N/A
Completed N=878
Disseminating Organizational SBI Services at Trauma Centers
Alcohol Abuse · alcohol dependence
Source: ClinicalTrials.gov NCT00607620 ↗
Enrolled (actual)
878
Serious AEs
0.2%
Results posted
Mar 2018
Primary outcomePrimary: Number of Participants With Hazardous Drinking — 292; 309; 201; 223 Participants
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.
Outcome Measures
| Outcome | Result | p-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 | — |
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.
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. Informational only — not medical advice.