MedPath

Randomized Controlled Trial of a Single-session Mechanism-focused Intervention for Suicidal Thoughts and Behaviors

Not Applicable
Recruiting
Conditions
Suicidal Ideation
Hopelessness
Wish to Live
Wish to Die
Registration Number
NCT05816317
Lead Sponsor
Shannon E. Sauer-Zavala
Brief Summary

Across multiple models of suicide risk, hopelessness and perceptions of social relatedness (i.e., lack of social connection/thwarted belongingness, perceived burdensomeness) have emerged as candidate mechanisms that maintain STBs. Although these mechanisms have garnered strong empirical support in predicting STBs, there has been virtually no integration with interventions aimed for individuals at acute risk for suicide. Thus, the overarching goal of the present proposal is to evaluate a mechanism-focused intervention that explicitly targets two core mechanisms implicated in the maintenance of STBs: hopelessness and negative perceptions of social relatedness. Given that the period immediately following hospital discharge presents the highest risk for suicide attempts and up to 70% of patients admitted for a suicide attempt do not attend their first outpatient appointment, the intervention will be evaluated on an inpatient unit. Additionally, most of the extant interventions for STBs are administered across multiple sessions (i.e., 4 sessions and up to one year); however treatments of this length are unlikely to be feasible in acute care settings. Fortunately, very brief suicide prevention interventions, are effective in reducing future suicide attempts and increasing the likelihood of attending follow-up treatments. Additionally, single-session interventions (not suicide specific) have been shown to reduce hopelessness immediately and at a one-month follow-up.

The present study is an RCT comparing a novel Single Session Mechanism Focused Intervention (SSMFI) for STBs to treatment-as-usual (TAU) on a psychiatric inpatient unit for patients admitted for suicidal ideation or attempt. The engagement of the putative processes (hopelessness and negative perceptions of social relatedness) that maintain STBs will be assessed, along with the feasibility and acceptability of SSMFI for STBs on an inpatient psychiatric unit.

Detailed Description

Not available

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
128
Inclusion Criteria
  • admitted for care to the Adult Inpatient Unit at Good Samaritan Hospital
  • endorse suicidal ideation and/or a recent suicide attempt (i.e., "a potentially self-injurious act committed with at least some wish to die") upon intake to the unit
  • 18 years of age; (4) English speaking
  • able to provide two methods for follow-up contact (i.e., phone number, email address) in order to complete study follow-up assessment.
Exclusion Criteria
  • current manic episode
  • acutely psychotic
  • actively detoxicating from substances
  • the inability to comprehend the intervention

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
Change in tntensity of suicidal ideationPre-intervention and directly after the intervention (i.e., 1 hour later)

RATE OVERALL INTENSITY OF YOUR SUICIDAL IDEATION RIGHT NOW: (scale from "1" Extremely low intensity to "5" Extremely high intensity)

Change in hopelessnessPre-intervention and directly after the intervention (i.e., 1 hour later)

How much are you feeling hopeless right now? (scale from "1" Not at all to "5" A lot)

Change in wisht to livePre-intervention and directly after the intervention (i.e., 1 hour later)

I wish to live this much: (scale from "0" Not at all to "8" Very much)

Change in wish to diePre-intervention and directly after the intervention (i.e., 1 hour later)

I wish to die this much: (scale from "0" Not at all to "8" Very much)

Change in Beck Hopelessness Scalepre-intervention, 1 week after the intervention is completed, 1 month after the intervention is completed

Hopelessness will be measured with the Beck Hopelessness Scale. Scores range from 0-20 and higher scores indicate greater levels of hopelessness.

Change in Interpersonal Needs Questionnairepre-intervention, 1 week after the intervention is completed, 1 month after the intervention is completed

Perceptions of social connectedness will be assessed with the Interpersonal Needs Questionnaire. Scores range from 0 to 107 with higher scores indicating less connection with others.

Secondary Outcome Measures
NameTimeMethod
Change in Columbia Suicide Severity Rating Scalepre-intervention, 1 week after the intervention is completed, 1 month after the intervention is completed

The self-report version of the Columbia Suicide Severity Rating Scale will be used to assess the presence of suicidal behaviors thoughts and behaviors. Participants are asked to respond Yes/No to 6 items that refer to various suicide related phenomena (thoughts, planning, intent, and behaviors). There is no total score for this measure.

Change in Adult Suicidal Ideation Questionnairepre-intervention, 1 week after the intervention is completed, 1 month after the intervention is completed

Intensity of suicidal ideation will be measured with the Adult Suicidal Ideation Questionnaire. Scores range from 0-150 and higher scores indicate greater intensity of suicidal ideation.

Trial Locations

Locations (1)

University of Kentucky

🇺🇸

Lexington, Kentucky, United States

© Copyright 2025. All Rights Reserved by MedPath