RECRUITING

Suicide Treatment Alternatives for Teens

Talk to us

Conditions

Suicidal IdeationSuicideSuicidalAdolescent

Quick Navigation

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

Quasi-Randomized trial to compare inpatient care versus outpatient crisis intervention clinic. This study plans to enroll up to 1,000 participants across 4 sites in a 5 years period.

Official Title

A Multi-Site Study to Compare the Outcomes of Psychiatric Treatment of Suicidal Adolescents in Different Treatment Settings

Quick Facts

Study Start:2019-11-04
Study Completion:2029-01
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT04089254

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 18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:CHILD, ADULT
Inclusion CriteriaExclusion Criteria
  1. 1. Adolescents that are 12 through 17 years old (including 17 year olds who will turn 18 years old during the course of the study).
  2. 2. Are brought to the Emergency Department (ED) due to suicidal thoughts or behaviors
  3. 3. Require a higher level of care (OCIC or Inpatient) indicated by clinician determination and a CHRT-SR score of 15 to 52.
  4. 4. The presence of a legal guardian
  5. 5. Capable of giving signed informed consent/assent, which includes compliance with the requirements and restrictions listed in the informed consent form (ICF) and in this protocol.
  1. 1. Adolescents with suicidal thoughts that place themselves at a serious imminent risk of suicide based on clinical judgment.
  2. 2. Adolescents who require 24 hour/day supervision but no adult can provide 24 hour/day supervision outside of the hospital
  3. 3. Adolescents without the ability to read and answer survey questions
  4. 4. Adolescents that are non-English speaking due to the scales and surveys that are used for this study only being available in English.

Contacts and Locations

Study Contact

Drew Barzman, MD
CONTACT
(513) 636-0807
drew.barzman@cchmc.org
Jennifer Combs, MSSA
CONTACT
(513) 803-0007
jennifer.combs@cchmc.org

Principal Investigator

Drew Barzman, MD
PRINCIPAL_INVESTIGATOR
Children's Hospital Medical Center, Cincinnati

Study Locations (Sites)

Northwell Health
Glen Oaks, New York, 11004
United States
Cincinnati Children's Hospital and Medical Center
Cincinnati, Ohio, 45229
United States
Nationwide Children's Hospital
Columbus, Ohio, 43205
United States
UT Southwestern Medical Center/Children's Health
Dallas, Texas, 75390
United States

Collaborators and Investigators

Sponsor: Children's Hospital Medical Center, Cincinnati

  • Drew Barzman, MD, PRINCIPAL_INVESTIGATOR, Children's Hospital Medical Center, Cincinnati

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 Date2019-11-04
Study Completion Date2029-01

Study Record Updates

Study Start Date2019-11-04
Study Completion Date2029-01

Terms related to this study

Keywords Provided by Researchers

  • Suicide
  • Suicidal
  • Adolescent

Additional Relevant MeSH Terms

  • Suicidal Ideation