MedPath

Effects of Anti-HIV Therapy on Nervous System Function

Completed
Conditions
HIV Infections
Registration Number
NCT00432003
Lead Sponsor
National Institute of Allergy and Infectious Diseases (NIAID)
Brief Summary

The purpose of this study is to observe the way two different anti-HIV treatment strategies affect nerve and brain function in adults with HIV.

Detailed Description

AIDS dementia complex (ADC) is a condition characterized by cognitive impairment, psychomotor slowing, and behavioral change. A milder form of ADC, called HIV minor cognitive/motor disorder (MCMD), is characterized by similar symptoms but has less of an impact on daily functioning. The neurocognitive impairment that results from ADC and MCMD carries an increased risk of poor drug adherence, morbidity, and mortality. It is unclear if highly active antiretroviral therapy (HAART) is effective in preserving neurocognitive function or in preventing or treating neurocognitive impairment. Distal symmetric sensory polyneuropathy (DSPN) and nucleoside-related neuropathy are two other serious conditions that HIV patients are at high risk for. DSPN is thought to be caused by active HIV infection; nucleoside-related neuropathy is thought to be caused by mitochondrial toxicity related to the use of certain antiretrovirals. These 2 conditions may lead to severe pain and discomfort in the feet. It is unknown what connection, if any, there is between DSPN and nucleoside-related neuropathy and the use of HAART. More data are needed on the natural history of these conditions.

This trial is a substudy of a study of management of antiretroviral therapy (SMART). In the SMART study, patients will participate in one of two strategies: a drug conservation (DC) strategy and a viral suppression (VS) strategy. Participants in the DC group will stop or defer HAART, then receive episodic HAART treatment for the minimum time needed to maintain a CD4 cell count of at least 250 cells/mm3. Participants in the VS group will receive HAART to maintain a viral load as low as possible, regardless of CD4 count. The purpose of this study is to compare changes in neurocognitive functioning and peripheral neuropathy symptoms between the 2 strategies of the SMART study.

Patients will participate in this substudy and the main SMART study at the same time. Within 45 days prior to randomization into the main SMART study, participants will have baseline data collected for this substudy. This data will include peripheral neuropathy assessments, treatments for symptoms of peripheral neuropathy. At selected study sites, additional measures will assess neurocognitive function, depression, alcohol and drug use, and education. At 6 months, 12 months, and every 12 months thereafter, peripheral neuropathy symptoms and treatment for the symptoms will be assessed; a pain questionnaire will also be completed. Participants will be followed until the SMART study ends.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
297
Inclusion Criteria
  • Coenrollment in the SMART study
Exclusion Criteria
  • Unable to comply with all study requirements

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
time to development of symptomatic peripheral neuropathy
Change in QNPZ-5 scores
change in peripheral neuropathy symptoms
Secondary Outcome Measures
NameTimeMethod
time to development of asymptomatic or symptomatic peripheral neuropathy
time to resolution of symptomatic peripheral neuropathy
chage in peripheral neuropathy symptoms
Time to neurocognitive impairment
time to development of ADC, stage 2 or greater

Trial Locations

Locations (45)

