NCT05061108

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

75
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
330

participants targeted

Target at P75+ for not_applicable hypertension

Timeline
4mo left

Started Aug 2022

Longer than P75 for not_applicable hypertension

Geographic Reach
1 country

1 active site

Status
active not recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress90%
Aug 2022Sep 2026

First Submitted

Initial submission to the registry

September 7, 2021

Completed
22 days until next milestone

First Posted

Study publicly available on registry

September 29, 2021

Completed
10 months until next milestone

Study Start

First participant enrolled

August 8, 2022

Completed
4.1 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 30, 2026

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

September 30, 2026

Last Updated

October 16, 2025

Status Verified

October 1, 2025

Enrollment Period

4.1 years

First QC Date

September 7, 2021

Last Update Submit

October 14, 2025

Conditions

Keywords

Health DisparitiesAfrican AmericanPrevention

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

EXPERIMENTAL

Randomized selection of recruited participants that will receive intervention

Behavioral: PAL2

Control

NO INTERVENTION

Randomized selection of recruited participants that will not receive intervention

Interventions

PAL2BEHAVIORAL

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

Also known as: Pragmatic personalized, adaptable approach to lifestyle and life circumstance
Intervention

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

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

Location

MeSH Terms

Conditions

Hypertension

Condition Hierarchy (Ancestors)

Vascular DiseasesCardiovascular Diseases

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

Locations