Clinical Trial

Rapid Personalization of Safety Plans for Psychiatrically Hospitalized Veterans at High-Risk for Suicide

Not Yet Recruiting
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Summary
Veterans psychiatrically hospitalized face significantly elevated suicide risk, particularly in the three months post-discharge. While Safety Planning is a required component of discharge planning, many safety plans lack personalization thereby reducing their effectiveness. The proposed intervention, Personalized Safety Plans (PSP), will be developed for rapid delivery on acute inpatient psychiatry units. PSP is a single-session intervention followed by twice monthly brief, personalized coaching sessions during the three-month high-risk discharge period. PSP will be iteratively refined and finalized in a case series (N = 15) then evaluated in a pilot randomized controlled trial (N = 96) comparing PSP to Safety Plans as Usual among psychiatrically hospitalized Veterans. Overall, the study aims to: 1) iteratively refine PSP; 2) examine PSP's preliminary effectiveness in reducing suicide ideation and increasing adaptive coping; 3) identify barriers and facilitators to implementation; and 4) develop a fidelity measure to support future personalization monitoring.
Protocol Amendment History 3 changes
notable Primary completion pushed: 2031-03-28 -> 2031-08-31 2026-05-07
minor Completion pushed: 2031-04-30 -> 2031-09-30 2026-05-07
critical Phase changed: Phase 1 -> not applicable 2026-04-10
Trial Details
NCT Number NCT07507786
Lead Sponsor VA Office of Research and Development
Conditions Suicide
Enrollment 111 participants
Start Date 2026-10-01
Primary Completion 2031-08-31 (estimated)
Study Completion 2031-09-30 (estimated)
Updated on ClinicalTrials.gov 2026-05-06