Actively Recruiting

Phase Not Applicable
Age: 12Years - 17Years
All Genders
NCT06486688

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

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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

Age: 12Years - 17Years
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

You will not qualify if you...

  • None; all adolescents with a Well Visit are eligible

AI-Screening

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Trial Site Locations

Total: 1 location

1

Kaiser Permanente Division of Research

Pleasanton, California, United States, 94588

Actively Recruiting

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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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