RECRUITING

Intensive Crisis Intervention

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Conditions

SuicideSuicidal IdeationSuicide, AttemptedSuicide and Self-harmSuicide Threat

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Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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.

Official Title

Intensive Crisis Intervention (ICI) for Adolescent Suicidal Behavior

Quick Facts

Study Start:2024-06-03
Study Completion:2026-07-31
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06476886

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:12 Years to 17 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:CHILD
Inclusion CriteriaExclusion Criteria
  1. 1. Youth between the ages of 12 years 0 months and 17 years 6 months at time of consent
  2. 2. Present to the Nationwide Children's Hospital (NCH) Psychiatric Crisis Department (PCD) or NCH Psychiatry Consult Liaison (CL) Service with suicidal ideation and/or behavior as the primary referral
  3. 3. Be eligible for admission to both YCSU and APIU based on PCD or CL clinician's clinical judgement
  4. 4. Patient and legal guardian must be willing to be admitted to either YCSU or APIU
  5. 5. Youth obtains a score of ≥23 on the Concise Health Risk Tracking Self-Report (CHRT-SR)
  6. 6. Youth resides with a primary caretaker who has legal authority to consent for participation in research
  7. 7. Legal guardian must attend the PCD or CL evaluation
  1. 1. Participants who are unable to understand study procedures (e.g., intellectual disability, actively psychotic)
  2. 2. Inability to speak or read English adequately to understand and complete study consent and procedures

Contacts and Locations

Study Contact

Jennifer L Hughes
CONTACT
614-722-6811
jennifer.hughes@nationwidechildrens.org
Anastasia Berg
CONTACT
614-355-7136
Stacie.berg@nationwidechildrens.org

Principal Investigator

Jennifer L Hughes
PRINCIPAL_INVESTIGATOR
Nationwide Children's Hospital

Study Locations (Sites)

Nationwide Children's Hospital
Columbus, Ohio, 43215
United States

Collaborators and Investigators

Sponsor: Jennifer Hughes

  • Jennifer L Hughes, PRINCIPAL_INVESTIGATOR, Nationwide Children's Hospital

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2024-06-03
Study Completion Date2026-07-31

Study Record Updates

Study Start Date2024-06-03
Study Completion Date2026-07-31

Terms related to this study

Additional Relevant MeSH Terms

  • Suicide
  • Suicidal Ideation
  • Suicide, Attempted
  • Suicide and Self-harm
  • Suicide Threat