Temple Univ. School of Medicine CRS

🇺🇸

Philadelphia, Pennsylvania, United States

Western Infectious Disease Consultants CRS

🇺🇸

Wheat Ridge, Colorado, United States

The Alfred Hosp., Clinical Research - Infectious Diseases Unit CRS

🇦🇺

Melbourne, Victoria, Australia

Instituto de Infectologia Emilio Ribas CRS

🇧🇷

Sao Paulo, Brazil

Windsor Regional Hosp., HIV Care Program CRS

🇨🇦

Windsor, Ontario, Canada

Burwood Road Gen. Practice CRS

🇦🇺

Burwood, New South Wales, Australia

Hosp. Universitario Prof. Edgard SantosCRS

🇧🇷

Salvador, Bahia, Brazil

Melbourne Sexual Health Ctr. CRS

🇦🇺

Carlton,, Victoria, Australia

St. Vincent's Hospital CRS

🇦🇺

Darlinghurst, New South Wales, Australia

Westmead Hospital CRS

🇦🇺

Westmead, New South Wales, Australia

Bamrasnaradura Institute CRS

🇹🇭

Muang, Nonthaburi, Thailand

Washington DC VAMC, Washington Regional AIDS Program, Infectious Diseases CRS

🇺🇸

Washington, District of Columbia, United States

Univ. of Florida, Div. of Infectious Diseases CRS

🇺🇸

Jacksonville, Florida, United States

SUNY Downstate Med. Ctr., HIV Ctr. for Women & Children CRS

🇺🇸

Brooklyn, New York, United States

Harlem Hospital Ctr./Columbia University CRS (Gordin CTU)

🇺🇸

New York, New York, United States

MediCorp, Infectious Disease Associates CRS

🇺🇸

Fredericksburg, Virginia, United States

Prahran Market Clinic CRS

🇦🇺

Melbourne, Victoria, Australia

Earl K. Long Med. Ctr., LSU - Mid City EIC Clinic CRS

🇺🇸

Baton Rouge, Louisiana, United States

Michigan State Univ., Infectious Disease Clinic CRS

🇺🇸

Lansing, Michigan, United States

Q.E. II Health Sciences Ctr., Captial District Authority, Victoria Gen. Hosp. CRS

🇨🇦

Halifax, Nova Scotia, Canada

Chulalongkorn University Hospital CRS

🇹🇭

Bangkok, Ratchathewi, Thailand

Sanpatong Hosp. CRS

🇹🇭

Chiang Mai, Thailand

Khon Kaen Univ., Srinagarind Hosp., Div. of Infectious Diseases & Tropical Medicine, Dept. of Medici

🇹🇭

Khon Kaen, Thailand

Mahidol Univ., Ramathibodi Hosp., Div of Infectious Disease CRS

🇹🇭

Bangkok, Ratchathewi, Thailand

Bronx-Lebanon Hosp. Ctr. CRS

🇺🇸

Bronx, New York, United States

The Research & Education Group-Portland CRS

🇺🇸

Portland, Oregon, United States

Oregon Health & Sciences Univ. Internal Medicine (L-475) CRS

🇺🇸

Portland, Oregon, United States

Univ. of Colorado Health Science Ctr. CRS

🇺🇸

Denver, Colorado, United States

Jacobi Med. Ctr., Ambulatory Care Pavillion CRS

🇺🇸

Bronx, New York, United States

Montefiore Med. Ctr., AIDS Ctr. CRS

🇺🇸

Bronx, New York, United States

Legacy Clinic Emanuel CRS

🇺🇸

Portland, Oregon, United States

Wayne State Univ. CRS

🇺🇸

Detroit, Michigan, United States

Bronx VAMC CRS

🇺🇸

Bronx, New York, United States

Univ. of Oklahoma Health Sciences Ctr., Div. of Infectious Diseases CRS

🇺🇸

Oklahoma City, Oklahoma, United States

Kaiser Immune Deficiency Clinic of Portland CRS

🇺🇸

Portland, Oregon, United States

Vernon Harris East End Community Health Ctr. CRS

🇺🇸

Richmond, Virginia, United States

Castro-Mission Health Ctr. CRS

🇺🇸

San Francisco, California, United States

Kaiser Permanente of Denver CRS

🇺🇸

Denver, Colorado, United States

Denver Public Health CRS

🇺🇸

Denver, Colorado, United States

Eastside Family Health Ctr. CRS

🇺🇸

Denver, Colorado, United States

Henry Ford Hosp. CRS

🇺🇸

Detroit, Michigan, United States

CrossOver Health Ctr. CRS

🇺🇸

Richmond, Virginia, United States

VCU Health Systems, Infectious Disease Clinic CRS

🇺🇸

Richmond, Virginia, United States

Virginia Commonwealth Univ. Medical Ctr. CRS

🇺🇸

Richmond, Virginia, United States

Med. College of Wisconsin, Infectious Disease Clinic CRS

🇺🇸

Milwaukee, Wisconsin, United States

© Copyright 2025. All Rights Reserved by MedPath