NCT06978959

Brief Summary

The investigators have designed a 5-week Family Navigator Plus (FN+) educational program to support foster parents in better understanding their youth's mental health needs and in finding mental health services. The purpose of this interventional study is to assess the the program's acceptability (e.g., satisfaction, barriers to participation, and burden), utility (e.g., how useful foster parents found the program to be), and feasibility (e.g., number referred who meet eligibility, time to complete assessments, self-reported feasibility). The investigators hypothesize that our program will be acceptable, useful, and feasible for foster parents of youth with mental health needs.

Trial Health

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
12

participants targeted

Target at below P25 for not_applicable

Timeline
32mo left

Started Jan 2026

Typical duration for not_applicable

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress11%
Jan 2026Dec 2028

First Submitted

Initial submission to the registry

May 1, 2025

Completed
17 days until next milestone

First Posted

Study publicly available on registry

May 18, 2025

Completed
8 months until next milestone

Study Start

First participant enrolled

January 12, 2026

Completed
1.6 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 31, 2027

Expected
1.3 years until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2028

Last Updated

January 27, 2026

Status Verified

January 1, 2026

Enrollment Period

1.6 years

First QC Date

May 1, 2025

Last Update Submit

January 23, 2026

Conditions

Keywords

foster parentsfamily navigatorpsychoeducation

Outcome Measures

Primary Outcomes (2)

  • Client Satisfaction Questionnaire (CSQ)

    The Client Satisfaction Questionnaire (CSQ-8) is an eight-item measure that assesses client satisfaction with services including its quality, utility, and relevance.

    Post-Intervention (Week 5) and 3 Month Follow Up (Week 18)

  • Post Session Questionnaire (PsQ)

    The PsQ is a measure we created to assess utility and relevance of session content and materials, and to assess if participants intended to use skills/information learned during that session.

    After Completing Each Session (Weeks 1 - 5)

Secondary Outcomes (5)

  • Parent Activation Measure - Mental Health

    Baseline (Week 1), Post-Intervention (Week 5), 3 month Follow Up (Week 18)

  • Barriers to Treatment Participation

    Baseline (Week 1), Post-Intervention (Week 5), 3 month Follow Up (Week 18)

  • PROMIS-Parent Proxy Pediatric Depressive Symptoms Short Form 8a (parent-report)

    Baseline (Week 1), Post-Intervention (Week 5), 3 month Follow Up (Week 18)

  • PROMIS-Parent Proxy Pediatric Anxiety Short Form 8a (parent-report)

    Baseline (Week 1), Post-Intervention (Week 5), 3 month Follow Up (Week 18)

  • Pediatric Symptoms Checklist - 17 (Parent Report)

    Baseline (Week 1), Post-Intervention (Week 5), 3 month Follow Up (Week 18)

Study Arms (1)

Foster Parents

EXPERIMENTAL

Participants will consist of adult (age 18 and older) foster parents of youth between the ages of 6 and 17 with mental health needs. Participants will be located in Illinois, and be either English or Spanish speaking. Participants will attend a 5-week educational program (one session per week) that aims to support them in understanding child behaviors, finding and access mental health services, communicating with providers, and using technology to find support.

Behavioral: FN+ Intervention

Interventions

Participants will attend 5 one-on-one sessions over the course of 5 weeks; they will meet with a family navigator over video conferencing software (e.g., Zoom). The purpose of each sessions are as follows: 1) Provide an overview of the program and help parents understand their perceptions of child behaviors, 2) Train parents to find, access, and overcome barriers to mental health services, 3) Build parent capacity in understanding how mental health treatment works and how to communicate with providers, 4) Help parents understand the common function of child behaviors, and 5) Train parents to find, evaluate, and use online mental health tools. Participants will complete measures of child symptoms, parent activation, barriers to treatment, and/or satisfaction with the program before the intervention, immediately after the intervention, and 3 months after completing the intervention.

Foster Parents

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Foster parent of a youth between the ages of 6 to 17 with mental health needs
  • Parent adopted child from foster care
  • Living in Illinois, United States
  • English or Spanish speaking
  • Has access to internet and videoconferencing

You may not qualify if:

  • \- Participated in the FN+ Focus Groups or PROACTIVE Parent Pilot Study

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Northwestern University

Chicago, Illinois, 60611, United States

RECRUITING

Related Publications (1)

  • Risser, H. J., Morford, A. E., Murphy, A. N., Pinkerton, L. M., Law, C., Yang, Y., ... & Boisseau, C. L. (2024). Feasibility and acceptability of a family navigator program to support foster parents of youth with mental health concerns. Children and Youth Services Review, 160, 107578.

    BACKGROUND

Study Officials

  • Heather J Risser, PhD

    Northwestern University

    PRINCIPAL INVESTIGATOR
  • Enrollment Contact, If interested in participation

    Northwestern University email FNplus@northwestern.edu

    STUDY DIRECTOR

Central Study Contacts

Christina L Boisseau, PhD

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
TREATMENT
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Assistant Professor

Study Record Dates

First Submitted

May 1, 2025

First Posted

May 18, 2025

Study Start

January 12, 2026

Primary Completion (Estimated)

August 31, 2027

Study Completion (Estimated)

December 31, 2028

Last Updated

January 27, 2026

Record last verified: 2026-01

Data Sharing

IPD Sharing
Will share

Per NIMH Data Sharing policy, de-identified IDP will be shared in the NIMH Data Archive (NDA, https://nda.nih.gov/)

Time Frame
Per NIMH Data Sharing policy
Access Criteria
Per NIMH Data Sharing policy
More information

Locations