Viewing Study NCT00183183



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Study NCT ID: NCT00183183
Status: COMPLETED
Last Update Posted: 2010-05-24
First Post: 2005-09-12

Brief Title: Impact of a Brief Motivational Interview on Drinking Behaviors of At Risk Drinkers Screened in the Emergency Room
Sponsor: UConn Health
Organization: UConn Health

Study Overview

Official Title: Alcohol Screening and Brief Intervention in the Emergency Department
Status: COMPLETED
Status Verified Date: 2010-05
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: Alcohol abuse is associated with injury chronic illness absenteeism from work and social costs to families and communities The goal of this project is to translate motivational interventions successful in the primary care setting to the Emergency Department ED environment by implementing screening brief intervention and referral to treatment SBIRT in order to reduce at-risk drinking among ED patients
Detailed Description: To evaluate the effectiveness of SBIRT in the emergency room setting ED patients meeting NIAAA criteria for high risk drinking were recruited from 14 sites nationwide control group-Spring 2004 intervention group-Summer 2004 26 of screened ED patients met inclusion criteria All enrollees received a list of local referral resources Intervention group patients also participated in a 15 minute negotiated interview and ED staff referred them directly for treatment if indicated Enrollees completed 3-month follow-up surveys with a telephone Interactive Voice Response IVR system A total of 1137 patients were enrolled across 14 sites 561 intervention 576 control with 62 male 37 Black and 38 White and a mean age of 37 At baseline intervention-i and control-c groups were similar in demographic characteristics and number of drinks on a typical day mean-i 500 mean-c 512 and maximum drinks on a given day in the past month mean-i 751 mean-c 733 The 3 month follow-up rate was 62 n687 the 6 month follow-up rate was 52 n567 The 12 month follow up is currently underway

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None
Secondary IDs
Secondary ID Type Domain Link
R21AA015123 NIH None None
NIH 5R21AA15123-02 US NIH GrantContract None httpsreporternihgovquickSearchR21AA015123