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

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ClinicalTrials.gov Identifier: NCT01300806
Recruitment Status : Completed
First Posted : February 23, 2011
Last Update Posted : May 22, 2013
Sponsor:
Information provided by (Responsible Party):
University of California, San Francisco

Brief 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.

Condition or disease
Substance Use

Detailed 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 Type : Observational
Actual Enrollment : 210 participants
Observational Model: Cohort
Time Perspective: Prospective
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

Resource links provided by the National Library of Medicine

MedlinePlus related topics: HIV/AIDS
U.S. FDA Resources

Group/Cohort
myHERO SBIRT
clinician administered SBIRT



Primary Outcome Measures :
  1. reduced substance use among HIV-positive people [ Time Frame: 6 months ]

Secondary Outcome Measures :
  1. technological innovation to improve the quality of medical care [ Time Frame: 6 months ]


Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Probability Sample
Study Population
primary care clinic patients
Criteria

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.


Information from the National Library of Medicine

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


Sponsors and Collaborators
University of California, San Francisco
Investigators
Principal Investigator: Carol Dawson Rose, PhD University of California, San Francisco

Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
Responsible Party: University of California, San Francisco
ClinicalTrials.gov Identifier: NCT01300806     History of Changes
Other Study ID Numbers: 09035355
First Posted: February 23, 2011    Key Record Dates
Last Update Posted: May 22, 2013
Last Verified: May 2013

Keywords provided by University of California, San Francisco:
HIV
harmful substance use