Preventing Suicidal Behavior in Youth
This study is looking at two different ways to help young people (ages 12-24) who are at risk for suicide and come to the emergency department. One approach is called Stanley Brown Safety Planning Intervention and Follow-up Contacts (SPI+), which helps people create a plan to prevent suicidal crises. The other is Interpersonal Psychotherapy for Adolescents Ultra Short Crisis Intervention (IPT-A SCI), a short therapy that teaches skills to prevent suicidal crises and addresses relationship problems. The study wants to see which of these interventions is more effective in reducing suicidal thoughts and behaviors. You might be able to join if you are between 12 and 24 years old and have a suicide risk during an acute care visit. The study aims to enroll 484 participants.
- Study design
- This is an interventional study comparing two behavioral interventions. It plans to enroll 484 participants aged 12 to 24.
- What's involved
- Participants will receive either the Stanley Brown Safety Planning Intervention in the emergency department with 3 follow-up contacts, or five sessions of Interpersonal Psychotherapy for Adolescents Ultra Short Crisis Intervention.
- Compensation
- Not stated in the trial record.
- Follow-up
- Your suicidal thoughts and behaviors will be checked at baseline, 3 months, 6 months, and 12 months after starting the study.
AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.
Preventing Suicidal Behavior With Diverse High-Risk Youth in Acute Care Settings
At a glance
Conditions
NCT06151158
Where you'd take part
This study runs at 6 sites. They're the same protocol — you choose where, and that choice sets who your contact draft is addressed to.
Childrens Hospital of Philadelphia
Philadelphia, Pennsylvaniastudy coordinator listed
Recruiting
Columbia University Irving Medical Center (CUMC)
New York, New Yorkstudy coordinator listed
Recruiting
Johns Hopkins All Children's Hospital
St. Petersburg, Floridastudy coordinator listed
Recruiting
Johns Hopkins University
Baltimore, Marylandstudy coordinator listed
Recruiting
University of North Carolina Medical Center
Chapel Hill, North Carolinastudy coordinator listed
Recruiting
Weill-Cornell Medicine
New York, New Yorkstudy coordinator listed
Recruiting
Sites open and close at different times, so the status above is per site — it can differ from the study's overall status.
Study leadership
- Holly C Wilcox, PhD · PRINCIPAL_INVESTIGATOR · Johns Hopkins Bloomberg School of Public Health
Who to contact
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Inclusion
Exclusion
What this trial measures
- Change in Suicidal ideation as assessed by the Suicide Assessment Five-step Evaluation and Triage (SAFE-T) with Columbia-Suicide Severity Rating Scale (C-SSRS) Recentbaseline, 3 months, 6 months, 12 months
Suicidal thoughts: measured using the Suicide Assessment Five-step Evaluation and Triage (SAFE-T) with Columbia-Suicide Severity Rating Scale (C-SSRS) Recent. Scores for suicidal ideation range from 0 to 5, with higher scores indicating more serious suicidal ideation, where 0 = "no suicidal thoughts"; 1= "wish to be dead"; 2 = "nonspecific active suicidal thoughts"; 3 = "suicidal thoughts with methods"; 4 = "suicidal intent"; and 5 = "suicidal intent with plan".
- Change in Suicidal behavior as assessed by the Suicide Assessment Five-step Evaluation and Triage (SAFE-T) with Columbia-Suicide Severity Rating Scale (C-SSRS) Recentbaseline, 3 months, 6 months, 12 months
Suicidal behavior with intent to die: measured using the Suicide Assessment Five-step Evaluation and Triage (SAFE-T) with Columbia-Suicide Severity Rating Scale (C-SSRS) Recent. Scored 0 to 1, with 1 indicating a suicide attempt since last assessment.
- Number of Suicides12 months
Measured through Death Records or Suicide from Office of Chief Medical Examiner, family report or medical record