Lifestyle Modification for the Treatment of Symptomatic Atrial Fibrillation (LIFE-AF)
NCT ID: NCT03785418
Last Updated: 2018-12-26
Study Results
Results pending
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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Recruitment Status
UNKNOWN
Clinical Phase
NA
Total Enrollment
60 participants
Study Classification
INTERVENTIONAL
Study Start Date
2018-10-29
Study Completion Date
2020-07-31
Brief Summary
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The purpose of this study is to evaluate the effectiveness of a lifestyle modification intervention focused on healthy eating, regular exercise and behavioural therapy to decrease the length and number of atrial fibrillation episodes as well as gain an understanding of the impact of these changes on the gut microbiome.
Detailed Description
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Proposed research:
This pilot study will evaluate the potential efficacy and feasibility of risk factor modification in patients with a known history of symptomatic paroxysmal and persistent AFIB (in sinus rhythm) by implementing current evidence-based lifestyle recommendations as well as gain an understanding of the impact of these changes in the gut microbiome.
Objectives:
This study aims to determine if a multicomponent risk factor modification intervention (dietary intervention, exercise regimen and behavioural therapy) implemented using a basic healthcare team reduces the burden of AFIB at 12 months by decreasing the length and number of AFIB episodes. This study aims to assess the impact of these interventions on AFIB-related symptoms, quality of life and rhythm status (documented on an implantable loop recorder \[ILR\]).This study aims to examine the gut microbiota and identify potential organisms which may be present in higher concentrations in patients with an elevated BMI and AFIB and how these organism levels may alter with dietary changes.
Study Design:
Baseline Screening \& Follow-Up Assessments and Procedures:
As part of our current clinical practice, all participants will undergo a clinical assessment which includes a 12-lead ECG and BP (this will be repeated at all follow-up visits: 1, 3, 6, and 12 months). Demographic data and body composition measurements (i.e. waist circumference) will also be obtained from participants' medical charts or from each participant directly. Screening for Diabetes mellitus, hyperlipidemia, obstructive sleep apnea and hypertension will also be completed at the first baseline visit.
If not checked within the prior 6 months, all participants will have a baseline blood sample drawn at the first baseline visit to test for baseline sodium (Na), potassium (K), urea, creatinine, free thyroxine (T4) and thyroid stimulating hormone (TSH) (this will be repeated at 12 months). HbA1C (prediabetes/Diabetes mellitus testing) and a fasting lipid profile (hyperlipidemia testing) will also be measured at baseline and repeated at 12 months if applicable (i.e. HbA1C in those with prediabetes or Diabetes mellitus and a fasting lipid profile in those with hyperlipidemia).
If not performed within the past 12 months, all participants will undergo a baseline transthoracic echocardiogram (TTE). A follow-up TTE will be repeated at the 12-month visit.
AFIB: At the first baseline visit and all follow-up visits, AFIB-related symptom burden (using the AFSS - Appendix I) and quality of life (using the AFEQT - Appendix II) will be assessed. All participants will undergo implantation of an implantable loop recorder (ILR) at their first baseline visit (Appendix VIII). This device will continually record the participants' heart rate and rhythm for a period of 12 months and will record any episodes of AFIB. These data will be downloaded by a technician during each follow-up visit (1, 3, 6, and 12 months) and stored in a secure manner. Principal and Co-Investigators will be blinded to these data. The ILR will be removed from participants during their final follow-up visit (at 12 months).
Apple Watch: All participants will be supplied with an Apple Watch in order to monitor their levels of physical activity (i.e. step counts and physical activity duration). For this reason, participants are required to own/have daily access to (i.e. provided by the research team) an iPhone to sync with the Apple Watch. The watch will be integrated with 2 apps (Cardiogram and Lose It) to record and keep track of physical activity, caloric intake and will also monitor heart rate. Participants will be trained on the use of the watch and apps. Participants will also be instructed to put this watch on first thing in the morning and not remove it until the evening when heading to bed throughout the duration of the trial. Participants will be asked to send data from the apps to the research team by email on a weekly basis. Participants will be asked to return the Apple Watch at their final follow-up visit (at 12 months).
Physical activity: Physical activity levels will be assessed using the IPAQ and MESA TWPAS Questionnaire at the first baseline visit. These questionnaires will also be administered at all follow-up visits (1, 3, 6, and 12 months). Participants will be asked to share data from the Cardiogram app with the research team on a weekly basis.
