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Clinical Trials/NCT04822636
NCT04822636
Recruiting
N/A

Family Mental Health Family Navigator

University of California, San Francisco1 site in 1 country150 target enrollmentJune 6, 2022
ConditionsMental Health

Overview

Phase
N/A
Intervention
Not specified
Conditions
Mental Health
Sponsor
University of California, San Francisco
Enrollment
150
Locations
1
Primary Endpoint
Treatment engagement
Status
Recruiting
Last Updated
last year

Overview

Brief Summary

This study will focus on developing and testing a family-based mental health navigator intervention, the Family Mental Health Navigator (FMHN), to evaluate whether the intervention combined with mHealth is preliminary efficacious in improving mental health service initiation and engagement for publicly-insured youth.

Detailed Description

The study will demonstrate how a family-based navigator intervention combined with mHealth may lead to improved mental health treatment initiation and engagement among publicly-insured youth. Publicly-insured youth have high rates of mental health symptoms relative to youth in the community, and are disproportionately racial and ethnic minorities, only perpetuating disparities in this population's mental health access and engagement. The proposed project will develop and test a family-based navigator intervention, the Family Mental Health Navigator (FMHN), a natural fit for improving publicly-insured youth's mental health service and clinical outcomes. The study will start with identifying the feasibility and acceptability of the FMHN intervention. Then, the study will determine whether the FMHN intervention improves publicly-insured youth mental health treatment initiation and engagement. Finally, the study will characterize patterns of pre- and post-service outcomes along the behavioral health services cascade of care, to further evaluate the feasibility, acceptability, and preliminary impact of the FMHN model.

Registry
clinicaltrials.gov
Start Date
June 6, 2022
End Date
April 1, 2026
Last Updated
last year
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • English-speaking and/or Spanish-speaking youth
  • Ages 6-17
  • Are currently receiving services at the San Francisco General Hospital
  • Are publicly insured
  • Have an involved caregiver/legal guardian for consent
  • Family has mobile phone access

Exclusion Criteria

  • Youth is not English-speaking nor Spanish-speaking
  • Caregiver has impairment that would preclude providing informed consent
  • Unavailable guardian for consent

Outcomes

Primary Outcomes

Treatment engagement

Time Frame: 12 months post enrollment

Engagement as measured by attendance in treatment for 6 or more weeks

Time to treatment referral

Time Frame: 12 months post enrollment

Number of days until treatment referral is made

Time to treatment initiation

Time Frame: 12 months post enrollment

Number of days until attendance at first treatment session

Study Sites (1)

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