Paroxysmal Atrial Fibrillation Clinical Trial
— Mental-AFOfficial title:
To Reduce Recurrence of Symptomatic Atrial Fibrillation and Improve Quality of Life After Catheter Ablation for Atrial Fibrillation by App-based Mental Training (Mental AF)
Verified date | March 2023 |
Source | Leipzig Heart Institute GmbH |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Atrial fibrillation (AF) is one of the most common heart rhythm disorders and it is associated with a variety of symptoms leading to a considerable deterioration in quality of life. The Mental-AF trial is intended to inquire if an app-based mental training can reduce the occurrence of symptomatic AF episodes within the blanking period, i.e. the first three months after catheter ablation for AF.
Status | Completed |
Enrollment | 183 |
Est. completion date | December 30, 2022 |
Est. primary completion date | January 15, 2022 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 88 Years |
Eligibility | Inclusion Criteria: - All patients undergoing AF ablation with symptomatic paroxysmal or chronic atrial fibrillation (EHRA II-IV) - Availability of smart phone with the capability to run android 5 or iOS 9 or newer versions - Capability to use mobile phone applications - Internet access - Consent to study participation Exclusion Criteria: - Patients < 18 years of age - Unavailability of smart phone running at least Android 5 or iOS 9 - Pregnancy |
Country | Name | City | State |
---|---|---|---|
Germany | Leipzig Heart Institute | Leipzig | Saxony |
Lead Sponsor | Collaborator |
---|---|
Leipzig Heart Institute GmbH | Heart Center Leipzig - University Hospital |
Germany,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Atrial Fibrillation (AF) 6 questionnaire score | Atrial fibrillation specific symptomatic outcome defined by AF 6 sum scores during the first 12 weeks following AF ablation, based on a 10-point Likert scale, ranging from 0 (no symptoms) to 10 (severe symptoms), sum scores ranging from 0 to 60. | 12 weeks, assessed weekly | |
Secondary | Atrial Fibrillation Effect on QualiTy of Life (AFEQT) score | Effects of AF on quality of Life, assessed by a 20-item questionnaire with 4 conceptual domains (daily Activities, treatment concern, symptoms and treatment satisfaction) on a 7-point Likert scale, responses ranging from 1 (no symptoms/limitations) to 7 (most severe limitations/symptoms), higher scores indicating better health status, the raw scores can be transformed to a 0 to 100 scale adjusting for missing data | Follow up (3 months) | |
Secondary | Patient-Reported Outcome Measurement Information System (PROMIS) Global Health 10 score | PROMIS Global Health questionnaire for the assessment of physical and mental health domains by 10 items using a 5-point Likert scale, ranging from (5) excellent to (1) poor. Higher scores indicate a healthier patient. | Follow up (3 months) | |
Secondary | Atrial fibrillation burden | Time in AF as assessed in 7-day-Holter | Follow up (3 months) | |
Secondary | Heart Rate | Heart Rate during blood pressure measurement | Follow up (3 months) | |
Secondary | Blood pressure | Office blood pressure measurement of diastolic and systolic blood pressure | Follow up (3 months) | |
Secondary | Atrial Fibrillation Effect on QualiTy of Life (AFEQT) score | Effects of AF on quality of Life, assessed by a 20-item questionnaire with 4 conceptual domains (daily Activities, treatment concern, symptoms and treatment satisfaction) on a 7-point Likert scale, responses ranging from 1 (no symptoms/limitations) to 7 (most severe limitations/symptoms), higher scores indicating better health status, the raw scores can be transformed to a 0 to 100 scale adjusting for missing data | Follow up at 12 months |
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