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临床试验/NCT04481295
NCT04481295招募中不适用

Effect of Pulmonary Rehabilitation Under Different Oxygen Concentration Using High-flow Nasal Cannula

National Hospital Organization Minami Kyoto Hospital1 个研究点 分布在 1 个国家目标入组 32 人开始时间: 2020年7月18日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
32
试验地点
1
主要终点
Change in the six-minutes walking distance prior to and following 4 weeks of pulmonary rehabilitation

研究概览

简要总结

The purpose of this study is to compare the exercise capacity between high SpO2 (Minimum SpO2 94-96%) value during pulmonary rehabilitation and low SpO2 (Minimum SpO2 84-86%) value during pulmonary rehabilitation for the patients with chronic respiratory failure receiving long-term oxygen therapy.

详细描述

In patients with chronic respiratory failure, pulmonary rehabilitation is recognized as an evidence-based treatment in improving exercise capacity, muscle strength, dyspnea, and quality of life. However, optimal SpO2 value during pulmonary rehabilitation in patients with chronic respiratory failure receiving long-term oxygen therapy is unclear.

The present study is randomized to compare the effect of exercise capacity between high SpO2 (Minimum SpO2 94-96%) value during pulmonary rehabilitation and low SpO2 (Minimum SpO2 84-86%) value during pulmonary rehabilitation for the patients with chronic respiratory failure receiving long-term oxygen therapy.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Other
盲法
Single (Participant)

入排标准

年龄范围
20 Years 至 90 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Subjects with chronic respiratory failure receiving long-term oxygen therapy for more than 3 months.

排除标准

  • •Subjects with severe cardiovascular disease, liver disease, neurological disease, and renal failure.
  • •Subjects with a history of hospitalization for pneumonia or exacerbation of respiratory failure within the last month.
  • •Subjects with changes in LTOT prescription flow within the last month
  • •Subjects who cannot undergo pulmonary rehabilitation due to severe heart failure, arteriosclerosis obliterans or spinal disease.

研究组 & 干预措施

High SpO2 group

Active Comparator

In this group, patients have undergone 4 weeks of pulmonary rehabilitation under the HFNC (FIO2 value that the minimum SpO2 value during pulmonary rehabilitation is 94-96%, and a flow of 10 L/min).

干预措施: High-flow nasal cannula (Other)

Low SpO2 group

Active Comparator

In this group, patients have undergone 4 weeks of pulmonary rehabilitation under the HFNC (FIO2 value that the minimum SpO2 value during pulmonary rehabilitation is 84-86%, and a flow of 10 L/min).

干预措施: Low SpO2 (Other)

结局指标

主要结局

Change in the six-minutes walking distance prior to and following 4 weeks of pulmonary rehabilitation

时间窗: four weeks

次要结局

  • Change in the nutritional status (body mass index(kg/m2) et.) prior to and following 4 weeks of pulmonary rehabilitation(four weeks)
  • Change in the six-minutes walking test (lowest SpO2 value etc.) prior to and following 4 weeks of pulmonary rehabilitation(four weeks)
  • Change in the body composition measured by InBody (muscle mass et.) prior to and following 4 weeks of pulmonary rehabilitation(four weeks)
  • Change in the constant-load exercise test (duration time etc.) prior to and following 4 weeks of pulmonary rehabilitation(four weeks)
  • Change in the incremental-exercise test (Maximum load value etc.) prior to and following 4 weeks of pulmonary rehabilitation(four weeks)
  • Change in the arterial blood gas (PaO2 value etc.) prior to and following 4 weeks of pulmonary rehabilitation(four weeks)
  • Change in the dyspnea (Modified Borg scale) prior to and following 4 weeks of pulmonary rehabilitation(four weeks)
  • Change in the inflammation marker (CRP etc.) prior to and following 4 weeks of pulmonary rehabilitation(four weeks)
  • Change in the sympathetic activity (Plasma catecholamine et.) prior to and following 4 weeks of pulmonary rehabilitation(four weeks)

研究者

发起方
National Hospital Organization Minami Kyoto Hospital
申办方类型
Other
责任方
Sponsor

研究点 (1)

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