Key result
Ongoing RCT evaluates adding behavioral weight loss to cardiac rehab for patients with AF and obesity.
Why the study?
Despite the potential to alleviate symptom burden and improve prognosis, few cardiac rehabilitation programs include targeted weight loss treatment for patients with AF and obesity.
Does adding a behavioral weight loss treatment to cardiac rehabilitation improve weight loss in adults with atrial fibrillation and obesity?
RCT (n=120)
Open-label
1:1 allocation stratified by sex
No
Does adding a behavioral weight loss treatment to cardiac rehabilitation improve weight loss in adults with atrial fibrillation and obesity?
This study protocol outlines an RCT to determine if adding a 'Small Changes' behavioral weight loss treatment to standard cardiac rehabilitation can achieve clinically meaningful weight loss in patients with atrial fibrillation and obesity.
Protocol tests behavioral weight loss addition to cardiac rehab in obese AF; leaves open efficacy until completion.
BACKGROUND: ) to alleviate symptom burden and improve prognosis, few cardiac rehabilitation (CR) programs include targeted weight loss treatment. AIMS: This RCT protocol will evaluate the efficacy of a "Small Changes" behavioral weight loss treatment (BWLT) to produce clinically relevant (≥ 10%) weight loss among patients with AF and obesity undergoing CR, relative to CR alone. Secondary aims are to establish efficacy of CR + BWLT for improving AF symptoms, AF risk factors, and health-related quality of life. METHODS: Adults (18 +) with AF and obesity will be recruited and randomized to receive CR + BWLT (intervention) or CR-only (control). Controls will receive CR consisting of supervised exercise and risk factor self-management for 12 weeks. The intervention group will receive CR plus BWLT (12 weekly, group-based virtual sessions, followed by 12 weeks of follow-up support). Weight and AF-risk factors will be assessed at pre-randomization, 12 weeks, 24 weeks, and 52 weeks. AF burden will be assessed using 30-s ECGs recorded bidaily and with AF symptoms. The primary endpoint of weight loss will be calculated from baseline to 52 weeks as a percentage of starting weight. Intention-to-treat analyses will compare the proportion in each group achieving ≥ 10% weight loss. Assuming success rates of 5% and 30% among controls and intervention groups, respectively, and a 30% loss to follow-up, 120 patients (60 per group) will provide 80% power to detect a difference using a two-sided independent test of proportions (alpha = 5%). IMPACT: This clinical trial will be the first to demonstrate that adding BWLT to CR promotes clinically meaningful weight loss among patients with AF and comorbid obesity. Findings will inform design and execution of a large efficacy trial of long-term (e.g., 5-year) clinical endpoints (e.g., AF severity, mortality). Implementing weight control interventions designed to target the AF substrate in CR could dramatically reduce morbidity and enhance quality of life among patients living with AF in Canada. TRIAL REGISTRATION: ClinicalTrials.gov registration number: NCT05600829. Registered October 31, 2022.
No takes yet. Share an insight, caveat, or question.
Williamson et al. (2024) conducted an RCT in Atrial fibrillation and obesity (n=120). Behavioral weight loss treatment (ASPIRE-AF) + Cardiac rehabilitation vs. Cardiac rehabilitation alone was evaluated on Proportion of patients achieving ≥ 10% body weight loss from baseline to 52-week follow-up. The BE-WEL in CR-AF study is an ongoing randomized controlled trial protocol evaluating whether adding a behavioral weight loss treatment to cardiac rehabilitation increases the proportion of patients with atrial fibrillation and obesity achieving ≥10% weight loss at 52 weeks.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: