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

StatusNot Yet Recruiting
PhaseNot applicable
Started

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Trial flagged as At Risk
Primary completion moved at least 2 months later Aug 31, 2031 → Oct 31, 2031
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Record History

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  1. Start date: Oct 1, 2026 to Dec 1, 2026 Show 4 more changesShow less
    • Primary completion pushed from Aug 31, 2031 to Oct 31, 2031
    • Study completion pushed from Sep 30, 2031 to Nov 30, 2031
    • Eligibility criteria expanded, about 8 words
    • Secondary endpoints: details revised at 3 of 3 entries
  2. Start date: May 1, 2026 to Oct 1, 2026
    • Primary completion pushed from Mar 28, 2031 to Aug 31, 2031
    • Study completion pushed from Apr 30, 2031 to Sep 30, 2031
    • Site contact updated
    v3
  3. Phase changed: Phase 1 → not applicable
    • Eligibility criteria shortened, about 10 words
    • Secondary endpoints: details revised at 3 of 3 entries
    v2
  4. Study First Submitted
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
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.
Trial Details
NCT Number NCT07507786
Lead Sponsor VA Office of Research and Development
Conditions
(from sponsor)		 Suicide
Related terms Suicide, Suicide Prevention
Enrollment 111 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov