RECRUITING

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

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

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

Official Title

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

Quick Facts

Study Start:2024-02-23
Study Completion:2027-04-01
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06223867

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * 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)
  2. * Cognitively and emotionally capable of consent and engaging in Jaspr app.
  3. * Reads English at 6th grade level.
  4. * Reliable telephone access.
  5. * Owns a smart phone
  6. * Lives in Massachusetts
  1. * Prisoners or in state custody
  2. * Adults unable to consent
  3. * Patient \<18 yeas
  4. * Enrolled subjects during the 12 month follow-up period

Contacts and Locations

Study Contact

Edwin D Boudreaux, PhD
CONTACT
508-334-3817
Edwin.Boudreaux@umassmed.edu
Mhd B Rahmoun, MD
CONTACT
Mhd.Rahmoun@umassmed.edu

Principal Investigator

Edwin D Boudreaux, PhD
PRINCIPAL_INVESTIGATOR
University of Massachusetts, Worcester

Study Locations (Sites)

UMass Memorial Health
Worcester, Massachusetts, 01655
United States

Collaborators and Investigators

Sponsor: University of Massachusetts, Worcester

  • Edwin D Boudreaux, PhD, PRINCIPAL_INVESTIGATOR, University of Massachusetts, Worcester

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2024-02-23
Study Completion Date2027-04-01

Study Record Updates

Study Start Date2024-02-23
Study Completion Date2027-04-01

Terms related to this study

Keywords Provided by Researchers

  • Suicide
  • Self-Harm
  • Attempt
  • Ideation
  • Suicidal thought
  • Suicidal plan
  • Crisis intervention
  • Suicide prevention
  • Emotional support
  • Mental Health
  • Behavioral Health
  • Psychiatry
  • Emergency Department
  • Technology
  • Mobile Application
  • Implementation
  • Safety Plan
  • Lethal Means

Additional Relevant MeSH Terms

  • Suicidal Ideation
  • Suicide Attempt
  • Self Harm