Efficacy, Effectiveness, and Implementation of Jaspr Health in Emergency Department- Part A
Evaluation of Efficacy, Effectiveness, and Implementation of Jaspr Health's Digital Platform in Emergency Department for Patients With Suicidal Risk- Part A: Randomized Controlled Trial
Who can join
Ages 18 and older · All sexes
Full eligibility criteria
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
About the study
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
What is being tested
- Jaspr App + JAH (device)
- ETAU (behavioral)
Sponsor: University of Massachusetts, Worcester · Participants: 670 · Started: Feb 23, 2024
Contact the study team
- Edwin D Boudreaux, PhD · Phone: 508-334-3817
Official record on ClinicalTrials.gov — NCT06223867
Locations in the U.S.
| Massachusetts | UMass Memorial Health, Worcester |
Conditions
From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.