Actively Recruiting
Centralized Virtual SBIRT for Pediatric Primary Care
Led by Kaiser Permanente · Updated on 2024-07-08
22320
Participants Needed
1
Research Sites
185 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Adolescent alcohol and other drug (AOD) use is a significant public health problem which contributes to high levels of mortality, morbidity and healthcare costs in young people, and identification and early intervention for these problems is critical to improving outcomes. Screening, Brief Intervention and Referral to Treatment (SBIRT) in pediatric primary care is an evidence-based strategy for addressing these problems, but has not been widely and systematically implemented, for a variety of reasons, including lack of training and staffing resources to support its implementation. This pragmatic, Type 1 Hybrid Comparative Effectiveness Implementation study will examine whether a centralized, virtually-delivered modality of SBIRT, rapidly accessible by multiple pediatric primary care clinics, can be cost-effectively implemented to improve early identification and treatment for AOD use and comorbid mental health problems among adolescents identified as being at high or severe risk of AOD use disorder during adolescent Well Visits.
CONDITIONS
Official Title
Centralized Virtual SBIRT for Pediatric Primary Care
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adolescents aged 12 through 17 years seen for a Well Visit
- At risk of alcohol or other drug use disorder defined as monthly or more frequent use OR any use plus depressive symptoms or suicidality in past two weeks
You will not qualify if you...
- None; all adolescents with a Well Visit are eligible
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Kaiser Permanente Division of Research
Pleasanton, California, United States, 94588
Actively Recruiting
Research Team
S
Stacy A Sterling, DrPH, MSW
CONTACT
M
Melanie Jackson-Morris
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
HEALTH_SERVICES_RESEARCH
Number of Arms
2
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