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.
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
- Conditions the study is for
- Patient With Atrial Fibrillation or High Stroke Risk
- 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.
South Korea1 site, 1 recruiting
- Recruiting
Severance Hospital, Yonsei University Health System
Seoul
Boyoung Joung, +82 02-2228-8447, cby6908@yuhs.ac
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 group | Role | What they receive |
|---|---|---|
| Patients with atrial fibrillation | Patients with previous diagnosis of atrial fibrillation Receives: Device: continous 3 day EKG monitoring with S-Patch Cardio | |
| Non-AF patients with high stroke risk | Non-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.
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)
Clinical outcome
composite outcome (all-cause mortality, stroke, transient ischemic accident, systemic embolism, cardiac arrest)
Measured: 1 year
Acquisition rate of ECG
Acquisition rate of ECG signal for 72 hours
Measured: Acquisition rate of ECG signal for 72 hours
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
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.
- First posted15 Nov 2021
- Study start15 Mar 2021
- Primary completionFeb 2023 (estimated)
- Study completionFeb 2023 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for Patient With Atrial Fibrillation or High Stroke RiskStudies of the same condition, open and under way.
- More trials run by Yonsei UniversityThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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
Sponsor and investigators
- Lead sponsor
- Yonsei University
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
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
Study at a glance
From the registry record, last updated by the sponsor on 15 Nov 2021. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Continuous EKG Monitoring Using S-Patch Ex : Prospective Observational Study (S-patch Registry)
- ClinicalTrials.gov ID
- NCT05119725
- Acronym / sponsor ID
- 1-2021-0002
- Keywords
- atrial fibrillation, stroke, risk, EKG, continuous
- Study type
- Observational
- Recruitment status
- Unknown status
- Enrolment
- 2,450 participants (estimated)
- Lead sponsor
- Yonsei UniversityUniversity, hospital or other
- Study start
- 15 Mar 2021 (actual)
- Primary completion
- Feb 2023 (estimated)
- Study completion
- Feb 2023 (estimated)
- First posted
- 15 Nov 2021 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
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
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
- Target follow-up
- 1 Year
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Patients with atrial fibrillation | – | Device: continous 3 day EKG monitoring with S-Patch CardioPatients with previous diagnosis of atrial fibrillation |
| Non-AF patients with high stroke risk | – | Device: continous 3 day EKG monitoring with S-Patch CardioNon-AF patients with high stroke risk |
Who may qualify
- Ages
- 19 years and older
- Sex
- All
- Age groups
- Adult, Older adult
- Study population
- Referred patients in tertiary care clinic
Key inclusion criteria (3 listed)
- Patients who are over the age of 19
- Those with previous diagnosis of atrial fibrillation
- Those without atrial fibrillation, but high stroke risk
Key exclusion criteria (2 listed)
- Those who refuse to participate in the trial.
- Those without internet connection
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| continous 3 day EKG monitoring with S-Patch Cardiocontinous 3 day EKG monitoring with S-Patch Cardio | Device | Non-AF patients with high stroke risk, Patients with atrial fibrillation |
Primary outcome
Number of partipants with atrial fibrillation
Time frame: At the end of continous ECG monitoring up to 72 hours
presence of atrial fibrillation
4 secondary outcomes
Clinical outcome
Time frame: 1 year
Acquisition rate of ECG
Time frame: Acquisition rate of ECG signal for 72 hours
Quality of Life
Time frame: At the enrollment
Cognitive function
Time frame: At the enrollment
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 15 Nov 2021.
- Derived from this study: PubMed 41548032Park 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.
- Individual participant dataSharing planned: No
Related trials for Patient With Atrial Fibrillation or High Stroke Risk
RecruitingPhase 4
AnticoaguLation ONE Year After Ablation of Atrial Fibrillation in Patients With Atrial Fibrillation (ALONE AF Study)
Atrial Fibrillation Patients With Moderate or High Stroke Risk Who Had Undergone Catheter Ablation of Atrial Fibrillation
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
1 site in 1 country: see every site and its status.
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.