Penn Medicine Healthy Heart

Sponsor
University of Pennsylvania (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT06062394
Collaborator
(none)
1,800
2
17

Study Details

Study Description

Brief Summary

To leverage access to patients across the primary care network, EPIC tools for identifying eligible patients, and the Way to Health platform to launch and enroll a program that will be evaluated in a clinical trial that is focused on changing patient behavior and powered to detect differences in improving blood pressure and cholesterol over 6 months for Penn Medicine patients in West/Southwest Philadelphia and Lancaster.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Penn Med Healthy Heart Program
N/A

Detailed Description

To leverage access to patients across the primary care network, EPIC tools for identifying eligible patients, and the Way to Health platform to launch and enroll Penn Medicine primary care patients into the Penn Medicine Healthy Heart, a six-month program for reduction of hypertension and hypercholesterolemia grounded in behavioral economics insights to increase uptake of and adherence to evidence-based interventions to reduce ASCVD risk. Penn Medicine Healthy Heart emphasizes proactive outreach and prevention outside of a traditional visit model using data assets to identify and risk stratify patients. The program aims to relieve overburdened PCPs through automated hovering technology coupled with a centralized, leveraged team of non-clinical navigators and nurse practitioners. The clinical trial will assess Penn Medicine Healthy Heart and will be powered to detect differences in improving blood pressure and cholesterol over 6 months for Penn Medicine patients in West/Southwest/Downtown Philadelphia and Lancaster, PA.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
1800 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Triple (Participant, Investigator, Outcomes Assessor)
Primary Purpose:
Health Services Research
Official Title:
Reducing Atherosclerotic Cardiovascular Disease (ASCVD) Through a Comprehensive Heart Disease Prevention Program (HDPP)
Anticipated Study Start Date :
Jan 1, 2024
Anticipated Primary Completion Date :
Nov 1, 2024
Anticipated Study Completion Date :
Jun 1, 2025

Arms and Interventions

Arm Intervention/Treatment
No Intervention: Usual Care

This group will not receive the intervention and will continue with usual care.

Experimental: Penn Med Healthy Heart Program

The Intervention group will receive the blood pressure monitor and move through the 4 HDPP modules of the intervention.

Behavioral: Penn Med Healthy Heart Program
Patients randomized to the intervention arm will be assigned a Patient Navigator (Clinical Research Coordinators, with support from Nurse Practitioners and a Medical Director) who will conduct an initial assessment with the patient to determine their main barriers to improving blood pressure and cholesterol control. The Patient Navigators will provide the patient with a home blood pressure cuff for remote monitoring, support from Way to Health text message reminders, referrals to established Penn Medicine smoking cessation programs, and referrals to nutrition and social workers as applicable. The Patient Navigators will help move the patients through four modules: Blood Pressure, Food Insecurity/Nutrition Screening, Statins, and Smoking Cessation. These modules provide patients with the chance to work on blood pressure, cholesterol control, access nutrition resources, and smoking cessation simultaneously or sequentially.
Other Names:
  • PMHH
  • HDPP
  • Outcome Measures

    Primary Outcome Measures

    1. Difference in mean Systolic Blood Pressure (SBP) [6-month period]

      Whether mean SBP is improved among those assigned to intervention vs those assigned to control

    2. Difference in mean LDL-c [6-month period]

      Whether mean LDL-c is improved among those assigned to intervention vs those assigned to control

    Secondary Outcome Measures

    1. Difference in mean Systolic Blood Pressure (SBP) [6-month period]

      Whether mean SBP is improved among those who engaged in the intervention i.e., the average improvement for intervention versus control for those who would have, counter-factually, engaged in the intervention if assigned intervention

    2. Difference in mean LDL-c [6-month period]

      Whether mean LDL-c is improved among those who engaged in the intervention i.e., the average improvement for intervention versus control for those who would have, counter-factually, engaged in the intervention if assigned intervention

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    35 Years to 80 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • On the Penn Medicine Primary Care Service Line registry

    • Last 2 Blood Pressure readings with Systolic Blood Pressure >=140 from any outpatient encounter in the last 12 months AND

    • ASCVD dx OR ASCVD risk score ≥10% OR Diabetes dx OR A1c ≥6.5 in last year OR Diabetes registry OR Last LDL ≥190 in past five years AND

    • Not on a statinor PCSK9, Inclisiran OR on a Low-intensity/moderate-intensity statin) with LDL >100

    Exclusion Criteria:
    • Patients on PCSK9 inhibitors

    • Documented statin allergy/ or intolerance in the EMR

    • Pregnancy

    • Breast feeding

    • Markedly shortened life expectancy including:

    1. metastatic cancer

    2. hospice

    3. End Stage Renal Disease

    4. Congestive Heart Failure

    5. Dementia

    • Is a non-English speaker requiring a translator

    Contacts and Locations

    Locations

    No locations specified.

    Sponsors and Collaborators

    • University of Pennsylvania

    Investigators

    • Principal Investigator: Kevin Volpp, MD, PhD, University of Pennsylvania

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    University of Pennsylvania
    ClinicalTrials.gov Identifier:
    NCT06062394
    Other Study ID Numbers:
    • 851832
    First Posted:
    Oct 2, 2023
    Last Update Posted:
    Oct 5, 2023
    Last Verified:
    Oct 1, 2023
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Oct 5, 2023