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NCT06704958 · ClinicalTrials.gov registry record · NA

Augmented Momentary Personal Ecological Risk Evaluation

A NA study of Suicidal Ideation and Self Harm, sponsored by University of Washington.

Recruiting
Registry status
NA
Development phase
50
Enrollment target
1
Study location

NCT06704958 is a NA study of Suicidal Ideation and Self Harm that is actively recruiting participants, run by University of Washington. The registered enrollment target is 50 participants, below the 267-participant average among 84 other Suicidal Ideation trials with a reported enrollment target (81% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT06704958, a NA study of Suicidal Ideation and Self Harm, is actively recruiting participants, sponsored by University of Washington.

RECRUITING
Registry status
NA
Development phase
50 participants
Enrollment target
1
Study location

Study 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.

Interventions

  • OTHER AMPERE EMA app

Study Locations (1)

Washington

  • University of Washington - Seattle

Trial Details

FieldValue
Enrollment Target 50 participants
Start Date 2025-09-25
Est. Completion 2026-07-01
Phase NA

Sponsor

University of Washington

1,048 total trials

What the Registry Record Tells You About NCT06704958

The ClinicalTrials.gov registry entry for NCT06704958 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 50 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 267-participant average among 84 other Suicidal Ideation trials with a reported enrollment target (81% lower). The listed sponsor is University of Washington, which has 1,048 total studies on file at ClinicalTrials.gov.

The record links to 2 conditions, with Suicidal Ideation appearing as the primary indexed condition, and to 1 intervention - of which AMPERE EMA app is the first listed.

NCT06704958 reports 1 study location spanning 1 distinct geographic area - top geographies include Washington.

Frequently Asked Questions

What is clinical trial NCT06704958 about?

NCT06704958 is a clinical study titled "Augmented Momentary Personal Ecological Risk Evaluation". 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...

What is the current status of trial NCT06704958?

This trial is currently recruiting. It is a NA study. The enrollment target is 50 participants. The study started on 2025-09-25. Estimated completion is 2026-07-01.

What conditions does trial NCT06704958 study?

This clinical trial studies the following conditions: Suicidal Ideation, Self Harm.

What interventions are being tested in trial NCT06704958?

The interventions under investigation include: AMPERE EMA app (OTHER).

Who is sponsoring clinical trial NCT06704958?

This trial is sponsored by University of Washington, which has 1,048 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06704958 being conducted?

This trial has 1 study location across Washington. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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