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临床试验/NCT05838911
NCT05838911已完成不适用

Does Neuromuscular Electrical Stimulation Benefit the Functional Ability of Elderly Patients With Chronic Obstructive Lung Disease

Beni-Suef University2 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2023年4月2日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
60
试验地点
2
主要终点
Muscle strength measurement

研究概览

简要总结

Background: Patients with COPD often experience skeletal muscle dysfunction. For those who are unable or unwilling to undertake physical training, neuromuscular electrical stimulation (NMES) may provide an alternative method of exercise training.

Objective: To investigate the effects of adding neuromuscular electrical stimulation of gluteus maximus, quadriceps and calf muscles to chest physiotherapy, compared to chest physiotherapy alone, on muscles strength (gluteus max., quadriceps, calf muscles), femoral blood flow physical and pulmonary function in severe COPD Patients.

详细描述

Material and methods

This study include a group of 60 patients (30 males and 30 females) diagnosed with severe COPD), their age is ranged 65-75 years, they will be randomly divided into two groups; study group (A) 30 patients and study group (B) 30 patients. Study group (A): The patients in this group will receive the chest physiotherapy program for 20 min each day, for five days a week for three consecutive weeks. Study group (B): The patients in this group will receive the same chest physiotherapy program combined with neuromuscular electrical stimulation of gluteus max., quadriceps, calf muscles, performed for 30 min /day for five days a week for three consecutive weeks. Femoral blood Flow, gluteus maximus, quadriceps and calf muscles strength and pulmonary function (FEV1/FVC) will be measured for both groups pre and post treatment.

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 (Investigator, Outcomes Assessor)

入排标准

年龄范围
65 Years 至 75 Years(Older Adult)
性别
All
接受健康志愿者

入选标准

  • A diagnosis of COPD with FEV1/FVC <50% predicted as per the GOLD guidelines.
  • Self-reported dyspnea and/or arm fatigue during at least one activity of daily living that required arm exercise.
  • Dyspnea and/or physical activity fatigue were self-reported by the Borg Scale.
  • Before entering in the study, all patients had their pulmonary function optimized with long-acting bronchodilators and corticosteroids.

排除标准

  • • Patients with unstable angina pectoris.
  • Progressive ventricular dysrhythmia.
  • Intermittent claudication.
  • Implanted cardiac pacemakers.
  • Uncontrolled diabetes mellitus.
  • Peripheral vascular disease.

结局指标

主要结局

Muscle strength measurement

时间窗: change from baseline to 3 weeks after intervention and 3 days as a follow-up

To determine the maximal muscle strength the Lafayette manual muscle test system (USER MANUAL) (MMT) Model 01163, White Plains, New York (10602) of gluteus maximus, quadriceps and calf muscles will be measured on right lower limb.

Six-minute walking test (Physical function assessment

时间窗: change from baseline to 3 weeks after intervention and 3 days as a follow-up

The six-minute walking distance (6MWD) was measured according to a standardized protocol. * Subjects were instructed to walk at their own pace along a 34.5-m corridor from one end to the other, covering as much ground as possible in the allotted time. * Subjects were allowed to stop and rest during the test, but they were instructed to resume walking as soon as they felt able to do

Pulmonary function test

时间窗: change from baseline to 3 weeks after intervention and 3 days as a follow-up

Pulmonary capacity and respiratory muscle functions will be assessed using the CPFS/D USB™ 187 Spirometer (Medical Graphics-MGC, St. Paul, MN, USA) with airflow being measured by a 188 calibrated Pitot tube (PreVent, Pneumotach). The participant completed at least three acceptable maximal forced and slow expiratory maneuvers after 15 min the inhalation of 400 mg of salbutamol 190 via a metered-dose inhaler. Forced vital capacity (FVC, L), forced expiratory volume in one second (FEV1, L), FEV1/ FVC, and inspiratory capacity (IC) will be measured according to American Thoracic Society standards

次要结局

  • Blood flow velocimetry measurement(change from baseline to 3 weeks after intervention and 3 days as a follow-up)

研究者

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

Ahmed Samir Abdelkhalik Youssef

lecturer at faculty of physical therapy

Beni-Suef University

研究点 (2)

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