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

Wake Forest University (WFU) logo

Wake Forest University (WFU)

Status

Active, not recruiting

Conditions

Acute Coronary Syndrome
Cardiovascular Diseases

Treatments

Other: Quality Surveillance Data Collection

Study type

Observational

Funder types

Other
Other U.S. Federal agency

Identifiers

NCT04617834
IRB00068612

Details and patient eligibility

About

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.

Full 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.

Enrollment

215 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

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

Trial design

215 participants in 1 patient group

Quality Surveillance Data
Description:
For this quality surveillance study, data will be collected retrospectively through electronic health record (EHR) queries for all eligible patients treated for acute cardiovascular symptoms by one of the study sites.
Treatment:
Other: Quality Surveillance Data Collection

Trial contacts and locations

4

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Central trial contact

Lauren Koehler, MS

Data sourced from clinicaltrials.gov

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