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RECRUITING NA

Preventing Suicidal Behavior With Diverse High-Risk Youth in Acute Care Settings

NCT06151158 · View on ClinicalTrials.gov ↗

Study Summary

The study will compare the effectiveness of two relatively brief and scalable evidence-based interventions: the Stanley Brown Safety Planning Intervention and Follow-up Contacts (SPI+), a suicide-specific intervention that helps people prevent suicidal crises from escalating, and Interpersonal Psychotherapy for Adolescents Ultra Short Crisis Intervention (IPT-A SCI), a psychotherapeutic crisis intervention treatment for suicidal adolescents that teaches youth skills to prevent suicidal crises and addresses interpersonal problems that lead to suicidal crises. The results will inform the future standard of care for youth at risk for suicide presenting in the ED setting. This project focuses on suicidal youth ages 12-19 in three ethnically and racially diverse urban areas: Philadelphia, Pennsylvania; Baltimore, Maryland; and upper Manhattan/lower Bronx in New York City.

Interventions

  • BEHAVIORAL Stanley Brown Safety Planning Intervention and Follow-up Contacts (SPI+)
  • BEHAVIORAL Interpersonal Psychotherapy for Adolescents Ultra Short Crisis Intervention (IPT-A SCI)

Study Locations (6)

New York

  • Columbia University Irving Medical Center (CUMC) — New York
  • Weill-Cornell Medicine — New York

Florida

  • Johns Hopkins All Children's Hospital — St. Petersburg

Maryland

  • Johns Hopkins University — Baltimore

North Carolina

  • University of North Carolina Medical Center — Chapel Hill

Pennsylvania

  • Childrens Hospital of Philadelphia — Philadelphia

Trial Details

FieldValue
Enrollment Target 1,000 participants
Start Date 2025-03-10
Est. Completion 2028-10-14
Phase NA

Sponsor

Johns Hopkins University

1,517 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06151158

The ClinicalTrials.gov registry entry for NCT06151158 describes a study currently listed as recruiting. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 1,000 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Johns Hopkins University, which has 1,517 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 4 conditions, with Suicide appearing as the primary indexed condition, and to 2 interventions — of which Stanley Brown Safety Planning Intervention and Follow-up Contacts (SPI+) is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT06151158 reports 6 study locations spanning 5 distinct geographic areas — top geographies include New York, Florida, Maryland. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT06151158 about?

NCT06151158 is a clinical study titled "Preventing Suicidal Behavior With Diverse High-Risk Youth in Acute Care Settings". The study will compare the effectiveness of two relatively brief and scalable evidence-based interventions: the Stanley Brown Safety Planning Intervention and Follow-up Contacts (SPI+), a suicide-specific intervention that helps people prevent suicidal crises from escalating, and Interpersonal Psych...

What is the current status of trial NCT06151158?

This trial is currently recruiting. It is a NA study. The enrollment target is 1,000 participants. The study started on 2025-03-10. Estimated completion is 2028-10-14.

What conditions does trial NCT06151158 study?

This clinical trial studies the following conditions: Suicide, Suicide, Attempted, Suicide Prevention, Suicide Ideation. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT06151158?

The interventions under investigation include: Stanley Brown Safety Planning Intervention and Follow-up Contacts (SPI+) (BEHAVIORAL), Interpersonal Psychotherapy for Adolescents Ultra Short Crisis Intervention (IPT-A SCI) (BEHAVIORAL). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT06151158?

This trial is sponsored by Johns Hopkins University, which has 1,517 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT06151158 being conducted?

This trial has 6 study locations across Florida, Maryland, New York, North Carolina, Pennsylvania. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial