Implementing a Brief Suicide Intervention for High Risk Youth With Front-Line Juvenile Justice Staff
Primary Purpose
Suicide and Self Harm
Status
Unknown status
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Safety planning
Sponsored by
About this trial
This is an interventional treatment trial for Suicide and Self Harm
Eligibility Criteria
Inclusion Criteria:
- Court-involved non-incarcerated (CINI) youth,
- ages 12-17
- Legal guardian available to consent for juvenile's participation,
- Juvenile is English speaking, and
- Juvenile flags in the caution or warning range of the MAYSI-2.
Inclusion for second cohort:
- Court-involved non-incarcerated (CINI) youth,
- ages 12-17
- Legal guardian available to consent for juvenile's participation,
- Juvenile is English speaking, and
- Juvenile does not flag in the caution or warning range of the MAYSI-2
Exclusion Criteria:
- observable cognitive, developmental delays, or psychosis that would interfere with completing consent, assessment or intervention, and
- Juvenile meets hospital level of care for imminent suicide risk.
Sites / Locations
- Rhode Island Family CourtRecruiting
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
No Intervention
Experimental
No Intervention
Arm Label
Pre-intervention
Safety Planning
Regression discontinuity
Arm Description
Pre-intervention baseline comparison
Intervention group
Subthreshold no intervention
Outcomes
Primary Outcome Measures
Self-Injurious Thoughts and Behaviors Interview 2.0 (SITBI 2.0) Short Form
Structured interview designed to assess the presence, frequency, and characteristics of a broad array of self-injurious thoughts and behaviors
Suicide Ideation Questionnaire (SIQ) - Junior
assesses the frequency of suicidal ideation
Child and Adolescent Services Assessment
parent report of utilization of MH services and operationalized as a composite score of suicide attempts and emergency interventions for acute suicidality assessed by the Child and Adolescent Services Assessment (CASA)
Treatment Attendance
Attendance at first treatment appointment and total number of treatment sessions attended will be collected by contacting each juveniles' treatment provider at the 3-month follow-up
Recidivism
Collateral data gathered from court database). Juveniles' recidivism rates (e.g., new arrests), description of related charges (e.g., substance-related, property) and time detained/incarcerated
Secondary Outcome Measures
Full Information
NCT ID
NCT02981420
First Posted
November 28, 2016
Last Updated
March 2, 2017
Sponsor
Rhode Island Hospital
Collaborators
National Institute of Mental Health (NIMH)
1. Study Identification
Unique Protocol Identification Number
NCT02981420
Brief Title
Implementing a Brief Suicide Intervention for High Risk Youth With Front-Line Juvenile Justice Staff
Official Title
Implementing a Brief Suicide Intervention for High Risk Youth With Front-Line Juvenile Justice Staff
Study Type
Interventional
2. Study Status
Record Verification Date
November 2016
Overall Recruitment Status
Unknown status
Study Start Date
December 2016 (undefined)
Primary Completion Date
May 2019 (Anticipated)
Study Completion Date
May 2020 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Rhode Island Hospital
Collaborators
National Institute of Mental Health (NIMH)
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
A youth's contact with the juvenile justice system represents an opportune moment for suicide screening and brief suicide intervention for indicated youth. This study will provide data on the novel implementation of an evidence-based brief suicide intervention, safety planning, administered by front-line juvenile court staff for suicidal court-involved non-incarcerated youth. Data will inform the dissemination and implementation of suicide brief interventions to be delivered by front-line staff at the time of mental health screening in the juvenile justice system. The proposed study is consistent with the NIMH Strategic Plan by testing an intervention for effectiveness in community settings (Strategy 3.3) and establishing a research-practice partnership to improve D&I of evidence-based MH services (4.2). The unique service delivery by JJ court staff also supports the NIMH goals to develop innovative service delivery models (Strategy 4.3) as well as validate a MH intervention for an underserved population (Strategy 4.1). This proposal also addresses the Healthy People 2020 goals of reducing suicide attempts (MHMD-2).
