What this study is
The overarching goal of this project is to expand access to evidence-based suicide risk assessment, safety planning, and intervention among patients at elevated suicide risk by implementing Jaspr in a real-world psychiatric setting.
What's being tested
- Jaspr
Intervention · BEHAVIORAL
Jaspr is a digital platform developed to "increase the delivery of suicide prevention evidence-based practices without adding to personnel needs in an effort to reduce suicidal behavior with an ultimate goal of saving lives." Jaspr includes the following evidence-based components: Comprehensive suicide assessment, crisis stability plans, and lethal means counseling, comfort and skills, and shared stories.
Study details
- Official title
- Expanding Access to Evidence-Based Suicide Risk Assessment and Intervention in a Crisis Stabilization Setting (Patient Informants and RCT)
- Sponsor
- Butler Hospital
- Conditions
- Suicide · Suicide Attempt · Randomized Controlled Trial (RCT)
- Enrolling
- 80 people
- Starts
- 2026-10-01
- Est. completion
- 2027-10-31
- Design
- Single-blind, randomized, parallel groups
- Record
- View on ClinicalTrials.gov ↗
Who can join
Age 18 Years and overSex ALLHealthy volunteers Not acceptedYou may qualify if
- Aged 18 and older
- Able to read, write, and understand English well enough to complete study procedures
- Presence of past-month active suicidal ideation (i.e., Columbia Suicide Severity Rating Scale [C-SSRS] screener >1) and/or past three-month suicidal behavior, verified by the C-SSRS screener
- Owns a smartphone compatible with downloading the Jaspr-at-Home app
You can't join if
- Medically or cognitively unable to participate in study procedures (e.g., current psychotic symptoms),
- Psychosocial factors influencing ability to complete study procedures (e.g., pending incarceration)
Sign in and we'll check these against your records.Full criteria on ClinicalTrials.gov ↗
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Study locations (2)
2 openButler Hospital
Providence, Rhode Island, United States
- Gabriela Tolentino · Contact555-555-5555GTolentino@carene.org
- Heather Schatten, PhD · Principal investigator
- Michael Armey, PhD · Sub-investigator
- Christopher Hughes, PhD · Sub-investigator
- Gemma Wallace, PhD · Sub-investigator
Brown University
Providence, Rhode Island, United States
Study team
Sponsor
Butler Hospital
Study ID BH-2339835
Frequently asked questions
The sponsor hasn't published answers to common questions for this trial.