Augmented Momentary Personal Ecological Risk Evaluation

Part of paid clinical trials in Seattle, Washington.

Sponsor
University of Washington
Study ID
NCT06704958
Status
Recruiting
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Conditions

  • Self Harm
  • Suicidal Ideation

Eligibility Criteria

Sex
ALL
Age
16 Years - 30 Years
Healthy Volunteers
Not accepted

Interventions

  • AMPERE EMA app — OTHER
    AMPERE EMA smartphone app using MyCap

Study Details

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.

Key Dates

Start date
Sep 25, 2025
Status verified
Nov 2025
Primary completion
Jun 1, 2026
Completion
Jul 1, 2026

Study Design

Enrollment
50 participants (estimated)
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
HEALTH_SERVICES_RESEARCH

Arms

  • Other: Use of AMPERE EMA prototype
    An EMA risk monitoring system using a smartphone EMA app to collect self-reported data from participating patients experiencing suicidal ideation.

Primary Outcome Measure

Acceptability of Intervention Scale (AIM) [ Time Frame: 2 month post-initiation of AMPERE EMA use ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
University of WashingtonSeattleWashington98195-

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By research site
University of Washington· Seattle, WA

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