search
Back to results

A Nurse-led Intervention to Extend the HIV Treatment Cascade for Cardiovascular Disease Prevention (EXTRA-CVD)

Primary Purpose

HIV/AIDS, Hypertension, Hyperlipidemias

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Multi-component intervention
General prevention education
Sponsored by
Case Western Reserve University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for HIV/AIDS focused on measuring Implementation Science, Cardiovascular Disease, Prevention

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Age ≥18 years
  2. Laboratory confirmed HIV+ diagnosis
  3. Undetectable HIV viral load: defined as the most recent HIV viral load <200 copies/mL, checked within the past year (assessed via chart abstraction)
  4. 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)
  5. 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:

  1. 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
  2. On anti-hypertensive medications solely for a non-hypertension indication (e.g. systolic heart failure)
  3. Severely hearing or speech impaired, or other disability that would limit participation in the intervention components
  4. In a nursing home and/or receiving in-patient psychiatric care
  5. Terminal illness with life expectancy < 4 months
  6. No reliable access to a telephone
  7. Pregnant, breast-feeding, or planning a pregnancy during the study period
  8. 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

Arm Type

Experimental

Active Comparator

Arm Label

Nurse Intervention

Education Control

Arm Description

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.

Outcomes

Primary Outcome Measures

Systolic blood pressure
Repeated measures across 4 time points (0, 4, 8, and 12 months)

Secondary Outcome Measures

Non high density lipoprotein (Non-HDL) cholesterol
Repeated measures across 4 time points (0, 4, 8, and 12 months)

Full Information

First Posted
August 20, 2018
Last Updated
July 17, 2023
Sponsor
Case Western Reserve University
Collaborators
Duke University, University Hospitals Cleveland Medical Center, MetroHealth Medical Center, National Heart, Lung, and Blood Institute (NHLBI), University of Washington
search

1. Study Identification

Unique Protocol Identification Number
NCT03643705
Brief Title
A Nurse-led Intervention to Extend the HIV Treatment Cascade for Cardiovascular Disease Prevention
Acronym
EXTRA-CVD
Official Title
A Nurse-led Intervention to Extend the HIV Treatment Cascade for Cardiovascular Disease Prevention
Study Type
Interventional

2. Study Status

Record Verification Date
July 2023
Overall Recruitment Status
Completed
Study Start Date
September 20, 2019 (Actual)
Primary Completion Date
January 15, 2023 (Actual)
Study Completion Date
January 15, 2023 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Case Western Reserve University
Collaborators
Duke University, University Hospitals Cleveland Medical Center, MetroHealth Medical Center, National Heart, Lung, and Blood Institute (NHLBI), University of Washington

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Strategies to improve uptake of cardiovascular disease preventive therapies among people living with HIV (PLHIV) are urgently needed. This study tests an innovative prevention nurse intervention to extend the HIV/AIDS treatment cascade for the treatment of hypertension and hyperlipidemia among PLHIV on suppressive antiretroviral therapy. This intervention may be scalable as an extension of ongoing HIV/AIDS treatment cascade initiatives in HIV specialty clinics nationwide.
Detailed Description
People living with HIV (PLHIV) are at increased risk for atherosclerotic cardiovascular disease (ASCVD); however, uptake of evidence based therapies to prevent ASCVD is sub-optimal. Reasons for under treatment may include low perceived risk, competing priorities for HIV specialist providers, and poor trust and communication with non-HIV primary care providers. This project proposes a nurse-led intervention to extend the HIV/AIDS treatment cascade-a widely adopted framework developed to improve access to high quality HIV care-for CVD prevention, specifically to improve control of blood pressure and hyperlipidemia in PLHIV on antiretroviral therapy who have suppressed HIV viral load. The study will be conducted in three racially and ethnically diverse clinic contexts [University Hospitals (Cleveland, OH), MetroHealth (Cleveland, OH) and Duke Health (Durham, NC)] that are broadly representative of HIV specialty care in the US. Using a mixed-methods clinical effectiveness trial design, this project will test the 12-month efficacy of a multi-component intervention among n=300 HIV+ adults on suppressive ART with hypertension and hyperlipidemia. Participants will be randomized 1:1 to intervention vs. education control. Control participants will receive general prevention education. The intervention will consist of four evidence-based components derived from prior studies in the general population: (1) nurse-led care coordination, (2) nurse-managed medication protocols and adherence support (3) home BP monitoring, and (4) electronic medical records (EMR) support tools. These components will be further adapted to the HIV specialty clinic context with key stakeholder input and using data from a mixed-methods study of current ASCVD preventive care practices at the three HIV clinic sites. A process evaluation of the prevention nurse intervention will be conducted, which will assess fidelity, dose, recruitment, reach, and context. Two key contextual process measures of interest will be changes in perceived ASCVD risk and changes in trust and communication between PLHIV participants and their HIV and non-HIV providers. If proven effective to reduce both blood pressure and cholesterol as postulated, this nurse-led intervention will have substantial clinical impact among high-risk PLHIV, potentially reducing ASCVD events by more than a quarter. This model is potentially scalable as an extension of HIV treatment cascade initiatives nationwide.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
HIV/AIDS, Hypertension, Hyperlipidemias
Keywords
Implementation Science, Cardiovascular Disease, Prevention

