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临床试验/NCT03027726
NCT03027726已完成不适用

Prevention of Diabetes in Overweight/Obese Preadolescent Children Through a Family-based Intervention Program Including Supervised Exercise; the PREDIKID Study

University of the Basque Country (UPV/EHU)2 个研究点 分布在 1 个国家目标入组 84 人开始时间: 2017年3月7日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
84
试验地点
2
主要终点
microRNA expression in circulating exosomes and in blood peripheral mononuclear cells

研究概览

简要总结

Background: The global pandemic obesity has led to increased risk for prediabetes and type 2 diabetes (T2D).

Objectives: (i) To evaluate the effect of a 22 weeks multidisciplinary intervention program including exercise on T2D risk in pre-adolescents with high risk to develop T2D, and (ii) To identify the profile of microRNA in circulating exosomes and in blood peripheral mononuclear cells in pre-adolescents with high risk to develop T2D and its response to a multidisciplinary intervention program including exercise.

详细描述

Background: The global pandemic obesity has led to increased risk for prediabetes and type 2 diabetes (T2D).

Objectives: (i) To evaluate the effect of a 22 weeks multidisciplinary intervention program including exercise on T2D risk in pre-adolescents with high risk to develop T2D, and (ii) To identify the profile of microRNA in circulating exosomes and in blood peripheral mononuclear cells in pre-adolescents with high risk to develop T2D and its response to a multidisciplinary intervention program including exercise.

Design, participants and methods: A total of 84 children with high risk of type 2 diabetes mellitus aged 8-12 years will be included and randomly assigned to control (N=42) or intervention (N=42) groups. The control group will receive a family-based lifestyle education and psycho-educational program (2 days/month), while the intervention group will attend the same lifestyle education and psycho-educational program plus the exercise program (3 days/week). The duration of training sessions will be 90 min of exercise, including warm-up, moderate to vigorous aerobic activities, and strength exercises. The following measurements will be evaluated at baseline prior to randomization and after the intervention: fasting, insulin glucose, and hemoglobin A1c; total and abdominal fat (dual X-ray absorptiometry); pancreatic, hepatic and visceral fat (magnetic resonance imaging); systolic and diastolic blood pressure; fasting leptin, adiponectin, fibroblast growth factor-21, fetuin-A, hs-C-reactive protein, tumor necrosis factor-alfa, interleukin (IL)-1beta and IL-6 and lipid profile; carotid intima-media thickness (ultrasonography), microRNA expression in circulating exosomes and in blood peripheral mononuclear cells (MiSeq-Illumina); functional peak aerobic capacity (cardiopulmonary exercise testing and 20m shuttle run test). Changes in dietary habits (food frequency questionnaire and two non-consecutive 24h recalls), physical activity and sleep (accelerometry); sex, age, socioeconomic status and pubertal status will be used as potential confounders.

Discussion/Conclusions: Early prevention and identification of children with high risk to develop T2D could help to reduce the morbidity and mortality associated with the disease.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
8 Years 至 12 Years(Child)
性别
All
接受健康志愿者

入选标准

  • Overweight/obese children aged between 8 and 12 years, meeting the international criteria for classification for T2D risk and having at least one parent or caregiver willing to participate in the program sessions will be included

排除标准

  • Children with any medical condition that could affect the results of the study or that limits physical activity will be excluded

结局指标

主要结局

microRNA expression in circulating exosomes and in blood peripheral mononuclear cells

时间窗: Baseline and at the end of the 22 weeks of intervention

The expression of miRNAs will be measured in circulating exosomes and in white blood cells (MiSeq-Ilumina)

Insulin resistance

时间窗: Baseline and at the end of the 22 weeks of intervention

The Homeostasis model assessment index will be calculated as fasting insulin concentration (microU/mL) x fasting glucose concentration (mmol/L)/22.5.

次要结局

  • Inflammation and biochemical cardiovascular disease risk factors(Baseline and at the end of the 22 weeks of intervention)
  • Ectopic fat: pancreatic and liver fat accumulation(Baseline and at the end of the 22 weeks of intervention)
  • Total, abdominal and visceral adiposity(Baseline and at the end of the 22 weeks of intervention)
  • Anthropometry and blood pressure(Baseline and at the end of the 22 weeks of intervention)
  • Cardiorespiratory fitness(Baseline and at the end of the 22 weeks of intervention)
  • Carotid intima-media thickness(Baseline and at the end of the 22 weeks of intervention)

研究者

发起方
University of the Basque Country (UPV/EHU)
申办方类型
Other
责任方
Principal Investigator
主要研究者

IDOIA LABAYEN

Professor

University of the Basque Country (UPV/EHU)

研究点 (2)

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