Search / Trial NCT00002409

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

Launched by GLAXO WELLCOME · Aug 30, 2001

Trial Information

Current as of December 06, 2024

Completed

Keywords

Drug Therapy, Combination Zidovudine Hiv Protease Inhibitors Lamivudine Patient Education Patient Compliance Reverse Transcriptase Inhibitors Anti Hiv Agents Viral Load Abacavir

ClinConnect Summary

Following initial screening, eligible patients are treated with open-label Combivir plus abacavir for 24 weeks. Patients are randomized to undergo the education intervention, Tools for Health and Empowerment (T.H.E.) course plus counseling, or routine counseling only (control group). Measurements and evaluations for assessment of immunologic effects, adherence, and health outcomes are performed at entry (Day 1) and at Weeks 2, 5, 8, 12, 16, and 24.

Gender

ALL

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.

Trial Officials

K Rawlings

Study Chair

About Glaxo Wellcome

Glaxo Wellcome, a leading global biopharmaceutical company, is dedicated to advancing healthcare through innovative research and development of new therapies. With a strong focus on addressing unmet medical needs, Glaxo Wellcome combines scientific excellence with a commitment to improving patient outcomes across various therapeutic areas, including respiratory, infectious diseases, and oncology. The company is recognized for its robust clinical trial portfolio, leveraging cutting-edge technology and collaborative partnerships to drive the development of transformative treatments. Glaxo Wellcome upholds the highest ethical standards in clinical research, ensuring patient safety and integrity throughout the trial process.

Locations

Miami, Florida, United States

Atlanta, Georgia, United States

Brooklyn, New York, United States

Washington, District Of Columbia, United States

Cincinnati, Ohio, United States

Memphis, Tennessee, United States

Los Angeles, California, United States

Oakland, California, United States

Tampa, Florida, United States

Newark, New Jersey, United States

Memphis, Tennessee, United States

Newark, New Jersey, United States

Los Angeles, California, United States

Washington, District Of Columbia, United States

Miami, Florida, United States

Chicago, Illinois, United States

Oak Park, Illinois, United States

Boston, Massachusetts, United States

Newark, New Jersey, United States

New York, New York, United States

Philadelphia, Pennsylvania, United States

Denmark, South Carolina, United States

Dallas, Texas, United States

Houston, Texas, United States

San Antonio, Texas, United States

People applied

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

Discussion 0

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