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临床试验/NCT03417908
NCT03417908Unknown不适用

Effects of Proprioceptive Neuromuscular Facilitation Applied to the Accessory Respiratory Muscles on Functional and Electromyographic Parameters in Patients With and Without COPD

Universidade Federal do Pampa2 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2017年12月4日最近更新:
适应症

试验速览

阶段
不适用
发起方
入组人数
60
试验地点
2
主要终点
Change in inspiratory capacity

研究概览

简要总结

To evaluate the activation of accessory respiratory muscles and the effects of stretching these muscles in patients with COPD.

详细描述

All subjects (sixty men) will perform spirometry, measure of inspiratory capacity (IC) and maximal inspiratory and expiratory pressures (MIP and MEP). Baseline blood pressure (BP), respiratory rate (RR), heart rate (HR), sensation of dyspnea (Borg Scale) and oxygen saturation (pulse oximetry, SpO2) will be collected prior to the performance of pulmonary function tests.

The electrical activity of the scalene (ESC), sternocleidomastoid (SCM) and external intercostal muscles (INTER) will be measured by surface electromyography (sEMG) at rest and during the maneuvers of IC, MIP and MEP.

Control group: The control group will perform isotonic concentric contraction of the biceps (two sets of five push-ups elbow in both arms) with the individual sitting in a chair with back support.

Intervention group: The contract-relax method of proprioceptive neuromuscular facilitation (PNF) technique will be used for stretching of ESC, ECM and external intercostals muscles. The contraction of agonist muscles against the resistance imposed by the physiotherapist (isometric contraction) is maintained for 6 seconds. After that, the patient will be asked to relax the muscles for 6 seconds without losing range of motion, and then the muscle will be lengthened. This procedure is repeated until the maximum amplitude of motion of the neck and upper limb is reached. The stretching will be performed on the right and left sides of the body.

Statistical analysis will be carried out with the Statistical Package for the Social Sciences, version 18.0 (SPSS Inc., Chicago, IL, USA). Normality of data distribution will be assessed by the Shapiro-Wilk test.

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 (Participant)

入排标准

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

入选标准

  • Control group: Men without respiratory symptoms and lung disease, with normal spirometry.
  • Interventional group: Men diagnosed with severe to very severe COPD (forced expiratory volume in one second / forced vital capacity - FEV1/FVC <0.7 and FEV1 <50% predicted after bronchodilator use); clinically stable over the past 4 weeks.

排除标准

  • History of fracture in the spine and / or upper limb
  • Herniated disc
  • Connective tissue disease
  • Ischemic heart disease or uncontrolled hypertension
  • Obesity (BMI> 30 kg/m2)
  • Aortic aneurysm
  • Recent abdominal or thoracic surgery
  • Retinal detachment

结局指标

主要结局

Change in inspiratory capacity

时间窗: One day

Change in inspiratory capacity

次要结局

  • Change in electromyographic activity of accessory respiratory muscles(One Day)
  • Change in maximal respiratory pressure (MIP and MEP)(One day)

研究者

发起方
Universidade Federal do Pampa
申办方类型
Other
责任方
Principal Investigator
主要研究者

Anelise Dumke

Professor

Universidade Federal do Pampa

研究点 (2)

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