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Impact of a Computer-Assisted SBIRT Program in an HIV Care Setting — SBIRT  

Substance Use Clinical Trial

Official title:
Impact of a Computer-Assisted SBIRT Program in an HIV Care Setting

Clinical Trial Summary

The goal of this research is to assess the impact of the "screening, brief intervention, and referral to treatment" (SBIRT) intervention strategy for harmful substance use among HIV-positive people.

Clinical Trial Description

The specific aims of the study are:

1. To assess the feasibility of conducting SBIRT using (1) a patient self-administered intervention embedded in a web-based Personal Health Record (PHR) compared to (2) a provider-administered SBIRT intervention guided by the Electronic Medical Record (EMR) during clinic appointments.

2. To examine the acceptability of web-based PHRs to conduct and communicate SBIRT compared to EMR-activated SBIRT conducted by clinic staff, from the perspective of the patient and the provider.

3. To assess the impact of SBIRT on risky drug and alcohol use in an HIV/AIDS population and subsequent effects on sexual risk behaviors and antiretroviral therapy (ART) adherence. ;

Study Design

Observational Model: Cohort, Time Perspective: Prospective

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01300806
Study type Observational
Source University of California, San Francisco
Contact
Status Completed
Phase N/A
Start date July 2010
Completion date May 2013
View Details
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