Augmented Momentary Personal Ecological Risk Evaluation
University of Washington
50 participants
Sep 25, 2025
INTERVENTIONAL
Conditions
Summary
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.
Eligibility
Inclusion Criteria3
- Young adults (age 16-30 years)
- Receiving care at University of Washington Primary Care for suicidal ideation as determined by Electronic Health Record problem list or PHQ-9 suicide risk item >0 in previous year and/or recent (past year) history of suicide attempt and/or active suicidal ideation.
- Ability to consent to participate
Exclusion Criteria4
- Age <16 or >30,
- Non-English speaking
- No smart phone access
- Any clinical medical/psychiatric condition, severity of that condition, or life situation that would compromise safe and voluntary study participation.
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Interventions
AMPERE EMA smartphone app using MyCap
Locations(1)
View Full Details on ClinicalTrials.gov
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NCT06704958