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Hativ® ELectrocardiogram monitoring on Patients with Sinus rhythm(HELP-S trial)

Not Applicable
Conditions
Diseases of the circulatory system
Registration Number
KCT0009304
Lead Sponsor
Hallym University Medical Center-Dongtan
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot yet recruiting
Sex
All
Target Recruitment
600
Inclusion Criteria

1) Adults with smartphones aged 19 years or older
2) Patients who exhibit sinus rhythm and are at a high risk for atrial fibrillation (determined by a risk factor score of =4 on C2HEST or HATCH)
3) The participant signed an informed consent for this study and is capable of comprehending and following the training and instructions

Exclusion Criteria

1) Patients with a physical disability who are unable to use a portable electrocardiogram (Hativ P30®)
2) Patients with an intracardiac device such as a pacemaker, ICD, CRT, VAD, etc.
3) Subjects who are unable to read the consent form (illiterate, foreigners, etc.)
4) Patients deemed unsuitable for participation in the study by the investigator.
5) Patients with previously diagnosed or treated atrial fibrillation
6) Patients taking amiodarone

Study & Design

Study Type
Observational Study
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Diagnostic yield
Secondary Outcome Measures
NameTimeMethod
Therapeutic intervention status;Cost-effectiveness;Satisfaction;Usability
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