Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
21 participants
OBSERVATIONAL
2010-08-01
2014-12-17
Brief Summary
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Detailed Description
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We plan to enroll 20 older HIV-infected patients (more than 50 years old) and 20 younger controls (20-40 years old), matched for gender and race/ethnicity. Participants will undergo a series of tests, at one comprehensive assessment. Demographic and medical history data will be abstracted from the medical record. Each participant will undergo a medical history and physical examination, and a battery of tests designed to evaluate neuropsychological function, activity, sleep patterns, frailty, emotional well-being and sexual health. These will consist of self-administered questionnaires and neuropsychological tests, as detailed in the Methods section. Innovative measures will be included such as an activity monitor worn by participants, and a Wii balance board to assess standing balance. Participants will be asked to keep a diary and wear the activity monitoring device for one month. Plasma and serum samples will be collected on one occasion for future testing of potential biomarkers.
Conditions
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Study Design
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COHORT
CROSS_SECTIONAL
Study Groups
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Aging in HIV
20-40 years of age or older than 50
Observational
No intervention
Interventions
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Observational
No intervention
Eligibility Criteria
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Inclusion Criteria
* 20-40 years of age or older than 50.
* If taking antiretroviral therapy, on stable therapy for the past 12 weeks and not anticipated to require a change in therapy during the following 6 weeks.
* If not taking antiretroviral therapy, not anticipated to initiate therapy in the next 6 weeks.
* Ability to provide written informed consent.
* Ability to complete the questionnaires in English.
Exclusion Criteria
* Any active psychiatric illness including schizophrenia, severe depression, or severe bipolar affective disorder that, in the opinion of the investigator, could confound performance of or the analysis of the test results.
* Active drug or alcohol abuse that, in the investigator's opinion, could compromise compliance with study procedures or confound the analysis of the test results.
* Major neurologic disease such as multiple sclerosis or stroke, active brain infection (except for HIV-1), brain neoplasm, or space-occupying brain lesion.
* Current delirium or intoxication.
* Pregnancy.
* Any other condition that, in the opinion of the investigator, is a contraindication to participation.
20 Years
75 Years
ALL
No
Sponsors
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National Institute of Mental Health (NIMH)
NIH
University of Nebraska
OTHER
Responsible Party
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Principal Investigators
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Susan Swindells, MBBS
Role: PRINCIPAL_INVESTIGATOR
University of Nebraska
Locations
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University of Nebraska Medical Center
Omaha, Nebraska, United States
Countries
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References
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Valcour V, Shikuma C, Shiramizu B, Watters M, Poff P, Selnes O, Holck P, Grove J, Sacktor N. Higher frequency of dementia in older HIV-1 individuals: the Hawaii Aging with HIV-1 Cohort. Neurology. 2004 Sep 14;63(5):822-7. doi: 10.1212/01.wnl.0000134665.58343.8d.
Related Links
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University of Nebraska Medical Center HIV Clinic
Other Identifiers
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0396-10-FB
Identifier Type: -
Identifier Source: org_study_id
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