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Status unknownNCT05119725Updated Nov 15, 2021

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

An observational study in Patient With Atrial Fibrillation or High Stroke Risk, sponsored by Yonsei University. Status unknown at 1 site in Korea, Republic of. Open to participants aged 19 Years and older. Per ClinicalTrials.gov, last updated 2021-11-15.

Sponsored by Yonsei University · Observational

The sponsor has not verified this record recently (last verified Nov 2021), so the status shown — last known as Recruiting — may be out of date.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
2,450
Ages
19 Years and older
Sex
All
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Study 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. 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.

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

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Conditions studied

  • Patient With Atrial Fibrillation or High Stroke Risk

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Keywords

  • atrial fibrillation
  • stroke
  • risk
  • EKG
  • continuous
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In context

Atrial Fibrillation

3,870 studies on the registry are indexed under Atrial Fibrillation; 924 are open to participants now.

This study's planned enrollment of 2,450 is above the median of 300 across 1,363 observational studies indexed under Atrial Fibrillation.

Browse Atrial Fibrillation studies →

Lead sponsor

Yonsei University is the lead sponsor of 1,387 studies on the registry; 232 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
19 Years and older
Sexes eligible
All
Sampling method
Non-probability sample

Study population

Referred patients in tertiary care clinic

Inclusion criteria

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

Exclusion criteria

Exclusion Criteria:

  1. Those who refuse to participate in the trial.
  2. Those without internet connection
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Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
2,450 participants (estimated)
Target follow-up
1 Year
Patient registry
Yes

Groups and cohorts

  • Patients with atrial fibrillation

    Patients with previous diagnosis of atrial fibrillation

    Device: continous 3 day EKG monitoring with S-Patch Cardio

  • Non-AF patients with high stroke risk

    Non-AF patients with high stroke risk

    Device: continous 3 day EKG monitoring with S-Patch Cardio

Interventions

  • Devicecontinous 3 day EKG monitoring with S-Patch Cardio

    continous 3 day EKG monitoring with S-Patch Cardio

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What researchers measure

Primary outcomes

  1. Number of partipants with atrial fibrillation

    presence of atrial fibrillation

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

Secondary outcomes

  1. Clinical outcome

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

    Time frame: 1 year

  2. Acquisition rate of ECG

    Acquisition rate of ECG signal for 72 hours

    Time frame: 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).

    Time frame: At the enrollment

  4. Cognitive function

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

    Time frame: At the enrollment

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Study locations

1 of 1 sites recruiting
  • Severance Hospital, Yonsei University Health System
    Seoul, Korea, Republic of
    Recruiting
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References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Nov 15, 2021, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT05119725
Lead sponsor
Yonsei University
Responsible party
Sponsor
First posted
Nov 15, 2021
Start date
Mar 15, 2021
Primary completion
Feb 2023 (estimated)
Completion
Feb 2023 (estimated)
Last update
Nov 15, 2021

Study contacts

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

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Nov 2021. You cannot join it, but the record below documents what was studied.

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