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Linkage, Empowerment, and Access to Prevent Hypertension (LEAPHTN)

Primary Purpose

Hypertension, Blood Pressure, Cardiovascular Disease Other

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
PAL2
Sponsored by
Wayne State University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Hypertension focused on measuring Health Disparities, African American, Prevention

Eligibility Criteria

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

Inclusion Criteria:

  1. Self-identification as Black, age >18 years, living in the city of Detroit
  2. Elevated BP systolic HTN: systolic BP 120-129 and/or diastolic BP <90 mm Hg upon screening
  3. Not currently taking medications for HTN
  4. Low cardiovascular risk as defined by 2017 AHA/ACC HTN guidelines (no diabetes, no chronic kidney disease, no established ASCVD, and a 10-year ASCVD risk <10%)2

Exclusion Criteria:

  1. Any clinical cardiovascular disease (e.g., coronary artery disease, heart failure, stroke, arrhythmia)
  2. Chronic kidney disease or glomerular filtration rate <60 ml/min on screening laboratory testing
  3. Diabetes or HbA1c ≥ 6.5% on screening laboratory testing
  4. LDL-C ≥ 190 mg/dL on screening laboratory testing (on or off medications)
  5. ASCVD risk score calculated ≥ 10% for 10 years by clinical calculator on screening2
  6. Inability or not willing to follow-up with PAL2 research or usual care limb and at 6 & 12-months at the MHU
  7. Taking any medications for diabetes, heart disease or kidney disease. Cholesterol medication is not an exclusion
  8. Inability to understand and sign informed consent

10. Chronic condition (e.g., cancer) with a potential life expectancy < 2 years

Sites / Locations

  • Wayne HealthRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Intervention

Control

Arm Description

Randomized selection of recruited participants that will receive intervention

Randomized selection of recruited participants that will not receive intervention

Outcomes

Primary Outcome Measures

Systolic BP levels will be significantly lower (by ≥4 mm Hg) in participants randomized to the PAL2 (active) intervention versus usual care (control) over the first 12 months of the trial
Resting seated systolic BP will be measured in the dominant upper arm by validated automated BP monitors using a standardized protocol in accordance with the methods in the 2017 American College of Cardiology (ACC)/American Heart Association (AHA) Hypertension guidelines. BP outcomes will be checked during months 6 and 12 of the trial

Secondary Outcome Measures

PAL2 (active) intervention will lower diastolic BP compared to usual care (control).
Resting seated diastolic BP will be measured in the dominant upper arm by validated automated BP monitors using a standardized protocol in accordance with the methods in the 2017 ACC/AHA Hypertension guidelines. BP outcomes will be checked during months 6 and 12 of the trial
PAL2 (active) intervention will lower the incidence of stage-1 hypertension compared to the control group over 1 year
Resting seated systolic and diastolic BPs will be measured in the dominant upper arm by validated automated BP monitors using a standardized protocol in accordance with the methods in the 2017 ACC/AHA Hypertension guidelines. BP outcomes will be checked during months 6 and 12 of the trial. Stage-1 hypertension is defined as a systolic BP ≥130 mm Hg and/or a diastolic BP ≥80 mm Hg.
The rates of adoption and sustainability of the PAL2 intervention will increase from baseline to 12 and 24 months, respectively.
Standardized surveys regarding the rate of compliance with the PAL2 intervention will be delivered at 6,12 and 24 months of the trial. These rates will be higher at 12 and 24 months versus 6 months

Full Information

First Posted
September 7, 2021
Last Updated
May 23, 2023
Sponsor
Wayne State University
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1. Study Identification

Unique Protocol Identification Number
NCT05061108
Brief Title
Linkage, Empowerment, and Access to Prevent Hypertension
Acronym
LEAPHTN
Official Title
Linkage, Empowerment, and Access to Prevent Hypertension (LEAP-HTN)
Study Type
Interventional

2. Study Status

Record Verification Date
May 2023
Overall Recruitment Status
Recruiting
Study Start Date
August 8, 2022 (Actual)
Primary Completion Date
September 30, 2025 (Anticipated)
Study Completion Date
September 30, 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Wayne State University

