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临床试验/NCT03082924
NCT03082924已完成不适用

Surface Diaphragm EMG Evaluate the Clinical Efficacy of Pulmonary Rehabilitation in Patients With Chronic Obstructive Pulmonary Disease: a Multi Center Prospective Randomized Controlled Study

Zhujiang Hospital1 个研究点 分布在 1 个国家目标入组 500 人开始时间: 2016年7月1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
500
试验地点
1
主要终点
Diaphragmatic function(composite outcome measure)

研究概览

简要总结

Pulmonary rehabilitation is recognized as a core component of the management of individuals with chronic obstructive respiratory disease, which has become first-line treatment besides drug therapy. However, in the current clinical evaluation system of pulmonary rehabilitation, there is still a lack of simple, objective index,which can be monitored at any time.Neural respiratory drive , as an important physiological index, is closely related to the symptoms and the severity of the disease. It may be a sensitive indicator to evaluate the effectiveness of pulmonary rehabilitation. Surface EMGdi can accurately evaluate neural respiratory drive , its detection is non-invasive, simple and safety . In recent years, with the development of signal detection and analysis technology, EMG recording is more stable, but as the related research samples were low, surface diaphragm EMG has not yet the establishment of standardization. Therefore, based on the previous work, the project was carried out in a multicenter randomized controlled study,in which the stable stage of COPD patients were included in different ways of pulmonary rehabilitation training, a comprehensive clinical assessment will be conducted before and after training. Compared with the traditional evaluation methods and standard esophageal diaphragmatic electromyography, surface EMGdi detect the changes of neural respiratory drive in patients with COPD,that can help to explore the application value of surface EMGdi in the assessment of chronic obstructive pulmonary disease with pulmonary rehabilitation, to provide a basis for the promotion of the diaphragm and the optimization of pulmonary rehabilitation program.

详细描述

The patients with COPD will participate in a rehabilitation program for 52 weeks.

Participants in the proposed study will be randomly programmed into one of four intervention groups:

  1. Neither cycle training nor inspiratory muscle training.
  2. Cycle training program alone (performing on calibrated stationary cycle ergometer).
  3. Inspiratory muscle training alone (performing on threshold loading device).
  4. Combined cycle training and inspiratory muscle training(performing on calibrated stationary cycle ergometer and threshold loading device).

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
None

入排标准

年龄范围
40 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients aged over 40 years old.
  • Patients with pulmonary function test of forced expiratory volume at one second(FEV1)/forced vital capacity(FVC) < 70%.
  • Patients in a clinically stable state
  • Patients who signed informed consent.
  • No participation in other pulmonary rehabilitation program within the previous 2 months.

排除标准

  • Patients with signs of an airway infection.
  • Patients with metabolic disease and serious cardiovascular disease.
  • Patients with Multiple pulmonary bulla.
  • Patients with poor compliance.

结局指标

主要结局

Diaphragmatic function(composite outcome measure)

时间窗: Change from baseline in diaphragm electromyogram.(8 weeks later, 26 weeks later, 52 weeks later)

Diaphragmatic function can be assessed by diaphragm electromyogram (EMGdi), which reflect the physiological activity of the diaphragm and indicate functional status of the central drive.

次要结局

  • Degree of dyspnea(composite outcome measure)(Change from baseline in degree of dyspnea.(8 weeks later, 26 weeks later, 52 weeks later))
  • Cardiopulmonary exercise test(composite outcome measure)(Change from baseline in cardiopulmonary exercise test.(8 weeks later, 26 weeks later, 52 weeks later))
  • Inspiratory muscle function(composite outcome measure)(Change from baseline in inspiratory muscle function.(8 weeks later, 26 weeks later, 52 weeks later))
  • Pulmonary Function(composite outcome measure)(Change from baseline in pulmonary function.(8 weeks later, 26 weeks later, 52 weeks later))
  • Exercise capacity(composite outcome measure)(Change from baseline in exercise performance.(8 weeks later, 26 weeks later, 52 weeks later))

研究者

发起方
Zhujiang Hospital
申办方类型
Other
责任方
Sponsor

研究点 (1)

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