se of Smartphone Application to Detect Atrial Fibrillation After Ablation Procedure

Not Applicable

• Conditions: Atrial Fibrillation; Cardiovascular - Other cardiovascular diseases

• Registration Number: ACTRN12622000887774
• Lead Sponsor: IVERSITY OF ADELAIDE

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2022-06-22
• Last Update Posted: 9 August 2022

Recruitment & Eligibility

• Status: ot yet recruiting
• Sex: All
• Target Recruitment: 98

Inclusion Criteria

•Patients with symptomatic AF undergoing AF ablation procedure
•Aged 18 years or older
•Owner of a smartphone

Exclusion Criteria

•Patients with implantable cardiac devices e.g pacemakers
•Inability to use a smartphone app due to physical, visual or cognitive impairment
•Unwilling or unable to comply fully with study procedures and follow-up

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Detection of post-ablation AF recurrence by the FibriCheck app[3-month, 6-month, 9-month and 12-month post ablation];Detection of post-ablation AF recurrence by Holter monitor[3-month, 6-month, 9-month and 12-month post ablation. Changes made prior to enrolment commencement]

Secondary Outcome Measures

Name	Time	Method
Adherence to the scheduled photoplethysmography (PPG) measurements - by accessing app analytics[3-month, 6-month, 9-month and 12-month post ablation. ];FibriCheck app usage questionnaire as reported by the participants using study-specific questionnaire[12-month post ablation]