Diet: The diets of all participants will be evaluated at the first baseline visit and follow-ups (1, 3, 6, and 12 months) using the Mediterranean Diet Score Tool. Participants will be asked to enter all food consumed into the Lose It app each day and send this information to the research team on a weekly basis. Only participants in the intervention group will be provided with the Mediterranean Diet Handout at baseline.
Gut microbiota: Participants will be provided with and trained on the use of "Poop" Kits. Stool samples will be collected (2nd baseline visit and at 1, 3, 6, and 12 months) and immediately stored at -80°C in Zymo collection devices. This deactivates active pathogens and preserves DNA for future extraction. Analyses will occur in the Centre for the Analysis of Genome Evolution and Function (CAGEF) at the University of Toronto, directed by Professor David Guttman. Microbial DNA will then be extracted from the frozen fecal samples and the 16S rRNA gene will be amplified. Analyses will be performed to determine levels of specific metabolites that have been strongly correlated to obesity and metabolic syndrome, namely monosaccharides and short-chain fatty acids (SCFAs).
Randomization: A randomization schedule will be prepared by the data coordinating centre at Queens University, Kingston, Ontario using a computerized random number-generator. Random allocation will be determined by a participant randomization software application (Dacima Software Inc., IWRS: Interactive Web Response System). Participants will be randomized on a 1:1 fashion between active intervention and control.
Experimental arm: Multicomponent Risk Factor Modification Baseline - 12 months: Active Lifestyle Intervention Participants in this intervention group will undergo the baseline and follow-up assessments described earlier. The specific components of the experimental arm will be tailored to the needs of the participants at their baseline visit for the study. Throughout the trial, participants in this group will be called weekly by a member of the research team to review and discuss each component of the lifestyle intervention (diet, exercise, and behavioural therapy). Details of each component are explained below.
Diet will be assessed (at baseline and all follow-up visits) using the Mediterranean Diet Score Tool (a 14-item questionnaire of adherence to the specified diet).Nutrition prescription will be based on a Mediterranean-style diet and individualized based on the participant's current weight and diet practices to optimize adherence. The diet will be comprised of recommended daily intakes of 50% carbohydrates, 35% unsaturated fats, and 15% protein. At baseline, basic information will be provided in written format using the Mediterranean Diet Handout. Data from the individuals' Apple Watches will be monitored and analyzed throughout the trial in order to assess compliance with these recommendations. Each participant will receive feedback and advice from the research assistant during weekly telephone sessions to motivate participants to make healthy changes to their diet in line with the Mediterranean Diet recommendations. Personal individual recommendations for changes to be introduced in the participant's diet in order to achieve a personalized goal. Research personnel will highlight the advantages of following this diet as opposed to the risks of not adhering to it. This approach has been successful in previous studies where behavioural intervention was used to help participants quit smoking.
Physical activity levels will be assessed (at baseline and all follow-up visits) using the IPAQ and MESA TWPAS. Exercise prescription was selected by investigators based on a recently published Harvard Medical School Health Report 'Starting to Exercise'. This report recommends individuals to perform 150 minutes of moderate aerobic exercise per week (equal to \>30 minutes/day, most days of the week). Data from the individuals' Apple Watches will be monitored and analyzed throughout the trial in order to assess compliance with these recommendations. Each participant will receive feedback and advice from the research assistant during weekly telephone sessions to motivate participants to gradually achieve higher levels of physical activity. Participants will be invited to attend an optional exercise class in which they walk along an indoor walking track for 60 minutes biweekly at Providence Care Hospital, supervised by a research assistant and monitored by a medically qualified Co-Investigator.
Comprehensive lifestyle intervention will include a structured behavioural change program that includes regular self-monitoring of food intake, by entering all food consumed into the Lose It app, which automatically calculates caloric intake, and physical activity. The qualified research assistant will facilitate participant engagement sessions by telephone on a weekly basis. During each session, the research assistant will assess the participant's current level of adherence to the diet and exercise recommendations and will motivate them to gradually achieve higher levels of exercise following the Harvard Medical School Health Report and to make healthy adjustments to their diet following the Mediterranean Diet Handout.
Control arm: Baseline - 12 months: Standard Clinical Practice In addition to receiving standard of care AFIB treatment, participants in the control arm of this trial will undergo all of the same baseline screening and follow-up assessments and procedures as the intervention arm but will receive no lifestyle intervention (no diet, exercise regimen, or behavioural therapy).
