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NCT06223867: Jaspr-PartA

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

Recruiting now NA Last updated 20 February 2026
What this trial tests

NA trial testing Jaspr App + JAH in Suicidal Ideation in 670 participants. Currently enrolling.

Timeline
23 February 2024
Primary endpoint
31 March 2028
31 March 2028

Quick facts

Lead sponsorUniversity of Massachusetts, Worcester
PhaseNA
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingsingle
Primary purposehealth services research
Enrollment670
Start date23 February 2024
Primary completion31 March 2028
Estimated completion31 March 2028
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

University of Massachusetts, Worcester

Who can join

18 and older, any sex, with Suicidal Ideation or Suicide Attempt. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Suicidal Ideation

Currently open trials in the same condition.

Other University of Massachusetts, Worcester trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06223867.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing