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临床试验/NCT01056081
NCT01056081已完成3 期

Inspiratory Muscle Training for Patients With Chronic Obstructive Pulmonary Disease Undergoing a Pulmonary Rehabilitation Program

Faculdade Evangelica do Parana0 个研究点目标入组 19 人开始时间: 2006年4月1日最近更新:
适应症

试验速览

阶段
3 期
状态
已完成
发起方
入组人数
19
主要终点
Inspiratory muscle strength

研究概览

简要总结

Uncertainty persists regarding the usefulness of incorporating inspiratory muscle training (IMT) in pulmonary rehabilitation programs for patients with chronic obstructive pulmonary disease. In this study the investigators investigate whether IMT associated with exercise training would be better than exercise training alone, with regard to exercise capacity, inspiratory muscle strength and dyspnea.

详细描述

Study design: A double-blind parallel controlled trial Setting: outpatient clinic Inclusion criteria: Subjects between 40 and 75 years of age referred by a physician to the Pulmonary Rehabilitation Program, with a clinical and spirometric diagnosis of moderate to severe COPD according to the Global Initiative for Chronic Obstructive Lung Disease (GOLD).

Outcome measurements: Inspiratory muscle strength (using maximal inspiratory pressure, MIP), exercise capacity (using six-minute walk test) and dyspnea were measured.

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
40 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Subjects with a clinical and spirometric diagnosis of moderate to severe COPD according to the Global Initiative for Chronic Obstructive Lung Disease (GOLD)
  • In a stable condition (without exacerbations or infections for at least a month)
  • Had to be former smokers (> 6 months without smoking)
  • subjects referred by a physician to the Pulmonary Rehabilitation Program

排除标准

  • Subjects with a known history of asthma, or severe and/or unstable heart disease or any other pathological condition that could impair their physical activities

结局指标

主要结局

Inspiratory muscle strength

时间窗: 8 weeks

次要结局

  • Exercise capacity(8 weeks)
  • Dyspnea(8 weeks)

研究者

发起方
Faculdade Evangelica do Parana
申办方类型
Other

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