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NCT01300806 Clinical Trial

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

Substance Use Clinical Trial

— SBIRT  

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

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT01300806
Other study ID # 09035355
Secondary ID
Status Completed
Phase N/A
First received February 17, 2010
Last updated May 20, 2013
Start date July 2010
Est. completion date May 2013

Study information
Verified date May 2013
Source University of California, San Francisco
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Observational

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.

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.

Recruitment information / eligibility
Status Completed
Enrollment 210
Est. completion date May 2013
Est. primary completion date May 2013
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- 18 years of age

- confirmed prior HIV+ serostatus

- ability to provide informed consent to be a participant over a 6 month period

- English or Spanish speaking

Exclusion Criteria:

Inability to answer questions with interviewer assistance. Not receiving primary care in clinic.

Study Design

Observational Model: Cohort, Time Perspective: Prospective

Related Conditions & MeSH terms

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
University of California, San Francisco

Outcome
Type Measure Description Time frame Safety issue
Primary reduced substance use among HIV-positive people 6 months No
Secondary technological innovation to improve the quality of medical care 6 months No
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