This pilot study will evaluate the potential efficacy and feasibility of risk factor modification in patients with a known history of symptomatic paroxysmal and persistent AFIB (in sinus rhythm) by implementing current evidence-based lifestyle recommendations as well as gain an understanding of the impact of these changes in the gut microbiome.
Objectives:
This study aims to determine if a multicomponent risk factor modification intervention (dietary intervention, exercise regimen and behavioural therapy) implemented using a basic healthcare team reduces the burden of AFIB at 12 months by decreasing the length and number of AFIB episodes. This study aims to assess the impact of these interventions on AFIB-related symptoms, quality of life and rhythm status (documented on an implantable loop recorder \[ILR\]).This study aims to examine the gut microbiota and identify potential organisms which may be present in higher concentrations in patients with an elevated BMI and AFIB and how these organism levels may alter with dietary changes.
Study Design:
Baseline Screening \& Follow-Up Assessments and Procedures:
As part of our current clinical practice, all participants will undergo a clinical assessment which includes a 12-lead ECG and BP (this will be repeated at all follow-up visits: 1, 3, 6, and 12 months). Demographic data and body composition measurements (i.e. waist circumference) will also be obtained from participants' medical charts or from each participant directly. Screening for Diabetes mellitus, hyperlipidemia, obstructive sleep apnea and hypertension will also be completed at the first baseline visit.
If not checked within the prior 6 months, all participants will have a baseline blood sample drawn at the first baseline visit to test for baseline sodium (Na), potassium (K), urea, creatinine, free thyroxine (T4) and thyroid stimulating hormone (TSH) (this will be repeated at 12 months). HbA1C (prediabetes/Diabetes mellitus testing) and a fasting lipid profile (hyperlipidemia testing) will also be measured at baseline and repeated at 12 months if applicable (i.e. HbA1C in those with prediabetes or Diabetes mellitus and a fasting lipid profile in those with hyperlipidemia).
If not performed within the past 12 months, all participants will undergo a baseline transthoracic echocardiogram (TTE). A follow-up TTE will be repeated at the 12-month visit.
AFIB: At the first baseline visit and all follow-up visits, AFIB-related symptom burden (using the AFSS - Appendix I) and quality of life (using the AFEQT - Appendix II) will be assessed. All participants will undergo implantation of an implantable loop recorder (ILR) at their first baseline visit (Appendix VIII). This device will continually record the participants' heart rate and rhythm for a period of 12 months and will record any episodes of AFIB. These data will be downloaded by a technician during each follow-up visit (1, 3, 6, and 12 months) and stored in a secure manner. Principal and Co-Investigators will be blinded to these data. The ILR will be removed from participants during their final follow-up visit (at 12 months).
Apple Watch: All participants will be supplied with an Apple Watch in order to monitor their levels of physical activity (i.e. step counts and physical activity duration). For this reason, participants are required to own/have daily access to (i.e. provided by the research team) an iPhone to sync with the Apple Watch. The watch will be integrated with 2 apps (Cardiogram and Lose It) to record and keep track of physical activity, caloric intake and will also monitor heart rate. Participants will be trained on the use of the watch and apps. Participants will also be instructed to put this watch on first thing in the morning and not remove it until the evening when heading to bed throughout the duration of the trial. Participants will be asked to send data from the apps to the research team by email on a weekly basis. Participants will be asked to return the Apple Watch at their final follow-up visit (at 12 months).
Physical activity: Physical activity levels will be assessed using the IPAQ and MESA TWPAS Questionnaire at the first baseline visit. These questionnaires will also be administered at all follow-up visits (1, 3, 6, and 12 months). Participants will be asked to share data from the Cardiogram app with the research team on a weekly basis.
Diet: The diets of all participants will be evaluated at the first baseline visit and follow-ups (1, 3, 6, and 12 months) using the Mediterranean Diet Score Tool. Participants will be asked to enter all food consumed into the Lose It app each day and send this information to the research team on a weekly basis. Only participants in the intervention group will be provided with the Mediterranean Diet Handout at baseline.
Gut microbiota: Participants will be provided with and trained on the use of "Poop" Kits. Stool samples will be collected (2nd baseline visit and at 1, 3, 6, and 12 months) and immediately stored at -80°C in Zymo collection devices. This deactivates active pathogens and preserves DNA for future extraction. Analyses will occur in the Centre for the Analysis of Genome Evolution and Function (CAGEF) at the University of Toronto, directed by Professor David Guttman. Microbial DNA will then be extracted from the frozen fecal samples and the 16S rRNA gene will be amplified. Analyses will be performed to determine levels of specific metabolites that have been strongly correlated to obesity and metabolic syndrome, namely monosaccharides and short-chain fatty acids (SCFAs).
