Hypertension Clinical Trial
— ASE-INNOVATEOfficial title:
Implementation of High Definition Screening Using Handheld Imaging and Digital Health Technologies Within a Learning Health System to Identify Cardiovascular Disease at the Point-of-care: The ASE-INNOVATE Program
Verified date | April 2024 |
Source | Scripps Health |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The need for new models of integrated care that can improve the efficiency of healthcare and reduce the costs are key priorities for health systems across the United States. Treatment costs for patients with at least one chronic medical or cardiovascular condition make up over 4-trillion dollars in spending on healthcare, with estimations of a population prevalence of 100-million affected individuals within the next decade. Therefore, the management of chronic conditions requires innovative and new implementation methods that improve outcomes, reduce costs, and increase healthcare efficiencies. Digital health, the use of mobile computing and communication technologies as an integral new models of care is seen as one potential solution. Despite the potential applications, there is limited data to support that new technologies improve healthcare outcomes. To do so requires; 1) robust methods to determine the impact of new technologies on healthcare outcomes and costs; and 2) evaluative mechanisms for how new devices are integrated into patient care. In this regard, the proposed clinical trial aims to advance the investigator's knowledge and to demonstrate the pragmatic utilization of new technologies within a learning healthcare system providing services to high-risk patient populations.
Status | Completed |
Enrollment | 374 |
Est. completion date | March 20, 2020 |
Est. primary completion date | December 20, 2019 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - All participants of the ASE 2018 Outreach Event who are at least 18 years old who are referred for a cardiac evaluation Exclusion Criteria: - Those not willing to consent |
Country | Name | City | State |
---|---|---|---|
United States | West Virgina University | Morgantown | West Virginia |
Lead Sponsor | Collaborator |
---|---|
Scripps Health | West Virginia University |
United States,
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* Note: There are 28 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Health Economic Outcomes | Economic difference between the total costs of care between randomized arms including; clinic visitations, hospitalizations, emergency room visitations, and diagnostic testing. Collected as cumulative diagnosis-related group (DRG) and current procedural terminology (CPT) amounts in United States Dollars | 180 days | |
Secondary | Mobile Cardiac Telemetry | Number of referrals for mobile cardiac telemetry monitoring between randomized arms | 180 days | |
Secondary | Health Economic Outcomes | Economic difference between the total costs of care between randomized arms including; clinic visitations, hospitalizations, emergency room visitations, and diagnostic testing. Collected as cumulative diagnosis-related group (DRG) and current procedural terminology (CPT) amounts in United States Dollars | 30 days | |
Secondary | Patient-Reported Outcome Measures | Veterans Research and Development Corporation-12 Patient Reported Outcomes (mean total score 50 +/- 10) where higher values are associated with greater mental and physical debility | 30 days | |
Secondary | Patient-Reported Outcome Measures | Veterans Research and Development Corporation-12 Patient Reported Outcomes (mean total score 50 +/- 10) where higher values are associated with greater mental and physical debility | 180 days | |
Secondary | Patient-Reported Experience Measures | Agency for Healthcare Research and Quality Consumer Assessment of Healthcare Providers and Systems (average scores and difference between randomized arms) where higher scores are associated with greater patient satisfaction and patient experience | 30 days | |
Secondary | Patient-Reported Experience Measures | Agency for Healthcare Research and Quality Consumer Assessment of Healthcare Providers and Systems (average scores and difference between randomized arms) where higher scores are associated with greater patient satisfaction and patient experience | 180 days | |
Secondary | Diagnostic Imaging | Number of referrals for diagnostic imaging with transthoracic echocardiography between randomized arms | 180 days | |
Secondary | Heart Failure | Incidence of heart failure diagnosed between randomized arms | 180 days | |
Secondary | Atrial Fibrillation | Incidence of atrial fibrillation diagnosed between randomized arms | 180 days | |
Secondary | Emergency Department Visitations | Percentage of patients presenting to the emergency department for a cardiac condition (example; myocardial infarction, heart failure, atrial fibrillation, and stroke) between randomized arms | 180 days | |
Secondary | Hospitalization | Percentage of patients hospitalized for a cardiac condition (example; myocardial infarction, heart failure, atrial fibrillation, and stroke) between randomized arms | 180 days | |
Secondary | Clinic Visitations | Percentage of patients presenting for a clinical visitation for a cardiac condition (example; myocardial infarction, heart failure, atrial fibrillation, and stroke) between randomized arms | 180 days | |
Secondary | Medical Therapy | Percentage of patients initiating medical therapy for a cardiac condition including: heart failure, coronary artery disease, atrial fibrillation, and/or hypertension between randomized arms | 180 days |
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