Neurocognitive Assessment in Youth Initiating HAART

Inclusion Criteria:

Groups 1 and 2 (If co-enrolling in ATN 061)

- HIV positive participants age 18 years and 0 days to 24 years and 364 days (the lower
age limit of this study is driven by the restriction of ATZ use to age 18 and
greater);

- Groups 1 and 2: CD4+ T cells above 350 cells/mm3 and HIV RNA >1,000 copies/ml, as
determined by two consecutive measures within 6 months of entry with the second
measure being collected at pre-entry to ATN 061;

- Infected with HIV after the age of nine via behavioral means;

- Naïve to ART except for HAART for PMTCT for six months or less with at least six
months since the time of exposure;

- HIV genotype without major resistance mutations to the recommended ATV-r based HAART
regimens;

- Able to provide written informed consent as determined by local Institutional Review
Boards;

- Fluent in English or Spanish.

Group 2, enrolled in ATN 071 and not ATN 061

- CD4+ T cells above 350 cells/mm3 and HIV RNA >1,000 copies/ml, as determined by most
recent laboratory evaluations available within 4 months prior to entry;

- Not prescribed HAART according to DHHS guidelines.

Groups 3 and 4:

- HIV positive participants age 18 years and 0 days to 24 years and 364 days;

- Infected with HIV after the of age nine via behavioral means;

- Naïve to ART except for HAART for PMTCT for six months or less with at least six
months since the time of exposure;

- Able to provide written informed consent as determined by local Institutional Review
Boards;

- Fluent in English or Spanish.

- CD4+ T cells < 350 cells/mm3, as determined by most recent laboratory evaluations
available within 4 months prior to entry.

Group 3 ONLY:

- Participant initiating HAART.

Group 4 ONLY:

- HAART has not been prescribed due to either participant's refusal to initiate HAART
or provider's concerns about participant's predicted inability to adhere to regimen.

Exclusion Criteria:

Groups 1 and 2:

- For Groups 1 and 2: any history of an AIDS-defining illness;

- Active drug or alcohol use or dependence that, in the opinion of the site personnel,
would interfere with meeting study requirements;

- History of cognitive or motor impairment due to non-HIV-related conditions (for
example, prematurity, cerebral palsy, closed head injury, CNS cancer or cranial
irradiation, etc.) or psychosis. Youth with diagnoses of learning disabilities or
attention deficit hyperactivity disorder will be allowed in the study;

- Enrollment of youth with chronic or acute medical conditions other than HIV that
could potentially impact upon neurocognitive functioning requires protocol chair
approval.

- Pregnancy at any time during the study including entry.