Atrial Fibrillation Lifestyle Project
NCT03724383 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 80
Last updated 2018-10-30
Summary
The objectives of the investigators are to demonstrate a reduction in frequency and symptoms of AF and improvements in cardiovascular risk factors following a lifestyle intervention in patients with paroxysmal AF. Participants will be randomized into control or intervention groups. The intervention will receive step trackers, diet counselling, an exercise program, and risk factor modification consultations. Controls will receive step trackers and care as usual. Testing will occur at baseline, six months, and one year.
Conditions
- Atrial Fibrillation Paroxysmal
Interventions
- BEHAVIORAL
-
Risk Factor Management Consult
Participants may be referred to an Internist to control risk factor management - this may require monthly visits until risk factor targets have been met.
- BEHAVIORAL
-
Diet Classes
Group nutrition sessions delivered two times per week (1 hr each), over a 3 month period (months 0 to 3 of intervention) delivered by a registered dietitian.
- BEHAVIORAL
-
Stress Management Classes
Group sessions delivered two times per week (1 hr each), over a 3 month period (months 0 to 3 of intervention). Techniques taught will include awareness, coping, and relaxation strategies.
- OTHER
-
Exercise Classes
Group sessions delivered two times per week (1 hr each), over 3 month period (months 3-6). Classes will include high intensity interval training, resistance training.
- OTHER
-
Home based exercise program
The interval and resistance training program will mirror the supervised exercise.
Sponsors & Collaborators
-
Vancouver Coastal Health
collaborator OTHER_GOV -
Vancouver Coastal Health Research Institute
collaborator OTHER -
University of British Columbia
collaborator OTHER -
Teddi Orenstein Lyall
lead OTHER
Principal Investigators
-
Teddi Orenstein Lyall, MD · University of British Columbia
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- DOUBLE
- Model
- PARALLEL
Eligibility
- Min Age
- 19 Years
- Max Age
- 75 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2018-09-06
- Primary Completion
- 2020-04-30
- Completion
- 2020-04-30
Countries
- Canada
Study Locations
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