Actively Recruiting
Intensive Case Management Between VA and Community Care for Suicide Prevention
Led by VA Eastern Colorado Health Care System · Updated on 2026-04-16
100
Participants Needed
1
Research Sites
147 weeks
Total Duration
On this page
Sponsors
V
VA Eastern Colorado Health Care System
Lead Sponsor
U
US Department of Veterans Affairs
Collaborating Sponsor
AI-Summary
What this Trial Is About
The goal of this randomized clinical trial is to build the evidence base for SUPERCEDE, a suicide prevention focused intensive case management intervention to increase access, improve care coordination, provide suicide prevention monitoring, and procure a timely response of VA mental health and suicide prevention services among VA-enrolled veterans receiving VA authorized community care. This phase is a hybrid effectiveness Type 1 randomized control trial, which will include 2 arms: the treatment intervention, SUPERCEDE, and the control intervention, present centered therapy. The main questions it aims to answer are:• This RCT will continue to build the evidence base for effectiveness and determine feasibility and acceptability for the previously piloted SUPERCEDE. • This RCT will improve the understanding of implementation of this intervention, both in VA and VA authorized community care organizations in preparation for broader implementation. Researchers will compare SUPERCEDE and present centered therapy to see if SUPERCEDE results in improved functioning and a decrease in suicidal ideation. Participants will be randomized to either SUPERCEDE or present centered therapy (PCT) plus a safety plan if warranted. SUPERCEDE is a suicide prevention case management intervention that combines BCBT-SP, a Crisis Response Plan (CRP), intensive case management to alleviate suicide risk factors, and VA authorized community care coordination. PCT is an active control condition often used in clinical trials of posttraumatic stress disorder. The intervention focuses on the present moment and encouraging the client to find solutions to their problems. In this trial, investigators will mirror the sessions of PCT to SUPERCEDE. Thus, the control group will receive 3 sessions, with an optional 3 additional sessions. Detailed Description For hypothesis 3a: Overall, 100 participants will be randomized to either SUPERCEDE or present centered therapy (PCT) plus a safety plan if warranted. SUPERCEDE is a suicide prevention case management intervention that combines BCBT-SP, a Crisis Response Plan, intensive case management to alleviate suicide risk factors, and VA authorized community care coordination. PCT is an active control condition often used in clinical trials of posttraumatic stress disorder. The intervention focuses on the present moment and encouraging the client to find solutions to their problems. In this trial, investigators will mirror the sessions of PCT to SUPERCEDE. Thus, the control group will receive 3 sessions, with an optional 3 additional sessions. The study therapist is trained in both SUPERCEDE and PCT. Recruitment. Eligible participants will be identified through the VA Rocky Mountain Regional (RMR) Medical Center the VA Corporate Data Warehouse (CDW), flyers and advertisements, or through clinician or community referral. A recruitment letter will be sent to participants identified in the CDW. Investigators will attempt to contact potential participants with a warm call by telephone (up to 3 times) after the letter is sent.
CONDITIONS
Official Title
Intensive Case Management Between VA and Community Care for Suicide Prevention
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Veterans enrolled in the VA Eastern Colorado Health Care System (ECHCS)
- Able to complete an online questionnaire
- Age 18 to 80 years
- Able to understand and provide virtual informed consent
- Receiving both VA care and VA authorized community care through the MISSION Act for any physical or mental health issue
- Veteran's non-VA care is authorized by the VA
- At risk for suicide as shown by any of the following: prior suicide attempt, suicidal thoughts in the past month, or current mental health symptoms (PHQ-9 >10 or PCL-5 >31)
- Reporting psychosocial challenges on the ACORN or Assessment of Needs measure
- Experiencing issues with VA community care coordination
- Receiving no or infrequent mental health services at the VA (less than once a month)
You will not qualify if you...
- At imminent risk of suicide or homicide requiring crisis intervention (eligible once stabilized)
- Unable or unwilling to participate in the intervention (e.g., unwilling to share VA community care information)
- No access to a device capable of telephone or video calls
- Any situation deemed inappropriate for this type of care by the principal investigator
AI-Screening
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Trial Site Locations
Total: 1 location
1
Eastern Colorado Healthcare System
Aurora, Colorado, United States, 80045
Actively Recruiting
Research Team
B
Bryann B DeBeer, PhD
CONTACT
P
Patricia D Russell, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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