parents will participate in 16 weekly group sessions to discuss common problems and how to address them. 2. The youth in the intervention will participate in a peer mentorship program called TeenAge Health Consultants (TAHC) consisting of 16 weekly virtual sessions where they interact with other youth to learn about important topics including how to deal with conflict, stay out of trouble, deal with stress, avoid drugs and other topics. Researchers will compare the intervention group to a control group that will receive the usual care to see if the intervention group shows improvement in symptoms compared to the usual care group.

Primary Outcome

Change in symptoms of post-traumatic stress disorder (PTSD) will be assessed using Posttraumatic Stress Disorder Reaction Index (PTSD-RI) for adolescents. PTSD scores will be dichotomized between meeting diagnostic criteria for PTSD (\>=35) and not meeting diagnostic criteria for PTSD (\<35).

Conditions Studied

Depression Anxiety Stress Disorders, Post-Traumatic Antisocial Personality Disorder Aggressive Behavior

Interventions

  • BEHAVIORAL RRF4H Combination Intervention

Study Locations (1)

Nebraska

  • Nile Lutheran Church - Omaha

Trial Details

FieldValue
Enrollment Target 308 participants
Start Date 2024-06-01
Est. Completion 2026-12-31
Phase NA
Washington University School of Medicine

1,502 total trials

What the registry record for NCT06176638 still lists

NCT06176638 is an interventional study that assigns participants to a tested intervention. The registered 308 participants enrollment target is mid-sized for trials with a published cap, below the 786-participant average among 679 other Depression trials with a reported enrollment target (61% lower).

The record links to 5 conditions, with Depression appearing as the primary indexed condition, and to 1 intervention - of which RRF4H Combination Intervention is the first listed.

NCT06176638 reports a single indexed study location in Nebraska.

Frequently Asked Questions

What is clinical trial NCT06176638 about?

NCT06176638 is a clinical study titled "Resettled Refugee Families for Healing". The goal of this type I hybrid effectiveness-implementation trial is to test a family strengthening (FS) model delivered through multiple family groups (MFG) combined with a virtual peer mentoring program called TeenAge Health Consultants (Virtual TAHC) aimed at addressing emotional and behavioral p...

What is the current status of trial NCT06176638?

This trial is currently active not recruiting. It is a NA study. The enrollment target is 308 participants. The study started on 2024-06-01. Estimated completion is 2026-12-31.

What conditions does trial NCT06176638 study?

This clinical trial studies the following conditions: Depression, Anxiety, Stress Disorders, Post-Traumatic, Antisocial Personality Disorder, Aggressive Behavior.

What interventions are being tested in trial NCT06176638?

The interventions under investigation include: RRF4H Combination Intervention (BEHAVIORAL).

Who is sponsoring clinical trial NCT06176638?

This trial is sponsored by Washington University School of Medicine, which has 1,502 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06176638 being conducted?

This trial has 1 study location across Nebraska. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Learn More About Clinical Trials

Similar trials for Depression

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT06176638's enrollment target sits among peer trials

308 136th of 679 higher than 544 of 679 other Depression trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Depression trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Related registry views

Source: ClinicalTrials.gov NCT06176638, the US trial registry maintained by the National Library of Medicine. NCT06176638 (mid enrollment · single site footprint · active not recruiting) retrieved and formatted by PlainTrial, see methodology.