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Enhancing Rural Health Via Cardiovascular Telehealth for Rural Patients Implementation (E-VICTORS)

Enhancing Rural Health Via Cardiovascular Telehealth for Rural Patients (E-VICTORS) Project

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04617834
Acronym
E-VICTORS
Enrollment
215
Registered
2020-11-05
Start date
2021-02-01
Completion date
2026-12-01
Last updated
2026-07-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute Coronary Syndrome, Cardiovascular Diseases

Keywords

acute chest pain, telehealth, implementation science, rural health

Brief summary

This pre-post study will evaluate the implementation of a cardiovascular telehealth platform, which will connect experts from the Wake Forest University Health Sciences (WFUHS) tertiary care center with Wilkes County Emergency Medical Services (WC-EMS) system, Wilkes Medical Center Emergency Department (ED), and The Wilkes County Health Department Public Health Community Clinic (PHCC) to improve cardiovascular care in this rural community.

Detailed description

This program aims to improve cardiovascular care for patients in Wilkes County by implementing a cardiovascular telehealth program designed to; a) assist WC- EMS paramedics with the early risk stratification (electrocardiogram (EKG) interpretation, vital signs, and risk scores), treatment, and transportation destination decisions in patients with acute chest pain or dyspnea, b) support Wilkes Medical Center (WMC) Emergency Department (ED) providers (physicians and advanced practice clinicians) in the evaluation, management, and disposition of patients with acute cardiovascular symptoms, and c) provide consultative expertise to the Primary Health Care Centers (PHCC) for patients seen following an EMS or ED encounter for cardiovascular symptoms.

Interventions

OTHERQuality Surveillance Data Collection

Data will be retrospectively collected through EHR queries

Sponsors

Wake Forest University Health Sciences
Lead SponsorOTHER
Health Resources and Services Administration (HRSA)
CollaboratorFED

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* age \> 18 years at time of index encounter * Cardiovascular symptoms (chest discomfort or dyspnea consistent with possible ACS) as indicated by the treating provider

Exclusion criteria

* Age \<18 * Traumatic chest pain * Dyspnea that is clearly from a non-cardiac etiology * Patients with hemodynamic instability SBP \< 90 mmHg, HR\>160 or \<40 bpm * Patients requiring intubation/mechanical ventilation

Design outcomes

Primary

MeasureTime frameDescription
Number of Emergency Department (ED) utilizationbaselineED utilization among patients with cardiovascular symptoms will be defined as the total number of cardiovascular-related ED admissions divided by the total number of unique individual patients receiving cardiovascular care during the project period.

Secondary

MeasureTime frameDescription
Number of Cardiovascular hospitalizationsBaselineCardiovascular hospitalizations will be defined as an inpatient or observation admission for cardiovascular conditions or symptoms based on Current Procedures Terminology (CPT) and International Classification of Diseases (ICD) codes
Number of Cardiovascular Inter-facility transfersBaselineCardiovascular Inter-facility transfers will be defined based on patients with cardiovascular symptoms or conditions transferred from Wilkes Medical Center (WMC) to another hospital.
Number of 30-day cardiovascular Emergency Department (ED) re-admissionsday 3030-day cardiovascular ED re-admissions will be defined as any cardiovascular related ED admission occurring during the 30 days following their initial/index ED encounter.
Number of 30-day cardiovascular hospital re-admissionsday 3030-day cardiovascular hospital re-admissions will be defined as any cardiovascular related hospital admission occurring during the 30 days following their index hospitalization.
Number of Adverse Eventsday 30 and Month 12Determine if telehealth implementation will result in improved sorting of cases for escalated and de-escalated care, reducing the number of adverse events.
Change in Cost - societal levelday 30 and Month 12Evaluate whether spending on healthcare (i.e., insurance payments) changes during the 30-day follow-up period.
Change in Cost - provider levelday 30 and Month 12Estimates will be obtained for the impact of the establishment of the telehealth program on the budget of the tertiary center.
Cost-effectivenessMonth 12 and Month 48Cost-effectiveness: will be evaluated at the societal level to inform the relative changes in patient outcomes and costs resulting from the telehealth program.
Cardiovascular telehealth consultation rateBaselineCardiovascular telehealth consultation rate will be assessed by identifying the total number of patients that received cardiovascular telehealth consultations at each originating site divided by the total number of patients at each originating site with cardiovascular symptoms.
Cardiovascular telehealth adoption rateMonth 12Adoption rate will be defined by the cardiovascular telehealth consultation rate at each originating site during the first 12 months following implementation of the cardiovascular telehealth service.
Cardiovascular telehealth sustainability rateMonth 24 - Month 48 post InterventionSustainability rate will be defined by the cardiovascular telehealth consultation rate at each site greater than 12 months after the availability of the cardiovascular telehealth service.

Countries

United States

Contacts

PRINCIPAL_INVESTIGATORSimon A Mahler, MD, MS

Wake Forest University Health Sciences

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 31, 2026