Impact of a Computer-Assisted SBIRT Program in an HIV Care Setting (SBIRT)
|ClinicalTrials.gov Identifier: NCT01300806|
Recruitment Status : Completed
First Posted : February 23, 2011
Last Update Posted : May 22, 2013
|Condition or disease|
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.
|Study Type :||Observational|
|Actual Enrollment :||210 participants|
|Official Title:||Impact of a Computer-Assisted SBIRT Program in an HIV Care Setting|
|Study Start Date :||July 2010|
|Actual Primary Completion Date :||May 2013|
|Actual Study Completion Date :||May 2013|
|clinician administered SBIRT|
- reduced substance use among HIV-positive people [ Time Frame: 6 months ]
- technological innovation to improve the quality of medical care [ Time Frame: 6 months ]
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01300806
|Principal Investigator:||Carol Dawson Rose, PhD||University of California, San Francisco|