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

Part of paid clinical trials in Aurora, Colorado.

Sponsor
University of Massachusetts, Worcester
Study ID
NCT06311591
Status
Enrolling By Invitation

Conditions

  • Self Harm
  • Suicidal Ideation
  • Suicide Attempt

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • Jaspr App — DEVICE
    Jaspr was designed to improve delivery of evidence-based, personalized suicide care in the ED. Jaspr (Dimeff, R44MH108222) is rooted in EBPs, including Collaborative Assessment and Management of Suicide (CAMS) and Dialectical Behavior Therapy (DBT). Briefly, Jaspr provides a patient interface, optimized for a tablet computer provided to the patient, which uses an avatar to administer: (1) the CAMS Suicide Status Form (SSF), an evidence-based suicide risk assessment; (2) crisis stabilization planning (CAMS' version of safety planning) or Stanley-Brown Safety Planning Intervention, depending on site choice; (3) lethal means safety counseling. Further, Jaspr teaches behavioral skills from DBT to manage imminent distress and has a library of over 40 racially and culturally diverse, inspirational videos of people with lived experience. Finally, Jaspr@home provides access to these resources after the visit during the high-risk transition to outpatient care.

Study Details

This Study will evaluate the implementation of 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

Key Dates

Start date
Nov 7, 2024
Status verified
Dec 2025
Primary completion
Jun 1, 2027
Completion
Jun 1, 2027

Study Design

Enrollment
27,908 participants (estimated)
Allocation
NON_RANDOMIZED
Intervention model
SEQUENTIAL
Primary purpose
HEALTH_SERVICES_RESEARCH

Arms

  • No Intervention: Enhanced Treatment as Usual (ETAU) Historical Control Group
    Enhanced Treatment As Usual (ETAU) Historical Control is defined as the treatment provided as part of routine clinical care in the participating EDs during a period of time when Jaspr was not being implemented.
  • Experimental: Jaspr Implementation Group
    This group will receive the enhanced treatment as usual (ETAU) provided as part of routine clinical care at the participating EDs. They will also be considered by their treating team for administration of Jaspr. Jaspr administers a Suicide Status Interview (SSI), Safety Planning, and Lethal means counseling, and allows open access to the Jaspr resource library. They can sign up to receive Jaspr at Home mobile app. Electronic Health Records (EHR) will be used to assess the outcomes in the 12 months following the index visit.

Primary Outcome Measure

Suicide composite, binary [ Time Frame: 12 months post enrollment ]

Locations (4)

FacilityCityStateZIPSite coordinators
UCHealth University of Colorado HospitalAuroraColorado80045-
UCHealth Memorial Hospital CentralColorado SpringsColorado80909-
Ohio State East HospitalColumbusOhio43210-
The Ohio State University Wexner Medical CenterColumbusOhio43210-

Find similar trials in Aurora, CO

By research site
UCHealth University of Colorado Hospital· Aurora, COUCHealth Memorial Hospital Central· Colorado Springs, COOhio State East Hospital· Columbus, OHThe Ohio State University Wexner Medical Center· Columbus, OH

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