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Effects of Mindfulness on Atrial Fibrillation

Primary Purpose

Atrial Fibrillation

Status
Unknown status
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
MUSE Headband
Sponsored by
Newmarket Electrophysiology Research Group Inc
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Atrial Fibrillation focused on measuring PVI, Atrial Fibrillation, MUSE Headband, Mindfulness

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age over 18
  • symptomatic persistent or paroxysmal AF awaiting ablation of AF

Exclusion Criteria:

  • Known Anxiety and Depression

Sites / Locations

  • Southlake Regional Health CentreRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Experimental

Arm Label

Control

Treatment Group

Arm Description

These patients will not receive a device, but have to fill out a quality of life questionnaire at the time of enrollment and 3 months after their procedure.

These patients will receive the device. they are expected to use it for at least 5 minutes per day. Patients in this arm will fill out a quality of life questionnaire at the time of enrollment and 3 months after their procedure.

Outcomes

Primary Outcome Measures

Quality of Life
patients in both arms will fill out a questionnaire for QoL 12 weeks after their ablation.

Secondary Outcome Measures

Full Information

First Posted
September 29, 2015
Last Updated
March 27, 2018
Sponsor
Newmarket Electrophysiology Research Group Inc
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1. Study Identification

Unique Protocol Identification Number
NCT02564302
Brief Title
Effects of Mindfulness on Atrial Fibrillation
Official Title
Effects of Monitored Mindfulness Training on Quality-of-life, Anxiety, and Depression in Patients Awaiting Ablation of Atrial Fibrillation
Study Type
Interventional

2. Study Status

Record Verification Date
March 2018
Overall Recruitment Status
Unknown status
Study Start Date
August 2015 (undefined)
Primary Completion Date
December 2018 (Anticipated)
Study Completion Date
May 2019 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Newmarket Electrophysiology Research Group Inc

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
This study aims to investigate the effect of MUSE (R) Headbands on patients with Atrial Fibrillation who is awaiting pulmonary vein isolation ablation procedure. Patients are randomized in 2 arms. The control arm will not be receiving the MUSE headband, whereas the treatment group obtains a device. Patients from both group will fill out a quality-of-life questionnaire at the time of enrollment and 3 months post PVI. Results from both arms will be evaluated and ultimately the effect of mindfulness using the headband will be evaluated in the aforementioned patient population.
Detailed Description
Background: Atrial fibrillation is the most common arrhythmic disorder and ablation of AF has become an important part of AF treatment. AF is associated with a large number of somatic symptoms like chest pain, fatigue, lightheadedness, palpitations, physical limitations, shortness of breath, irregular rhythm and heart rate but also with psychological comorbidities such as anxiety and depression [1]. In recent years, the severity of these comorbidities has become more apparent in AF patients. For instance, Sears and colleagues found a positive correlation between the number of AF symptoms reported and the number of negative emotions experienced [2]. Since there is prospective data on the effects of AF ablation on long term mortality and morbidity, reduction of AF related symptoms and improvement of quality of life (QoL) is still a major goal of AF ablation [3,4]. Mindful meditation (MM) is a basic form of meditation that involves focusing on one thing internally or externally. Being fully present in the moment is the goal of MM. Practicing MM teaches relaxation and concentration on experiencing bodily sensations such as breathing patterns. Mindfulness is independent of environmental stimuli; it is a state of mind that can be achieved at any time [5]. Studies show that, with practice, this form of meditation can provide both long- and short-term positive effects with respect to reduction in anxiety and depression[6,7]. Immediate and transferable benefits for AF patients include self-regulated attention, heightened perception of internal states, reduced stress and anxiety symptoms, and increased overall well-being. Mindfulness training can heighten meta-cognitive processing, which can improve a person's ability to control adverse thoughts and feelings. Consistent mindful meditation training can induce neuroplasticity[7,8]. The amygdala is a crucial brain structure that is hyperactive during perceived stressful conditions [8]. Being able to utilize skills to control emotions in stressful situations will be beneficial in controlling psychological hyperactivity. Studies show after mindful-attention training there is a decrease in amygdala activity even when in a non-meditative state [6]. This is proof that skills obtained during meditation have lasting positive neural effects. In another study, Holzel et al. found that after eight weeks of MM training, there was a significant correlation between a decrease in subjective stress and a decrease in amygdala's gray matter density. Therefore, a reduction in stress output is positively correlated with gray matter density. MM training induces brain changes in the amygdala and resting state connectivity, which have impacts on cognition such as an increase in attentional control and executive function [9]. Neurofeedback training (NFT) is a method where participants are hooked up to an EEG which allows participants to see how active their brain is and monitor neural changes in real-time. NFT is proven to significantly enhance the positive effects of MM training and have a positive effect on depression[10,11]. The present study is going to investigate the psychological and physiological benefits of mindful meditation (MM) training in patients with atrial fibrillation (AF) using a system for real-time-neurofeedback. Rationale for study design: Although there is growing evidence that there might also positive prognostic effects especially on stroke risk [12,13] treatment of AF related symptoms is still one of the major targets of AF ablation. Lakkireddy and colleagues showed that yoga could improve symptoms and QoL as well as anxiety and depression scores [14] in AF patients, illustrating that alternative therapy can be highly effective in AF and be a valuable addition to somatic therapy like AF-ablation. In this study investigators want to investigate the effects of mindfulness meditation that is supported by the MUSE™ headband which is a device that provides neurofeedback during the meditation. This way investigators seek not only to improve the effects of the meditation but also will be able to monitor therapy compliance via the implemented software. Since patients with AF are a very heterogeneous group and AF burden, comorbidities as well as symptom perception can differ significantly investigators chose to investigate the less diverse group of patients with symptomatic AF that are scheduled for AF ablation. By applying prospective randomization investigators avoid the risk of a significant bias in baseline patient characteristics and comorbidities. Study design and aims: A total number of 60 patients waiting for an AF ablation for symptomatic AF will be included into this prospective, randomized pilot study. All patients will undergo assessment of QoL, anxiety and depression using 3 self-reporting scales for QoL, anxiety and depression at baseline and after 12 weeks. The scales are listed in Appendix A. At baseline patients will be 1:1 randomized to be either part of the intervention (Group 1) or control (Group 2) group. Patients in Group 1 will be supplied with the MUSE™ headband (InteraXon Inc., Toronto, Canada) that is a tool for mindfulness meditation with neurofeedback. Patients in Group 2 will not undergo any study-related treatment. The aim of this study will be to investigate the effects of mindfulness meditation with neurofeedback on QoL, anxiety and depression in patients awaiting AF ablation. The results of the study will also be the basis of future studies further investigating the Statistical analysis: The primary endpoint will be expressed as mean or median test result where applicable. The secondary endpoint will be measured by the individual duration of use of the device in group 1. The Shapiro-Wilks-test will be used to test for normality of distribution and the Mann-Whitney-U test will be applied for comparison of means. Study-timeline and Budget: Our institution is a high volume centre for AF ablations that performs 300-350 procedures per year. Because of the non-invasive character of the MUSE-device investigators expect a high recruitment rate and plan to complete enrollment of the 60 patients within 6 months. With a follow-time of 3 months investigators expect to complete patient inclusion and follow-up after 9 months. Data analysis will take approximately 4 weeks resulting in a total study duration of 10 months. InteraXon Inc. will provide 30 MUSE™ headbands for the study time.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Atrial Fibrillation
Keywords
PVI, Atrial Fibrillation, MUSE Headband, Mindfulness

