Qin Yuan , John Oginni , Ning Liao , Hui He , Zan Gao
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引用次数: 0
摘要
背景全世界每年约有 170 万妇女被诊断出患有乳腺癌。确诊后定期参加体育锻炼对健康大有裨益，可改善乳腺癌幸存者（BCS）的预后和整体健康相关生活质量（HRQoL）。尽管有这些益处，但中国乳腺癌幸存者中坚持建议的中度至剧烈运动水平的比例很低。健身可穿戴设备和应用程序等电子健康技术提供了一个机会，可通过提供个性化的锻炼计划改善 BCS 的医疗保健。所有参与者都将获得华为智能手环，并被分为 1) 个性化干预组，接受每日 PA 跟踪和反馈；2) 对照组，接受标准护理。主要结果为运动量，次要结果包括生物标志物、体重和身体成分、功能性健身、心身健康、生活质量和个人信念。结果将在基线、6 个月和 12 个月（终点）进行评估。成功的结果将彻底改变中国 BCS 的 PA 计划，为未来的电子健康干预提供一个模式。
Promoting precision health using fitness wearable and apps among breast cancer survivors: Protocols of a smart health management trial
Background
Annually, approximately 1.7 million women are diagnosed with breast cancer worldwide. Engaging in regular physical activity (PA) post-diagnosis brings significant health benefits, enhancing breast cancer survivors' (BCS) prognosis and overall health-related quality of life (HRQoL). Despite these benefits, a low percentage of Chinese BCS adhere to the recommended moderate-to-vigorous PA levels. This highlights the need for innovative PA interventions tailored for BCS management. eHealth technology, such as fitness wearables and apps, presents an opportunity to improve BCS healthcare by offering personalized exercise programs.
Methods
This study focuses on developing a precision eHealth PA program for 200 Chinese BCS in Guangdong Province, using a custom micro-application and a smart band for a 12-month trial. All participants will receive a Huawei Smart Band and be divided into 1) a personalized intervention group, receiving daily PA tracking and feedback, and 2) a control group receiving standard care. The primary outcome is PA and secondary outcomes include biomarkers, weight and body composition, functional fitness, HRQoL, and individual beliefs. Outcomes will be assessed at baseline, 6 months, and 12 months (endpoint). Successful outcomes could revolutionize PA programs for Chinese BCS, providing a model for future eHealth interventions.
期刊介绍：
Contemporary Clinical Trials is an international peer reviewed journal that publishes manuscripts pertaining to all aspects of clinical trials, including, but not limited to, design, conduct, analysis, regulation and ethics. Manuscripts submitted should appeal to a readership drawn from disciplines including medicine, biostatistics, epidemiology, computer science, management science, behavioural science, pharmaceutical science, and bioethics. Full-length papers and short communications not exceeding 1,500 words, as well as systemic reviews of clinical trials and methodologies will be published. Perspectives/commentaries on current issues and the impact of clinical trials on the practice of medicine and health policy are also welcome.
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