Impact of a Computer-Assisted SBIRT Program in an HIV Care Setting
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.
|Study Design:||Observational Model: Cohort
Time Perspective: Prospective
|Official Title:||Impact of a Computer-Assisted SBIRT Program in an HIV Care Setting|
- reduced substance use among HIV-positive people [ Time Frame: 6 months ] [ Designated as safety issue: No ]
- technological innovation to improve the quality of medical care [ Time Frame: 6 months ] [ Designated as safety issue: No ]
|Study Start Date:||July 2010|
|Study Completion Date:||May 2013|
|Primary Completion Date:||May 2013 (Final data collection date for primary outcome measure)|
|clinician administered SBIRT|
The specific aims of the study are:
- 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.
- 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.
- 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.
Please refer to this study by its ClinicalTrials.gov identifier: NCT01300806
|Principal Investigator:||Carol Dawson Rose, PhD||University of California, San Francisco|