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
60 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Control
Arm Type
No Intervention
Arm Description
These patients will not receive a device, but have to fill out a quality of life questionnaire at the time of enrollment and 3 months after their procedure.
Arm Title
Treatment Group
Arm Type
Experimental
Arm Description
These patients will receive the device. they are expected to use it for at least 5 minutes per day. Patients in this arm will fill out a quality of life questionnaire at the time of enrollment and 3 months after their procedure.
Intervention Type
Device
Intervention Name(s)
MUSE Headband
Intervention Description
MUSE Headband will help patients with mindfulness.
Primary Outcome Measure Information:
Title
Quality of Life
Description
patients in both arms will fill out a questionnaire for QoL 12 weeks after their ablation.
Time Frame
12 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age over 18 symptomatic persistent or paroxysmal AF awaiting ablation of AF Exclusion Criteria: Known Anxiety and Depression
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Pouria Alipour, BSc
Phone
9058954521
Ext
5012
Email
palipour@southlakeregional.org
First Name & Middle Initial & Last Name or Official Title & Degree
Annette Nath, RN
Phone
9058954521
Ext
2945
Email
anath@southlakeregional.org
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Atul Verma, MD
Organizational Affiliation
Newmarket Electrophysiology Research Group
Official's Role
Study Director
Facility Information:
Facility Name
Southlake Regional Health Centre
City
Newmarket
State/Province
Ontario
ZIP/Postal Code
L3Y 2P9
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Pouria Alipour, BSc
Phone
905-895-4521
Ext
5012
Email
PAlipour@southlakeregional.org
First Name & Middle Initial & Last Name & Degree
Annette Nath, RN
Phone
905-895-4521
Ext
2945
Email
ANath@southlakeregional.org
First Name & Middle Initial & Last Name & Degree
Atul Verma, MD
First Name & Middle Initial & Last Name & Degree
Pouria Alipour, BSc

12. IPD Sharing Statement

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Effects of Mindfulness on Atrial Fibrillation

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