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临床试验/NCT00890669
NCT00890669已完成不适用

Treadmill Walking Training With Additional Body Load Improves Quality of Life in Subjects With Parkinson's Disease

Universidade Federal de Sao Carlos2 个研究点 分布在 1 个国家目标入组 9 人开始时间: 2007年8月1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
9
试验地点
2
主要终点
The quality of life was measured through Parkinson Disease Questionnaire (PDQ-39).

研究概览

简要总结

Parkinson's disease (PD) causes motor and non-motor impairments that affect the quality of life of the subjects. The purpose was to assess the effects of treadmill walking training with additional body load on the quality of life and motor symptoms of the subjects with PD.

Methods: Nine subjects with PD, Hoehn and Yahr stages 2 through 3, not demented and with capability to ambulate independently voluntarily participate in this study. The training program was divided into three phases (A1-B-A2): treadmill training with additional body load (A1), control condition (conventional physical therapy group) (B) and treadmill training with load again (A2). Each phase lasted six weeks. The quality of life and motor symptoms were assessed by PDQ-39 and UPDRS, respectively. Both evaluations and training were performed during on-phase of the medication cycle.

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
51 Years 至 81 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Hoehn and Yahr (H-Y) stages 2 through 3
  • Absence of dementia (Mini-Mental Status Examination - MMSE, defined according to educational level)
  • Capacity to ambulate independently for at least 10 meters

排除标准

  • Change medication (dopaminergic) during the study period
  • Use treadmill for at least six months prior to the study
  • Other neurologic problems or musculoskeletal, cardiovascular and respiratory disease or uncorrected visual deficit that could represent risk and interfere in the accomplishment of the training

结局指标

主要结局

The quality of life was measured through Parkinson Disease Questionnaire (PDQ-39).

时间窗: 4 times, once before treatment, and 3 after each treatment phase.

次要结局

未报告次要终点

研究者

发起方
Universidade Federal de Sao Carlos
申办方类型
Other

研究点 (2)

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