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临床试验/NCT06848478
NCT06848478招募中不适用

Level Up! (The Combined and Independent Effects of Exercise Training and Dietary Enhancement on Cardiometabolic Health in Adolescents With Obesity)

Arkansas Children's Hospital Research Institute6 个研究点 分布在 1 个国家目标入组 120 人开始时间: 2026年6月4日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
120
试验地点
6
主要终点
Group differences in composite score of cardiometabolic health changes over time.

研究概览

简要总结

The goal of this clinical trial is to learn how exercise and diet quality affect the health of adolescents with obesity. The main questions it aims to answer are:

  • Does exercise improve cardiometabolic health in adolescents with obesity?
  • Does enriching the diet with fruits and vegetables improve cardiometabolic health in adolescents with obesity?
  • Do exercise and a fruit and vegetable diet together provide greater health benefits than either one alone in adolescents with obesity?

Researchers will compare four groups to see how exercise and diet impact health:

  • Standard Care Group: Receives the usual care for obesity.
  • Exercise Group: Receives weekly exercise coaching and participates in a 12-week exercise program.
  • Diet Group: Receives weekly dietary coaching and eats a diet enriched with fruits and vegetables for 12 weeks.
  • Combined Exercise and Diet Group: Receives both exercise and dietary programs, namely weekly exercise and dietary coaching, participation in a 12-week exercise program, and daily consumption of fruits and vegetables for 12 weeks.

During the 12-week study, participants will attend three study visits to:

  • Provide blood, stool, and urine samples.
  • Answer questions about health, sleep, diet, and physical activity.
  • Undergo body scans to measure fat, lean, and bone mass.
  • Complete blood vessel function and liver fat content assessments.
  • Assess resting exergy expenditure.
  • Complete fitness tests.
  • Wear a fitness tracker to monitor physical activity and sleep patterns.

详细描述

The Level Up! study is a 12-week randomized controlled trial designed to investigate the independent and combined effects of exercise training and dietary enrichment on cardiometabolic health in adolescents with obesity. The study will enroll adolescents participating in an obesity treatment program. Participants will be randomly assigned to one of four groups: standard of care, exercise, dietary, or combined exercise and dietary intervention.

Each participant will attend three assessment visits at baseline, week 6, and week 12 at the Arkansas Children's Nutrition Center (ACNC). The following key measurements will be conducted:

  • Body Composition: Dual-Energy X-ray Absorptiometry (DXA)
  • Metabolic Profile: Fasting blood markers, including glucose, lipid profile, and insulin resistance
  • Vascular Function: Brachial artery flow-mediated dilation (ultrasound)
  • Liver Fat Content: Elastography
  • Continuous Glucose Monitoring: Interstitial sensor-based glucose measurement
  • Resting Metabolic Rate: Indirect calorimetry
  • Aerobic Capacity: Cardiopulmonary exercise test (spirometry)
  • Muscle Strength: Dynamometry
  • Physical Activity & Sleep: Accelerometry
  • Dietary Intake: 3-day food records

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Factorial
主要目的
Basic Science
盲法
Single (Outcomes Assessor)

入排标准

年龄范围
13 Years 至 17 Years(Child)
性别
All
接受健康志愿者

入选标准

  • Male or female aged 13 to 17 years.
  • Newly enrolled in a weight management program.
  • Excessive weight: Class I obesity I (≥95% percentile to < 120% of the 95th percentile), class II Obesity (≥120 to <140% of the 95th percentile, or BMI ≥35 to < 40 g/m2).
  • Less than 60 min/day of moderate to vigorous physical activity.
  • Fruit intake ≤ 1.5 cup equivalent per day.
  • Vegetable intake ≤ 1.5 cup equivalent per day.
  • Medical release.

排除标准

  • Type 2 diabetes mellitus.
  • Asthma that requires daily use of inhalers to keep symptoms under control.
  • Asthma that requires the use of rescue inhalers (e.g., albuterol) >2 days per week
  • Exercise-induced asthma.
  • Autism spectrum disorder (e.g., Autistic disorder, Rett disorder, Asperger disorder, childhood disintegrative disorder, pervasive developmental disorder not otherwise specified (PDD-NOS).
  • Epilepsy.
  • Chronic kidney disease.
  • Hormonal disease (e.g., hypothyroidism and growth hormone deficiency).
  • Autoimmune diseases (e.g., lupus, thyroiditis, juvenile idiopathic arthritis).
  • Bleeding disorders (e.g., hemophilia).
  • Chronic infections (e.g., HIV, hepatitis B, hepatitis C).
  • Other pre-existing medical conditions or medications as determined by the investigators to affect the outcomes of interest.
  • Pregnancy.
  • Dislike of > 1 study product assessed at the initial visit.
  • Parent/child refusal to have blood drawn.
  • Refusal to authorize study investigators to access data from the clinical records.

研究组 & 干预措施

Control

No Intervention

Participants receive the standard of care for treating Class I and II obesity.

Exercise intervention

Experimental

In addition to the standard of care, participants engage in exercise coaching and a 12-week exercise program, encompassing three 60-minute supervised sessions per week.

干预措施: Exercise Intervention (Behavioral)

Nutritional Intervention

Experimental

In addition to the standard of care, participants receive dietary coaching and engage in a 12-week daily dietary program enriched with a blend of fruits and vegetables.

干预措施: Nutritional Intervention (Behavioral)

Exercise and Nutritional Intervention

Experimental

In addition to the standard of care, participants receive a combined exercise and dietary intervention, as described in the other two intervention arms.

干预措施: Exercise Intervention (Behavioral)

Exercise and Nutritional Intervention

Experimental

In addition to the standard of care, participants receive a combined exercise and dietary intervention, as described in the other two intervention arms.

干预措施: Nutritional Intervention (Behavioral)

结局指标

主要结局

Group differences in composite score of cardiometabolic health changes over time.

时间窗: Baseline, 6 weeks, and 12 weeks.

The primary outcome is a composite score of cardiometabolic health status. The score is calculated as the mean of specific z-scores for the following markers: fasting triglycerides (mg/dL), total cholesterol/HDL-cholesterol ratio, HOMA2-IR, systolic blood pressure (mmHg), fat-mass-index \[whole-body fat mass (kg)/height² (m²)\], and inverse peak oxygen uptake (mL O₂/kg/min). The composite score is computed as the mean of the standardized z-scores for each marker, providing an overall measure of cardiometabolic health status.

次要结局

  • Group differences in low-density lipoprotein (LDL) cholesterol (mg/dL) changes over time.(Baseline, 6 weeks, and 12 weeks.)
  • Group differences in fow-mediated dilation (%) changes over time.(Baseline, 6 weeks, and 12 weeks.)
  • Group differences in liver steatosis (dB/m) changes over time.(Baseline and 12 weeks.)
  • Group differences in appendicular lean mass index changes over time.(Baseline, 6 weeks, and 12 weeks.)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (6)

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