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
298 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Nurse Intervention
Arm Type
Experimental
Arm Description
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.
Arm Title
Education Control
Arm Type
Active Comparator
Arm Description
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.
Intervention Type
Other
Intervention Name(s)
Multi-component intervention
Intervention Description
4 components as described
Intervention Type
Other
Intervention Name(s)
General prevention education
Intervention Description
General education as described
Primary Outcome Measure Information:
Title
Systolic blood pressure
Description
Repeated measures across 4 time points (0, 4, 8, and 12 months)
Time Frame
12 months
Secondary Outcome Measure Information:
Title
Non high density lipoprotein (Non-HDL) cholesterol
Description
Repeated measures across 4 time points (0, 4, 8, and 12 months)
Time Frame
12 months
Other Pre-specified Outcome Measures:
Title
% of subjects in each hypertension cascade category
Description
Ordinal 4-level variable across 4 time points (0, 4, 8, and 12 months). The hypertension cascade tool consists of mutually exclusive categories as follows: 1=undiagnosed hypertension; 2=hypertension diagnosed; 3=hypertension diagnosed and appropriately managed; 4=hypertension diagnosed, appropriately managed, and blood pressure target achieved.
Time Frame
12 months
Title
% of subjects in each hyperlipidemia cascade category
Description
Ordinal 4-level variable across 4 time points (0, 4, 8, and 12 months). The hypercholesterolemia cascade tool consists of ordered categories as follows: 1=undiagnosed hyperlipidemia; 2=hyperlipidemia diagnosed; 3=hyperlipidemia diagnosed and appropriately managed; 4=hyperlipidemia diagnosed, appropriately managed, and non-HDL cholesterol target achieved.
Time Frame
12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
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 >130 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 >130mg/dL or on cholesterol lowering medication 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 100mg/dL 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 Non-English Speaking
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Chris T Longenecker, MD
Organizational Affiliation
University of Washington
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Allison R Webel, RN PhD
Organizational Affiliation
University of Washington
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Hayden Bosworth, PhD
Organizational Affiliation
Duke University
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Barb Gripshover, MD
Organizational Affiliation
Case Western Reserve University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Duke Health
City
Durham
State/Province
North Carolina
ZIP/Postal Code
27710
Country
United States
Facility Name
University Hospitals Cleveland Medical Center
City
Cleveland
State/Province
Ohio
ZIP/Postal Code
44106
Country
United States
Facility Name
MetroHealth Medical Center
City
Cleveland
State/Province
Ohio
ZIP/Postal Code
44109
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
In collaboration with the National Institutes of Health funding body, we will develop a process to facilitate providing other investigators with access to appropriately de-identified study data. We will make the following available upon request after the primary manuscript is published: de-identified data set, trial description information, data collection forms, and data structure.
IPD Sharing Time Frame
After publication of the primary manuscript
IPD Sharing Access Criteria
Data will be made available upon request or on a data share site after publication of the primary manuscript.
Citations:
PubMed Identifier
33579396
Citation
Schexnayder J, Longenecker CT, Muiruri C, Bosworth HB, Gebhardt D, Gonzales SE, Hanson JE, Hileman CO, Okeke NL, Sico IP, Vedanthan R, Webel AR. Understanding constraints on integrated care for people with HIV and multimorbid cardiovascular conditions: an application of the Theoretical Domains Framework. Implement Sci Commun. 2021 Feb 12;2(1):17. doi: 10.1186/s43058-021-00114-z.
Results Reference
derived
PubMed Identifier
33228623
Citation
Webel AR, Schexnayder J, Rentrope CR, Bosworth HB, Hileman CO, Okeke NL, Vedanthan R, Longenecker CT. The influence of healthcare financing on cardiovascular disease prevention in people living with HIV. BMC Public Health. 2020 Nov 23;20(1):1768. doi: 10.1186/s12889-020-09896-8.
Results Reference
derived
PubMed Identifier
31419622
Citation
Okeke NL, Webel AR, Bosworth HB, Aifah A, Bloomfield GS, Choi EW, Gonzales S, Hale S, Hileman CO, Lopez-Kidwell V, Muiruri C, Oakes M, Schexnayder J, Smith V, Vedanthan R, Longenecker CT. Rationale and design of a nurse-led intervention to extend the HIV treatment cascade for cardiovascular disease prevention trial (EXTRA-CVD). Am Heart J. 2019 Oct;216:91-101. doi: 10.1016/j.ahj.2019.07.005. Epub 2019 Jul 18.
Results Reference
derived

Learn more about this trial

A Nurse-led Intervention to Extend the HIV Treatment Cascade for Cardiovascular Disease Prevention

We'll reach out to this number within 24 hrs