The Effect of Teaching HIV-Infected Patients About HIV and Treatment
HIV Infections

About this trial
This is an interventional treatment trial for HIV Infections focused on measuring Drug Therapy, Combination, Zidovudine, HIV Protease Inhibitors, Lamivudine, Patient Education, Patient Compliance, Reverse Transcriptase Inhibitors, Anti-HIV Agents, Viral Load, abacavir
Eligibility Criteria
Inclusion Criteria Patients must have: Documented and confirmed HIV infection. Limited or no experience with antiretrovirals. CD4+ lymphocyte cell count of 50 cells/mm3 or more 14 days prior to study drug administration. HIV-1 plasma RNA above 40 copies/ml and less than 100,000 copies/ml within 14 days prior to study drug administration. Ability to read, comprehend, and record information in fifth-grade English. Ability to attend the 4 sessions of T.H.E. course on Weeks 1-4. Exclusion Criteria Co-existing Condition: Patients with the following symptoms or conditions are excluded: Patients suffering from a serious medical condition such as diabetes, congestive heart failure, cardiomyopathy, or other cardiac dysfunction which would compromise the safety of the patient. Malabsorption syndrome or other gastrointestinal dysfunction which may interfere with drug absorption or render the patient unable to take oral medication. Acute or chronic active hepatitis. Concurrent Treatment: Excluded: Treatment with foscarnet or other agents with required documented activity against HIV-1 in vitro. Patients with the following prior conditions are excluded: A clinical diagnosis of AIDS, according to the 1993 Centers for Disease Control (CDC) AIDS surveillance definition. (CD4 cell counts below 200 cells/mm3 will not be considered AIDS-defining.) History of allergy to any study drug. Prior Medication: Excluded: History of antiretroviral use. Patients with a history of sequential nucleoside monotherapy will be excluded, as will patients with a total antiretroviral history exceeding 6 months. Required treatment with immunomodulating agents, such as systemic corticosteroids, interleukins, vaccines, or interferons, within 4 weeks prior to study entry, or an HIV immunotherapeutic vaccine within 3 months prior to entry. Asthmatic patients using inhaled corticosteroids are eligible for enrollment. Prior Treatment: Excluded: Radiation therapy or cytotoxic chemotherapeutic agents received within 4 weeks prior to entry. Risk Behavior: Excluded: Current alcohol or illicit drug use which may interfere with the ability to comply with dosing schedule and protocol evaluation and assessment.
Sites / Locations
- AIDS Healthcare Foundation
- Oasis Clinic / King Drew Med Ctr
- Robert Scott MD
- Georgetown Univ Med Ctr
- Whitman Walker Clinic/Elizabeth Taylor Med Ctr
- Univ of Miami School of Medicine
- Specialty Med Care Ctrs of South Florida Inc
- Saint Josephs Comprehensive Research Institute
- AIDS Research Consortium of Atlanta
- Rush Med College / Dept of Infectious Diseases
- Encounter Med Group
- New England Med Ctr / Div of Geo Med & Infect Disease
- Jeffrey Bomser Clinic / NJCR
- UMDNJ / Dept of Ob/Gyn
- Newark Community Health Ctr
- Addiction Research and Treatment Corp
- Bentley-Salick Med Practice
- Holmes Hosp / Univ of Cincinnati Med Ctr
- Allegheny Univ of the Hlth Sciences / Div of Infect Diseases
- Carolina Family Care/Denmark Med Ctr / P O Box 278
- Univ of Tennessee
- Univ of Tennessee / Div of Infect Dis / Dept of Med
- Southeast Dallas Health Ctr
- Therapeutic Concepts
- Santa Rosa Med Ctr / Baptist Med Ctr