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临床试验/NCT04886843
NCT04886843已完成不适用

The Effects Of Cold Application To The Intact Side In Addition Cross Training With NMES On Dorsiflexor Muscle Strength In Hemiplegia

Istanbul Physical Medicine Rehabilitation Training and Research Hospital2 个研究点 分布在 1 个国家目标入组 25 人开始时间: 2020年1月23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
25
试验地点
2
主要终点
Change of ankle dorsiflexor isometric muscle strength

研究概览

简要总结

The aim of this study is to investigate whether a cold application to the contralateral (affected side) extremity in addition to unilateral neuromuscular electrical stimulation (NMES) application has a facilitating effect on muscle strength in post-stroke hemiplegia patients.

详细描述

In this prospective randomized controlled single-blind study, a total of 25 patients, 16 men, and 9 women were included according to inclusion and exclusion criteria. Patients were randomly assigned to the experimental group (n=12) or the control group (n=13). NMES has applied to the non-affected side ankle dorsiflexors five sessions for a week in both groups. In addition to the experimental group, the cold application was applied on the affected side dorsiflexor muscle skin. The cold application was done on a moist towel for five minutes using a cold pack. A five-minute break was given and a further 5-minute cold application was repeated. The cold application was done simultaneously with NMES. A conventional rehabilitation program was applied to all patients by a physiotherapist. Before and after treatment, both ankle dorsiflexor strength was measured with a force sensor. For force measurements, a force transducer (FC2211-0000-0100-L Compression Load Cell, TE Connectivity company, France) was used. Force transducer signals were received with a data acquisition device (POWERLAB® data acquisition system ADInstruments, Oxford, UK) and evaluated offline on the computer. The measurement values were expressed in kilogram.force (kg.f) and this value was normalized according to body weight.

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
Double (Participant, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 85 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Cases with stroke duration ≥1 month
  • Brunnstrom stage ≥4 for lower limb
  • Unilateral stroke
  • Ability to walk at least 10 m (FAC ≥3)
  • Cooperating with the examination and tests

排除标准

  • Cold allergy
  • Active inflammatory, rheumatological, or infectious disease
  • Presence of lower extremity fracture
  • Severe spasticity (MAS> 3) in ankle dorsiflexors
  • Peripheral nerve lesions such as polyneuropathy, radiculopathy
  • Parent rhythm/conduction block problem in the heart
  • Uncontrollable hypertension (Maxima >140 mmHg, Minima >90 mmHg)
  • Have a contracture on the ankle joint
  • The presence of skin lesions in the application area
  • Finding or suspected active deep vein thrombosis

结局指标

主要结局

Change of ankle dorsiflexor isometric muscle strength

时间窗: Change from Baseline ankle dorsiflexor isometric muscle strength at 6 days

Force transducer used for measuring maximum voluntary ankle dorsiflexion force. The force unit is kilogram.force

次要结局

  • Change of Lower Extremity Brunnstrom Score(Change from Baseline Lower Extremity Brunnstrom Score at 6 days)
  • Change of Modified Ashworth Scale Score(Change from Baseline Modified Ashworth Scale Score at 6 days)
  • Change of Functional Ambulation Scale Score(Change from Baseline Functional Ambulation Scale Score at 6 days)
  • Change of Timed Up and Go Test Score(Change from Baseline Change of Timed Up and Go Test Score at 6 days)

研究者

发起方
Istanbul Physical Medicine Rehabilitation Training and Research Hospital
申办方类型
Other Gov
责任方
Sponsor

研究点 (2)

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