Adapting a Brief Suicide Intervention for Pediatric Primary Care
This study is testing a new suicide prevention intervention for young people in pediatric primary care clinics. The intervention, called "Pilot Intervention," is based on proven methods like the SAFETY-Acute program. It will be compared to the usual care provided in these clinics. The study aims to see if this new intervention is practical and acceptable for adolescents aged 10 to 18 who are at risk for suicide, and for their healthcare providers. You might be able to join if you are between 10 and 18 years old, speak English, and have current or recent suicide risk, but are not in immediate crisis. The main goal is to understand how well the intervention works and if it needs further changes. The study plans to enroll 48 participants, but its current status is unclear.
- Study design
- This study is an interventional pilot study involving 48 participants aged 10-18. It compares a new suicide prevention intervention to usual care in three primary care clinics.
- What's involved
- Participants and providers will complete measures approximately two weeks after completing the intervention.
- Compensation
- Not stated in the trial record.
- Follow-up
- Participants are followed for approximately two weeks after completing the intervention.
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Adapting a Brief Suicide Intervention for Pediatric Primary Care: Enhancing Uptake and Impact
At a glance
Conditions
NCT06499740
Where you'd take part
This study runs at 3 sites. They're the same protocol — you choose where, and that choice sets who your contact draft is addressed to.
Northwest Pediatrics
Centralia, Washingtonstudy coordinator listed
Recruiting
Olympia Pediatrics
Olympia, Washingtonstudy coordinator listed
Recruiting
Richmond Pediatrics
Mountlake Terrace, Washingtonstudy 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
- Sarah Danzo, PhD · PRINCIPAL_INVESTIGATOR · University of Washington
Who to contact
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Inclusion
Exclusion
What this trial measures
- Feasibility of Intervention MeasureParticipant and providers complete approximately 2 weeks after completing intervention
Feasibility of the intervention (includes 4 items scored on a 5 point likert scale with higher scores representing greater feasibility.)
- Acceptability of Intervention MeasureParticipant and providers complete approximately 2 weeks after completing intervention
Participant rated acceptability of the intervention (includes 4 items scored on a 5 point likert scale with higher scores representing greater acceptability.)
- Intervention Appropriateness MeasureParticipant and providers complete approximately 2 weeks after completing intervention
Participant rated appropriateness of the intervention (includes 4 items scored on a 5 point likert scale with higher scores representing greater appropriateness.)
- Client Satisfaction QuestionnaireParticipant completes approximately 2 weeks after completing intervention
Participant rated satisfaction with the intervention (includes 8 items scored on a 4 point likert scale with higher scores representing greater satisfaction.)
- Intervention Usability ScaleProvider completes approximately 2 weeks after completing intervention
Participant rated intervention usability (includes 10 items scored on a 5 point likert scale with greater total score representing greater usability).