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Recruiting NCT05180344

Feasibility, Acceptability, and Preliminary Efficacy of a Novel Personalized Mobile Intervention for Suicide - Open Trial (2)

No phase Interventional Suicide Suicide and Self-harm Suicide, Attempted Suicidal Ideation

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Mobile Application to Prevent Suicide (MAPS).
Who it may be relevant to
Registry conditions: Suicide, Suicide and Self-harm, Suicide, Attempted, Suicidal Ideation. Basic parameters: 18 years — 26 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United States
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Official title

Feasibility, Acceptability, and Preliminary Efficacy of a Novel Personalized Mobile Intervention for Suicide

Overview

The primary aim of this grant is to conduct pilot testing on a novel personalized mobile intervention for suicide - Mobile Application to Prevent Suicide (MAPS) - and to establish feasibility, acceptability, safety, and primary outcomes (i.e., suicidal ideation and behavior; re-hospitalization).

Interventions

  • Behavioral Mobile Application to Prevent Suicide (MAPS)
    Safety Planning Intervention, ecological momentary intervention smartphone app system, and bidirectional communication with study clinician.

Primary outcome measures

  • Acceptability of Research (Recruitment) [Time frame: Baseline]
  • Acceptability of Research (Recruitment) [Time frame: 1 month]
  • Acceptability of Research Procedures [Time frame: 1 month]
  • Patient Satisfaction [Time frame: 1 month]
  • Acceptability of MAPS Intervention [Time frame: 1 month]
  • Satisfaction with MAPS Intervention [Time frame: 4 weeks]
  • Ecological Momentary Assessment (EMA) Adherence [Time frame: 4 weeks]
Secondary outcome measures (2)
  • Suicidal Ideation and Behavior [Time frame: 1 month]
  • Rehospitalization [Time frame: 1 month]

Eligibility criteria

Inclusion criteria

  • Suicidal ideation and/or suicidal behavior in the past month verified by the C-SSRS
  • Between the ages of 18 and 26
  • English proficiency
  • Comfortable with smartphone technology
  • Deemed by the treatment team to be stable enough to complete study procedures

Exclusion criteria

  • Current psychotic or manic symptoms severe enough to interfere with study procedures

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Non-randomized
Model
Single group
Masking
Open label
Primary purpose
Treatment

Study locations

United States · 1 center
  • Butler Hospital — Providence

Identifiers

NCT: NCT05180344 · 1710-001 · SRG-1-119-18

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