- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03586895
e-Connect: A Service System Intervention for Justice Youth at Risk for Suicide
Study Overview
Detailed Description
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Katherine Elkington, PhD
- Phone Number: 16467746965
- Email: ke2143@cumc.columbia.edu
Study Contact Backup
- Name: Mihir Topiwala
- Phone Number: 6467745781
- Email: mihir.topiwala@nyspi.columbia.edu
Study Locations
-
-
New York
-
New York, New York, United States, 10032
- New York State Psychiatric Institute
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Sample: County Probation Leadership (Executive and Supervisory) and Line (Juvenile Probation Officers) Staff
Inclusion Criteria: Probation Officers ages 21-70 years old with active employment at the probation department working with youth, or supervise those working with youth in one of the following capacities: probation supervision, assessment, and referral, or engage in work that is related to policies, procedures, and decisions around these activities in 10 site counties
Exclusion Criteria: There are no exclusionary criteria and no special classes of participants.
Sample: Youth on Probation
Inclusion Criteria: All new intakes ages 10-18 years old
Exclusion Criteria: There are no exclusionary criteria and no special classes of participants.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Non-Randomized
- Interventional Model: Sequential Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: e-Connect
County receives training and materials and subsequently begins the e-Connect intervention
|
e-Connect
|
No Intervention: Standard of care
Counties use the standard of care and there is no intervention in practices.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Behavioral health treatment initiation
Time Frame: Monthly in years 2- 5
|
Date of first behavioral health appointment/contact extracted from state management information system (MIS)
|
Monthly in years 2- 5
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Behavioral health referral
Time Frame: Day one of probation
|
Clinically appropriate referral made by probation officer to behavioral health provider, based on screening results, indicated by referral date extracted from MIS
|
Day one of probation
|
Youth screened for risk of suicide
Time Frame: Day one of probation
|
Evidence-based screening tool self administered by youth
|
Day one of probation
|
Family Experience and Fidelity of e-Connect
Time Frame: Bimonthly years 2-5
|
PO completes family debriefing checklist: family receptivity to screening results and referral plan
|
Bimonthly years 2-5
|
e-Connect Sustainability
Time Frame: end of implementation through sustainment period, monthly
|
Ongoing use of e-Connect during post implementation phase
|
end of implementation through sustainment period, monthly
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Suicidal Behavior, Non-Suicidal Self-Injury (NSSI), BH knowledge
Time Frame: Years 1-5
|
Measured during pre-post quizzes following web-based training modules; developed for study
|
Years 1-5
|
Perceived importance of screening and referral to BH - Baseline Phase services
Time Frame: 2 months
|
Subscales for screening - Measure assessing perceived importance of activities associated with screening, referral and linkage - developed by JJTRIALS research cooperative.
|
2 months
|
Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Katherine Elkington, PhD, Columbia University/New York State Psychiatric Institute
Publications and helpful links
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 7588
- R01MH113599 (U.S. NIH Grant/Contract)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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