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临床试验/NCT02479373
NCT02479373已完成不适用

"Joint Fitness": A Double-Armed Controlled Intervention to Assess the Safety and Effectiveness of Resistance Exercise Training on Muscle, Bone, Strength, Symptoms, Quality of Life and Biological Parameters in Children and Young Adults With JIA

Johns Hopkins University2 个研究点 分布在 1 个国家目标入组 33 人开始时间: 2012年7月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
33
试验地点
2
主要终点
Change in BMI

研究概览

简要总结

This research is being done to see if resistance exercise (RE) is safe and has a positive effect on children and young adults with juvenile idiopathic arthritis (JIA).

JIA is an inflammatory autoimmune disease that can cause severe impairment and disability. JIA can cause bone loss and decreased muscle strength. The medications used to treat JIA can also have negative effects on growth and development, strength, and ability to function. RE is performing movements in a slow and controlled fashion (i.e., no speeding up or using force in the lifting and lowering of the weight) to lessen force on the joints and tissues. This study will be using Ren-Ex exercise equipment to perform RE.

Currently the American College of Rheumatology recommends exercise for patients with arthritis. This exercise includes range of motion exercise to protect joint mobility as well as low resistance and aerobic exercise (AE) to protect muscle mass, bone health, and fitness. However, a recent study showed no major differences in functionality or quality of life between patients who performed AE and those who did not perform AE. There is a need for more data on the impact of RE on children with JIA. Children and young adults aged 10 to 21 with juvenile idiopathic arthritis may join.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Supportive Care

入排标准

年龄范围
10 Years 至 21 Years(Child, Adult)
性别
All
接受健康志愿者

入选标准

  • American College of Rheumatology criteria for polyarticular JIA
  • Stable medical therapy

排除标准

  • Non-English speaking
  • Pregnancy
  • Currently breast feeding
  • Cognitive impairment as determined by PI (patient is not responsible for making their own health care decisions)

结局指标

主要结局

Change in BMI

时间窗: Baseline and 12 weeks

Change in Lower and upper extremity strength testing

时间窗: Baseline and 12 weeks

Isokinetic strength testing with a Biodex dynamometer to measure peak torque

Change in Total Body Dual-Emission X-ray Absorptiometry (DEXA) Scan

时间窗: Baseline and 12 weeks

Total and lean body mass and fat mass will be determined

次要结局

  • Change in Erythrocyte sedimentation rate (ESR)(Baseline and 12 weeks)
  • Number of Participants with Adverse Events as a Measure of Safety and Tolerability(Baseline and 12 weeks)
  • Change in Quality of Life(Baseline and 12 weeks)
  • Change in C-reactive protein (CRP)(Baseline and 12 weeks)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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