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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01683227
Other study ID # 1RC1DA028031-01
Secondary ID
Status Completed
Phase N/A
First received September 7, 2012
Last updated April 18, 2016
Start date April 2010
Est. completion date August 2012

Study information

Verified date April 2016
Source San Diego State University
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

Screening, Brief Intervention, and Referral to Treatment (SBIRT) is a comprehensive, integrated public health approach to identify and deliver a spectrum of early detection and intervention services for substance use in general medical care settings. These settings, such as emergency department visits, offer a potential "teachable moment" because patients may have perceptions of vulnerability about their health, and therefore be particularly receptive to screening and counseling. There is mounting scientific evidence suggesting SBIRT is effective in reducing alcohol use at varying levels of severity in a myriad of health care settings including primary care, emergency departments, and trauma centers. Although the SBIRT approach has shown promise for alcohol, relatively little is known about its effectiveness for adult illicit drug use specifically.

This will be among the first studies to rigorously test the SBIRT approach for drug use. It will evaluate the effectiveness of SBIRT for drug use and related factors for 700 multi-ethnic ED patients using a two-group randomized repeated-measures design in which biologically-validated drug use abstinence and related outcomes of an intervention group are compared to those of an attention-placebo control group. Over a 14-month period, bilingual/bicultural Health Educators recruited participants who reported past 30-day illicit drug use in excess of risky alcohol use from the waiting areas of two large hospital's ED and trauma units. Following consent procedures and standardized baseline assessments, Health Educators randomly assigned participants to one of the two conditions. The intervention group received "Life Shift," an SBIRT drug use intervention matched to the participant's drug use risk level. The control group received the same type and quantity of intervention in an unrelated area—Driving and Traffic Safety ("Shift Gears" program), also matched to their driving/traffic risk level. A 6-month face-to-face follow-up visit by trained measurement technicians blind to the participant's assigned condition collected standardized self-report past 30-day drug use measures (ASI-Lite)and hair samples for validating self-reported abstinence. Additional outcome variables are changes in the frequency of drug use, functional status measures (i.e., medical problems, psychiatric problems, and alcohol use), and health care utilization.


Recruitment information / eligibility

Status Completed
Enrollment 700
Est. completion date August 2012
Est. primary completion date June 2011
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years to 100 Years
Eligibility Inclusion Criteria:

- 18 or over

- speak English or Spanish

- competent to give consent and interact

- drug use risk higher than alcohol use risk

Exclusion Criteria:

- under 18

- non english or spanish speaker

- no telephone where one can be reached

- too injured/sick to participate

- alcohol use risk higher than drug use risk

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Factorial Assignment, Masking: Double Blind (Subject, Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Behavioral:
Screening/motivational drug intervention
Screening and brief motivational intervention delivered in the ER to reduce drug use
Motivational placebo intervention
Screening and brief motivational intervention delivered in the ER to reduce driving and traffic risk

Locations

Country Name City State
United States Scripps Mercy Emergency Department and Trauma Unit San Diego California
United States UCSD Emergency Department and Trauma Unit San Diego California

Sponsors (1)

Lead Sponsor Collaborator
San Diego State University

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary past 30 day drug use abstinence Based on the addiction severity index-Lite 6 months post intervention No
Secondary Frequency of drug use Based on composite score from the Addiction Severity Index-Lite 6 months post intervention No
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