Detailed Description
Suicide and suicidal behaviors among youth in the United States represents a significant public health problem. Youth involved in the juvenile justice system have a greater burden of risk factors associated with suicide ideation and behaviors as compared to their non-justice involved peers, placing these youth at greater risk for suicide. Thus, the overall goal of this Mentored Patient-Oriented Research Career Development Award (K23) is to support the applicant in developing the skills to launch an independent research program focused on the dissemination and implementation of evidence-based interventions for court-involved non-incarcerated (CINI) youth involved in the juvenile justice system to reduce psychiatric morbidity. Specific training goals are: (1) engage in intensive clinical and research training to increase my expertise in conducting brief interventions for adolescent suicide, (2) develop expertise in dissemination and implementation strategies and research in the juvenile justice system, (3) achieve skills in mixed-method research methodology including design and analysis of studies to support causal inference when randomization is not possible. The applicant will pursue these goals through a combination of mentoring, didactics, and practical experience. Specific training goals for this 5-year-period will be achieved under the mentorship of Drs. Anthony Spirito (Brown University), Marina Tolou-Shams (UCSF), Gina Vincent (UMASS Medical School), and Peter Friedmann (Baystate Health). The objective of the proposed research study is to 1) identify individual-, administrative-, and system-level factors that promote or hinder uptake of a brief suicide intervention conducted by front-line juvenile justice staff with CINI youth and 2) implement an evidence-based brief intervention, safety planning, for suicidal CINI youth and evaluate its utility with these youth. In the Treatment Adaptation phase, 12 juvenile justice stakeholders will be interviewed pre- and post-intervention implementation, as well as 24 youth and 24 caregivers 3-months post-intervention, about the acceptability of the brief intervention in the juvenile court setting. In the Treatment Trial phase, we will examine the effectiveness of a safety planning intervention for indicated suicidal youth in reducing suicidal ideation, in reducing suicidal events (suicide attempts as well as emergency evaluations and psychiatric hospitalizations for suicidality), increased engagement in outpatient mental health treatment, and improved youth motivation for treatment. CINI juveniles, ages 12-17, (N=100 for baseline (historical control) cohort; N=100 for efficacy trial; N=100 for alternative causal design) and a caregiver will be recruited from the juvenile court to participate in the current study. CINI juveniles in the efficacy trial will receive the evidenced-based brief suicide intervention as part of standard of care and will be compared to historical control and alternative causal design. Baseline data will be collected as part of routine care. Youth and a caregiver will be re-assessed at 3 months subsequent to the juvenile's initial court appointment.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Suicide and Self Harm
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
300 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Pre-intervention
Arm Type
No Intervention
Arm Description
Pre-intervention baseline comparison
Arm Title
Safety Planning
Arm Type
Experimental
Arm Description
Intervention group
Arm Title
Regression discontinuity
Arm Type
No Intervention
Arm Description
Subthreshold no intervention
Intervention Type
Behavioral
Intervention Name(s)
Safety planning
Intervention Description
Safety Planning Intervention. This brief one-session intervention, based on cognitive behavioral principles, is designed to help individuals identify a concrete list of coping strategies and social supports that youth can utilize preceding or during a crisis to lower imminent risk of suicidal behavior. In youth who also report nonsuicidal self-injurious behavior (NSSI), the safety plan will address both suicidal and nonsuicidal behavior. The plan helps youth identify possible triggers to SI/crisis including self-monitoring of suicidal thoughts, feelings, and behaviors; advance planning to remove lethal means; determine distress tolerance/emotion regulation skills that may be helpful; identify accessible social supports to target hopelessness/sense of isolation; reinforce the commitment to seek treatment; and, how and where to access emergency care.
Primary Outcome Measure Information:
Title
Self-Injurious Thoughts and Behaviors Interview 2.0 (SITBI 2.0) Short Form
Description
Structured interview designed to assess the presence, frequency, and characteristics of a broad array of self-injurious thoughts and behaviors
Time Frame
3 months
Title
Suicide Ideation Questionnaire (SIQ) - Junior
Description
assesses the frequency of suicidal ideation
Time Frame
3 months
Title
Child and Adolescent Services Assessment
Description
parent report of utilization of MH services and operationalized as a composite score of suicide attempts and emergency interventions for acute suicidality assessed by the Child and Adolescent Services Assessment (CASA)
Time Frame
3 months
Title
Treatment Attendance
Description
Attendance at first treatment appointment and total number of treatment sessions attended will be collected by contacting each juveniles' treatment provider at the 3-month follow-up
Time Frame
3 months
Title
Recidivism
Description
Collateral data gathered from court database). Juveniles' recidivism rates (e.g., new arrests), description of related charges (e.g., substance-related, property) and time detained/incarcerated
Time Frame
3 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
12 Years
Maximum Age & Unit of Time
17 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Court-involved non-incarcerated (CINI) youth,
ages 12-17
Legal guardian available to consent for juvenile's participation,
Juvenile is English speaking, and
Juvenile flags in the caution or warning range of the MAYSI-2.
Inclusion for second cohort:
Court-involved non-incarcerated (CINI) youth,
ages 12-17
Legal guardian available to consent for juvenile's participation,
Juvenile is English speaking, and
Juvenile does not flag in the caution or warning range of the MAYSI-2
Exclusion Criteria:
observable cognitive, developmental delays, or psychosis that would interfere with completing consent, assessment or intervention, and
Juvenile meets hospital level of care for imminent suicide risk.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Kathleen Kemp, Ph.D.
Phone
4017938269
Email
kkemp@lifespan.org
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Kathleen Kemp, Ph.D.
Organizational Affiliation
RIH/Brown University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Rhode Island Family Court
City
Providence
State/Province
Rhode Island
ZIP/Postal Code
02903
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Kathleen Kemp, Ph.D.
Phone
203-619-1692
Email
kkemp@lifespan.org
12. IPD Sharing Statement
Plan to Share IPD
No
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Implementing a Brief Suicide Intervention for High Risk Youth With Front-Line Juvenile Justice Staff
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