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| Sponsor: | Centers for Disease Control and Prevention |
|---|---|
| Collaborators: |
The Miriam Hospital Minneapolis Medical Research Foundation Washington University School of Medicine Denver Infectious Disease Consultants, PLLC |
| Information provided by: | Centers for Disease Control and Prevention |
| ClinicalTrials.gov Identifier: | NCT00146419 |
Purpose
The SUN Study is a Centers for Disease Control and Prevention (CDC)-sponsored multi-site prospective observational cohort study designed to better understand the incidence and etiology of metabolic and other complications related to effective HIV treatment and longer survival. The SUN Study is also providing a platform to evaluate a behavioral intervention designed to reduce HIV transmission through prevention counseling in routine care.
| Condition | Intervention |
|---|---|
|
HIV Infections Sexually Transmitted Diseases |
Behavioral: Reduction in behaviors capable of sexually transmitting HIV |
| Study Type: | Observational |
| Study Design: | Cohort, Prospective |
| Official Title: | Study to Understand the Natural History of HIV/AIDS in the Era of Effective Therapy (SUN Study) |
| Enrollment: | 699 |
| Study Start Date: | March 2004 |
Effective antiretroviral therapy has significantly improved and prolonged the lives of HIV-infected persons. However, antiretroviral use has also been associated with a diverse array of "unnatural" metabolic complications and other adverse medical conditions. These problems, together with subsequent longer survival, have increased patients' risk for developing renal, hepatic, cardiovascular, neurological, rheumatologic, and other end-organ diseases, and cancers. Longer survival is also increasing the pool of HIV-infected persons capable of transmitting the virus, which could accelerate the pace of the U.S. epidemic; however, the ability of physicians caring for HIV-infected persons to incorporate prevention into their clinical practices and the effectiveness of this intervention have not been extensively evaluated.
The goals of the Study to Understand the Natural History of HIV and AIDS ("SUN" Study) are:
The SUN Study is designed to enroll and follow for 5 or more years a cohort of up to 1,000 HIV-infected adults at HIV specialty care centers in four U.S. cities: Denver, Minneapolis, Providence, and St. Louis. Data will be gathered through longitudinal real-time chart review, biannual physical examination (e.g., body mass index [BMI], blood pressure), repeated non-invasive imaging (e.g., dual energy x-ray absortiometry [DEXA] scanning, carotid ultrasonography) and regularly scheduled laboratory testing (e.g., serum lipids, pap smears, and urinary microalbumin). Data collection and quality control will be managed by Cerner Corporation. After sufficient enrollment, (circa 200 persons per site) a structured prevention program to reduce HIV transmission will be introduced. The impact of this intervention will be evaluated both subjectively (e.g., self-reported change in behavior on an audio computer-assisted self-interviewing [ACASI] questionnaire) and objectively (e.g., change in sexually transmitted disease [STD] incidence).
Outcomes include determination of the incidence of therapy-related metabolic complications and other adverse conditions associated with longer survival, identification of risk factors for these complications and conditions, and reduction in both reported and objective measures of risky sexual behavior.
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | Yes |
| Sampling Method: | Non-Probability Sample |
HIV-infected persons receiving care at HIV-specialty clinics
Inclusion Criteria:
For highly active antiretroviral therapy (HAART)-naïve subjects (i.e. persons with no prior substantial antiretroviral [ARV] exposure):
For HAART-exposed subjects (i.e. persons who have taken or are taking HAART at the time of enrollment):
Subject's previous and/or current treatment with ARVs has consisted only of HAART (of any duration and in any number of regimens) defined as:
Exclusion Criteria:
Within the past 60 days subject has:
Footnotes:
Contacts and Locations| United States, Colorado | |
| Denver Infectious Disease Consultants | |
| Denver, Colorado, United States, 80220 | |
| University of Colorado Health Sciences Center | |
| Denver, Colorado, United States, 80220 | |
| United States, Minnesota | |
| Hennepin County Medical Center | |
| Minneapolis, Minnesota, United States, 55404 | |
| Abbott Northwestern Hospital | |
| Minneapolis, Minnesota, United States, 55407 | |
| Park-Nicollet Institute | |
| Minneapolis, Minnesota, United States, 55416 | |
| United States, Missouri | |
| Washington University School of Medicine | |
| St. Louis, Missouri, United States, 63108 | |
| United States, Rhode Island | |
| The Miriam Hospital | |
| Providence, Rhode Island, United States, 02905 | |
| United States, Virginia | |
| Cerner Corporation | |
| McLean, Virginia, United States, 22182 | |
| Principal Investigator: | Charles Carpenter, M.D. | The Miriam Hospital |
| Principal Investigator: | Keith Henry, M.D. | Minneapolis Medical Research Foundation |
| Principal Investigator: | Kristin Mondy, M.D. | Washington University School of Medicine |
| Principal Investigator: | John H Hammer, M.D. | Denver Infectious Disease Consultants, PLLC |
More Information
| Responsible Party: | CDC ( John T. Brooks ) |
| Study ID Numbers: | CDC-NCHSTP-3979, 200-2002-00610, 200-2002-00611, 200-2002-00612, 200-2002-00613 |
| Study First Received: | September 1, 2005 |
| Last Updated: | January 6, 2010 |
| ClinicalTrials.gov Identifier: | NCT00146419 History of Changes |
| Health Authority: | United States: Federal Government |
|
Treatment Experienced Treatment Naive |
|
RNA Virus Infections Sexually Transmitted Diseases, Viral Slow Virus Diseases Immune System Diseases Acquired Immunodeficiency Syndrome Infection Genital Diseases, Male |
Immunologic Deficiency Syndromes Genital Diseases, Female Virus Diseases HIV Infections Sexually Transmitted Diseases Lentivirus Infections Retroviridae Infections |