耳穴按压与间歇性低碳水化合物饮食治疗超重或肥胖伴有胃热湿阻综合征的儿童:一项随机对照试验方案

IF 1.5 Q3 HEALTH CARE SCIENCES & SERVICES JMIR Research Protocols Pub Date : 2025-03-03 DOI:10.2196/59856
Wen Sun, Jingwei He, Wenqin Wang, Chen Lu, Yating Lin, Yalan Dou, Weili Yan, Jian Yu
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引用次数: 0

摘要

背景:儿童期肥胖经常持续到成年,并与以后生活中心血管疾病的风险增加和早期发病有关。行为改变策略已被提出作为儿童和青少年肥胖的一线体重管理方法。非药物干预,如中医耳指压治疗和间歇性低碳水化合物饮食(ILCD),正在越来越多地研究在年轻肥胖人群。然而,关于儿童体重控制和降低心脏代谢风险的有效性和安全性的高质量证据有限。目的:本研究旨在比较中医耳压治疗(TAAT)与ILCD治疗超重或肥胖胃热湿阻证患儿降低心脏代谢风险的效果。方法:随机对照试验。研究对象为在某三级儿童医院中医科肥胖门诊就诊的超重或肥胖儿童。符合条件的参与者必须满足以下条件:(1)年龄在6 - 18岁之间,(2)体重超重,(3)有胃热湿阻综合征。招募的儿童将以3:1的比例随机接受TAAT或自我管理的ILCD,为期1个月:TAAT组150人,ILCD组50人。主要观察指标是从治疗开始到1个月结束时体重的变化。次要结局分别为1个月和3个月时的体重、腰围、腰高比、BMI、血压、体脂含量、肝肾功能指标、糖代谢指标、肠道菌群、中医证候评分。采用意向治疗策略进行初步统计分析。采用广义线性模型比较各组间体重变化差异,以基线体重为协变量,以高斯函数表示族函数,恒等函数表示联结函数,得到体重变化平均差异及其95% CI的估计值。结果:该研究方案已获得机构伦理委员会批准,并于2023年5月5日在ClinicalTrials.gov上注册。招聘于2023年6月开始,预计将于2025年12月完成。截至2024年11月,我们已经招募了112名参与者。结论:这项随机对照试验将为TAAT与ILCD在超重或肥胖伴有胃热湿阻综合征的儿童中降低体重和改善心脏代谢风险的治疗效果和安全性提供证据。探索性目标包括基于生物样本的两种干预措施的潜在机制。试验注册:ClinicalTrials.gov NCT05847478。https://clinicaltrials.gov/study/NCT05847478.International注册报告标识符(irrid): DERR1-10.2196/59856。
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Auricular Acupressure Versus an Intermittent Low-Carbohydrate Diet in Children With Overweight or Obesity With Gastric-Heat and Dampness-Obstruction Syndrome: Protocol for a Randomized Controlled Trial.

Background: Childhood obesity frequently persists into adulthood and is associated with an increased risk and earlier onset of cardiovascular disease in later life. Behavioral change strategies have been proposed as the first-line weight management approach for children and adolescents with obesity. Nonpharmacological interventions, such as traditional Chinese medicine (TCM) auricular acupressure treatment and intermittent low-carbohydrate diet (ILCD), are increasingly being investigated in the young obese population. However, there is limited high-quality evidence about effectiveness and safety in weight control and reducing cardiometabolic risk in the pediatric population.

Objective: This study aimed to compare the effect of cardiometabolic risk reduction between TCM auricular acupressure treatment (TAAT) and ILCD in children with overweight or obesity with gastric-heat and dampness-obstruction syndrome.

Methods: This is a randomized controlled trial. Eligible participants are children with overweight or obesity and enrolled at the obesity clinic of the department of TCM at a tertiary children's hospital. Eligible participants must meet the following criteria: (1) be aged between 6 and 18 years, (2) be overweight, and (3) have gastric-heat and dampness-obstruction syndrome. Recruited children will be randomized 3:1 to receive either TAAT or a self-administered ILCD for 1 month: 150 in the TAAT group and 50 in the ILCD group. The primary outcome is the change in body weight from the beginning of treatment to the end of 1 month. Secondary outcomes included body weight, waist circumference, waist-to-height ratio, BMI, blood pressure, body fat content, indexes of liver and renal function, indexes of glucose metabolism, gut microbiota, and TCM syndrome scores at the end of 1 month and 3 months, respectively. Primary statistical analyses were conducted using the intention-to-treat strategy. A generalized linear model was used to compare the difference in weight change between the groups, with the baseline body weight as the covariate, to obtain the estimate of the mean difference in body weight change and its 95% CI, using Gaussian for family function and identity for link function.

Results: The study protocol was approved by the institutional ethical committee and registered on ClinicalTrials.gov on May 5, 2023, before recruitment. Recruitment began in June 2023 and is expected to be completed by December 2025. As of November 2024, we have enrolled 112 participants.

Conclusions: This randomized controlled trial will provide evidence on the treatment effects and safety of TAAT versus ILCD among children with overweight or obesity with gastric-heat and dampness-obstruction syndrome, in reducing body weight and improving cardiometabolic risks. Exploratory aims include potential underlying mechanisms of the 2 kinds of interventions, based on biosamples.

Trial registration: ClinicalTrials.gov NCT05847478. https://clinicaltrials.gov/study/NCT05847478.

International registered report identifier (irrid): DERR1-10.2196/59856.

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