BRITEPath- Phase 2

NCT ID: NCT04672798

Last Updated: 2023-06-05

Study Results

Results available

Outcome measurements, participant flow, baseline characteristics, and adverse events have been published for this study.

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Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

101 participants

Study Classification

INTERVENTIONAL

Study Start Date

2020-11-05

Study Completion Date

2022-07-31

Brief Summary

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BRITEPath (BP) aims to support co-located mental health clinicians in the development of a high quality, effective, and personalized safety plan for referred patients who screen positive for depression and/or suicidal ideation.

BRITEPath utilizes BRITE, a safety planning and emotion regulation app that is loaded on the patient's smart phone and has previously been shown to be well accepted and to reduce suicide attempts compared to usual care in psychiatric inpatients (HR = 0.49). To support mental health clinicians in the development of effective safety plans, study investigators will develop Guide2Brite (G2B), which provides step-by-step instructions for the mental health clinician on how to populate BRITE onto the patient's smartphone and BRITEBoard, a clinician dashboard that tracks patient symptoms, app use, and rating on helpfulness of different interventions assessed through BRITE.

Detailed Description

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BRITEPath has 3 components: 1) BRITE, an emotion regulation and safety planning phone app that is delivered by a co-located mental health (MH) clinician to adolescents at the time of their first therapy appointment; 2) Guide2Brite, which will guide the co-located MH clinician in working with the adolescent to population content onto BRITE; and 3) BRITEBoard, which is a clinician dashboard delivered to the MH clinician and PCP.

Assignment of Interventions: This study will utilize a 1:1 randomization scheme to randomize participants to receive BRITEPath intervention or Treatment as Usual (TAU).

Hypothesis: The use of BRITEPath will decrease depressive symptoms, distress, and suicidality (any self-injurious ideation, urges, or behavior) as well as improve overall functioning compared to TAU.

Conditions

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Depression Suicidal Ideation

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

This study will use a parallel study design, where participants are randomized into two groups, BRITEPath or TAU, and will receive interventions in parallel.
Primary Study Purpose

HEALTH_SERVICES_RESEARCH

Blinding Strategy

SINGLE

Outcome Assessors
Outcomes assessors will be masked to the intervention condition at follow-up assessment time points.

Study Groups

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BRITEPath

Participants will receive the components in BRITEPath from a mental health (MH) clinical trained by the study staff/PI's on how to implement BRITE safety planning with fidelity.

First, the MH clinician will review possible barriers to implementation of the safety plan and problem-solve appropriately with patient and parent(s); (2) BRITE is the emotion regulation/safety planning app loaded on the patient's smartphone that populated with support from Guide2BRITE; and (3) BRITEBoard, a clinician dashboard that shows app use, change in distress and symptoms ratings, and can be used for shared decision making with parents, patients, and PCPs. Clinicians will review adolescent's skill development and app content with parents. Prior to discharge or following acute increases in suicide risk.

Group Type EXPERIMENTAL

BRITEPath

Intervention Type BEHAVIORAL

BRITEPath will guide co-located mental health clinicians in the use of an emotion regulation and safety planning app (BRITE) to be loaded on the phone of depressed and suicidal adolescents in order to improve depression and reduce the likelihood of a suicide attempt.

Treatment As Usual (TAU)

Participants in the TAU group will receive treatment from their mental health clinician which may include safety planning.

Group Type ACTIVE_COMPARATOR

Treatment As Usual (TAU)

Intervention Type BEHAVIORAL

Participants in this group will receive usual care from their mental health care provider.

Interventions

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BRITEPath

BRITEPath will guide co-located mental health clinicians in the use of an emotion regulation and safety planning app (BRITE) to be loaded on the phone of depressed and suicidal adolescents in order to improve depression and reduce the likelihood of a suicide attempt.

Intervention Type BEHAVIORAL

Treatment As Usual (TAU)

Participants in this group will receive usual care from their mental health care provider.

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

1. Youth aged 12-26yo
2. Own a device (e.g. smartphone, iPod, tablet) with capability to download BRITE app
3. Biological or adoptive parent is willing to provide informed consent for teen to participate
4. Youth speaks and understands English
5. Positive PHQ score or provider determines youth has depressive symptoms based on clinical interaction and refers youth to the study (in cases when PHQ is not available and study staff will complete the PHQ during the screening) OR Provider can refer if they are unclear if symptoms are depressive and PHQ scoring will be used to determine youth's eligibility. OR Screening Wizard screening questionnaire (which includes the PHQ and depressive symptom questions) indicates depression OR provider/parent have concern that youth/patient has a mood or behavioral problem
6. Family agrees to see an (embedded) MH therapist at the practice
7. PHQ scores: Score of 8 or higher on PHQ-8 -or- Score of 1 or higher on #9 of PHQ-9 suicidality item

Exclusion Criteria

1. Non English speaking
2. No parent willing to provide informed consent
3. No cell phone capability of downloading BRITE app
4. Is currently experiencing mania or psychosis
5. Evidence of an intellectual or developmental disorder (IDD)
6. Life threatening medical condition that requires immediate treatment (including emergent suicidality, homicidally, abuse/neglect, or other mental or physical condition)
7. Other cognitive or medical condition preventing youth from understanding study and/or participating.
8. Currently receiving MH treatment/currently satisfied with treatment
Minimum Eligible Age

12 Years

Maximum Eligible Age

26 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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Stephanie Stepp

Associate Professor of Psychiatry and Psychology

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Stephanie Stepp, PhD

Role: PRINCIPAL_INVESTIGATOR

University of Pittsburgh

David Brent, MD

Role: STUDY_DIRECTOR

University of Pittsburgh

Locations

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Henry Ford Health System

Detroit, Michigan, United States

Site Status

Northwell Hospital

Hyde Park, New York, United States

Site Status

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

Moon Township, Pennsylvania, United States

Site Status

STAR- Center

Pittsburgh, Pennsylvania, United States

Site Status

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

Wexford, Pennsylvania, United States

Site Status

Seattle Children's Hospital

Seattle, Washington, United States

Site Status

Countries

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United States

Provided Documents

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Document Type: Study Protocol and Statistical Analysis Plan

View Document

Document Type: Informed Consent Form

View Document

Other Identifiers

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P50MH115838-02

Identifier Type: NIH

Identifier Source: secondary_id

View Link

STUDY20110359

Identifier Type: -

Identifier Source: org_study_id

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