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Clinical Trials/NCT05180344
NCT05180344RecruitingNot Applicable

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

Butler Hospital2 sites in 1 country10 target enrollmentStarted: July 25, 2024Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Enrollment
10
Locations
2
Primary Endpoint
Acceptability of Research (Recruitment)

Study Overview

Brief Summary

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).

Study Design

Study Type
Interventional
Allocation
Non Randomized
Intervention Model
Single Group
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to 26 Years (Adult)
Sex
All
Accepts Healthy Volunteers
No

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

Outcomes

Primary Outcomes

Acceptability of Research (Recruitment)

Time Frame: 1 month

Measured by dropout rate.

Acceptability of Research Procedures

Time Frame: 1 month

Feedback on qualitative interview

Patient Satisfaction

Time Frame: 1 month

Measured using the Client Satisfaction Questionnaire, a self-report measure of satisfaction with treatment. Scores range from 8 to 32, with higher scores representing higher satisfaction.

Acceptability of MAPS Intervention

Time Frame: 1 month

Feedback on qualitative interview.

Satisfaction with MAPS Intervention

Time Frame: 4 weeks

Measured by protocol completion rate.

Ecological Momentary Assessment (EMA) Adherence

Time Frame: 4 weeks

Number of assessments completed out of total.

Secondary Outcomes

  • Suicidal Ideation and Behavior(1 month)
  • Rehospitalization(1 month)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (2)

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