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临床试验/NCT01410279
NCT01410279Unknown不适用

Inspiratory Muscle Training Effect on the Functional Capacity and the Quality of Life in Chronic Pulmonary Hypertension

Hospital de Clinicas de Porto Alegre2 个研究点 分布在 1 个国家目标入组 34 人开始时间: 2009年12月最近更新:
适应症

试验速览

阶段
不适用
入组人数
34
试验地点
2
主要终点
The distance traveled in meters in the six minutes walk test after 8 weeks the inspiratory muscle training

研究概览

简要总结

The purpose of this study is evaluate the effect the inspiratory muscle training on the functional capacity of patients with pulmonary hypertension.

详细描述

Pulmonary hypertension (PH) is a syndrome, in the case of hemodynamic alteration of a number of diseases and processes, such as the progressive increase in pulmonary vascular resistance, right heart failure and early death. Frequently patients with PH have reduced functional capacity, quality of life and survival. It was demonstrated recently that patients with HP also have inspiratory muscle weakness, possibly further increase the fatigue and dyspnea during exercise. To meet this need, inspiratory muscle training can lead to significant improvement in respiratory muscle strength, exercise tolerance and dyspnea, thus resulting in reduction of discomfort during activities of daily living, increase in exercise capacity and improved quality of life in different situations.

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 (Outcomes Assessor)

入排标准

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

入选标准

  • Clinical diagnosis pulmonary hypertension
  • World Health Organization (WHO) functional class II to IV
  • inspiratory muscle weakness

排除标准

  • chronic obstructive pulmonary disease
  • orthopedic and neurological disease

结局指标

主要结局

The distance traveled in meters in the six minutes walk test after 8 weeks the inspiratory muscle training

时间窗: patients will be monitored throughout the training protocol for 8 weeks

次要结局

  • Increase in score of quality of life questionnaire after 8 weeks the inspiratory muscle training(patients will be monitored throughout the training protocol for 8 weeks)

研究者

申办方类型
Other

研究点 (2)

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