Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT06223867

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

Led by University of Massachusetts, Worcester · Updated on 2026-02-20

670

Participants Needed

1

Research Sites

214 weeks

Total Duration

On this page

Sponsors

U

University of Massachusetts, Worcester

Lead Sponsor

O

Ohio State University

Collaborating Sponsor

AI-Summary

What this Trial Is About

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

CONDITIONS

Official Title

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

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Positive for suicide risk on the Patient Safety Screener in the ED (active suicidal ideation in 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
  • Has reliable telephone access
  • Owns a smartphone
  • Lives in Massachusetts
Not Eligible

You will not qualify if you...

  • Prisoners or in state custody
  • Adults unable to consent
  • Patients younger than 18 years
  • Subjects enrolled during the 12 month follow-up period

AI-Screening

AI-Powered Screening

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Trial Site Locations

Total: 1 location

1

UMass Memorial Health

Worcester, Massachusetts, United States, 01655

Actively Recruiting

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Research Team

E

Edwin D Boudreaux, PhD

CONTACT

M

Mhd B Rahmoun, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

HEALTH_SERVICES_RESEARCH

Number of Arms

2

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