Purpose

CROWN is a two-arm, cluster-randomized pilot trial testing the feasibility and preliminary efficacy of a salon-based cardiovascular intervention - training stylists as Heart Health Stylists to conduct in-salon blood pressure screenings, home monitoring with telehealth support, community health-worker coaching, and pharmacist-led medication management - among Black and Hispanic women with hypertension.

Condition

Eligibility

Eligible Ages
Between 18 Years and 79 Years
Eligible Sex
Female
Accepts Healthy Volunteers
Yes

Inclusion Criteria

Women are eligible if: - At least 18 years old - Self-identify as Black/African American or Hispanic - Have an average seated systolic blood pressure of 130 mmHg or higher on initial salon screening, and - Have visited the participating salons at least twice in the past six months.

Exclusion Criteria

Women are excluded if: - Pregnant or planning pregnancy during the study period - Have end-stage renal disease requiring dialysis - Have serious medical conditions limiting life expectancy to less than 12 months - Currently participating in other cardiovascular intervention studies - Have severe cognitive impairment, impeding informed consent - Unable to operate blood pressure monitoring equipment after training - Plan to relocate outside the study area within 6 months - Have documented adverse reactions to blood pressure cuff usage.

Study Design

Phase
N/A
Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel Assignment
Primary Purpose
Prevention
Masking
Single (Outcomes Assessor)
Masking Description
Outcomes assessors and data analysts will be masked to treatment allocation.

Arm Groups

ArmDescriptionAssigned Intervention
Experimental
CROWN Intervention Arm
Participants will receive in-salon blood pressure screenings by trained stylists, a home blood pressure monitor connected to a telemonitoring app, community health worker coaching, pharmacist medication support, and digital social needs screening with referrals.
  • Behavioral: CROWN Intervention
    CROWN Intervention includes: 1. Private BP screenings in salon "Heart Health Stations" by trained Heart Health Stylists 2. Free Omron home BP monitor paired with a mobile app for twice-daily telemonitoring 3. In-depth coaching sessions + monthly check-ins with a community health worker 4. Bi-weekly medication review and adherence support by a clinical pharmacist 5. Digital social-needs screening (AHC HRSN) with referral to community resources
Active Comparator
Enhanced Usual Care Arm
Participants will receive in-salon blood pressure screenings, a free Omron home monitor, printed cardiovascular health materials, and standard referrals to social and health services, without telemonitoring, coaching, or pharmacist support.
  • Behavioral: Enhanced Usual Care
    Enhanced Usual Care include: 1. Private BP screenings in salon "Heart Health Stations" by Heart Health Stylists 2. Printed cardiovascular health brochures 3. Free home blood pressure monitor (no app integration) 4. Standard referrals to social and health services

Recruiting Locations

Johns Hopkins University
Baltimore, Maryland 21205
Contact:
Oluwabunmi Ogungbe
410-614-1519
oogungb3@jh.edu

More Details

Status
Recruiting
Sponsor
Johns Hopkins University

Study Contact

Oluwabunmi Ogungbe, PhD, MPH, RN
4106141519
oogungb3@jh.edu

Detailed Description

CROWN is a six-month, cluster-randomized pilot trial enrolling approximately 12 beauty salons. In intervention salons, trained Heart Health Stylists provide weekly private blood pressure screenings. Participants recruited from the intervention salons will receive a home blood pressure monitor linked to a mobile app, as well as community health worker coaching sessions and pharmacist medication support. Participants in the enhanced usual care salons will receive only printed educational materials and a home blood pressure monitor. Eligibility (age ≥18, self-identified Black or Hispanic, Systolic Blood Pressure (SBP) ≥130/80) will be confirmed via three standardized BP measurements, medical history review, and medication assessment in private salon alcoves or by phone. Assessments at baseline, 12, and 24 weeks include seated blood pressure (BP), weight, point-of-care hemoglobin A1c, and lipid panels, as well as surveys of health behaviors and social needs. Participants will receive gift cards, and retain the home monitor at the end of the study. The primary outcome is the change in systolic blood pressure; secondary outcomes include blood pressure control rates, adherence, lifestyle behaviors, and social needs resolution, with end-of-study qualitative interviews assessing acceptability.

Notice

Study information shown on this site is derived from ClinicalTrials.gov (a public registry operated by the National Institutes of Health). The listing of studies provided is not certain to be all studies for which you might be eligible. Furthermore, study eligibility requirements can be difficult to understand and may change over time, so it is wise to speak with your medical care provider and individual research study teams when making decisions related to participation.