Mental Health Care Coordination for Transition Aged Youth

Sponsor
Children's National Research Institute (Other)
Overall Status
Completed
CT.gov ID
NCT03336892
Collaborator
Health Resources and Services Administration (HRSA) (U.S. Fed)
220
2
43

Study Details

Study Description

Brief Summary

This study seeks to quantify the impact of recommended mental health care coordination practices on patient experiences of care, (i.e. satisfaction, stigma, quality of mental health care), evaluate the efficiency and effectiveness of the intervention (i.e. care coordination, timing, unmet needs), and assess mental health outcomes (i.e. symptoms and functioning, involvement with law enforcement/juvenile justice system; rates of substance use /abuse, service utilization) in a population of 16-22 year-old youth receiving primary care in a D.C. urban academic adolescent medicine practice, using standardized outcome measures.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Mental Health Care Coordination
N/A

Detailed Description

In the maternal and child health field, there is increasing awareness of modifiable health conditions that appear early in the life course and impact development and wellness throughout the life span. Special opportunities exist in vulnerable populations with serious mental health conditions to better understand what life course events can facilitate attainment of optimal health and development. One such opportunity is making sure youth with serious emotional disturbance/serious mental illness receive the mental health services they need.

Unfortunately, untreated mental illness among adolescents and young adults is a major public health problem. Particularly concerning is the fact that 80% of youth with serious emotional disturbance/serious mental illness are not receiving needed mental health services and unmet mental health needs are even higher among certain populations, including minority youth. Youth with untreated mental health problems face a number of challenges that are exacerbated when left untreated. For example, youth with serious mental illness tend to have more difficulties in school and more involvement with the criminal justice system than their peers. These youth also face more challenges successfully transitioning to adulthood and becoming productive members of society.

Untreated mental illness tends to lead to more intensive and costly treatment down the road. There are many barriers to accessing mental health services, including stigma and difficulty navigating a complex mental health system, which contribute to unmet mental health needs. Additionally, youth may be so significantly impaired that expecting them to access mental treatment without some supportive services is unrealistic.

In light of these facts, it becomes urgent to implement recommended standards for mental health integration and evaluate their impact on mental health outcomes. The Center for Integrated Health Solutions in a joint Health Resources and Services Administration (HRSA)-Substance Abuse and Mental Health Services Administration (SAMHSA) effort recently released expanded joint principles for behavioral health integration. In this model, coordinated care is defined by primary and behavioral health care provided at different locations in the medical neighborhood, but care is coordinated through enhanced communication across the two disciplines. This report makes available an important standard for establishing integrated mental health care coordination practices within a primary care setting, but also demands careful evaluation.

This study seeks to quantify the impact of recommended mental health care coordination practices on patient experiences of care, (i.e. satisfaction, stigma, quality of mental health care), evaluate the efficiency/effectiveness of the intervention (i.e. care coordination, timing, unmet needs), and assess mental health outcomes (i.e. symptoms and functioning, involvement with law enforcement/juvenile justice system; rates of substance use /abuse, service utilization) in a population of 16-22 year-old youth receiving primary care in a D.C. urban academic adolescent medicine practice, using standardized outcome measures.

Study Design

Study Type:
Interventional
Actual Enrollment :
220 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Participant)
Primary Purpose:
Health Services Research
Official Title:
Mental Health Care Coordination for Transition Aged Youth With Serious Emotional Disturbance/Serious Mental Illness
Actual Study Start Date :
Apr 1, 2016
Actual Primary Completion Date :
Mar 31, 2019
Actual Study Completion Date :
Oct 31, 2019

Arms and Interventions

Arm Intervention/Treatment
Experimental: Intervention

Enhanced usual care with written mental health resources and system navigation information in addition to individualized mental health care coordination by a dedicated specially trained mental health care coordinator.

Behavioral: Mental Health Care Coordination
Enhanced usual care with written mental health resources and system navigation information in addition to individualized mental health care coordination by a dedicated specially trained mental health care coordinator.

No Intervention: Control

Enhanced usual care with written mental health resources and system navigation information.

Outcome Measures

Primary Outcome Measures

  1. Connection to mental healthcare [2 years]

    Number of study participants self-reported receiving mental health care services since enrollment

Secondary Outcome Measures

  1. Patient Experiences [2 years]

    Experience of Care and Health Outcomes (ECHO) Survey

  2. Depression symptoms [2 years]

    PHQ-9 Questionnaire

  3. Mental Health Stigma [2 years]

    Internalized Stigma of Mental Illness (ISMI) Questionnaire

  4. Patterns of substance use [2 years]

    Youth Risk Behavior Survey (YRBS) Questionnaire

  5. Adverse Childhood Events [2 years]

    Philadelphia ACE Survey

Eligibility Criteria

Criteria

Ages Eligible for Study:
16 Years to 22 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • has a diagnosis of serious emotional disturbance/serious mental illness

  • has not received outpatient mental health services in the past 30 days

Exclusion Criteria:
  • does not have a diagnosis of serious emotional disturbance/serious mental illness

  • has received outpatient mental health services in the past 30 days

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Children's National Research Institute
  • Health Resources and Services Administration (HRSA)

Investigators

  • Principal Investigator: Lisa K Tuchman, MD, MPH, Children's National Research Institute

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Lisa Tuchman, Principal Investigator, Children's National Research Institute
ClinicalTrials.gov Identifier:
NCT03336892
Other Study ID Numbers:
  • Pro7512
  • R40MC29453
First Posted:
Nov 8, 2017
Last Update Posted:
Feb 23, 2021
Last Verified:
Feb 1, 2021
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Lisa Tuchman, Principal Investigator, Children's National Research Institute

Study Results

No Results Posted as of Feb 23, 2021