Actively Recruiting

Phase Not Applicable
Age: 12Years - 17Years
All Genders
NCT06476886

Intensive Crisis Intervention

Led by Jennifer Hughes · Updated on 2025-08-07

213

Participants Needed

1

Research Sites

112 weeks

Total Duration

On this page

Sponsors

J

Jennifer Hughes

Lead Sponsor

N

National Institute of Mental Health (NIMH)

Collaborating Sponsor

AI-Summary

What this Trial Is About

The study's purpose is to improve the clinical management of severe crises experienced by youth with psychiatric disorders by examining a brief, evidence-based alternative to inpatient psychiatric care.

CONDITIONS

Official Title

Intensive Crisis Intervention

Who Can Participate

Age: 12Years - 17Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Youth between the ages of 12 years 0 months and 17 years 6 months at time of consent
  • Present to the Nationwide Children's Hospital Psychiatric Crisis Department or Psychiatry Consult Liaison Service with suicidal ideation and/or behavior as the primary referral
  • Eligible for admission to both the Youth Crisis Stabilization Unit and Adolescent Psychiatric Inpatient Unit based on clinical judgment
  • Patient and legal guardian willing to be admitted to either unit
  • Youth has a score of 23 or higher on the Concise Health Risk Tracking Self-Report
  • Youth resides with a primary caretaker who can legally consent for research participation
  • Legal guardian attends the evaluation at Psychiatric Crisis Department or Consult Liaison Service
Not Eligible

You will not qualify if you...

  • Unable to understand study procedures due to intellectual disability or active psychosis
  • Cannot speak or read English well enough to understand and complete study consent and procedures

AI-Screening

AI-Powered Screening

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Trial Site Locations

Total: 1 location

1

Nationwide Children's Hospital

Columbus, Ohio, United States, 43215

Actively Recruiting

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Research Team

J

Jennifer L Hughes

CONTACT

A

Anastasia Berg

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

3

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