Randomization: A randomization schedule will be prepared by the data coordinating centre at Queens University, Kingston, Ontario using a computerized random number-generator. Random allocation will be determined by a participant randomization software application (Dacima Software Inc., IWRS: Interactive Web Response System). Participants will be randomized on a 1:1 fashion between active intervention and control.
Experimental arm: Multicomponent Risk Factor Modification Baseline - 12 months: Active Lifestyle Intervention Participants in this intervention group will undergo the baseline and follow-up assessments described earlier. The specific components of the experimental arm will be tailored to the needs of the participants at their baseline visit for the study. Throughout the trial, participants in this group will be called weekly by a member of the research team to review and discuss each component of the lifestyle intervention (diet, exercise, and behavioural therapy). Details of each component are explained below.
Diet will be assessed (at baseline and all follow-up visits) using the Mediterranean Diet Score Tool (a 14-item questionnaire of adherence to the specified diet).Nutrition prescription will be based on a Mediterranean-style diet and individualized based on the participant's current weight and diet practices to optimize adherence. The diet will be comprised of recommended daily intakes of 50% carbohydrates, 35% unsaturated fats, and 15% protein. At baseline, basic information will be provided in written format using the Mediterranean Diet Handout. Data from the individuals' Apple Watches will be monitored and analyzed throughout the trial in order to assess compliance with these recommendations. Each participant will receive feedback and advice from the research assistant during weekly telephone sessions to motivate participants to make healthy changes to their diet in line with the Mediterranean Diet recommendations. Personal individual recommendations for changes to be introduced in the participant's diet in order to achieve a personalized goal. Research personnel will highlight the advantages of following this diet as opposed to the risks of not adhering to it. This approach has been successful in previous studies where behavioural intervention was used to help participants quit smoking.
Physical activity levels will be assessed (at baseline and all follow-up visits) using the IPAQ and MESA TWPAS. Exercise prescription was selected by investigators based on a recently published Harvard Medical School Health Report 'Starting to Exercise'. This report recommends individuals to perform 150 minutes of moderate aerobic exercise per week (equal to \>30 minutes/day, most days of the week). Data from the individuals' Apple Watches will be monitored and analyzed throughout the trial in order to assess compliance with these recommendations. Each participant will receive feedback and advice from the research assistant during weekly telephone sessions to motivate participants to gradually achieve higher levels of physical activity. Participants will be invited to attend an optional exercise class in which they walk along an indoor walking track for 60 minutes biweekly at Providence Care Hospital, supervised by a research assistant and monitored by a medically qualified Co-Investigator.
Comprehensive lifestyle intervention will include a structured behavioural change program that includes regular self-monitoring of food intake, by entering all food consumed into the Lose It app, which automatically calculates caloric intake, and physical activity. The qualified research assistant will facilitate participant engagement sessions by telephone on a weekly basis. During each session, the research assistant will assess the participant's current level of adherence to the diet and exercise recommendations and will motivate them to gradually achieve higher levels of exercise following the Harvard Medical School Health Report and to make healthy adjustments to their diet following the Mediterranean Diet Handout.
Control arm: Baseline - 12 months: Standard Clinical Practice In addition to receiving standard of care AFIB treatment, participants in the control arm of this trial will undergo all of the same baseline screening and follow-up assessments and procedures as the intervention arm but will receive no lifestyle intervention (no diet, exercise regimen, or behavioural therapy).
Conditions
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Atrial Fibrillation
Keywords
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Atrial Fibrillation
Study Design
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Allocation Method
RANDOMIZED
Intervention Model
PARALLEL
A randomization schedule will be prepared by the data coordinating centre at Queen's University, Kingston, Ontario using a computerized random number-generator. Random allocation will be determined by a patient randomization software application. Participants will be randomized on a 1:1 fashion between active intervention and control.
Primary Study Purpose
TREATMENT
Blinding Strategy
SINGLE
Outcome Assessors
Data downloaded from the participants' implantable loop recorders will not be available to the investigators nor anyone involved in direct patient interaction in the study. A blinded event committee composed of three physicians with a specialization in cardiology, who are not directly involved in the research study, will have access to this data.
Study Groups
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Experimental Arm
Multicomponent Risk Factor Modification Intervention focused on healthy eating, regular exercise and behavioural therapy
Group Type
EXPERIMENTAL
Multicomponent Risk Factor Modification
Intervention Type
BEHAVIORAL
Healthy eating, regular exercise and behavioural therapy.
