Comparing outpatient crisis intervention to inpatient care for suicidal teens
Official title: A Multi-Site Study to Compare the Outcomes of Psychiatric Treatment of Suicidal Adolescents in Different Treatment Settings
Run by Children's Hospital Medical Center, Cincinnati · NCT04089254 · Data updated 2026-11-12
This study tests whether an outpatient crisis intervention program can help suicidal teens just as well as staying in the hospital.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 12 Years to 18 Years |
| Sex | All |
| Enrollment | 1000 (estimated) |
| Sponsor | Children's Hospital Medical Center, Cincinnati Academic / other |
| Locations | 4 sites (Glen Oaks, New York and 3 other locations) |
| Status | Recruiting |
| Started | November 4, 2019 |
| Main results expected | January 2028 |
| Study ends | January 2029 |
| Registry record updated | July 5, 2024 |
| Trial ID | NCT04089254 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are adolescents aged 12 to 17 who are brought to the Emergency Department due to suicidal thoughts or behaviors and require a higher level of care.
✕Probably not a fit
Patients who are at serious imminent risk of suicide or require constant supervision may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This study evaluates the effectiveness of an Outpatient Crisis Intervention Clinic (OCIC) compared to traditional inpatient care for adolescents experiencing suicidal ideation. It aims to enroll up to 1,000 participants across four sites over five years, measuring outcomes such as the time to first recurrence of suicidal events and overall treatment satisfaction. The study will also analyze clinical and socioeconomic factors that may influence treatment outcomes, helping to guide families and clinicians in making informed decisions about care settings for suicidal adolescents.
Why it matters
Potential benefit: If successful, this study could lead to improved treatment outcomes and satisfaction for adolescents experiencing suicidal thoughts.
How similar studies have gone: Other studies have shown promise in evaluating outpatient interventions for mental health crises, suggesting potential for success in this approach.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: 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. Are brought to the Emergency Department (ED) due to suicidal thoughts or behaviors 3. Require a higher level of care (OCIC or Inpatient) indicated by clinician determination and a CHRT-SR score of 15 to 52. 4. The presence of a legal guardian 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. Exclusion Criteria: 1. Adolescents with suicidal thoughts that place themselves at a serious imminent risk of suicide based on clinical judgment. 2. Adolescents who require 24 hour/day supervision but no adult can provide 24 hour/day supervision outside of the hospital 3. Adolescents without the ability to read and answer survey questions 4. Adolescents that are non-English speaking due to the scales and surveys that are used for this study only being available in English.
Where it's running
-
Northwell Health
Glen Oaks, New York, United States Recruiting -
Cincinnati Children's Hospital and Medical Center
Cincinnati, Ohio, United States Recruiting -
Nationwide Children's Hospital
Columbus, Ohio, United States Recruiting -
UT Southwestern Medical Center/Children's Health
Dallas, Texas, United States Not yet recruiting
Study contacts
- Principal investigator: Drew Barzman, MD — Children's Hospital Medical Center, Cincinnati
- Study coordinator: Drew Barzman, MD
- Email: drew.barzman@cchmc.org
- Phone: (513) 636-0807
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
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This observational study looks at whether financial hardship and social isolation are linked to depression, suicidal thoughts, and loneliness among French university students.
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Ketamine with DBT for suicidality in adults with treatment-resistant depression or bipolar disorder and BPD
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.