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临床试验/NCT01014663
NCT01014663已完成不适用

Comparison of Non-contact Boxing Training and Traditional Therapeutic Exercise on Functional Outcomes in Persons With Parkinson's Disease

University of Indianapolis2 个研究点 分布在 1 个国家目标入组 31 人开始时间: 2009年9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
31
试验地点
2
主要终点
Mobility: Measured with the Timed Up and Go Test; Four-Square Step Test; Six-Minute Walk Test; Berg Balance Scale; Functional Reach Test

研究概览

简要总结

The primary purpose of this study is to compare the effects of a non-traditional boxing training program to a traditional therapeutic exercise program on activity and participation outcomes in persons with Parkinson's disease. Thirty participants will be randomly assigned to participate in either non-contact boxing training or traditional therapeutic exercise for 36 sessions over 12 weeks. Participants will be measured immediately before (pre-test) and after (post-test) the intervention.

详细描述

Physical therapists commonly treat patients with Parkinson's disease. Typical clinical interventions used by physical therapists including strengthening, stretching and aerobic training have been shown to improve function and quality of life of persons with Parkinson's disease. Alternative exercise interventions that incorporate non-traditional concepts, such as tango dance, tai chi and taiji have also been found to lead to improvements in function in persons with Parkinson's disease. It is important that comparisons between different types of exercise programs for persons with Parkinson's disease be explored in order to determine effective options for care.

Here in Indianapolis, Indiana, individuals with Parkinson's disease have a unique opportunity for alternative exercise with the recent development of the popular non-contact boxing training program offered by the Rock Steady Boxing Foundation. Therefore, the purpose of this study is to compare the effects of the non-traditional boxing training program to a traditional therapeutic exercise program on activity and participation outcomes in persons with Parkinson's disease.

Thirty participants with Parkinson's disease will be recruited from Central Indiana. All potential participants will be screened to determine eligibility for the study. Participants who are eligible and give consent will be randomly assigned to participate in either the non-contact boxing training or the traditional therapeutic exercise program for 36 sessions lasting over 12 weeks with 60-90 minutes of exercise each session. Participants will be measured immediately before (pre-test) and after (post-test) the intervention period.

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
Single (Outcomes Assessor)

入排标准

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

入选标准

  • diagnosis of Parkinson's disease
  • currently not receiving physical therapy services
  • medically stable with a physician release stating approval to enter an exercise program
  • independently ambulatory in the home setting with or without the use of an assistive device
  • able to follow at least three step verbal commands
  • available for the entire period of the study
  • have transportation to and from training and measurement sessions

排除标准

  • preexisting neurological conditions other than Parkinson's disease
  • current musculoskeletal conditions that would limit participation in either training program
  • significant orthopedic surgery within the past six months
  • past brain surgery or brain stimulator implant
  • currently known pregnant
  • pre-existing cardiovascular conditioner that would prohibit participation in an exercise program

结局指标

主要结局

Mobility: Measured with the Timed Up and Go Test; Four-Square Step Test; Six-Minute Walk Test; Berg Balance Scale; Functional Reach Test

时间窗: Each outcome measures is assessed at pre-test (immediately before intervention), post-test (immediately after the 12 week intervention).

次要结局

  • Participation: measured with the Activities Specific Balance Confidence Scale and the Parkinson's disease Quality of Life Scale(Each outcome measures is assessed at pre-test (immediately before intervention), post-test (immediately after the 12 week intervention).)

研究者

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

Stephanie Miller

Associate Professor

University of Indianapolis

研究点 (2)

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