ClinicalTrials.Veeva

Menu

Advancing Student Suicide Interventions With Scalable Technologies (ASSIST)

University of Massachusetts, Amherst logo

University of Massachusetts, Amherst

Status

Invitation-only

Conditions

Suicide Attempt
Suicidal Ideation
Self-Harm

Treatments

Device: Jaspr
Behavioral: Behavioral support

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT07211373
UMassIRB6366
P50MH129701 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

Mobile-based applications, such as JasprHealth, can deliver evidence-based skills intended to reduce imminent suicide risk (e.g., reducing means access), improve emotional states (e.g., via distraction and coaching to act opposite to emotions), and reduce feelings of social isolation (e.g., via shared stories), but user engagement is a barrier. The aim of this study was to examine the effects of a technological application resource (Jaspr) relative to human augmentation (Jaspr+, e.g., motivationally focused orientation plus prompts) on acceptability, preliminary effectiveness, and engagement among college students who screen positive for suicide risk.

Full description

Mobile-based applications, such as Jaspr Health, can deliver evidence-based skills intended to reduce imminent suicide risk (e.g., reducing means access), improve emotional states (e.g., via distraction and coaching to act opposite to emotions), and reduce feelings of social isolation (e.g., via shared stories). Although mobile-device-delivered interventions hold the potential to make interventions widely accessible, user engagement presents a substantial barrier to efficacy. This study, ASSIST: Advancing Student Suicide Interventions with Scalable Technologies, aims to improve engagement with mobile-delivered suicide prevention applications, with the ultimate goal of reducing suicidal thoughts and behaviors in college students. Including human elements alongside Jaspr Health has the potential to improve the uptake of this evidence-based, accessible mobile-device-delivered intervention.

The aim of this study was is to examine the effects of the technological application resource Jaspr tablet application with access to Jaspr at Home (JAH) vs. Jaspr+ human augmentation (e.g., motivationally focused orientation plus prompts) on acceptability, preliminary effectiveness, and engagement among 50 college students who screen positive for suicide risk (n=25 per condition) over the course of 2 months. Candidate mechanisms (e.g., coping skills, self-stigma) will also be assessed. Participants were randomized via the Redcap randomization module, stratified by site.

Enrollment

50 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Recent suicidal thoughts or behavior (i.e., past 2-week suicidal ideation or past 6-month suicidal behaviors)
  • Current UMass Amherst or University of Wisconsin Madison undergraduate student
  • 18 years of age or older
  • Ability to understand written or spoken English
  • Owning a mobile device
  • Ability to understand and consent to study procedures

Exclusion criteria

  • No recent suicidal thoughts or behaviors (i.e., past 2-week suicidal ideation or past 6-month suicidal behaviors)
  • Not a current UMass Amherst or University of Wisconsin Madison undergraduate student
  • Under 18 years of age
  • Inability to understand written or spoken English
  • Does not own a mobile device

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

50 participants in 2 patient groups

Jaspr
Experimental group
Description:
Subjects in this arm will complete a guided Safety Planning, and Lethal means counseling on the Jaspr app before open access to the Jaspr resource library. Subjects can sign up to receive Jaspr At Home (JAH) mobile app. Subjects will have continue to have access to treatment as usual through their respective university clinics.
Treatment:
Device: Jaspr
Jaspr+
Experimental group
Description:
Subjects in this arm will complete a guided Safety Planning, and Lethal means counseling on the Jaspr app before open access to the Jaspr resource library. This will be guided by motivational interviewing principles. Subjects can sign up to receive Jaspr At Home (JAH0 mobile app. Subjects will be prompted with their personalized goals as reminders to use the Jaspr at home app. Subjects will have continue to have access to treatment as usual through their respective university clinics.
Treatment:
Behavioral: Behavioral support
Device: Jaspr

Trial documents
1

Trial contacts and locations

1

Loading...

Central trial contact

Study Coordinator; Katherine L Dixon-Gordon, PhD

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems