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Veterans Coordinated Community Care (3C) Study

Targeted Intensive Case Management of Veterans at Risk of Suicide Post Inpatient Hospitalization

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05272176
Acronym
3C
Enrollment
850
Registered
2022-03-09
Start date
2022-01-11
Completion date
2026-06-30
Last updated
2026-07-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Suicide

Keywords

Veterans, Suicide Prevention, Behavioral Symptoms, Case Management

Brief summary

Veterans Coordinated Community Care (3C) Study will recruit 850 Veterans at risk for suicide post inpatient hospitalization. Each participant will be randomly assigned to treatment as usual (TAU) or TAU plus the Coping Long Term with Active Suicide Program (CLASP), with follow-up for 6 months after discharge. Outcomes include suicide-related behaviors (including deaths due to suicide, opioid overdose, or other substance-related accidents; and nonfatal suicide attempts) and suicidal ideation and functioning.

Detailed description

Suicide is a problem of great public health importance. The great majority of suicides occur among people with psychiatric disorders, and among psychiatric patients, those recently discharged from psychiatric hospitalization have highest suicide risk. Intensive post-discharge case management programs have been shown to reduce post-discharge suicides, but the rarity of these events even among recently-hospitalized patients makes it infeasible to argue for universal implementation of intensive post-discharge case management. Researchers propose to address this problem by carrying out a pragmatic trial among psychiatric inpatients in the Veterans Health Administration (VHA) healthcare system judged to be at high risk of post-discharge suicide (based on a validated prediction model). Researchers will evaluate the effects of a scalable remote post-discharge moderate intensity adjunctive intervention, the Coping Long Term with Active Suicide Program (CLASP), and carry out a heterogeneity of treatment effects (HTE) analysis to determine how these effects vary as a function of patient characteristics and features of the post-discharge treatment environment. Patients in the CLASP treatment will be asked to nominate a significant other (SO) to participate in the program with them. SO participation is optional. The aim of this research is to conduct a multi-site randomized controlled trial (N=850) of the CLASP intervention compared to treatment as usual for Veterans at risk for suicide post inpatient hospitalization. Assessments will occur at baseline and 6 months post discharge. Medical, administrative, and vital records will be obtained for each participant. The primary outcome of this study will be post-discharge suicide-related behaviors (including deaths due to suicide, opioid overdose, or other substance-related accidents; and nonfatal suicide attempts) in the 6 months post-discharge. Researchers will also evaluate secondary outcomes involving patient suicidal ideation and functioning.

Interventions

BEHAVIORALCoping Long Term with Active Suicide Program (CLASP)

Telehealth-based case management intervention designed to reduce suicidal behavior among individuals at high risk for suicide across the transition from inpatient hospitalization to the community.

Sponsors

Brown University
Lead SponsorOTHER
Harvard University
CollaboratorOTHER
Canandaigua VA Medical Center
CollaboratorFED
West Virginia University
CollaboratorOTHER
The Warren Alpert Foundation
CollaboratorUNKNOWN

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Inpatient Veteran at high-risk for post-discharge suicide (as flagged by the study's validated prediction model) * 18 years or older * Access to a telephone after discharge.

Exclusion criteria

* Impaired decision-making capacity * Limited or no English language proficiency * Terminal illness

Design outcomes

Primary

MeasureTime frameDescription
Veterans Affairs Healthcare System (VAHS) health and administrative records on suicide related behaviors6 months after dischargeSuicide related behaviors that include deaths due to suicide, opioid overdose, or other substance-related accidents; and nonfatal suicide attempts.
3C Suicide Outcome Measure6 months after dischargeStudy specific aggregate measure (3C Suicide Outcome Measure) containing selected items from the Columbia-Suicide Severity Rating Scale (C-SSRS), Self-Injurious Thoughts and Behaviors Interview (SITBI), and Suicidal Behaviors Questionnaire (SBQ).

Secondary

MeasureTime frameDescription
Veterans Affairs Healthcare System (VAHS) health and administrative records on suicidal ideation and functioning6 months after dischargeSuicidal ideation and functioning identified through VAHS health and administrative records
3C Suicidal Ideation and Functioning Outcome Measure6 months after dischargeStudy specific aggregate measure (3C Suicidal Ideation and Functioning Outcome Measure) containing selected items from the Columbia-Suicide Severity Rating Scale (C-SSRS), Self-Injurious Thoughts and Behaviors Interview (SITBI), and Suicidal Behaviors Questionnaire (SBQ), P4 Screener, Suicide Attempt Beliefs Scale (SABS), Brief Reasons for Living Inventory 10-Item Version (BRFL-10), Suicide-Related Coping Scale, and Acquired Capability for Suicide Scale

Countries

United States

Contacts

PRINCIPAL_INVESTIGATORLauren Weinstock, PhD

Brown University

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 16, 2026