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临床试验/NCT03702517
NCT03702517已完成不适用

Efficacy of Lateral Stair Walking Training in Patients With Chronic Stroke: a Pilot Randomized Controlled Study

Kaohsiung Veterans General Hospital.0 个研究点目标入组 30 人开始时间: 2016年1月3日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
30
主要终点
muscle strength

研究概览

简要总结

The experimental group received 15 minutes of lateral stair walking exercise and 30 minutes of traditional physiotherapy (strengthening exercise, balance training and gait training) each time.

The measures were done by one experience physical therapist (not involve in the intervention) before receiving the intervention and at weeks four, eight, and twelve. It took 45 minutes for each subject to complete all measures each time.

详细描述

For lateral stair walking training, the dynamic stair trainer features four steps. The height can be adjusted from 0 to 16.5 centimeters, the stair was 0.74 m in width, with each step being 16 cm deep and 10 cm long. The experimental group received different heights of lateral stair walking training according to the patients' ability. The patients went up the stairs with the affected leg up first and they went down stairs with the sound leg leading first. For safety, the subjects held a handrail during the lateral stair walking exercise. The control group received traditional physiotherapy (strengthening exercise, balance training and gait training) for 30 minutes. Both the experimental group and control group received the intervention once a week for 12 weeks. All the interventions were done by the same physical therapist.

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 (Investigator)

入排标准

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

入选标准

  • •subjects who were diagnosed with stroke within 6 months to 6 years by a neurologist or physiatrists,
  • •computerized tomography scan or magnetic resonance imaging scan showed unilateral brain damage,
  • •no obvious cognitive impairment,
  • •no serious bone and joint problems
  • •could follow the instructions and steps of the experiment
  • •walked 15 meters independently.

排除标准

  • •cognitively impaired,
  • •visually impairedor
  • •unable to receive training due to other diseases (lung, heart, gastrointestinal tract, bone and muscle, nervous system etc.)

研究组 & 干预措施

lateral stair walking exercise

Experimental

The experimental group received 15 minutes of lateral stair walking exercise

干预措施: lateral stair walking exercise (Device)

lateral stair walking exercise

Experimental

The experimental group received 15 minutes of lateral stair walking exercise

干预措施: traditional physiotherapy (Device)

traditional physiotherapy

Active Comparator

strengthening exercise, balance training and gait training

干预措施: lateral stair walking exercise (Device)

traditional physiotherapy

Active Comparator

strengthening exercise, balance training and gait training

干预措施: traditional physiotherapy (Device)

结局指标

主要结局

muscle strength

时间窗: Both the experimental group and control group received the intervention once a week for 12 weeks.The measures were done by one experience physical therapist before receiving the intervention and at weeks four, eight, and twelve.

Mycroft 3 hand-held dynamometer18: It has good reliability. Muscle strength can be measured in Newton's. It is applied in assessing the muscle strength of subjects.

次要结局

  • Timed up and go test (TUG)(Both the experimental group and control group received the intervention once a week for 12 weeks.The measures were done by one experience physical therapist before receiving the intervention and at weeks four, eight, and twelve.)
  • The Brunnstrom motor recovery stage of Lower extremity (LE):(Both the experimental group and control group received the intervention once a week for 12 weeks.The measures were done by one experience physical therapist before receiving the intervention and at weeks four, eight, and twelve.)
  • Barthel index for Activities of Daily Living (ADL)(Both the experimental group and control group received the intervention once a week for 12 weeks.The measures were done by one experience physical therapist before receiving the intervention and at weeks four, eight, and twelve.)
  • Reha Gait® for gait parameters.(Both the experimental group and control group received the intervention once a week for 12 weeks.The measures were done by one experience physical therapist before receiving the intervention and at weeks four, eight, and twelve.)
  • active range of motion (AROM)(Both the experimental group and control group received the intervention once a week for 12 weeks.The measures were done by one experience physical therapist before receiving the intervention and at weeks four, eight, and twelve.)
  • The postural assessment scale for stroke patients (PASS)(Both the experimental group and control group received the intervention once a week for 12 weeks.The measures were done by one experience physical therapist before receiving the intervention and at weeks four, eight, and twelve.)
  • Passive range of motion (PROM)(Both the experimental group and control group received the intervention once a week for 12 weeks.The measures were done by one experience physical therapist before receiving the intervention and at weeks four, eight, and twelve.)
  • Fugal-Meyer assessment for Lower extremity,(Both the experimental group and control group received the intervention once a week for 12 weeks.The measures were done by one experience physical therapist before receiving the intervention and at weeks four, eight, and twelve.)

研究者

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

Wan-Yun Huang

Physical Therapist, Principal Investigator, Assistant Professor)

Kaohsiung Veterans General Hospital.

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