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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05324566
Other study ID # 21-001964
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date May 5, 2021
Est. completion date June 2024

Study information

Verified date August 2023
Source Mayo Clinic
Contact Jennifer Dugan, BA
Phone 507-538-1125
Email dugan.jennifer@mayo.edu
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

The purpose of the study is to determine if the Electrocardiograms (ECGs) and symptoms data obtained from an Apple Watch and transmitted to Mayo Clinic are of sufficient quality to guide a person's care.


Description:

1. Patients who have the Mayo Clinic patient app and iOS 14 or higher who are 18 years of age or older will be invited to enroll. 2. Patient will undergo email survey to assess ownership of Apple Watch v4 or later, and subsequent willingness to participate in the study. Those who agree will undergo digital consent and enrollment. 3. A customized Mayo Clinic Study App will be available to download to their iOS device and will be used to test whether it is feasible to access ECGs and symptoms data patients have collected using their personal Apple watch that are saved on the patient's phone. The study app will facilitate transmission of past and future patient-recorded watch ECGs. 4. The patient ECGs and self-reported symptoms data will be uploaded to the AI Dashboard in the patient's medical record (ECG rhythm classification facilitated by Apple ECG program). 5. We will perform a retrospective review of electronic medical record data from enrolled subjects to assess the quality of the Apple Watch obtained ECGs, assess the results from the AI-ECG dashboard using obtained watch ECGs, and compare these results to prior or subsequently obtained 12 lead ECGs. 6. Data analysis will be performed with steps to ensure patient confidentiality. Data will be transmitted using similar protocols as with current app data, and all data will be saved in the secure Mayo Clinic electronic environment (called the UDP). 7. All patients' watch data will be compared to AI dashboard data. Additionally, clinical data in the EMR (such as blood tests, echocardiograms, and other data recorded for routine medical care) will be used to assess the utility of the watch ECG quality for AI algorithms (such as determining whether a weak heart pump is present, for example).


Recruitment information / eligibility

Status Recruiting
Enrollment 1000000
Est. completion date June 2024
Est. primary completion date June 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Using the Mayo patient iPhone app. (determined automatically via Mayo software). Exclusion Criteria: - Inability to provide informed consent.

Study Design


Locations

Country Name City State
United States Mayo Clinic Rochester Rochester Minnesota

Sponsors (1)

Lead Sponsor Collaborator
Mayo Clinic

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Number of patient-triggered Apple Watch ECGs recorded Total number of patient-triggered Apple Watch ECGs recorded and uploaded by individual patients over the study period. 12 months
Primary Frequency of medical providers accessing Apple Watch data Number of times a medical provider accesses the Apple Watch data via electronic medical record-linked ECG dashboard. 12 months
Primary Number of Apple Watch ECGs of acceptable quality A sample of Apple Watch ECGs will undergo manual review by ECG technicians and rated using a standard data form for signal quality and diagnostic utility, summarized as the percent of "acceptable" ECGs. 12 months
Primary Performance of Artificial Intelligence ECG algorithms for disease prediction with Apple Watch ECGs Artificial Intelligence ECG algorithms to predict various cardiac pathologies will be applied to Apple Watch ECGs. Accuracy and performance of AI algorithm models will be assessed by comparing AI predicted disease and patient's given medical diagnosis in the electronic medical record. 12 months
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