Adapting a Brief Suicide Intervention for Pediatric Primary Care: Enhancing Uptake and Impact

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age10+
SponsorUniversity of Washington

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

48 Participants
are divided into 2 treatment groups

Sponsors and collaborators

University of Washington

Lead sponsor

National Institute of Mental Health (NIMH)

Collaborator