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Recruiting NCT07350161

Implementation of a Caregiver-Report Suicide-Risk Screener in Children Under Age 8 in a Behavioral Health Center

No phase Interventional Information Dissemination

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: SITB information.
Who it may be relevant to
Registry conditions: Information Dissemination. Basic parameters: from 18 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 →
Official title

Implementation of a Caregiver-Report Suicide-Risk Screener in Children Under Age 8 in a Behavioral Health Center: A Pilot Study

Overview

This project addresses the pressing need for tools to identify suicidal thoughts and behaviors in children aged 4-7. Although young children can experience STBs, current screening tools and guidelines often overlook this age group, partly due to challenges in directly assessing young children. The investigators developed a promising caregiver-report screener that identified at-risk children. This study will evaluate the screener's feasibility and effectiveness in clinical settings, gather feedback from clinicians and caregivers, and refine the screening process. The goal is to facilitate early intervention, improving mental health care and outcomes for young children.

Detailed description

This project aims to evaluate the feasibility, acceptability, and efficacy of a caregiver-report suicide risk (STB) screening tool for children under age 8. Despite the rising rates of STBs in young children, tools for identifying at-risk individuals in this age group are limited, and significant resistance remains to screening children for STBs. Given the challenges in directly assessing young children and the lack of validated tools, the investigators developed a caregiver-report screener to detect early signs of STBs. Preliminary data indicate that this screener is both sensitive and specific, showing promise in identifying at-risk children. The proposed study will evaluate the implementation of this screener in a child behavioral health clinic, obtaining qualitative and quantitative feedback from both clinicians and caregivers to refine the screener and its integration into clinical workflows. Additionally, the investigators will assess how clinicians use the screener results in diagnostic and treatment planning. This study will provide critical insights into barriers and best practices for STB screening in young children, ultimately improving early identification and clinical care for at-risk youth.

Interventions

  • Other SITB information
    childhood SITB information

Primary outcome measures

  • Clinician report of SITB screen acceptability [Time frame: From time of intervention until the follow-up interviews 3-4 months later.]
Secondary outcome measures (2)
  • Clinician report of hesitancies regarding use of SITB screen [Time frame: From time of intervention until the follow-up interviews 3-4 months later.]
  • Clinicians' incorporation of SITB Screen in Child Treatment Plans [Time frame: From time of intervention until the follow-up interviews 3-4 months later.]

Eligibility criteria

Inclusion criteria

  • licensed mental health clinician (e.g., LPC, LMSW, LCSW, MD) in the Hermann Center
  • provides care to children 4-7 years of age
  • provides care through the Early Child Intervention, Early Psychiatric Care, or Trauma Response program
  • must be currently seeing and/or accepting new patients

Exclusion criteria

  • none

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

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Single blind
Primary purpose
Screening

Study locations

United States · 1 center
  • Washington University School of Medicine — St Louis

Identifiers

NCT: NCT07350161 · 202501012 · UL1TR002345

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