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

NCT ID: NCT06506344

Last Updated: 2025-12-09

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Clinical Phase

NA

Total Enrollment

5250 participants

Study Classification

INTERVENTIONAL

Study Start Date

2024-06-24

Study Completion Date

2027-07-31

Brief Summary

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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

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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.

Conditions

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Suicide Prevention

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

HEALTH_SERVICES_RESEARCH

Blinding Strategy

NONE

Study Groups

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5S Trial

Participants will receive an intervention aimed at suicide prevention in this group.

Group Type EXPERIMENTAL

5S Trial

Intervention Type BEHAVIORAL

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.

No-Contact Control Group

Participants will be able to engage with healthcare services as usual and will have no knowledge of their involvement in the study.

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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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.

Intervention Type BEHAVIORAL

Eligibility Criteria

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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
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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National Institute of Mental Health (NIMH)

NIH

Sponsor Role collaborator

Michigan State University

OTHER

Sponsor Role collaborator

HealthPartners Institute

OTHER

Sponsor Role collaborator

Brown University

OTHER

Sponsor Role collaborator

Henry Ford Health System

OTHER

Sponsor Role lead

Responsible Party

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Brian Ahmedani

Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Brian Ahmedani, PhD, MSW

Role: PRINCIPAL_INVESTIGATOR

Henry Ford Health

Lauren Weinstock, PhD

Role: PRINCIPAL_INVESTIGATOR

Brown University

Rebecca Rossom, MD, MS

Role: PRINCIPAL_INVESTIGATOR

HealthPartners Institute

Locations

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Henry Ford Health

Detroit, Michigan, United States

Site Status RECRUITING

HealthPartners Institute

Bloomington, Minnesota, United States

Site Status RECRUITING

Countries

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United States

Central Contacts

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Diane Wisnieski, MSW

Role: CONTACT

313-319-6084

Facility Contacts

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Diane Wisnieski, MSW

Role: primary

313-319-6084

Caitlin Borgert-Spaniol, MA

Role: primary

952-883-5421

Other Identifiers

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5P50MH127512-02

Identifier Type: NIH

Identifier Source: org_study_id

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