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

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Henry Ford Health

Status

Enrolling

Conditions

Suicide Prevention

Treatments

Behavioral: 5S Trial

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT06506344
5P50MH127512-02 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

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.

Full 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.

Enrollment

5,250 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

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

Trial design

Primary purpose

Health Services Research

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

5,250 participants in 2 patient groups

5S Trial
Experimental group
Description:
Participants will receive an intervention aimed at suicide prevention in this group.
Treatment:
Behavioral: 5S Trial
No-Contact Control Group
No Intervention group
Description:
Participants will be able to engage with healthcare services as usual and will have no knowledge of their involvement in the study.

Trial contacts and locations

2

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Central trial contact

Diane Wisnieski, MSW

Data sourced from clinicaltrials.gov

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