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Recruiting NCT06506344

Syncing Screening and Services for Suicide Prevention Across Health and Jail Systems

No phase Interventional Suicide Prevention

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: 5S Trial.
Who it may be relevant to
Registry conditions: Suicide Prevention. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United States
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Project 1 (Signature): Syncing Screening and Services for Suicide Prevention Across Health and Jail Systems

Overview

This study aims to harmonize jail release record data with electronic health record data in order to connect patients to an evidence-based suicide prevention and clinical care pathway upon jail release.

Detailed description

This study is designed to test the effectiveness of a care pathway delivered at the time of jail release, to increase behavioral health services engagement and prevent suicide attempt. There are 3 primary aims of this study: (1) Examine the effectiveness of the intervention on suicide attempt outcomes. (2) Evaluate the impact of the intervention on behavioral health utilization mechanisms. (3) Evaluate implementation outcomes and processes to guide future implementation and research, including: cost and cost-effectiveness; scalability; sustainability; feasibility, acceptability, and appropriateness to providers/systems; and implementation strategies.

Interventions

  • Behavioral 5S Trial
    Participants will receive caring contacts/recruitment outreach, suicide risk screening, suicide safety planning, and, if indicated, connection to healthcare services, resources and the CLASP virtual outreach intervention.

Primary outcome measures

  • Composite measures of suicide attempt and death [Time frame: 6-months from jail release date]

Eligibility criteria

Inclusion criteria

  • 18 years of age or older
  • Released from jail between February 2021 and July of 2028
  • Had a prior primary care visit or behavioral health visit at a participating health system in the past 3 years

Exclusion criteria

  • Does not currently reside in the same state as the study site (i.e.- Michigan, Minnesota)
  • Would require a translator to participate in the research according to EHR data
  • Previously requested to be excluded from research

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Open label
Primary purpose
Health services research

Study locations

United States · 2 centers
  • Henry Ford Health — Detroit
  • HealthPartners Institute — Bloomington

Publications

  • Wisnieski DM, Rossom RC, Weinstock LM, Johnson J, Miley K, Gaudiano BA, Benz MB, Borgert-Spaniol C, Graves HR, Norwood R, Kazan R, Starkey C, Kim H, Fletcher L, Kane S, Hu Y, Farrell Z, Strong S, Yeh HH, Miller T, Jones R, Morey K, Ahmedani BK. Study protocol for a type I hybrid effectiveness trial of strategies to prevent suicide attempts among adults recently released from jail. Contemp Clin Tri PMID 41407099

Identifiers

NCT: NCT06506344 · 5P50MH127512-02

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