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N/A N=878 Randomized Double-blind Treatment

Disseminating Organizational SBI Services at Trauma Centers

Alcohol Abuse · Alcohol Dependence

Enrolled (actual)
878
Serious AEs
0.2%
Results posted
Mar 2018
Primary outcome: Primary: Number of Participants With Hazardous Drinking — 292; 309; 201; 223 Participants

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Brief Intervention (Behavioral)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
University of Washington
Primary completion
Sep 2012

Outcome Measures

OutcomeResultp-value
PRIMARY
Number of Participants With Hazardous Drinking
292; 309; 201; 223; 166; 198
PRIMARY
Alcohol Use Problems
3.3; 3.38; 2.99; 3.08
SECONDARY
Number of Abstinent Days
74.2; 73.4; 75.5; 71.3
SECONDARY
Number of Binge Drinking Days
9.4; 10.6; 9.4; 11.4
SECONDARY
Alcohol Use Problems
3.3; 3.38; 2.99; 3.08

Summary

The goal of the Disseminating Organizational Screening and Brief Interventions Services (DO-SBIS) investigation is to capitalize on the unique opportunity afforded by the American College of Surgeons' mandate by taking early steps to insure high quality, evidence-based SBI services are implemented and outcomes are assessed. In the first phase of the investigation, SBI services will be assessed for all 190 level I trauma centers in the United States. In the second phase of the investigation, 20 level I trauma centers will be selected for randomization to intervention or control conditions.

Eligibility Criteria

Inclusion Criteria

  • For provider subjects: staff at trauma centers selected by study
  • For patient subjects: admitted to trauma centers selected by study, positive blood alcohol levels, able to provide two follow-up contacts

Exclusion Criteria

  • For Providers: Once a trauma center is selected for participation, providers will be selected from existing hospital staff.
  • For Patients: Patients so severely injured that they cannot participate in study procedures will be excluded;
  • Patients who are admitted after self-inflicted injury, or are psychotic and therefore require more intensive acute interventions, will not be included in the study;
  • Injured hospitalized prisoners are excluded.
  • Children under the age of 18 are excluded.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT00607620). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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