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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01680614
Other study ID # 2011-8155
Secondary ID
Status Completed
Phase N/A
First received September 4, 2012
Last updated October 24, 2017
Start date January 1, 2013
Est. completion date June 29, 2015

Study information

Verified date October 2017
Source University of California, Irvine
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

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.


Recruitment information / eligibility

Status Completed
Enrollment 2114
Est. completion date June 29, 2015
Est. primary completion date June 1, 2015
Accepts healthy volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- 18 years or older

- Trauma and ED patients

Exclusion Criteria:

- Under the age of 18

- Intoxicated

- Psychiatric

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
CASI


Locations

Country Name City State
United States UC Irvine Medical Center Orange California

Sponsors (1)

Lead Sponsor Collaborator
University of California, Irvine

Country where clinical trial is conducted

United States, 

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