Efficacy, Effectiveness, and Implementation of Jaspr Health in Emergency Department- Part A
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorUniversity of Massachusetts, Worcester
About this trial
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
Eligibility criteria
Qualifiers
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.
Disqualifiers
Prisoners or in state custody
Adults unable to consent
Patient <18 yeas
Enrolled subjects during the 12 month follow-up period
Trial design
Treatments tested in this trial
- Jaspr App + JAH
- ETAU
Treatment groups
670 Participants
are divided into 2 treatment groupsSponsors and collaborators
University of Massachusetts, Worcester
Lead sponsor
Ohio State University
Collaborator
Evidence-Based Practice Institute, Seattle, WA
Collaborator
Worcester Polytechnic Institute
Collaborator
National Institute of Mental Health (NIMH)
Collaborator
University of Colorado, Denver
Collaborator
Source ClinicalTrials.gov