[09]一项评估亨廷顿舞蹈病运动结果的新试验设计

M. Busse, L. Quinn, C. Drew, R. Williams-Thomas, P. Dimitropoulou, R. Playle, K. Hamana, B. Griffin, R. Reilmann, M. Kelson, A. Rosser
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引用次数: 0

摘要

背景和目的在亨廷顿病(HD)群体中,在短期内对亨廷顿病进行运动干预方面取得了一些成功。为了推动这一领域的发展,我们现在需要进行长期随访研究,以阐明运动和体育活动对疾病进展的潜在影响。有效利用现有数据和考虑患者偏好对于评估招募和保留具有挑战性的非药物干预措施至关重要。方法:在PACE-HD中,我们采用了一项队列试验设计,涉及欧洲和美国的六个Enroll-HD站点。该设计包括对一组明显HD患者(n=120)的身体健康和活动进行纵向评估,并在3个地点(n=60)进行为期12个月的运动与常规护理的随机对照试验(RCT)。干预措施包括一个有目标设定的体育活动指导计划,一本相关的工作手册,以及提供运动器材和FitBit设备,用于自我监测运动。评估包括健康测试和使用可穿戴技术来捕获和量化大型HD队列中身体活动的剂量(频率、持续时间和强度)。被分配到常规活动组的随机对照试验参与者和观察队列的参与者将提供他们年度注册- hd评估的参考数据(n=90),我们将利用这些数据来评估随机分配到支持运动组的参与者(n=30)的运动效果。如果设计被证明是可行的,它将为在现有的入组队列支持下对HD运动进行强有力的评估铺平道路。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
J09 A new trial design for evaluating exercise outcomes in huntington’s disease
Background and aims Across the Huntington’s Disease (HD) communities, there has been some success in delivering exercise interventions in HD over the short term. In order to move the field forward we now need studies with longer term follow-up to elucidate the potential effect of exercise and physical activity on disease progression. The efficient use of existing data and consideration of patient preferences is critical for evaluation of non-drug interventions where recruitment and retention are challenging. Methods In PACE-HD we utilise a Trial-within-a-Cohort design involving six Enroll-HD sites across Europe and USA. This design involves longitudinal evaluation of physical fitness and activity in a cohort of people with manifest HD (n=120) and a nested randomized trial (RCT) at 3 sites (n=60) of 12-months exercise compared to usual care. The intervention incorporates a physical activity coaching program with goal setting, an associated workbook, and provision of exercise equipment and FitBit devices for self-monitoring of exercise. Assessments include fitness testing and the use of wearable technologies to capture and quantify dose (frequency, duration, intensity) of physical activity in a large HD cohort. Participants in the RCT allocated to usual activity and those from the observational cohort will provide reference data (n=90) from their annual Enroll-HD assessments that we will utilise to evaluate exercise effects in those randomized to supported exercise (n=30). Outcomes Should the design prove to be feasible, it will pave the way for robust evaluation of exercise in HD supported by the existing Enroll cohort.
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