4. Oversight

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

5. Study Description

Brief Summary
Brief Summary: Black adults have a higher incidence of hypertension (HTN) and a greater risk of HTN-related cardiovascular disease (CVD) compared with White adults. Even mild elevations in blood (BP) above 115/75 mm Hg are associated with increased CVD risk. Accordingly, emphasis is being placed on early interventions for high BP, particularly in those who are low cardiovascular risk(systolic BP 110-139 and diastolic BP < 90 mm Hg), for participants lifestyle modification is recommended. Although lifestyle modifications are effective to lower BP, implementation is suboptimal in Black communities, especially those participants residing in low-income urban settings. Pervasive negative social determinants of health (SDoH), such as poor access to healthcare, food insecurity, limited availability of healthy foods, lack of safe places to engage in physical activity, and low health literacy are major drivers of inequities in HTN and a critical barrier to implementation of recommended lifestyle modifications in Black communities. To achieve health equity, effective strategies must address negative SDoH that are root causes of racial disparities in health outcomes as clearly demonstrated by the coronavirus disease (COVID-19) pandemic. Predominantly Black cities like Detroit, Michigan, where the mortality rate from heart disease is nearly twice the national average, have been devastated by COVID-19. To address this, the investigators developed an innovative mobile health unit (MHU) program that uses geospatial health and social vulnerability data to direct deployment of testing and vaccination services to communities with highest needs. Since April 2020, the investigators conducted 500 events with 220 community partners where 40,000 people have been tested or vaccinated for COVID in MHUs. Using a hybrid type I effectiveness-implementation design in the proposed Linkage, Empowerment, and Access to Prevent Hypertension (LEAP-HTN) study, the investigators will implement a novel approach that links low cardiovascular risk Black adult participants without stage-2 hypertension to collaborative care delivered in deprived neighborhoods by community health workers (CHWs) using a personalized, adaptable approach to lifestyle and life circumstance (PAL2) intervention. The investigators will leverage our MHU program, layering on top of existing services to streamline access for screening, recruitment and all ongoing follow-up throughout the study period. Our specific aims are: AIM 1: To compare the effect of PAL2 intervention versus usual care (MHU engagement without PAL2) on systolic BP reduction and prevention of stage 2 HTN (systolic BP ≥ 140 mm Hg and/or diastolic BP >90 mm Hg) among 500 Black adults with baseline untreated systolic BPs below stage 2 (ranging 110-139 mm Hg) and a diastolic BP < 90 mm Hg. Hypothesis (H) 1a: Systolic BP (primary outcome) will be reduced more in those randomized to PAL2 intervention versus usual care at 6 and 12 months. H1b: Diastolic BP levels and the incidence of stage 2 HTN (systolic BP ≥ 140 mm Hg and/or diastolic BP >90 mmm Hg) at 6 and 12 months (secondary outcomes) will be lower in participants randomized to the PAL2 intervention versus usual care. AIM 2: To use the RE-AIM framework to assess the reach, adoption, effectiveness, sustainability and cost of LEAP-HTN at 12 months post-randomization. H2a: The rates of adoption and sustainability of the PAL2 intervention will increase from baseline to 12 and up to 24 months in subjects with available data, respectively. H2b: PAL2 intervention will be more cost-effective than usual care at 12 months and projected to be more cost-effective at 10 years. Health Equity Impact: Targeted deployment of MHUs and PAL2 can mitigate several key adverse SDoH. LEAP-HTN contributes to the RESTORE Network by testing a sustainable and scalable approach to advance health equity and prevent HTN in Black adults participants. If successful, the use of MHU can be easily implemented in similar urban Black communities across the U.S.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hypertension, Blood Pressure, Cardiovascular Disease Other
Keywords
Health Disparities, African American, Prevention

