Neurocognitive Effects and Tolerability of Efavirenz in Aging HIV-infected Individuals ("SHAC Neuro Study")

NCT ID: NCT01985399

Last Updated: 2016-10-17

Basic Information

• Recruitment Status: COMPLETED
• Total Enrollment: 100 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2013-12-31
• Study Completion Date: 2015-12-31

Brief Summary

Investigators hypothesize that older HIV-infected individuals (i.e., >50 years old) on efavirenz (EFV)-containing antiretroviral therapy (ART) will have significantly worse neurocognitive function than older individuals on non-EFV-containing ART.

Detailed Description

With the aging of the HIV-infected population in the United States and elsewhere, neurocognitive dysfunction will likely become an increasingly common problem. Older individuals could be at increased risk for efavirenz-associated adverse effects due to impaired metabolism, increased drug-drug interactions, and lower physiologic reserve, but there are few data on the long-term safety of efavirenz (and other antiretrovirals) in older individuals with HIV.

The Stanford HIV Aging Cohort (SHAC) is an ideal setting to study potential neurologic effects of antiretrovirals in aging patients. SHAC is an ongoing longitudinal study initiated in 2008 to evaluate aging in virologically-suppressed HIV-infected individuals. The cohort is supported through multiple grants including a grant from the State of California's HIV Research Program as well as a NIH supplemental grant. As of September 2013, approximately 150 virologically-suppressed HIV-infected adults have been enrolled. In addition to enrolling patients with good adherence to ART, the cohort purposefully excludes subjects with active substance abuse, unstable medical conditions, and psychiatric illnesses to limit potential confounding the study end points. Recently, an NIH supplemental grant (AI069556) was received which will expand the SHAC to 300 HIV-infected subjects. The median age of the subjects in the cohort is in the mid-50's allowing an ample number of older subjects for our planned studies.

Conditions

HIV; AIDS

Study Design

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

Study Groups

EFV containing ARV regimen

Pts on Efavirenz containing ARV regimen will have neuropsychological testing performed

Neuropsychological testing

Intervention Type: BEHAVIORAL

Neuropsychological testing

Non -EFV ontaning ARV regimen

Pts on a Non-Efavirenz containing ARVregimen will have neuropsychological testing measures performed

Neuropsychological testing

Intervention Type: BEHAVIORAL

Neuropsychological testing

Interventions

Neuropsychological testing

Neuropsychological testing

Intervention Type: BEHAVIORAL

Eligibility Criteria

Inclusion Criteria

• Enrollment into SHAC (Stanford HIV Aging cohort)
• Age over 50 years of age
• Stable antiretroviral therapy containing EFV- or PI-containing ART (but not both) for at least 6 months
• HIV RNA levels of <200 copies/mL for at least 6 months excluding blips (i.e., a single measurement between 200-500 copies/mL preceded and followed by measurements of <200 copies/mL) while on ART.

Exclusion Criteria

• Completed treatment for any acute systemic infection (other than HIV-1) less than four weeks before study entry
• Any active brain infection (except for HIV-1), brain neoplasm, or space-occupying brain lesion.
• Any active psychiatric illness including schizophrenia, severe depression, or severe bipolar affective disorder that, in the opinion of the investigator, could confound the analysis of the neuropsychological test results.
• Active drug or alcohol abuse that, in the investigator's opinion, could prevent compliance with study procedures or confound the analysis of study endpoints.
• Hospitalization within 30 days of study entry
• Receipt of systemic chemotherapy within 30 days of study entry
• Unable to provide informed consent

• Minimum Eligible Age: 50 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Janssen Services, LLC

INDUSTRY

Sponsor Role: collaborator

Stanford University

OTHER

Sponsor Role: lead

Responsible Party

Philip Grant

Principle Investigator

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Philip Grant, MD

Role: PRINCIPAL_INVESTIGATOR

Stanford University

Locations

Stanford University AIDS Clinical Trials Unit

Palo Alto, California, United States

Countries

United States

Other Identifiers

SHAC Neuro Study

Identifier Type: -

Identifier Source: org_study_id