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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04067427
Other study ID # MAF2019
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date August 16, 2019
Est. completion date December 30, 2022

Study information

Verified date March 2023
Source Leipzig Heart Institute GmbH
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.


Description:

To explore the potential of a daily app-based mindfulness mental training in improving AF symptoms, assessed by self-reported outcome measures, i.e. the AF 6 questionnaire, AF Effect on QualiTy of Life (AFEQT) and Patient Reported Outcome Measurement Information System (PROMIS) Global Health questionnaires, as well as in reducing AF burden in 7-day-Holter, within the first 12 weeks following AF ablation.


Recruitment information / eligibility

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

Study Design


Intervention

Other:
Mental training
App-based mental training

Locations

Country Name City State
Germany Leipzig Heart Institute Leipzig Saxony

Sponsors (2)

Lead Sponsor Collaborator
Leipzig Heart Institute GmbH Heart Center Leipzig - University Hospital

Country where clinical trial is conducted

Germany, 

Outcome

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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