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 ]
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01300806
|Principal Investigator:||Carol Dawson Rose, PhD||University of California, San Francisco|