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A Cardiometabolic Health Program Linked With Clinical-Community Support and Mobile Health Telemonitoring to Reduce Health Disparities (LINKED-HEARTS)

Primary Purpose

Hypertension, High Blood Pressure, Diabetes

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
LINKED-HEARTS Program
Sponsored by
Johns Hopkins University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Hypertension

Eligibility Criteria

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

Inclusion Criteria:

  1. 18 years of age as of date of data extraction,
  2. Self-identify as non-Hispanic white, non-Hispanic Black/African American and/or Hispanic,
  3. Diagnosis of Hypertension (HTN) defined by International Classification of Diseases, Tenth code (ICD-10 code) and elevated systolic blood pressure (SBP) measure (≥140 mm Hg) on their most recent clinic visit.
  4. Diagnosis of diabetes or chronic kidney disease (both defined by ICD-10 code), in addition to HTN
  5. Receives primary medical care at one of the participating health systems
  6. Have a Maryland home address

Exclusion Criteria:

  1. Age <18 years
  2. Diagnosis of end-stage renal disease (ESRD) treated with dialysis
  3. Serious medical condition which either limits life expectancy or requires active management (e.g., cancer)
  4. Cognitive impairment or other condition preventing participation in the intervention
  5. Upper arm circumference >50 cm (maximum limit of the extra-large BP cuff)
  6. Planning to leave the practice or move out of the geographic area in 24 months
  7. No longer consider the practice site their location for primary care
  8. Unwillingness to provide informed consent

Sites / Locations

  • Choptank Community Health SystemsRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

LINKED-HEARTS Program

Enhanced Usual Care

Arm Description

Patients in the LINKED-HEARTS Program will be trained to measure their blood pressure with an Omron 10 series device using the Sphygmo telemonitoring app. The physician, pharmacist and Community Health Worker will have access to transmit data. Community Health Workers will provide education on managing blood pressure; reinforce positive blood pressure self-management behaviors; deliver knowledge and skills to promote healthy chronic conditions; assist with linking clinical and administrative services; and link participants with community resources. The study pharmacist will conduct telehealth visits, optimize pharmacologic therapy. The pharmacists will assess and address medication adherence to improve hypertension and diabetes control.

Patients in the Enhanced Usual Care Arm, will receive care as usual from their primary care provider and will be trained to measure their blood pressure with an Omron 10 series device. The staff in each participating community health center practice will be trained in blood pressure measurement best practices.

Outcomes

Primary Outcome Measures

Blood Pressure Control as assessed by percentage of participants with controlled Blood Pressure
Percent of patients with controlled Blood Pressure (<140/90 mm Hg).

Secondary Outcome Measures

Change in Systolic Blood Pressure
Change from baseline in mean systolic blood pressure in millimeters of mercury (mmHg).
Change in Diastolic blood pressure
Change from baseline in diastolic blood pressure in mmHg.
Mean change in Hemoglobin A1c
Mean change from baseline in hemoglobin A1c (percent) in patients with a diagnosis of diabetes.
Percent with Hemoglobin A1c < 7.0
Change from baseline in the percent with hemoglobin A1c < 7.0 in patients with a diagnosis of diabetes.
Change in Body Mass Index (BMI)
Change from baseline in BMI (Kg/m^2).
Mean change in Estimated Glomerular Filtration Rate
Mean change from baseline in Estimated Glomerular Filtration Rate.
Change in Health-Related Quality of Life as assessed by the PROMIS 29
This outcome will be measured using Patient-Reported Outcomes Measurement Information System®, (PROMIS) 29 Profile v. 2.0

Full Information

First Posted
April 4, 2022
Last Updated
October 19, 2023
Sponsor
Johns Hopkins University
Collaborators
National Institute on Minority Health and Health Disparities (NIMHD)
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1. Study Identification

Unique Protocol Identification Number
NCT05321368
Brief Title
A Cardiometabolic Health Program Linked With Clinical-Community Support and Mobile Health Telemonitoring to Reduce Health Disparities
Acronym
LINKED-HEARTS
Official Title
A Cardiometabolic Health Program Linked With Clinical-Community Support and Mobile Health Telemonitoring to Reduce Health Disparities
Study Type
Interventional

2. Study Status

Record Verification Date
October 2023
Overall Recruitment Status
Recruiting
Study Start Date
October 16, 2023 (Actual)
Primary Completion Date
October 1, 2025 (Anticipated)
Study Completion Date
September 1, 2026 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Johns Hopkins University
Collaborators
National Institute on Minority Health and Health Disparities (NIMHD)

