HOME  | CONTACT  | PATIENT LOGIN  | CLINIC LOGIN  | FAQ
  • PATIENTS &
    HEALTHY VOLUNTEERS
  • INVESTIGATORS
  • CROS / SPONSORS
  • CAREERS
  • TRIAL ALERTS

TRIALS SEARCH
      
  • HEALTH NEWS

  • RSS FEEDS

  • ABOUT TRIALS

  • LINK TO US


View Clinical Trial (Medical Research Study)


Disseminating Organizational SBI Services (DO-SBIS) at Trauma Centers

Signup
Browse Studies

City:   Seattle
State:   Washington
Zip Code:   98122
Conditions:   Alcohol Abuse - Alcohol Dependence
Purpose:   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.
Study Summary:   Each year in the United States approximately 2.5 million individuals are so severely injured that they require inpatient hospital admission. The integration of screening and brief interventions (SBI) into acute injury care has the potential to markedly increase the number of patients who receive needed services and has been a longstanding public health objective. In January of 2005 the American College of Surgeons, the primary agency responsible for developing trauma center requirements, passed a landmark resolution mandating that level I trauma centers must screen injured patients for an alcohol use disorder, and provide an intervention to those who screen positive. Preliminary studies suggest that there is a substantial risk that the SBI mandate will be implemented with marked variability and that low quality SBI procedures could become the default standard of trauma center care. Providers at each intervention trauma center will receive workshop training and ongoing telephone coaching in the delivery of evidence-based motivational interviewing (MI) intervention; MI training will be embedded within evidence-based organizational development activities that aim to facilitate the integration of SBI services into routine trauma center care. Control trauma centers will implement SBI care as usual. The investigation hypothesizes that intervention trauma centers, when compared to control trauma centers, will demonstrate higher quality SBI, as evidenced by greater provider proficiency in SBI delivery, significant reductions in 6- and 12-month post-injury alcohol use in patients receiving SBI, and enhanced organizational acceptance of SBI services. Without DO-SBIS baseline data on SBI services and follow-up RCT data on patient, provider, and organizational outcomes, a critical opportunity to provide empiric support of a historic policy decision to require alcohol services at level I trauma centers could be lost. The DO-SBIS interdisciplinary research group includes trauma surgery opinion leaders who are dedicated to implementing future policy mandates that derive from the DO-SBIS research program. Future mandates will aim to strengthen and refine trauma center delivery of evidence-based SBI services. The dissemination of high quality SBI services at level I trauma centers has the potential to influence alcohol policy in other health care settings nationwide.
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.
NCT ID:   NCT00607620
Primary Contact:   Principal Investigator
Douglas F Zatzick, MD
University of Washington

Jennifer Stubbs, BS
Phone: 206-744-1756
Email: jens2@u.washington.edu
Backup Contact:   N/A
Location Contact:   Seattle, Washington 98122
United States

DOUGLAS ZATZICK
Phone: 206-744-1756
Email: DZATZICK@U.WASHINGTON.EDU

Site Status: Recruiting

Data Source:   ClinicalTrials.gov
Date Processed:   May 19, 2013
Modifications to this listing:   Only selected fields are shown, please use the link below to view all information about this clinical trial.
Click to view Full Listing


If you would like to be contacted by the clinical trial representative please enter your contact information, then click "I Am Interested In This Study"
First Name:  
Last Name:  
Email Address:  
Confirm Email:    
Daytime Phone (eg. 555-555-5555):  
City:  
State:
Zip Code:    
Best Time to Call:  
Questions/Comments:  
  • NEARBY STUDIES

Within 25 Miles

Antidepressant Induced Sexual Dysfunction - Seattle WA

Bipolar Disorder - Seattle WA

Pediatric Depression - Kirkland WA

Pediatric Depression - Seattle WA

Generalized Anxiety Disorder - Seattle WA

Crohn's Disease - Seattle WA

Depression - Seattle WA

Treatment Resistant Depression - Seattle WA

Gout - Port Orchard WA

Binge Eating Disorder - Seattle WA

Multiple Sclerosis - Seattle WA

Low Back Pain and Constipation - Bothell WA

Anti-Depressant Induced Sexual Dysfunction - Seattle WA

Uncontrolled Angina (Adult Stem Cell Research) - Seattle WA

Uncontrolled Angina (Adult Stem Cell Research) - Seattle WA

Irritable Bowel Syndrome (with diarrhea) - Seattle WA

Brain Tumor (Glioblastoma) - Seattle WA

Chronic Sciatic Pain - Bellevue WA

Adult ADHD - Seattle WA

Within 50 Miles

Postherpetic Neuralgia (Post-shingles pain) - Tacoma WA

Within 100 Miles

Irritable Bowel Syndrome (with diarrhea) - Wenatchee WA

 
Clinical Connections Home | Investigators | CROs / Sponsors | Clinical Trials Notification | Search Clinical Trials | About Clinical Trials | Links | Terms And Conditions | Sitemap | Suggestions / Feedback
© 1998-2013 | All trademarks are property of their legal owners. | All Rights Reserved

ClinicalConnection.com is a resource that provides individuals with information regarding clinical trials that are being conducted worldwide.

ClinicalConnection.com does not conduct these clinical trials nor endorse them. Please consult your doctor or physician before participating.