Control Arm
Standard Clinical Practice
Group Type
NO_INTERVENTION
No interventions assigned to this group
Interventions
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Multicomponent Risk Factor Modification
Healthy eating, regular exercise and behavioural therapy.
Intervention Type
BEHAVIORAL
Eligibility Criteria
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Inclusion Criteria
* paroxysmal or persistent AFIB (in sinus rhythm at the time of randomization)
* BMI \> 30 kg/m\^2 or a waist circumference greater than 100 cm (male) or 90 cm (female)
* have daily access to an iPhone
* have at least one of the following risk factors:hypertension, diabetes or pre-diabetes, hyperlipidemia, smoker, obstructive sleep apnea
* BMI \> 30 kg/m\^2 or a waist circumference greater than 100 cm (male) or 90 cm (female)
* have daily access to an iPhone
* have at least one of the following risk factors:hypertension, diabetes or pre-diabetes, hyperlipidemia, smoker, obstructive sleep apnea
Exclusion Criteria
* Permanent AFIB (AFIB lasting \> 1 year)
* Prior or actively on waiting list for catheter ablation for AFIB
* History of unstable angina not corrected with revascularization
* Left ventricular ejection fraction \<30%
* Left atrial size \>5.5 cm
* New York Heart Association (NYHA) classification IV heart failure
* Moderate or severe cardiac valvular lesion (stenosis or regurgitation) on echocardiography or valvular lesion requiring intervention.
* Participation in a cardiac rehabilitation program within the last year
* Serious underlying psychiatric disorder: e.g. eating disorder, severe psychotic disorder with recent (3 month) hospitalization or psychiatric illness requiring supervised care precluding full independent function.
* Participants who are unable or unwilling to provide fully informed consent.
* Currently performing exercise training 150 minutes/week of moderate to vigorous physical activity
* Gastrointestinal malabsorption disorder: A previously diagnosed gastrointestinal malabsorption disorder interfering with macro or micronutrient absorption.
* If receiving warfarin and unstable international normalized ratio (INR) defined as persistently outside of the therapeutic range (2.0-3.0) for greater than 14 consecutive days.
* Other non-cardiovascular medical conditions making 1-year survival unlikely.
* Prior or actively on waiting list for catheter ablation for AFIB
* History of unstable angina not corrected with revascularization
* Left ventricular ejection fraction \<30%
* Left atrial size \>5.5 cm
* New York Heart Association (NYHA) classification IV heart failure
* Moderate or severe cardiac valvular lesion (stenosis or regurgitation) on echocardiography or valvular lesion requiring intervention.
* Participation in a cardiac rehabilitation program within the last year
* Serious underlying psychiatric disorder: e.g. eating disorder, severe psychotic disorder with recent (3 month) hospitalization or psychiatric illness requiring supervised care precluding full independent function.
* Participants who are unable or unwilling to provide fully informed consent.
* Currently performing exercise training 150 minutes/week of moderate to vigorous physical activity
* Gastrointestinal malabsorption disorder: A previously diagnosed gastrointestinal malabsorption disorder interfering with macro or micronutrient absorption.
* If receiving warfarin and unstable international normalized ratio (INR) defined as persistently outside of the therapeutic range (2.0-3.0) for greater than 14 consecutive days.
* Other non-cardiovascular medical conditions making 1-year survival unlikely.
Minimum Eligible Age
18 Years
Eligible Sex
ALL
Accepts Healthy Volunteers
No
Sponsors
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Abbott
INDUSTRY
Sponsor Role
collaborator
University of Toronto
OTHER
Sponsor Role
collaborator
Dr. Benedict Glover
OTHER
Sponsor Role
lead
Responsible Party
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Dr. Benedict Glover
Principal Investigator, Chief of Cardiac Arrhythmia Service, Department of Medicine
Responsibility Role
SPONSOR_INVESTIGATOR
Principal Investigators
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Benedict M Glover, MD
Role: PRINCIPAL_INVESTIGATOR
Queen's University
Christopher Simpson, MD
Role: PRINCIPAL_INVESTIGATOR
Queen's Unviersity
Locations
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Kingston Health Sciences Centre
Kingston, Ontario, Canada
Site Status
RECRUITING
Countries
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Canada
Central Contacts
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Facility Contacts
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Christopher Simpson, MD
Role: primary
Milena A Bullen, BScH
Role: backup
References
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Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
6022511
Identifier Type: -
Identifier Source: org_study_id