4. Oversight

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

5. Study Description

Brief Summary
The LINKED- HEARTS Program is a multi-level project that intervenes at the practice level by linking home blood pressure monitoring (HBPM) with a telemonitoring platform (Sphygmo). The program incorporates team-based care by including community health workers (CHWs) and pharmacists to improve the outcomes of multiple chronic conditions (reduced blood pressure (BP), lower blood sugar, and improved kidney function). The LINKED-HEARTS Program will recruit a total of 600 adults with uncontrolled hypertension (BP ≥ 140/90 mm Hg) AND either type 2 diabetes or chronic kidney disease (CKD) across 16 community health centers or primary care practices serving high-risk adults. This cluster-randomized trial consists of two arms: (1) enhanced "usual care arm," wherein patients will be provided with Omron 10 series home BP monitors and will be managed by the patients' primary care clinicians as usual; and (2) the "intervention arm" which will integrate HBPM telemonitoring, a CHW intervention and provider-level interventions into the usual clinical care to improve BP control and provide support for self-management of chronic conditions. The study pharmacist will conduct telehealth, use the Sphygmo app and the Pharmacist Patient Care Process to collaborate with other providers to optimize pharmacologic therapy to improve hypertension outcomes and with payors to ensure consistent access to drug therapy.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hypertension, High Blood Pressure, Diabetes, Chronic Kidney Diseases

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
LINKED-HEARTS Program
Arm Type
Experimental
Arm Description
Patients in the LINKED-HEARTS Program will be trained to measure their blood pressure with an Omron 10 series device using the Sphygmo telemonitoring app. The physician, pharmacist and Community Health Worker will have access to transmit data. Community Health Workers will provide education on managing blood pressure; reinforce positive blood pressure self-management behaviors; deliver knowledge and skills to promote healthy chronic conditions; assist with linking clinical and administrative services; and link participants with community resources. The study pharmacist will conduct telehealth visits, optimize pharmacologic therapy. The pharmacists will assess and address medication adherence to improve hypertension and diabetes control.
Arm Title
Enhanced Usual Care
Arm Type
No Intervention
Arm Description
Patients in the Enhanced Usual Care Arm, will receive care as usual from their primary care provider and will be trained to measure their blood pressure with an Omron 10 series device. The staff in each participating community health center practice will be trained in blood pressure measurement best practices.
Intervention Type
Behavioral
Intervention Name(s)
LINKED-HEARTS Program
Intervention Description
The intervention arm will include training on home blood pressure monitoring, Sphygmo blood pressure telemonitoring app, Community Health Worker visit for education, counseling on lifestyles modification and Pharmacist to collaborate with other providers to optimize pharmacologic therapy to improve hypertension outcomes and with payors to ensure consistent access to drug therapy.
Primary Outcome Measure Information:
Title
Blood Pressure Control as assessed by percentage of participants with controlled Blood Pressure
Description
Percent of patients with controlled Blood Pressure (<140/90 mm Hg).
Time Frame
12 months
Secondary Outcome Measure Information:
Title
Change in Systolic Blood Pressure
Description
Change from baseline in mean systolic blood pressure in millimeters of mercury (mmHg).
Time Frame
Baseline and 12 months
Title
Change in Diastolic blood pressure
Description
Change from baseline in diastolic blood pressure in mmHg.
Time Frame
Baseline and 12 months
Title
Mean change in Hemoglobin A1c
Description
Mean change from baseline in hemoglobin A1c (percent) in patients with a diagnosis of diabetes.
Time Frame
Baseline and 12 months
Title
Percent with Hemoglobin A1c < 7.0
Description
Change from baseline in the percent with hemoglobin A1c < 7.0 in patients with a diagnosis of diabetes.
Time Frame
Baseline and 12 months
Title
Change in Body Mass Index (BMI)
Description
Change from baseline in BMI (Kg/m^2).
Time Frame
Baseline and 12 months
Title
Mean change in Estimated Glomerular Filtration Rate
Description
Mean change from baseline in Estimated Glomerular Filtration Rate.
Time Frame
Baseline and 12 months
Title
Change in Health-Related Quality of Life as assessed by the PROMIS 29
Description
This outcome will be measured using Patient-Reported Outcomes Measurement Information System®, (PROMIS) 29 Profile v. 2.0
Time Frame
12 months and 24 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 18 years of age as of date of data extraction, Self-identify as non-Hispanic white, non-Hispanic Black/African American and/or Hispanic, Diagnosis of Hypertension (HTN) defined by International Classification of Diseases, Tenth code (ICD-10 code) and elevated systolic blood pressure (SBP) measure (≥140 mm Hg) on their most recent clinic visit. Diagnosis of diabetes or chronic kidney disease (both defined by ICD-10 code), in addition to HTN Receives primary medical care at one of the participating health systems Have a Maryland home address Exclusion Criteria: Age <18 years Diagnosis of end-stage renal disease (ESRD) treated with dialysis Serious medical condition which either limits life expectancy or requires active management (e.g., cancer) Cognitive impairment or other condition preventing participation in the intervention Upper arm circumference >50 cm (maximum limit of the extra-large BP cuff) Planning to leave the practice or move out of the geographic area in 24 months No longer consider the practice site their location for primary care Unwillingness to provide informed consent
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Yvonne Commodore-Mensah, PhD, MSH
Phone
443-614-1519
Email
ycommod1@jhu.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Yvonne Commodore-Mensah, PhD, MSH, RN
Organizational Affiliation
JHU School Of Nursing
Official's Role
Principal Investigator
Facility Information:
Facility Name
Choptank Community Health Systems
City
Denton
State/Province
Maryland
ZIP/Postal Code
21629
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Susan Johnson

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

A Cardiometabolic Health Program Linked With Clinical-Community Support and Mobile Health Telemonitoring to Reduce Health Disparities

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