Key result
This protocol outlines a randomized controlled trial to evaluate the effect of a 24-week moderate exercise training program on functional capacity in patients with an implantable cardioverter defibrillator.
Why the study?
Data on the safety and efficacy of exercise training in patients with implantable cardioverter defibrillators are sparse and have not been extensively studied.
Does moderate exercise training improve functional capacity in patients with an implantable cardioverter defibrillator?
RCT (n=70)
Random allocation
No
Does moderate exercise training improve functional capacity in patients with an implantable cardioverter defibrillator?
Answers are grounded in this paper and cite their sources.
This protocol describes a planned randomized controlled trial to assess whether a 24-week home-based moderate exercise program improves functional capacity in patients with an ICD and reduced ejection fraction.
BACKGROUND: Cardiac rehabilitation programs are planned to reduce the physiological and psychological stress of Cardiovascular Disease, decrease the risk of mortality secondary to CVD, improve cardiovascular function, and help patients to achieve their highest quality of life. However, data on the safety and efficacy of exercise training (ET) in patients with implantable cardioverter defibrillators (ICDs) is sparse. Exercise interventions in those with an ICD have not been extensively studied. MATERIALS AND METHODS: A randomized controlled trial will be conducted to determine the effects of moderate ET on the functional capacity of patients with an Implantable cardioverter defibrillator with age group of >18 years, NYHA with grade II and III, EF ≤50%, No evidence of ICD discharge for past 3 months with minimum post-ICD implantation period of a minimum of 3 months. This study includes a total of 70 patients. Random allocation will be used to randomize participants into two groups (35 in each). Home-based walking exercises in the form of aerobic walking will be advised to patients with ICD. They will be advised to walk within the target heart rate for 1 to 24 weeks, which is divided into two components. Initial components included 1-8 weeks of exercise as an Aerobic conditioning component, which includes 1 hour/day x 5 days/week, followed by 9 to 24 weeks as an Aerobic maintenance component, which includes 30 minutes/day x 5 days/week. Adherence to the home walking program with the pulse, spo2, and BP will be tracked using a smartwatch, home exercise log book, and telephone follow-up (if less than 35km - monthly home visit will be done). Functional capacity will be assessed using a 6-minute walk test at baseline and at 6-month intervals. CONCLUSION: This study will identify the safety and efficacy of ET among patients with ICD, which will contribute to the important evidence base for cardiac rehabilitation among this group of patients.
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Ramamoorthy et al. (2024) conducted an RCT in Implantable cardioverter defibrillator (n=70). Moderate exercise training (home-based aerobic walking) vs. Control was evaluated on Functional capacity assessed using a 6-minute walk test. This protocol outlines a randomized controlled trial to evaluate the effect of a 24-week moderate exercise training program on functional capacity in patients with an implantable cardioverter defibrillator.
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