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The Efficacy of Computerized Alcohol Screening and Intervention (CASI) in At-Risk Emergency Department and Trauma Patients

The recruitment status of this study is unknown because the information has not been verified recently.
Verified September 2012 by University of California, Irvine.
Recruitment status was  Recruiting
Sponsor:
Information provided by (Responsible Party):
Shahram Lotfipour, University of California, Irvine
ClinicalTrials.gov Identifier:
NCT01680614
First received: September 4, 2012
Last updated: September 6, 2012
Last verified: September 2012
  Purpose

The purpose of this research is to examine the effectiveness of computerized alcohol screening and brief intervention in the UC Irvine Medical Center Emergency Department (ED) and Trauma Patients. Brief interventions have a high potential impact in ED and Trauma populations. Computerized alcohol screening and brief intervention (CASI) is a fast and easy to use tool for patients and healthcare providers. CASI mitigates barriers to proper screening and intervention, including time, availability of trained personnel, patient comfort, and language barriers. CASI provides the Alcohol Use Disorders Identification Test (AUDIT) followed by a brief intervention and customized alcohol intake recomendations for the patient.

The intervention of this study will be the addition of a brief CASI questionnaire to the standard of care for a random subset of subjects. All subjects who screen positive for hazardous alcohol use will be followed up and reassessed for alcohol use. The researchers hypothesize that the addition of CASI will lead to a decrease in alcohol intake within three months. The basis of this research is evidence of the effectiveness in the CASI system, the growing public health issue of alcohol abuse, the need to be able to provide effective screening and brief intervention in the high volume ED settings, and findings that the primary method to reduce traumatic death is prevention.


Condition Intervention
Alcohol Consumption
Behavioral: CASI

Study Type: Observational
Study Design: Observational Model: Cohort
Time Perspective: Prospective

Resource links provided by NLM:


Further study details as provided by University of California, Irvine:

Groups/Cohorts Assigned Interventions
At Risk Adult Drinkers
CASI
Behavioral: CASI

  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Sampling Method:   Probability Sample
Study Population

Emergency Department

Criteria

Inclusion Criteria:

  • 18 years or older
  • Trauma and ED patients

Exclusion Criteria:

  • Under the age of 18
  • Intoxicated
  • Psychiatric
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT01680614

Locations
United States, California
UC Irvine Medical Center Recruiting
Orange, California, United States, 92868
Contact: Shahram Lotfipour, MD    714-456-2326    shl@uci.edu   
Sponsors and Collaborators
University of California, Irvine
  More Information

Additional Information:
No publications provided

Responsible Party: Shahram Lotfipour, Principal Investigator, University of California, Irvine
ClinicalTrials.gov Identifier: NCT01680614     History of Changes
Other Study ID Numbers: 2011-8155
Study First Received: September 4, 2012
Last Updated: September 6, 2012
Health Authority: United States: Institutional Review Board

Additional relevant MeSH terms:
Alcohol Drinking
Drinking Behavior

ClinicalTrials.gov processed this record on November 20, 2014