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Feasibility, Acceptability, and Preliminary Efficacy of a Novel Personalized Mobile Intervention for Suicide - Open Trial (2)

StatusRecruiting
PhaseNot applicable
Started
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Record status
This record was last updated July 17, 2025 (before its estimated October 1, 2025 completion). Its status may not reflect the trial's current state.

Record History

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  1. Minor Primary and study completion dates: May 31, 2025 to Oct 1, 2025v8
  2. Notable Trial status: Not Yet Recruiting to Recruitingv7 Show 4 more changesShow less
    • Start date changed from estimate of Jul 1, 2024 to Jul 25, 2024
    • Interventions: Mobile Application to Prevent Suicide (MAPS) (Behavioral), Treatment as Usual + Ecological Momentary Assessment (TAU + EMA) (Behavioral) to Mobile Application to Prevent Suicide (MAPS) (Behavioral)
    • Site details revised
    • Study title expanded, about 1 word
  3. Notable Primary and study completion dates: May 31, 2024 to May 31, 2025
    • Start date: Mar 1, 2024 to Jul 1, 2024
    v6
  4. Notable Enrollment target: 40 to 10v5 Show 4 more changesShow less
    • Start date: Sep 1, 2023 to Mar 1, 2024
    • Primary and study completion dates: May 1, 2024 to May 31, 2024
    • Secondary endpoints: details revised at 1 of 2 entries
    • Study arms: 2 to 1
  5. Notable Primary and study completion dates: Aug 31, 2023 to May 1, 2024
    • Start date: Oct 1, 2022 to Sep 1, 2023
    v4
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  1. Notable Start date: Aug 1, 2022 to Oct 1, 2022v3
  2. Notable Start date: Feb 1, 2022 to Aug 1, 2022v2
  1. Minor Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • 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.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
30 trials monitored
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The primary aim of this grant is to conduct pilot testing on a novel personalized mobile intervention for suicide - Mobile Application to Prevent Suicide (MAPS) - and to establish feasibility, acceptability, safety, and primary outcomes (i.e., suicidal ideation and behavior; re-hospitalization).
Trial Details
NCT Number NCT05180344
Lead Sponsor Butler Hospital
Collaborators: American Foundation for Suicide Prevention
Conditions
(from sponsor)
Suicide, Suicide and Self-harm, Suicide, Attempted, Suicidal Ideation
Related terms Self-Injurious Behavior, Suicidal Ideation, Suicide, Suicide, Attempted
Enrollment 10 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov