Suicide Prevention Intervention for At-Risk Individuals in Transition
SPIRIT
Suicide Risk Reduction in the Year Following Jail Release: the SPIRIT Trial (Suicide Prevention Intervention for At-Risk Individuals in Transition)
1 other identifier
interventional
800
1 country
2
Brief Summary
The four year SPIRIT Trial, or Suicide Prevention Intervention for at-Risk Individuals in Transition, will recruit 800 pretrial jail detainees at risk for suicide. Each participant will be randomly assigned to today's standard care or to Safety Planning Intervention (SPI) method and then followed for one year after release. Outcomes include suicide events, suicide attempts and ideation, psychiatric symptoms, functioning, treatment utilization, problem-solving, belongingness, and cost-effectiveness.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Apr 2016
Longer than P75 for not_applicable
2 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
April 1, 2016
CompletedFirst Submitted
Initial submission to the registry
April 26, 2016
CompletedFirst Posted
Study publicly available on registry
May 3, 2016
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 31, 2019
CompletedStudy Completion
Last participant's last visit for all outcomes
December 31, 2019
CompletedResults Posted
Study results publicly available
December 10, 2025
CompletedDecember 10, 2025
November 1, 2025
3.8 years
April 26, 2016
October 27, 2025
November 25, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Suicide Events
Number of suicide events (a composite of attempts, behaviors, suicide-related hospitalizations, and suicide deaths) in the year following jail release. Events are identified through self-report, hospital records, and death records.
One year after jail release
Secondary Outcomes (9)
Suicide Attempts
One year after release from jail
Weeks of Active Suicide Ideation
One year after release from jail
Severity of Suicide Ideation
Assessed 1, 4, 8, and 12 months after release from jail, 12 months reported.
Time to First Suicide Event
One year after release from jail
Psychiatric Symptoms
Assessed 1, 4, 8, and 12 months after release from jail, 12 months reported.
- +4 more secondary outcomes
Study Arms (2)
Safety Planning Intervention
EXPERIMENTALBrown and Stanley's Safety Planning Intervention (SPI) is a brief, adjunctive intervention designed to reduce subsequent suicidal behavior in high-risk populations. The core element of SPI is the collaborative development of the Safety Plan, which is a prioritized written list of coping strategies and supports that individuals can use during or preceding suicidal crises. In this study, safety planning will occur during pretrial jail detention, with telephone follow-up in the community to conduct risk assessment, review the Safety Plan, problem-solve obstacles to treatment, and assist with linkage to services.
Standard Care
NO INTERVENTIONStandard Care for pretrial jail detainees is assessment of risk and stabilization to the extent possible during their jail detention. No post-release community follow-up is typically provided. This study will augment standard care with regular assessment and emergency referral post-release, as well as provision of a list of community resources.
Interventions
Brown and Stanley's Safety Planning Intervention (SPI) is a brief, adjunctive intervention designed to reduce subsequent suicidal behavior in high-risk populations. The core element of SPI is the collaborative development of the Safety Plan, which is a prioritized written list of coping strategies and supports that individuals can use during or preceding suicidal crises. In this study, safety planning will occur during pretrial jail detention, with telephone follow-up in the community to conduct risk assessment, review the Safety Plan, problem-solve obstacles to treatment, and assist with linkage to services.
Eligibility Criteria
You may qualify if:
- Unsentenced male and female pretrial jail detainees
- + years of age
- at risk for suicide, operationalized as a response of "yes" on item 4 or greater on the initial 5 C-SSRS screening questions, indicating the presence of at least some active suicide ideation with some intent to act in the past month (i.e., individuals at higher risk, such as those who report intent with specific plan and/or suicide attempt/s in the last month, will also be included);
- speak and understand English well enough to understand questionnaires when they are read aloud.
You may not qualify if:
- expects to be sentenced and serve their sentence before being released to the community
- cannot provide the name and contact information of at least two locator persons
- does not have access to any telephone.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Michigan State Universitylead
- Brown Universitycollaborator
Study Sites (2)
Genesee County Jail
Flint, Michigan, 48502, United States
Rhode Island Department of Corrections
Cranston, Rhode Island, 02879, United States
Related Publications (1)
Weinstock LM, Jones RN, Miller TR, Brown GK, Arias SA, Graves HR, Miller IW, Cerbo L, Rexroth J, Fitting H, Russell D, Kubiak S, Stein MD, Matkovic C, Yen S, Gaudiano BA, Johnson JE. Safety Planning vs Standard Care for Suicide Prevention After Pretrial Jail Detention: A Randomized Clinical Trial. JAMA Netw Open. 2025 Nov 3;8(11):e2543156. doi: 10.1001/jamanetworkopen.2025.43156.
PMID: 41212557DERIVED
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Results Point of Contact
- Title
- Dr. Jennifer Johnson
- Organization
- Michigan State University
Study Officials
- PRINCIPAL INVESTIGATOR
Jennifer Johnson, PhD
Michigan State University
- PRINCIPAL INVESTIGATOR
Lauren Weinstock, PhD
Brown University
Publication Agreements
- PI is Sponsor Employee
- No
- Restrictive Agreement
- No
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal Investigator
Study Record Dates
First Submitted
April 26, 2016
First Posted
May 3, 2016
Study Start
April 1, 2016
Primary Completion
December 31, 2019
Study Completion
December 31, 2019
Last Updated
December 10, 2025
Results First Posted
December 10, 2025
Record last verified: 2025-11
Data Sharing
- IPD Sharing
- Will share
De-identified data will be made available through relevant NIH and NIJ repositories after the trial has ended.