Adherence-Suppression-Resistance Relationships for Atripla Compared to Historical Antiretroviral Regimens

NCT ID: NCT01006005

Last Updated: 2023-11-08

Basic Information

• Recruitment Status: COMPLETED
• Total Enrollment: 51 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2007-07-31
• Study Completion Date: 2008-06-30

Brief Summary

The study is recruiting 50 patients initiating or switching to Atripla and comparing them to 250 individuals previously followed in a prospective study of HIV+ low income individuals recruited from homeless shelters, single room occupancy hotels and free meal food lines as part of the UCSF Reach Study. Adherence will be measured through monthly unannounced pill counts and electronic medication monitors.

Conditions

HIV Infections; Adherence

Study Design

• Observational Model Type: COHORT
• Study Time Perspective: PROSPECTIVE

Eligibility Criteria

Inclusion Criteria

• 18+ years old;
• HIV+;
• Initiating Atripla within 6-months of recruitment;
• Lives in the Tenderloin, South of Market, or Mission District San Francisco;
• Capable of providing informed consent; and
• Willing to complete all study procedures.

Exclusion Criteria

• Intoxication, cognitive dysfunction or psychosis will preclude potential subjects from informed consent.

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

University of California, San Francisco

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Other Identifiers

IN-US-177-0106

Identifier Type: -

Identifier Source: org_study_id