A Nurse-led Intervention to Extend the HIV Treatment Cascade for Cardiovascular Disease Prevention (EXTRA-CVD)
HIV/AIDS, Hypertension, Hyperlipidemias
About this trial
This is an interventional supportive care trial for HIV/AIDS focused on measuring Implementation Science, Cardiovascular Disease, Prevention
Eligibility Criteria
Inclusion Criteria:
- Age ≥18 years
- Laboratory confirmed HIV+ diagnosis
- Undetectable HIV viral load: defined as the most recent HIV viral load <200 copies/mL, checked within the past year (assessed via chart abstraction)
- Hypertension: defined as systolic blood pressure >140 mmHg on ≥ 2 occasions in the past 12 months or on an antihypertensive medication (assessed via chart abstraction)
- Hyperlipidemia: defined as a non-high-density lipoprotein cholesterol level that is greater than the National Lipid Association target [130mg/dl for moderate to high risk (≥ 2 major risk factors) or 100mg/dl for very high risk (known ASCVD or diabetes + ≥2 major risk factors)]. Major risk factors include HIV, Age >45 men or >55 women, family history of early coronary artery disease, smoking, hypertension, low high-density lipoprotein cholesterol. By design, all participants in our study will be ≥ moderate risk.
Exclusion Criteria:
- On lipid-lowering medication solely for cardiovascular disease prevention with evidence of pre-medication non-high-density lipoprotein cholesterol which was already below National Lipid Association target
- On anti-hypertensive medications solely for a non-hypertension indication (e.g. systolic heart failure)
- Severely hearing or speech impaired, or other disability that would limit participation in the intervention components
- In a nursing home and/or receiving in-patient psychiatric care
- Terminal illness with life expectancy < 4 months
- No reliable access to a telephone
- Pregnant, breast-feeding, or planning a pregnancy during the study period
- Planning to move out of the area in the next 12 months
Sites / Locations
- Duke Health
- University Hospitals Cleveland Medical Center
- MetroHealth Medical Center
Arms of the Study
Arm 1
Arm 2
Experimental
Active Comparator
Nurse Intervention
Education Control
This multi-component intervention will consist of four evidence-based components delivered at 4 in-person visits (0, 4, 8, and 12 months) and by telephone contact: (1) nurse-led care coordination, (2) nurse-managed medication protocols and adherence support (3) home blood pressure monitoring, and (4) electronic medical records support tools.
Participants in the education control arm will receive general prevention education delivered at 4 in-person visits (0, 4, 8, and 12 months), which will consist of evidence-based material on diet, exercise, smoking, sexually transmitted infections, and cancer prevention.