RecruitingNot Applicable

Efficacy, Effectiveness, and Implementation of Jaspr Health in Emergency Department- Part A

United States670 participantsStarted 2024-02-23

Plain-language summary

This Study will comprehensively evaluate a multi-component suicide prevention technology (Jaspr Health) that facilitates delivery of suicided-related evidence-based practices (EBPs) while replacing wasted waiting time with productive time in the Emergency Departments (EDs). The EBPs satisfy several key performance elements for systems adopting Zero Suicide. A Complementary Randomized Controlled Trial and Real-World Study for Efficacy, Effectiveness, and Implementation Study Design (CREID) will be used

Who can participate

Age range18 Years

SexALL

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Inclusion Criteria: * Positive for suicide risk on the Patient Safety Screener in the ED (active suicidal ideation int the past 2 weeks, or suicidal attempt in the past 6 months) * Cognitively and emotionally capable of consent and engaging in Jaspr app. * Reads English at 6th grade level. * Reliable telephone access. * Owns a smart phone * Lives in Massachusetts Exclusion Criteria: * Prisoners or in state custody * Adults unable to consent * Patient \<18 yeas * Enrolled subjects during the 12 month follow-up period

What they're measuring

Suicide composite, binary

Timeframe: 12 months after enrollment

Trial details

NCT IDNCT06223867

SponsorUniversity of Massachusetts, Worcester

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2028-03-31

Contact for this trial

Edwin D Boudreaux, PhD

508-334-3817 Edwin.Boudreaux@umassmed.edu

View on ClinicalTrials.gov More Suicidal Ideation trials