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
500 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Intervention
Arm Type
Experimental
Arm Description
Randomized selection of recruited participants that will receive intervention
Arm Title
Control
Arm Type
No Intervention
Arm Description
Randomized selection of recruited participants that will not receive intervention
Intervention Type
Behavioral
Intervention Name(s)
PAL2
Other Intervention Name(s)
Pragmatic personalized, adaptable approach to lifestyle and life circumstance
Intervention Description
Community health worked based intervention to mitigate psychosocial and life circumstance barriers to optimize health promotion coupled with high blood pressure and lifestyle disease state education
Primary Outcome Measure Information:
Title
Systolic BP levels will be significantly lower (by ≥4 mm Hg) in participants randomized to the PAL2 (active) intervention versus usual care (control) over the first 12 months of the trial
Description
Resting seated systolic BP will be measured in the dominant upper arm by validated automated BP monitors using a standardized protocol in accordance with the methods in the 2017 American College of Cardiology (ACC)/American Heart Association (AHA) Hypertension guidelines. BP outcomes will be checked during months 6 and 12 of the trial
Time Frame
12 months
Secondary Outcome Measure Information:
Title
PAL2 (active) intervention will lower diastolic BP compared to usual care (control).
Description
Resting seated diastolic BP will be measured in the dominant upper arm by validated automated BP monitors using a standardized protocol in accordance with the methods in the 2017 ACC/AHA Hypertension guidelines. BP outcomes will be checked during months 6 and 12 of the trial
Time Frame
12 Months
Title
PAL2 (active) intervention will lower the incidence of stage-1 hypertension compared to the control group over 1 year
Description
Resting seated systolic and diastolic BPs will be measured in the dominant upper arm by validated automated BP monitors using a standardized protocol in accordance with the methods in the 2017 ACC/AHA Hypertension guidelines. BP outcomes will be checked during months 6 and 12 of the trial. Stage-1 hypertension is defined as a systolic BP ≥130 mm Hg and/or a diastolic BP ≥80 mm Hg.
Time Frame
12 months
Title
The rates of adoption and sustainability of the PAL2 intervention will increase from baseline to 12 and 24 months, respectively.
Description
Standardized surveys regarding the rate of compliance with the PAL2 intervention will be delivered at 6,12 and 24 months of the trial. These rates will be higher at 12 and 24 months versus 6 months
Time Frame
24 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Self-identification as Black, age ≥18 years, living in the Detroit-area Systolic BP 110-139 and diastolic BP <90 mm Hg upon screening Not currently taking medications for HTN Low cardiovascular risk as defined by 2017 AHA/ACC HTN guidelines (no diabetes, no chronic kidney disease, no established ASCVD 10-year ASCVD risk <10% if systolic BP is in stage-1 hypertension range (130-139 mm Hg and < 65 years old Exclusion Criteria: Any clinical cardiovascular disease (e.g., coronary artery disease, heart failure, stroke, arrhythmia) Chronic kidney disease or glomerular filtration rate <60 ml/min on screening laboratory testing Diabetes or HbA1c ≥ 6.5% on screening laboratory testing LDL-C ≥ 190 mg/dL on screening laboratory testing (on or off medications) ASCVD risk score calculated ≥ 10% for 10 years by clinical calculator on screening (if stage-1 systolic HTN only)2 Inability or not willing to follow-up with PAL2 research or usual care limb and at 6 & 12-months at the MHU Taking any medications for diabetes, heart disease or kidney disease. Cholesterol medication is not an exclusion Inability to understand and sign informed consent 10. Chronic condition (e.g., cancer) with a potential life expectancy < 2 years
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Phillip Levy, MD
Phone
313-577-1214
Email
plevy@med.wayne.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Andrea L Jones
Phone
734-448-9803
Email
andjones@med.wayne.edu
Facility Information:
Facility Name
Wayne Health
City
Detroit
State/Province
Michigan
ZIP/Postal Code
48201
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Andrea Jones
Phone
313-448-9803
Email
andjones@med.wayne.edu
First Name & Middle Initial & Last Name & Degree
Phillip Levy, MD
First Name & Middle Initial & Last Name & Degree
Robert Brook, MD

12. IPD Sharing Statement

Plan to Share IPD
Undecided

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