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Completed

NCT Number: NCT00385632

Effects of Two Anti-HIV Drug Regimens on Quality of Life and Health Care Use Among SMART Study Participants

The purpose of this study is to compare the effects of two different anti-HIV drug regimens on quality of life and health care utilization among SMART study participants.

Completed

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Key information

Age range

13 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

UCSF, Fresno, School of Medicine, Dept. of Internal Medicine CRS, Fresno, California, United States

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About this study

Advances in antiretroviral therapy (ART) have dramatically reduced mortality and morbidity rates for HIV infected people. However, HIV infection is a costly disease to treat. With improvement in survival, quality of life and the long-term cost of HIV treatment have become increasingly important to the majority of individuals infected with HIV. Different HIV treatment regimens may lead to variations in quality of life and health care costs over the course of treatment. In the SMART study, participants were randomly assigned to one of two treatment groups:

  • Group 1 participants followed a drug conservation (DC) regimen in which ART was stopped or deferred until CD4 cell count dropped below 250 cells/mm3, initiated until CD4 cell count was at least 350 cells/mm3, and then followed by episodic ART based on CD4 cell count.
  • Group 2 participants followed a viral suppression (VS) regimen in which ART was continued to keep viral loads as low as possible, regardless of CD4 cell count.

The purpose of this study is to compare how the DC and VS regimens affect quality of life, symptom severity, health care utilization, and resulting costs among SMART study participants.

At baseline, participants will complete questionnaires regarding quality of life, symptoms, health care utilization, current insurance, and socioeconomic status. Body appearance and signs of HIV disease progression will also be assessed at this time. Follow-up evaluations on quality of life and symptoms will be repeated at Months 4, 8, and 12 and annually thereafter. Follow-up evaluations of all other baseline measures will occur once a year.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Coenrollment in the SMART study
  • Parent or guardian willing to provide informed consent, if applicable

Treatment and study plan

Antiretroviral Regimens

Drug

Various antiretroviral therapy combinations already being administered to participants

Primary outcomes

  1. Quality of life as assessed by self-administered questionnaires, a symptom severity survey, and an assessment of body appearance

    Time frame: Throughout study

  2. Self-reported healthcare utilization

    Time frame: Throughout study

  3. Recorded medications used by participants

    Time frame: Throughout study

  4. Cost of treating HIV/AIDS

    Time frame: Throughout study

Sponsors and collaborators

Lead sponsor

National Institute of Allergy and Infectious Diseases (NIAID)

Nih

Collaborators

  • Community Programs for Clinical Research on AIDS

Registry information

Official study title

Quality of Life and Healthcare Utilization Substudy

Important dates

Study start
2002
Primary completion
2008
Study completion
2008
First posted
Oct 11, 2006
Registry last updated
Apr 21, 2014

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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