Actively Recruiting
Augmented Momentary Personal Ecological Risk Evaluation
Led by University of Washington · Updated on 2025-11-26
50
Participants Needed
1
Research Sites
39 weeks
Total Duration
On this page
Sponsors
U
University of Washington
Lead Sponsor
N
National Institute of Mental Health (NIMH)
Collaborating Sponsor
AI-Summary
What this Trial Is About
The goal of this intervention study is to co-design and test an Ecological Momentary Assessment (EMA) prototype tool with young adults aged 16-30 experiencing suicidality to see if it is an acceptable and usable clinical tool for risk management. The main study aims are: * To co-design a prototype EMA suicide risk monitoring system with patients and health care provider input using Human Centered Design (HCD) methods. * To test the developed EMA protype with providers and their young adult patients aged 16-30 experiencing suicidality to determine if the EMA prototype is an acceptable and usable clinical tool. Young adult participants receiving care for active suicidal ideation will * Download and use the EMA prototype for a total of two months. * Complete 3 online surveys at 0, 1 and 2 months after enrolled in the study.
CONDITIONS
Official Title
Augmented Momentary Personal Ecological Risk Evaluation
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Young adults aged 16 to 30 years
- Receiving care at University of Washington Primary Care for suicidal ideation as indicated by Electronic Health Record or recent suicidal behavior
- Ability to consent to participate in the study
You will not qualify if you...
- Younger than 16 or older than 30 years
- Non-English speaking
- No access to a smartphone
- Any medical or psychiatric condition or life situation that would prevent safe and voluntary participation
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
University of Washington
Seattle, Washington, United States, 98195
Actively Recruiting
Research Team
M
Mindy Vredevoogd, MS
CONTACT
T
Tess Grover, BA
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
HEALTH_SERVICES_RESEARCH
Number of Arms
1
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