THRIVE: A Recovery-Focused Suicide Prevention Intervention in Crisis Stabilization Centers
THRIVE
THRIVE: Hybrid Randomized Effectiveness-Implementation Trial of a Recovery-Focused Suicide Prevention Intervention for Crisis Stabilization Centers
2 other identifiers
interventional
552
1 country
3
Brief Summary
Suicide is a major public health concern in the United States, with more than 1.4 million adults attempting suicide and nearly 50,000 adults dying by suicide each year. The launch of the national 3-digit 988 Suicide \& Crisis Lifeline in 2022 has strengthened the crisis care system by emphasizing the need for people in crisis to have someone to call, someone to respond, and somewhere to go. Community-based Crisis Stabilization Centers (CSCs) are an important part of the crisis care system, providing short-term crisis stabilization services and an alternative to Emergency Department care. However, suicide risk can remain high after discharge from CSCs, and no brief, effective, recovery-focused interventions are currently available for this setting. This study will evaluate the effectiveness of THRIVE (Toward Hope, Recovery, Interpersonal Growth, Values, and Engagement) in CSCs. THRIVE is a recovery-focused intervention designed for adults receiving care for suicide risk . THRIVE includes one 60-minute psychotherapy group (focused on belonging, giving, meaningful living, and recovery) delivered during the CSC stay and up to six peer-led recovery coaching calls during the weeks following discharge. This multi-site Hybrid Type 1 randomized effectiveness-implementation trial will enroll 552 participants and compare care as usual (CAU) in CSCs to CAU plus THRIVE (CAU + THRIVE). The primary purpose of this study is to determine whether THRIVE reduces suicide risk events (SREs) following CSC discharge, including crisis care re-admissions, escalation to higher levels of care, suicide attempts, and suicide deaths. The study will also examine barriers and facilitators that may influence the adoption and implementation of THRIVE in community-based crisis settings.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Oct 2026
Longer than P75 for not_applicable
3 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
First Submitted
Initial submission to the registry
August 14, 2026
CompletedFirst Posted
Study publicly available on registry
August 25, 2026
CompletedStudy Start
First participant enrolled
October 15, 2026
ExpectedPrimary Completion
Last participant's last visit for primary outcome
October 1, 2030
Study Completion
Last participant's last visit for all outcomes
October 1, 2031
August 25, 2026
August 1, 2026
4 years
August 14, 2026
August 21, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Total Suicide Risk Events (SREs) per Arm
Suicide Risk Events (SREs) is the total aggregate number of crisis care contacts for suicide risk (e.g., crisis center re-admissions, care escalations to the emergency department or inpatient units, suicide attempts, suicide deaths) in the 12-months post-discharge. We will include SREs discovered through three sources: 1) Participant follow-up surveys, including the Columbia Suicide Severity Rating Scale; 2) Electronic Health Record data; 3) Claims data. We will apply a pre-set codebook with adjudication rules to determine whether post-discharge SREs are suicide-related or non-suicide related. Each participant will be ascribed one numeric value (e.g., "3"; "12") representing the total number of SREs occurring post-discharge based on all available data . To assess differences in the number of SREs according to arm, a generalized linear model (GLM) will be fit.
12 Months
Study Arms (2)
Care as Usual + THRIVE
EXPERIMENTALBehavioral: THRIVE Toward Hope, Recovery, Interpersonal Growth, Values and Engagement (THRIVE), is a brief, suicide-specific, narrative, recovery-focused, 60 minute group psychotherapy intervention followed by up to 6 peer-led recovery coaching phone calls. THRIVE includes five components: 1) Creating a Safe Space for Disclosure; 2) Psychoeducation on Suicide Recovery; 3) Sharing the Suicide Narrative; 4) Completing the Meaningful Living Plan; 5) Taking Action on the Meaningful Living Plan in the Community. Behavioral: Usual Care Care as Usual in Crisis Stabilization Centers includes medication management, the safety planning Intervention, group psychoeducation, individual counseling, discharge planning, and community referral linkages
Care as Usual
ACTIVE COMPARATORCare as Usual in the Crisis Stabilization Centers includes medication management, the safety planning Intervention, individual counseling, group psychoeducation, discharge planning, and community referral linkages.
Interventions
Care as Usual in the Crisis Stabilization Centers includes medication management, the safety planning Intervention, individual counseling, group psychoeducation, discharge planning, and community referral linkages.
Toward Hope, Recovery, Interpersonal Growth, Values and Engagement (THRIVE), is a brief, suicide-specific, narrative, recovery-focused, 60 minute group psychotherapy intervention followed by up to 6 peer-led recovery coaching phone calls. THRIVE includes five components: 1) Creating a Safe Space for Disclosure; 2) Psychoeducation on Suicide Recovery; 3) Sharing the Suicide narrative; 4) Completing the Meaningful Living Plan; 5) Taking Action on the Meaningful Living Plan in the Community.
Eligibility Criteria
You may qualify if:
- Admission to CSC with suicidal crisis, as defined by active suicide ideation ascertained by the Columbia Suicide-Severity Rating scale (C-SSRS), which the sites already routinely administer
- Ability and willingness to provide information and permission to contact at least one person in case of emergency or inability to reach the participant for follow-up.
You may not qualify if:
- Under age 18.
- Inability to communicate with the researcher in English.
- Acute psychiatric instability (e.g., psychotic symptoms) prohibiting participation in psychotherapy.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (3)
Wellstone
Huntsville, Alabama, 35802, United States
Connections Health Solutions
Phoenix, Arizona, 85007, United States
Mental Health Cooperative
Nashville, Tennessee, 35756, United States
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Jennifer D Lockman, PhD
University of Alabama at Birmingham
Central Study Contacts
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
August 14, 2026
First Posted
August 25, 2026
Study Start (Estimated)
October 15, 2026
Primary Completion (Estimated)
October 1, 2030
Study Completion (Estimated)
October 1, 2031
Last Updated
August 25, 2026
Record last verified: 2026-08
Data Sharing
- IPD Sharing
- Will share
- Shared Documents
- SAP, ICF, ANALYTIC CODE
- Time Frame
- De-identified data will be made available for sharing as soon as is possible, no later than at the time of an associated peer-reviewed publication or the end of the grant award period, whichever occurs first. Data will continue to be available following the end of the award period. Individuals may access it by applying.
- Access Criteria
- Deidentified data will be deposited into the National Data Archive (NDA) and Open Science Framework (OSF) data repositories, which will restrict access to the data to qualified investigators who request access to the data. NDA and OSF will approve sharing requests at their discretion.
We will share de-identified IPD according to our comprehensive NIMH Data Management and Sharing Plan