RECRUITING

Artificial Intelligence (AI) Enabled, Cloud-based ECG Diagnostic Solution (ZBPro) Feasibility Testing

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

The proposed research is to address the accessibility and affordability of technology to capture symptomatic and asymptomatic cardiac events via Long-Term Continuous Electrocardiogram Monitoring (LTCM), and to provide physicians with full access to their patients' recorded data in a timely manner. We adopt an FDA cleared single- lead OEM patch Holter made of flexible material to make long-term wearing more comfortable and more patient compliant. The patch transmits the recorded data to our cloud-based platform: ZBPro™, where our innovative technologies reside. Our proprietary AI algorithms with innovative human interaction tools, which were developed under the National Science Foundation (NSF) Small Business Innovation Research (SBIR) Phase I (Award #: 2025951) Award analyze and interpret the recorded data to detect and annotate arrhythmia/cardiac events, and generates daily reports for physician review. The feasibility of our algorithms has been verified using ZBeats' proprietary ECG database based on the standard ANSI/AAMI EC57. Data collection and transmission has been verified in the office environment. This proposed observational study will utilize a multidisciplinary collaboration of ZBeats Inc. (ZBTS), Stony Brook University (SBU), and Lankenau Medical Center (LMC). The study will enroll patients undergoing ECG monitoring. The primary outcome measure will be the ability to capture cardiac arrhythmias and events from participants. The prescribed FDA-cleared device will serve as the ground truth (GT) for our analyses. The detected arrhythmias and events from our solution will be compared with the findings from the ground truth to obtain our system's detection rate. The goal is to achieve a detection rate of \>80% to be deemed successful.

Official Title

Feasibility Testing of a Novel AI-enabled, Cloud-based ECG Diagnostic Solution to Enable Fast and Affordable Diagnosis in Long-term Continuous Ambulatory ECG Monitoring

Quick Facts

Study Start:2023-08-30
Study Completion:2024-05
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06013917

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. 1. Patients who are \> 18 years of age
  2. 2. Patients who are from one of the clinical collaborators practices
  3. 3. Patients who are prescribed to undergo ECG monitoring using an FDA-cleared monitoring device
  4. 4. Patients who are post TAVR procedure, a recent history of stroke/TIA, or having cardiac related symptoms
  5. 5. Patients who are comfortable using a smartphone or have someone in the home to help with data transmission
  6. 6. Patients who have manual dexterity to be able to recharge the phone battery or someone in the home to help them
  7. 7. Patients who are English speaking
  1. 1. Patients who are \<18 years of age
  2. 2. Patients who are not being prescribed with cardiac monitor testing
  3. 3. Patients who refuse to sign informed consent
  4. 4. Patients who are unable to provide informed consent
  5. 5. Patients who have a pacemaker implanted
  6. 6. Patients who are presenting with any dermatitis or infected skin over left anterior thorax
  7. 7. Patients who have a history of reaction to a prior cardiac monitor device
  8. 8. Patients who are uncomfortable having a cell phone at home for the duration of study participation
  9. 9. Patients who non-English speaking

Contacts and Locations

Study Contact

Bin Fang, PhD
CONTACT
6312202463
bin.fang@zbeats.co
Ashutosh Yaligar, MBA
CONTACT
5182219417
ashutosh.yaligar@zbeats.co

Principal Investigator

Puja Parikh, MD
PRINCIPAL_INVESTIGATOR
Stony Brook University

Study Locations (Sites)

Stony Brook University
Stony Brook, New York, 11794
United States

Collaborators and Investigators

Sponsor: ZBeats INC

  • Puja Parikh, MD, PRINCIPAL_INVESTIGATOR, Stony Brook University

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2023-08-30
Study Completion Date2024-05

Study Record Updates

Study Start Date2023-08-30
Study Completion Date2024-05

Terms related to this study

Keywords Provided by Researchers

  • Artificial Intelligence
  • Cardiac Monitoring

Additional Relevant MeSH Terms

  • Arrhythmias, Cardiac