N/A
N=249
Observational Study to Compare Outcomes of Different Psychiatric Treatment of Suicidal Adolescents
Suicidal Ideation
Bottom Line
View on ClinicalTrials.gov: NCT04625686 ↗Enrolled (actual)
249
Serious AEs
19.3%
Results posted
Jan 2025
Primary outcome: Primary: Number of Recurrent Suicidal Events Measured by Treatment Arm — 0.66; 0.45; 0.20; 0.60 hospitalizations
Study Design & Population
- Study type
- Observational
- Phase
- N/A
- Interventions
- Mental Health Treatment (Behavioral)
- Age
- Pediatric, Adult · 12+ yrs
- Sex
- All
- Sponsor
- Children's Hospital Medical Center, Cincinnati
- Primary completion
- Dec 2021
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Number of Recurrent Suicidal Events Measured by Treatment Arm |
0.66; 0.45; 0.20; 0.60 | — |
| SECONDARY Which Treatment Leads to Better Life Satisfaction |
15.75; 16.74; 15.4; 14 | — |
Summary
To address the unmet need of optimizing the treatment and management for adolescent suicidality, the investigators propose to evaluate the effectiveness and safety of telehealth services compared to inpatient and OCIC for suicidal adolescents in target population. To achieve this goal, the investigators propose a multi- site study to compare telehealth, OCIC, and inpatient care, and see which can lead to a lower risk of a suicidal event (primary outcome) as well as higher treatment satisfaction (TS) and satisfaction with life (SL) (secondary outcomes) of both the legal guardians/parents and patients.
Eligibility Criteria
Inclusion Criteria
- Adolescents that are 12 through 18 years old.
- Adolescents that are brought to the Emergency Department for crisis evaluation due to suicidal thoughts or behaviors.
- Require a higher level of care.
- The presence of a legal guardian for consent.
- 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
- Adolescents with suicidal thoughts who had prior OCIC treatment in the past 12 months.
- Adolescents without the ability to answer survey questions.
- Adolescents that are non-English speaking due to the scales and surveys that are used for this study only being available in English.
Data sourced from ClinicalTrials.gov (NCT04625686). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.