Evaluation of a brief, scalable module to mitigate suicidal ideation among youth
Full Description
Project Summary
Suicidal ideation (SI) is prevalent and impairing in youth and can lead to restrictive and
intensive care. There is a critical need to develop and test scalable brief interventions
conducive to enhancing least-restrictive, cost-efficient, and accessible support, and which
target drivers of SI in youth. This R61/R33 application addresses this need via a brief
intervention module for youth experiencing subacute SI (i.e., SI which does not necessitate
intensive, restrictive services) which targets an established driver of SI, perceived
burdensomeness toward others (PB). This R61/R33 proposal builds on pilot findings by first
demonstrating the ability of the brief module to engage the target now in a rigorous
randomized controlled trial (RCT; R61) and then evaluating the module embedded within a
larger CBT protocol in preparation for a larger clinical trial (R33). We will measure the target
using established and novel measures recently developed and validated by the MPIs with an
eye toward establishing multimethod measurement of PB for a possible larger clinical trial.
The proposed intervention module addresses current empirical and clinical gaps in the
following ways: The intervention module (1) precisely targets a suicide-related interpersonal
risk factor, leveraging the MPIs recent clinical trial findings and in congruence with a large
body of work on suicide etiology and theory; (2) is easily combined with standard therapies via
simplicity from a streamlined manual and intuitive concepts, (3) and is highly scalable via a
cognitive-behavioral approach with high resource efficiency (e.g., minimal therapist training,
little session time needed). The study is therefore congruent with NIMH Strategy 3.2.A:
“Developing multi-modal intervention strategies that combine the simultaneous application of
established or novel [psychosocial interventions] to selectively access specific therapeutic
targets.”
Grant Number: 5R61MH137300-02
NIH Institute/Center: NIH
Principal Investigator: Victor Buitron
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