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临床试验/NCT01857791
NCT01857791Unknown不适用

Efficacy of a Clinic-based, Multi- Disciplinary, Pediatric Weight Management Program

University of Vermont2 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2011年1月最近更新:
适应症

试验速览

阶段
不适用
入组人数
40
试验地点
2
主要终点
weight loss

研究概览

简要总结

Childhood obesity has more than tripled in the past 30 years. From 1980 to 2008, the prevalence of obesity among adolescents aged 12 to 18 years, increased from 5.0% to 18.1%.1 Although several pediatric weight management programs are available, access to these programs may not always be possible.

The proposed study will be an ongoing research program with approximately 40 children ages 12-18 years enrolled into the study over a year. All study participants will participate in a baseline evaluation which will include body composition measures, aerobic testing, as well as nutrition and physical activity questionnaires. Study participants will be assigned to the clinic-based group. The clinic- based group will participate in a 12-week multi-disciplinary weight management program. All study participants will then participate in a 12-week follow-up evaluation similar to the baseline visit. New participants will be enrolled every 12 weeks. Every 12 weeks, active participants (those that have completed a minimum of 12 weeks) will have the option to continue in the program or, discontinue their active participation in the program and enroll into the maintenance phase which will consist of measures only every 12 weeks.

The objective of the proposed study includes examining the efficacy of the clinic-based, multi-disciplinary, pediatric weight management program.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
12 Years 至 18 Years(Child, Adult)
性别
All
接受健康志愿者

入选标准

  • Phone screening
  • Approval to participate in a weight management program from the child's pediatrician
  • Children between the ages of 12 and 18 years
  • Children overweight (>85th-<95th BMI percentile) or obese (>95th BMI percentile)

排除标准

  • Children with evidence of significant cardiovascular disease or cardiac arrhythmias
  • Children with liver disease
  • Children on chronic use of medications including diuretics, steroids and adrenergic-stimulating agents
  • Children with emotional problems such as clinical depression or other diagnosed psychological condition and currently use prescription medication for psychological conditions
  • Children with evidence of family and/or medical neglect or physical, mental or sexual child abuse

结局指标

主要结局

weight loss

时间窗: 12 weeks

Body weight will be measured at baseline and at 12-weeks. Mean percentage weight change will be assessed following the 12-week intervention.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Connie Tompkins, PhD

Assistant Professor

University of Vermont

研究点 (2)

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