Bridging the Gap to Improve Mental Health Treatment Utilization

NCT ID: NCT04558489

Last Updated: 2022-01-11

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

WITHDRAWN

Clinical Phase

NA

Study Classification

INTERVENTIONAL

Study Start Date

2021-12-30

Study Completion Date

2022-04-01

Brief Summary

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Bridging the Gap aims to improve access to effective mental health treatment in a primary care setting through utilization of single session growth mindset interventions for parents and for youths. This project will also utilize focus groups and qualitative interviews to gain feedback on a single session online intervention in a rural pediatric primary care practice.

Detailed Description

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Bridging the Gap purposes to collect feedback on a single session growth mindset intervention (GMI) for parents and for youths designed to instill beliefs that personal traits (including mental health problems) are malleable. Feedback will also be collected to identify ways to improve implementing single session interventions (SSIs) in a primary care setting as well as identifying the impact on work-flow of this GMI. Patients presenting with depression and/or anxiety will all receive the GMI and will have the option of participating in focus groups/interviews pre and post-intervention to provide feedback on the intervention. Providers at this rural pediatric primary care practice will also have the chance to participate in focus groups/interviews pre and post-intervention implementation.

Assignment of Interventions: As an open trial, all participants will be assigned to the intervention arm and will receive the GMI.

This study is an open trial pilot project to collect feedback on a single session growth mindset intervention (GMI) (n=25 youth/caretaker dyads). Feedback from pre and post-intervention focus groups/interviews will be collected for 8 parents, 8 youth, and 8 treatment providers.

The aims of the study are to:

1. Collect feedback from providers, parents, and participants pre and post- GMI to identify ways to improve implementing single session interventions (SSIs) in a primary care setting.
2. Identify the impact on work-flow of using an online single session called Growth Mindset Intervention in a primary care setting.

Conditions

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Depression Anxiety Adolescent Behavior Suicidal Ideation

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

This study will use an open trial design, where all participants will receive the Growth Mindset Intervention.
Primary Study Purpose

HEALTH_SERVICES_RESEARCH

Blinding Strategy

NONE

Study Groups

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IPR + GMI

Participants receiving IPR + GMI will complete a 30-minute on-line intervention via qualtrics that covers the following topics: (1) Educate youth and caregiver that thoughts and emotions are not fixed but are malleable and subject to change; (2) provide youth and families with a brief intervention that instills hopefulness through an action plan for managing internalizing symptoms; (3) assist with developing system of support to access during times of distress; and (4) educate the caregiver on the importance of these interventions.

Group Type EXPERIMENTAL

IPR + GMI

Intervention Type BEHAVIORAL

The IPR + GMI intervention aims to impact reported hopelessness, attitudes to treatment, and view of self as changeable as well as targets treatment attendance and utilization.

Interventions

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IPR + GMI

The IPR + GMI intervention aims to impact reported hopelessness, attitudes to treatment, and view of self as changeable as well as targets treatment attendance and utilization.

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* Patients presenting with depression and/or anxiety, as identified by the patient, parent, or provider
* 10-18 years old
* CBT is recommended by provider. Receipt of mental health services upon enrollment will be monitored but will not preclude participation
* Participants must reside with a legal guardian
* English speaking

Exclusion Criteria

* Participants will be excluded if they have conditions that might impair their ability to effectively engage in Bridging the Gap, i.e
* Those in a current manic episode
* Those in a current psychotic episode
* Those diagnosed with Autism Spectrum Disorder
* Those who have issues with substance abuse
* Participants with current involvement with child welfare.
Minimum Eligible Age

10 Years

Maximum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Kaiser Foundation Research Institute

OTHER

Sponsor Role collaborator

National Institute of Mental Health (NIMH)

NIH

Sponsor Role collaborator

University of Pittsburgh

OTHER

Sponsor Role lead

Responsible Party

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Tina R Goldstein

Associate Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Tina Goldstein, PhD

Role: PRINCIPAL_INVESTIGATOR

University of Pittsburgh

David Brent, MD

Role: STUDY_DIRECTOR

University of Pittsburgh

Locations

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Children's Community Pediatrics (CCP- Armstrong Kittanning) of Children's Hospital of Pittsburgh of UPMC

Kittanning, Pennsylvania, United States

Site Status

Countries

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United States

Other Identifiers

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P50MH115838-02

Identifier Type: NIH

Identifier Source: secondary_id

View Link

STUDY19110071

Identifier Type: -

Identifier Source: org_study_id

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