Clinical trial Recruiting at 1 site Interventional Ages 10 and up

Scaling up e-Connect in Juvenile Probation Settings

Official title: Scaling up eConnect in Juvenile Probation Settings: a Hybrid Implementation Effectiveness Trial of a Digital Suicide Risk/Behavior Identification and linkage-to Treatment System

Run by New York State Psychiatric Institute · NCT05541926 · Data updated 2026-11-12

This project tests a plan to expand e-Connect, an evidence-based suicide risk and cross-system linkage program, across nine Indiana counties to see if it can be adopted widely and cost-effectively in juvenile probation settings.

Quick facts

Study typeInterventional
Ages10 Years and up
SexAll
Enrollment3629 (estimated)
SponsorNew York State Psychiatric Institute
Academic / other
Locations1 site (New York, New York)
StatusRecruiting
StartedMay 2, 2023
Main results expectedApril 30, 2028
Study endsAugust 31, 2028
Registry record updatedJune 30, 2026
Trial IDNCT05541926 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal participants are county probation staff, treatment staff, and local facilitators in participating sites who are adults fluent in English and employed by the partnering agencies.

Probably not a fit

Participants not directly benefiting may include youth not currently receiving e-Connect services within the system, as the study focuses on system-wide implementation.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

The study uses a stepped-wedge, implementation-effectiveness design to scale up an evidence-based suicide risk identification and cross-system linkage program (e-Connect) in juvenile justice settings. Guided by the GPM and EPIS frameworks, it involves External Facilitators helping Local Facilitators in nine counties to transfer knowledge and skills for sustained use. The project has three phases: preparation for scale-up, scale-up implementation and sustainment, and an effectiveness/outcome evaluation. Data will address clinical outcomes related to identification of service needs and cross-system referrals, as well as implementation costs. The work builds on a prior efficacy trial and aims to determine real-world feasibility, acceptability, and impact in a new system and geography.

Why it matters

Potential benefit: If successful, the approach could enable broader, more reliable identification of at-risk youth and improved linkage to services within juvenile justice settings.

How similar studies have gone: Previous feasibility work on e-Connect in another state provides a foundation, with this study expanding scale-up to a new jurisdiction and design.

Who can join: the full rules

Show full inclusion / exclusion criteria
Sample: County Probation Staff

Inclusion Criteria:

* All probation agency leadership and officers employed by the partnering sites who are (a) at least 18 years of age and (b) conversant in English in participating study counties are eligible

Exclusion Criteria:

* There are no exclusionary criteria and no special classes of participants.

Sample: County Treatment Staff

Inclusion Criteria:

* All treatment staff (agency directors, supervisors and clinical line staff) employed by participating treatment agencies who are at least 18 years of age and conversant in English in participating study counties will be asked to participate

Exclusion Criteria:

* There are no exclusionary criteria and no special classes of participants.

Sample: Local Facilitators

Inclusion Criteria:

* All county/local Justice Diversion Alternatives Initiative (JDAI) representatives that work with partnering sites who (a) are at least 18 years of age and (b) conversant in English in participating study counties are eligible

Exclusion Criteria:

* There are no exclusionary criteria and no special classes of participants.

Sample: Probation Youth

Inclusion Criteria:

* All youth who are on probation who are (a) 10-18 years of age and (b) conversant in English in participating study counties are eligible;

Exclusion Criteria:

* There are no exclusionary criteria and no special classes of participants.

Where it's running

  • Columbia University and New York State Psychiatric Instititute
    New York, New York, United States
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

  • Friends and family training for those at risk of suicide

    A six-week program tests whether training for caregivers can help them support a loved one at risk of suicide while also taking care of their own mental health.

    Recruiting Unity Health Toronto · Toronto, Ontario · NCT07902089

  • Inhaled DMT for major depressive disorder

    This trial tests whether inhaled DMT can quickly ease depressive symptoms and reduce suicide risk in adults with major depressive disorder.

    Recruiting Phase 2 Universidade Federal do Rio Grande do Norte · Fortaleza, Ceará and 4 other locations · NCT07562191

  • Suicide risk and learned suicide ability in people with mood disorders

    This project will try to identify which biological, psychological, social, and clinical factors relate to suicide risk and the learned ability for suicide in people aged 16–60 with mood disorders by collecting blood, urine, and questionnaire data.

    Recruiting Tianjin Anding Hospital · Tianjin, Tianjin Municipality · NCT07523490

  • Combining the Youth-Nominated Support Team with CBT for Black adolescents at acute suicide risk

    This project will test whether adding a computer-assisted Youth-Nominated Support Team to Cognitive Behavioral Therapy for Suicide Prevention helps Black adolescents (ages 12-17) who come to an urban emergency setting with suicidal thoughts or self-injury.

    Recruiting at 2 sites University of Michigan · Detroit, Michigan and 1 other locations · NCT07506460

  • Remote case management to prevent suicide after psychiatric hospital discharge

    This project will test whether a 6-month remote program called Pathfinding helps active-duty Army soldiers reduce suicidal behavior after leaving inpatient psychiatric care.

    Recruiting Uniformed Services University of the Health Sciences · Bethesda, Maryland · NCT07404787

  • Text reminders to help parents keep teens safe after a suicide-related ED visit

    This study tests whether sending parents text messages can help them reduce their teen’s access to lethal means and increase safety practices after a suicide-related emergency visit.

    Recruiting University of Texas Southwestern Medical Center · Dallas, Texas · NCT07383714

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.