Preventing Suicidal Behavior With Diverse High-Risk Youth in Acute Care Settings

Recruiting N/A Interventional Study
Suicide, Attempted Suicide Ideation Suicide Suicide Prevention
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
Ready to participate?

Review the details below, then apply to join this clinical trial.

At a Glance
Age
12 – 24
Sex
Any
Study type
Interventional
Purpose
Prevention
Participants needed
484 (estimated)
Sponsor
Johns Hopkins University · Other
Think this trial could be right for you?

Answer a few quick questions to see if you may meet the eligibility requirements.

Check Your Eligibility
About This Trial
The study will compare the effectiveness of two relatively brief and scalable evidence-based interventions: the Stanley Brown Safety Planning Intervention and Follow-up Contacts (SPI+), a suicide-specific intervention that helps people prevent suicidal crises from escalating, and Interpersonal Psychotherapy for Adolescents Ultra Short Crisis Intervention (IPT-A SCI), a psychotherapeutic crisis int…
Trial Locations
Loading…

Loading trial locations…

Eligibility Criteria
Inclusion Criteria: * Suicide Risk During Acute Care Visit (At least one item in risk assessment is required; check all that apply): \_\_\_ Chief complaint of suicide-related concern (via Medical Record/Other), \_\_\_ Active suicidal ideation endorsed in past 1 month on validated suicide screener, …
Contacts

Holly C Wilcox, PhD

4103700081

hwilcox1@jhmi.edu

CONTACT

Catherine Grela

2408058868

agrelam1@jh.edu

CONTACT