Actively Recruiting

Phase Not Applicable
Age: 16Years - 20Years
All Genders
ID06019377

Pilot Testing an Intervention to Enhance Coping and Increase Mental Health Help-seeking Among Transition-age Youth in Foster Care

Led by Portland State University ยท Updated on 2025-02-28

106

Participants Needed

1

Research Sites

17 weeks

Total Duration

On this page

Sponsors

P

Portland State University

Lead Sponsor

N

National Institute of Mental Health (NIMH)

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are evaluating a program called Stronger Youth Networks and Coping (SYNC) to help young people transitioning from foster care improve their mental health and use of services. This study focuses on foster youth aged 16 to 20 who face behavioral health risks such as depression, anxiety, and PTSD. SYNC aims to increase coping skills, emotional regulation, and willingness to seek help, addressing challenges like limited support and negative views on mental health care. The study compares two groups: one receiving the SYNC intervention plus usual child welfare services, and the other receiving typical services alone. The SYNC program consists of eight weekly 90-minute online group sessions led by a facilitator and a peer with foster care experience. Usual services include federally funded transition planning and life skills training. The study will first test SYNC with two small groups, then conduct a randomized trial with 80 participants to evaluate its impact on coping, help-seeking attitudes, and mental health symptoms. Participants will join remotely and complete assessments before and after the intervention, and again six months later. Researchers will measure changes in coping flexibility, help-seeking intentions, emotional regulation, and mental health service use. The program's materials and procedures will be refined for future larger trials. The total participation duration includes the 8-week intervention and follow-up assessments at post-intervention and six months later.

CONDITIONS

Brief Title

Intervention to Enhance Coping and Help-seeking Among Youth in Foster Care

Who Can Participate

Age: 16Years - 20Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Eligible to receive federally-funded transition-related services in Oregon (ages 16-20 and in foster care at least 90 days after turning 14)
  • Indicated behavioral health risk shown by child welfare records such as DSM diagnoses, psychotropic medication use, emotional-behavioral disability, or residential placement
Not Eligible

You will not qualify if you...

  • Unable to actively participate due to non-English speaking or significant developmental disabilities
  • Participation contraindicated due to current crisis or placement that does not allow involvement

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Outpatient Treatment

Duration - 8 weeks

Participants assigned to the intervention group attend 8 weekly remote 90-minute group sessions led by a facilitator and a near-peer with lived foster care experience, focusing on coping skills and help-seeking strategies. Participants assigned to the services-as-usual group continue with typical child welfare services including life skills and transition planning support.

8 weekly remote group sessions for the intervention group; services-as-usual continue for the comparison group

Follow-up

Duration - 6 months after program completion

Participants are assessed immediately after program completion and again 6 months later to evaluate coping, help-seeking intentions, and mental health self-efficacy.

2 assessment visits (immediately post-program and at 6 months follow-up)

Trial Site Locations

Total: 1 location

1

Portland State University

Portland, Oregon, United States, 97201

Actively Recruiting

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Research Team

J

Jennifer Blakeslee, PhD,MSW,BS

R

Rebecca A Miller, M.Ed, BA

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

2

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