跳至主要内容
临床试验/NCT06776731
NCT06776731招募中不适用

Hyperoxia During Outpatient Pulmonary Rehabilitation in Chronic Lung Disease - Does it Matter?

Eastern Switzerland University of Applied Sciences2 个研究点 分布在 1 个国家目标入组 32 人开始时间: 2025年1月6日最近更新:
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
2
主要终点
Constant Work Rate Exercise Test Endurance time

研究概览

简要总结

Chronic obstructive pulmonary disease (COPD) is a global burden. Treatment options have improved in recent years, pulmonary rehabilitation plays a key role. Oxygen therapy is recommended in patients with a low saturation at rest, but no clear guidance is given for patients who desaturate during exercise. The effect of ambulatory oxygen during exercise is not yet completely understood, especially in those patients with exercise-induced desaturation.

Aim: Evaluate the effect of supplemental oxygen therapy during a 3-months long ambulatory pulmonary rehabilitation program on exercise endurance. Patients will either receive supplemental oxygen therapy or room air during exercise training.

Methods: A total of 32 patients with a confirmed diagnosis of COPD undergoing pulmonary rehabilitation will be included (male and female : aged ≥ 18 years; stable condition > 3 weeks (e.g. no exacerbations); resting oxygen saturation (SpO2) ≥ 88% and exercise induced hypoxemia defined by a fall in SpO2 by ≥ 4% and/ or below 90% during a 6-minute walking test). 3-months comprehensive PR for both intervention and control group including: education and awareness, instruction on inhalation therapies, smoking cessation counselling, respiratory and skeletal muscle training in groups, guided walks / cycle ergometer training. The intervention group will be trained using SSOT and the control group will receive sham air (ambient air). Patients and assessors will be blinded. Between group difference in cycling constant work rate exercise test (CWRET) time from baseline to 3 months SSOT (5l/min) vs ambient air will be the primary outcome of this study.

Data will be summarized by means (SD) and medians (quartiles) for normal and non-normal distributions. Effects of treatment will be evaluated by mean differences with 95% confidence intervals, T-tests or Wilcoxon matched pair tests as appropriate. A p-value threshold of <0.05 or a confidence interval not including zero will be considered as statistically significant. Analyses will be performed according to the intention to treat principle.

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, Care Provider)

入排标准

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

入选标准

  • We will include male and female with a confirmed diagnosis of COPD (post-bronchodilator forced expiratory volume in one second (FEV1) / forced vital capacity (FVC) ratio of <0.7; a greater than 10 pack-year smoking history)
  • undergoing pulmonary rehabilitation
  • aged ≥ 18 years
  • stable condition > 3 weeks (e.g. no exacerbations)
  • resting oxygen saturation (SpO2) ≥ 88%
  • exercise induced hypoxemia defined by a fall in SpO2 by ≥ 4% and/ or below 90% during a 6MWT
  • informed consent as documented by signature.

排除标准

  • Severe daytime resting hypoxemia (SpO2 < 88% )
  • long-term oxygen therapy, unstable condition requiring adaptation of pharmacologic and other treatment modalities or requirement of intensive care or relevant severe concomitant disease
  • inability to follow the procedures of the study, e.g. due to language problems, psychological disorders, neurological or orthopedic problems with walking disability or inability to ride a bicycle
  • women who are pregnant or breast feeding; enrolment in another clinical trial with active treatment.

研究组 & 干预措施

Endurance training with 5l/ min room air applied via nasal cannula.

Placebo Comparator

Endurance training with 5l/ min room air applied via nasal cannula with an Everflo oxygen concentrator.

干预措施: Room Air (placebo) (Other)

Endurance training with 5l/ min Oxygen Therapy applied via nasal cannula.

Experimental

Endurance training with 5l/ min Oxygen Therapy applied via nasal cannula with an Everflo oxygen concentrator..

干预措施: Oxygen (Other)

结局指标

主要结局

Constant Work Rate Exercise Test Endurance time

时间窗: 3 months

Constant Work Rate Exercise Test Endurance time measured with Constant Work Rate Exercise Test (CWRET) (75% of the maximal work rate from the maximal ramp exercise test)

Constant Work Rate Exercise Test Endurance time

时间窗: 3 months

Constant Work Rate Exercise Test Endurance time measured with Constant Work Rate Exercise Test (CWRET) (75% of the maximal work rate from the maximal ramp exercise test)

次要结局

  • SpO2(3 months)
  • Heart rate(3 months)
  • Borg scale(3 months)
  • Constant Work Rate Exercise Test Endurance time(6 months)
  • 6 minute walk test (6MWT)(3 months)
  • 6 minute walk test (6MWT)(3 months)
  • Heart rate(3 months)
  • SpO2(3 months)
  • Borg scale(3 months)
  • Constant Work Rate Exercise Test Endurance time(6 months)

研究者

发起方
Eastern Switzerland University of Applied Sciences
申办方类型
Other
责任方
Sponsor

研究点 (2)

Loading locations...

相似试验