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The Cleveland Cardiometabolic Cohort

Observational Study of Cardiometabolic Risk in HIV Infected Subjects After Initiation of Antiretroviral Therapy: The Cleveland Cardiometabolic Cohort

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03059121
Enrollment
56
Registered
2017-02-23
Start date
2016-09-01
Completion date
2025-05-19
Last updated
2026-01-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

HIV, Lipodystrophy

Keywords

HIV, Lipodystrophy

Brief summary

In this observational study, the investigators will examine the changes in body composition in HIV-infected subjects before and after initiation of HIV treatment, and look at the correlations with changes in cardiometabolic indices such as endothelial function and coronary calcium scoring.

Detailed description

The effects of lifestyle factors on body composition changes after antiretroviral therapy (ART) are unknown, and as such, investigators will use this prospective observational cohort to study relationships between lifestyle factors, including diet, physical activity and illicit drug use, with changes in body composition after ART. In addition, the effect of the body fat changes will be correlated to changes in cardiometabolic indices such as endothelial function and coronary calcium scoring.

Interventions

Sponsors

University Hospitals Cleveland Medical Center
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
16 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* HIV-1 infection as documented by any licensed ELISA test kit and confirmed by Western blot at any time prior to study entry. HIV-1 culture, HIV-1 antigen, plasma HIV-1 RNA, or a second antibody test by a method other than ELISA is acceptable as an alternative confirmatory test * Provides written informed consent and is capable of reading and comprehending the informed consent * Is not currently taking antiretroviral therapy and has never been on such treatments in the past. Exception would be for subjects who had been in the past on ≤30 days cumulative antiretrovirals, as long as these were stopped \>6 months prior to study entry * Is planning on starting antiretroviral therapy as part of routine clinic care

Exclusion criteria

* Pregnancy or lactation

Design outcomes

Primary

MeasureTime frameDescription
Body composition measuresBaseline, 6-month, 1 year, 2 year, 3 year, 4 year, 5 yearAssessed using DEXA (dual energy x-ray absorptiometry) scans which will be quantifying total body fat

Secondary

MeasureTime frameDescription
Resting Energy Expenditure (REE) measuresBaseline, 6-month, 1 year, 2 year, 3 year, 4 year, 5 yearAssessed using a BodyGem REE calculator (values in KCal)
endothelial function measuresBaseline, 6-month, 1 year, 2 year, 3 year, 4 year, 5 yearAssessed using EndoPAT (values reported as a reactive hyperemia index RHI)
calcium score measuresBaseline, 6-month, 1 year, 2 year, 3 year, 4 year, 5 yearAssessed using CT scans
central obesityBaseline, 6-month, 1 year, 2 year, 3 year, 4 year, 5 yearmeasured with waist circumference using a tape measure (in cm)
Lipids measuresBaseline, 6-month, 1 year, 2 year, 3 year, 4 year, 5 yearused measuring blood levels of triglycerides (mg/dL); serum high-density lipoprotein (mg/dL) ; cholesterol (mg/dL); low density lipoprotein (mg/dL)
Fasting plasma glucose measuresBaseline, 6-month, 1 year, 2 year, 3 year, 4 year, 5 yearfasting plasma glucose test is performed after a person has fasted for at least 8 hours (measured in mg/dL)
Metabolic syndromeBaseline, 6-month, 1 year, 2 year, 3 year, 4 year, 5 yearMetabolic syndrome will be defined using the following measures: central obesity, serum triglycerides , serum high-density lipoprotein (HDL); cholesterol levels and fasting plasma glucose

Countries

United States

Contacts

PRINCIPAL_INVESTIGATORGrace McComsey, MD

University Hospitals Cleveland Medical Center

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026