Linkage, Empowerment, and Access to Prevent Hypertension
LEAPHTN
1 other identifier
interventional
330
1 country
1
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable hypertension
Started Aug 2022
Longer than P75 for not_applicable hypertension
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
September 7, 2021
CompletedFirst Posted
Study publicly available on registry
September 29, 2021
CompletedStudy Start
First participant enrolled
August 8, 2022
CompletedPrimary Completion
Last participant's last visit for primary outcome
September 30, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
September 30, 2026
October 16, 2025
October 1, 2025
4.1 years
September 7, 2021
October 14, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
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
12 months
Secondary Outcomes (3)
PAL2 (active) intervention will lower diastolic BP compared to usual care (control).
12 Months
PAL2 (active) intervention will lower the incidence of stage-1 hypertension compared to the control group over 1 year
12 months
The rates of adoption and sustainability of the PAL2 intervention will increase from baseline to 12 and 24 months, respectively.
24 months
Study Arms (2)
Intervention
EXPERIMENTALRandomized selection of recruited participants that will receive intervention
Control
NO INTERVENTIONRandomized selection of recruited participants that will not receive intervention
Interventions
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
Eligibility Criteria
You may qualify if:
- 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
- year ASCVD risk \<10% if systolic BP is in stage-1 hypertension range (130-139 mm Hg and \< 65 years old
You may not qualify if:
- 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
- Inability to understand and sign informed consent
- \. Chronic condition (e.g., cancer) with a potential life expectancy \< 2 years
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Wayne Health Mobile Units
Detroit, Michigan, 48201, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- PREVENTION
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Professor, Assistant Vice President for Translational Sciences and Clinical Research Innovation
Study Record Dates
First Submitted
September 7, 2021
First Posted
September 29, 2021
Study Start
August 8, 2022
Primary Completion (Estimated)
September 30, 2026
Study Completion (Estimated)
September 30, 2026
Last Updated
October 16, 2025
Record last verified: 2025-10