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Patient With Atrial Fibrillation or High Stroke RiskNCT05119725

Continuous EKG Monitoring Using S-Patch Ex : Prospective Observational Study (S-patch Registry)

An observational study of Patient With Atrial Fibrillation or High Stroke Risk, run by Yonsei University at 1 site in South Korea.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

Atrial fibrillation (AF) is associated with increased mortality and morbidity, and is a dominant, yet preventable, cause of cardioembolic stroke, which has more severe outcomes than other ischaemic stroke causes if left untreated. Read more about this study

Who is it for?
Ages 19 years and older
What is being tested?
continous 3 day EKG monitoring with S-Patch Cardio
Type of treatment
Medical device
How many people
2,450 participants
Where
1 siteSouth Korea
Study dates
15 Mar 2021to Feb 2023
How long will I take part?
1 Year
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 19 years and older
  • All sexes
  • Adult, Older adult

Study population: Referred patients in tertiary care clinic

Who may be able to join

  • Patients who are over the age of 19
  • Those with previous diagnosis of atrial fibrillation
  • Those without atrial fibrillation, but high stroke risk

Who cannot join

  • Those who refuse to participate in the trial.
  • Those without internet connection

Trial locations and contacts

1 site in 1 country.

Boyoung Joung contact

+82 02-2228-8447

cby6908@yuhs.ac

South Korea1 site, 1 recruiting
  • Severance Hospital, Yonsei University Health System

    Seoul

    Boyoung Joung, +82 02-2228-8447, cby6908@yuhs.ac

    Recruiting

Other trials in South Korea

About this study

Atrial fibrillation (AF) is associated with increased mortality and morbidity, and is a dominant, yet preventable, cause of cardioembolic stroke, which has more severe outcomes than other ischaemic stroke causes if left untreated. Approximately 10% of ischemic strokes are associated with AF (AF) first diagnosed at the time of stroke. Detecting asymptomatic AF would provide an opportunity to prevent these strokes by instituting appropriate anticoagulation.

Early diagnosis of AF might enable oral anticoagulant therapy and prevent unwanted consequences of undetected disease, leading to the suggestion that screening for AF might be beneficial in populations at risk. However, there is still debate about whether screen-detected AF bears a similar stroke and mortality risk profile to clinically detected AF, particularly when AF screening is done at a higher intensity than single-time point.

Read more

The absence of studies reporting on hard clinical endpoints in AF screening has led to differences in recommendations globally. Most notably, systematic screening for AF is to be considered according to 2020 European guidelines, whereas the US Preventive Services Task Force concluded that current evidence is insufficient to assess the balance of benefits and harms of screening for AF.

The incidence of screen-detected AF strongly depends on the population screened and duration/intensity of screening. Single-time point screening of a general population ≥65 years of age detects undiagnosed AF in 1.4%, and the AF detected is largely persistent. In a large population-based study of individuals 75 to 76 years of age, a more intense 2-week screening program using twice-daily intermittent handheld ECG recordings identified AF in 3.0% (0.5% on the initial ECG4). The identical protocol restricted to those with ≥1 additional stroke risk factor identified 7.4% with AF.

This study was designed in to two arms. The purpose of Arm 1 is to upgrade the artificial intelligence by collecting the continued ECG monitoring data in patients with previous diagnosed AF. The purpose of Arm 2 is to investigate the detection rate of AF using systematic, intensive AF screening with continuous ECG monitoring and the rate of clinical outcome in individuals at high risk during one year follow-up.

Read the detailed description

Arm 1 Patients with AF are examined with 72 hour continued ECG monitoring Arm 2 Patients with high stroke risk (CHA2DS2-VASc score >=2) are examined with 72 hour continued ECG monitoring

Being tested
continous 3 day EKG monitoring with S-Patch Cardio
Keywords
atrial fibrillation, stroke, risk, EKG, continuous
Medical subject headings
Atrial Fibrillation, Stroke

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • continous 3 day EKG monitoring with S-Patch CardioDevice

    continous 3 day EKG monitoring with S-Patch Cardio

Study groups in NCT05119725
Study groupRoleWhat they receive
Patients with atrial fibrillationPatients with previous diagnosis of atrial fibrillation
Receives: Device: continous 3 day EKG monitoring with S-Patch Cardio
Non-AF patients with high stroke riskNon-AF patients with high stroke risk
Receives: Device: continous 3 day EKG monitoring with S-Patch Cardio

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Number of partipants with atrial fibrillation

    presence of atrial fibrillation

    Measured: At the end of continous ECG monitoring up to 72 hours

Secondary outcomes (4)
  1. Clinical outcome

    composite outcome (all-cause mortality, stroke, transient ischemic accident, systemic embolism, cardiac arrest)

    Measured: 1 year

  2. Acquisition rate of ECG

    Acquisition rate of ECG signal for 72 hours

    Measured: Acquisition rate of ECG signal for 72 hours

  3. Quality of Life

    Atrial Fibrillation Effect on Quality-of-life (AFEQT) questionnaire: 20 questions, scare from 1 (better outcome) to 7 (worse outcome).

    Measured: At the enrollment

  4. Cognitive function

    Korean Dementia Screening Questionnaire (KDSQ) questionnaire: 25 questions, scare form 1 (better oucome) to 3 (worse outcome)

    Measured: At the enrollment

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted15 Nov 2021
  2. Study start15 Mar 2021
  3. Primary completionFeb 2023 (estimated)
  4. Study completionFeb 2023 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
2,450 participants (estimated)
Target duration
1 Year
IDs, dates and publications
ClinicalTrials.gov ID
NCT05119725
Sponsor's protocol ID
1-2021-0002
Status last verified
Nov 2021
First submitted
20 Oct 2021
Last updated
15 Nov 2021
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Publications

  • Park SH, Jin JH, Kim J, Lee D, Kim D, Jang J, Yu HT, You SC, Joung B. Wearable device derived electrocardiographic age and its association with atrial fibrillation. NPJ Digit Med. 2026 Jan 17;9(1):157. doi: 10.1038/s41746-026-02344-8.

    PubMed 41548032

Questions about this trial

What is this clinical trial studying?

An observational study of Patient With Atrial Fibrillation or High Stroke Risk, run by Yonsei University at 1 site in South Korea.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 15 Nov 2021. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in South Korea. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

Contact Boyoung Joung (+82 02-2228-8447, cby6908@yuhs.ac), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Number of partipants with atrial fibrillation (time frame: At the end of continous ECG monitoring up to 72 hours). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT05119725, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 15 Nov 2021.

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