About this trial
Suicide is a leading cause of death among adolescents in the United States and improving access to high quality just-in-time suicide interventions to reduce risk has important public health implications. Integrating such interventions into routinely accessed settings, such as pediatric primary care, holds promise; however, many clinicians in these settings fail to adequately screen or intervene in youth suicidal thoughts and behaviors, representing a key barrier to reducing suicide. The proposed study is a pre-post quasi-experimental pilot feasibility and preliminary efficacy trial of a suicide prevention intervention informed by evidence based interventions including the SAFETY-Acute suicide prevention intervention implemented in 3 pediatric primary care clinics.
Eligibility criteria
Qualifiers
adolescent between the ages of 10 and 18 years old
speaks fluent English
current or past low to moderate suicide risk (denies current plan with intent to kill self)
Disqualifiers
high suicide risk (endorses current plan and intent)
does not speak fluent English
does not have a primary care provider
has a child who meets inclusion criteria
Trial design
Treatments tested in this trial
- Pilot Intervention
- Treatment as Usual
Treatment groups
Sponsors and collaborators
University of Washington
Lead sponsor
National Institute of Mental Health (NIMH)
Collaborator