Suicidal Ideation, Suicide, Suicide and Self-harm, Suicide, Attempted
Conditions
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).
Interventions
Safety Planning Intervention, ecological momentary intervention smartphone app system, and bidirectional communication with study clinician.
Sponsors
American Foundation for Suicide Prevention (AFSP)
Butler Hospital
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to 26 Years
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
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Ecological Momentary Assessment (EMA) Adherence | 4 weeks | Number of assessments completed out of total. |
| Acceptability of MAPS Intervention | 1 month | Feedback on qualitative interview. |
| Satisfaction with MAPS Intervention | 4 weeks | Measured by protocol completion rate. |
| Acceptability of Research (Recruitment) | Baseline | Measured by recruitment rate. |
| Acceptability of Research (Dropout) | 1 month | Measured by dropout rate. |
| Acceptability of Research Procedures | 1 month | Feedback on qualitative interview |
| Patient Satisfaction | 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. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Rehospitalization | 1 month | Will be assessed using the Treatment History Interview and medical records review. |
| Suicidal Ideation and Behavior | 1 month | Will be assessed using the Columbia Suicide Severity Rating Scale, items from the Modified Scale for Suicidal Ideation, and ecological momentary assessment of suicidal ideation and behavior. The Columbia Suicide Severity Rating Scale can provide presence/absence of suicidal ideation and suicidal behavior, as well as a suicidal ideation score ranging from 0 to 5 with higher scores representing more severe ideation, and a suicidal ideation intensity rating from 0-25 with higher scores representing more intense ideation. |
Countries
United States
Outcome results
None listed