Clinical Trials Directory

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UnknownNCT05006105

Early Detection of Atrial Fibrillation Using Mobile Technology in Cryptogenic Stroke Patients

Early Detection of Atrial Fibrillation Using Mobile Technology in Cryptogenic Stroke Patients - REMOTE Study

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
225 (estimated)
Sponsor
Ziekenhuis Oost-Limburg · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to demonstrate the added value of mobile health (mHealth) to detect atrial fibrillation (AF) early in the care path of cryptogenic stroke and transient ischemic attack (TIA) patients.

Detailed description

The use of photoplethysmography (PPG)-based mHealth (with smartphone and smartwatch) is compared to the guideline-recommended insertable loop recorders (ILR) in the detection of AF in cryptogenic stroke or TIA patients.

Conditions

Interventions

TypeNameDescription
DEVICEseven-day ECG HolterParticipants receive a seven-day ECG Holter after hospital discharge.
DEVICE24-hour blood pressure monitorParticipants receive a 24-hour blood pressure monitor, approximately four weeks after hospital discharge.
OTHERQuestionnaire: vision of mHealthParticipants receive a questionnaire concerning their vision of mHealth, approximately four weeks after hospital discharge.
OTHERQuestionnaire: user experience & feeling of safetyParticipants receive a questionnaire concerning their user experience and feeling of safety of using mHealth, after using mHealth for six months.
DEVICEInsertable loop recorderParticipants receive an insertable loop recorder, approximately six weeks after hospital discharge.

Timeline

Start date
2020-10-12
Primary completion
2025-02-01
Completion
2025-02-01
First posted
2021-08-16
Last updated
2022-09-16

Locations

2 sites across 1 country: Belgium

Source: ClinicalTrials.gov record NCT05006105. Inclusion in this directory is not an endorsement.