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A Lifestyle-based, PhysiCal AcTIVity IntErvention for Patients With Symptomatic Atrial Fibrillation (the ACTIVE-AF Study).

A comparison of a lifestyle-based physical activity intervention with usual care on arrhythmia burden and symptom severity in patients with atrial fibrillation.

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12615000734561
Acronym
ACTIVE-AF
Enrollment
120
Registered
2015-07-16
Start date
2015-11-04
Completion date
2019-12-20
Last updated
2021-11-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief summary

We have recently shown that increasing fitness improves arrhythmia outcomes in patients with atrial fibrillation, a common heart rhythm disorder. In this study, we intend to evaluate a goal-directed, lifestyle based physical activity intervention for the reduction of AF burden and symptom severity. We hypothesise that our physical activity intervention will lower arrhythmia burden and improve symptom severity when compared to standard medical care alone.

Interventions

The physical activity intervention is designed to increase physical activity towards a weekly target of 210 minutes of moderate-intensity (Rating of Perceived Exertion <14 or <75% Heart rate reserve) physical activity. Vigorous activity (Rating of Perceived Exertion >14 or >75% Heart rate reserve), such as running may be used to substitute moderate activity at a ratio of 1:2 (i.e. 10 minutes of vigorous activity would equate to 20 minutes of moderate activity). This level of activity exceeds the

The physical activity intervention is designed to increase physical activity towards a weekly target of 210 minutes of moderate-intensity (Rating of Perceived Exertion <14 or <75% Heart rate reserve) physical activity. Vigorous activity (Rating of Perceived Exertion >14 or >75% Heart rate reserve), such as running may be used to substitute moderate activity at a ratio of 1:2 (i.e. 10 minutes of vigorous activity would equate to 20 minutes of moderate activity). This level of activity exceeds the American Heart Association Physical Activity guidelines (Haskell et al., 2007). The rationale for this intervention is based on the LOOK AHEAD study in which a target of 200 minutes per week was used, resulting in significant weight loss and improvements in cardiorespiratory fitness and traditional cardiovascular risk factors (Jakicic et al., 2009; Wing et al., 2013). The incremental benefit on health with a higher exercise dose is also supported by large epidemiological studies (Wen et al., 2012, Lancet). The program includes a weekly, 45-minute individual session (0-3 months) with an exercise physiologist (Dr Elliott), decreasing to fortnightly from 3-6 months. Within each session, participants will undertake supervised exercise training, discuss strategies to improve weekly PA and goal setting will be agreed between the health professional and the patient. Patients will maintain a journal detailing their physical activity and exercise habits. If required, additional sessions will be scheduled. 24-hour telephone and email support will be accessible to the patient. Participants will be asked to maintain a food diary and to adopt a diet consisting of high protein, low glycemic index foods.

Sponsors

University of Adelaide
Lead SponsorUniversity

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Treatment

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

- Symptomatic Paroxysmal or Persistent AF - Aged >18 years and <80 years - Current physical activity levels <60 minutes per week.

Exclusion criteria

- Previous AF ablation - Permanent AF - History of myocardial infarction or cardiac surgery in past 12 months. - Autoimmune or systemic inflammatory disease. - Decompensated heart failure. - Unable to exercise due to an existing musculoskeletal disorder.

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 12, 2026