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临床试验/NCT03840044
NCT03840044已完成不适用

The Effect of Physical Exercise in a Cold Air Environment on Normal Volunteers and Asthmatic Patients

KU Leuven2 个研究点 分布在 1 个国家目标入组 45 人开始时间: 2019年6月3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
KU Leuven
入组人数
45
试验地点
2
主要终点
Change in Forced Expiratory Volume in 1 seconds (FEV1)

研究概览

简要总结

The purpose of the study is to compare airway physiologic reactions to physical exercise in a cold air environment (-5°C, 60% relative humidity) between normal volunteers and subjects with mild/moderate asthma. For this purpose, the investigators intend to evaluate the effect of a cold air exercise test on the Forced Expiratory Volume in 1 second (FEV1), respiratory symptoms, functional airway integrity, local and systemic inflammation and on the airway microbiome.

This study also features as an exploratory study for a subsequent interventional study in order to establish the feasibility of the cold air exercise protocol and to determine the extent of the effects in subjects with mild/moderate asthma.

详细描述

It is already demonstrated that exercising during cold air exposure and at a high altitude may induce asthmatic symptoms, a variable degree of airway obstruction and increased neutrophilic airway inflammation in asthmatic patients. Therefore, in this project, the investigators want to evaluate the feasibility, of a shorter standardized "cold air exercise test" (a submaximal exercise challenge in a controlled cold air (-5°C, relative humidity 60%) environment) and to compare the respiratory physiologic reactions to physical exercise during cold exposure between healthy volunteers and asthmatic patients. For this purpose, they intend to evaluate the effect of a cold air exercise test on FEV1, respiratory symptoms, functional airway integrity, local and systemic inflammation and on the airway microbiome.

This study features as an exploratory study for a subsequent interventional study, that will assess the protective effect of azithromycin versus placebo on the cold air exercise induced changes in patients with mild/moderate asthma (ALASCAIR2 study). The present preparatory study is needed to standardize the cold air exercise test in a controlled environment so that it would be possible to use it as challenge test in an interventional study and to identify the most appropriate design for such a study.

The primary objective of this study is to compare the proportional change in FEV1, pre to post a 90 minutes submaximal exercise in a cold air environment between healthy volunteers versus mild/moderate asthmatics, calculated as a time-weighted average over the 30 minutes post-exposure.

The primary endpoint is the change in FEV1, calculated as a time-weighted average over the 30 minutes after the cold exercise test. At each time point (pre-exposure, 5' post-exposure, and at 15, 25 and 35 minutes post-exposure), FEV1 (L) will be measured in triplicate.

They want to evaluate whether the exercise test in a cold air environment produces respiratory symptoms (such as nasal discharge or obstruction, dyspnea, cough and/or mucus production, etc.), has an impact on airway integrity (nasal patency, airflow obstruction, lung ventilation inhomogeneity & small airway dysfunction, bronchial hyperreactivity, cough reflex hypersensitivity), induces local or systemic inflammatory changes (biomarkers in nasal fluid, sputum and blood) or changes to the airway microbiome (in nasal fluid and sputum) in healthy volunteers and in mild/moderate asthmatics. The study group also want to compare the observed changes induced by the cold air exercise test between the healthy volunteers and the mild/moderate asthmatics.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Basic Science
盲法
None

入排标准

年龄范围
18 Years 至 60 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

结局指标

主要结局

Change in Forced Expiratory Volume in 1 seconds (FEV1)

时间窗: pre-, 5, 15, 25 and 35 minutes, 24 hours and 1 week post-exposure

Change in FEV1, calculated as a time-weighted average over the 35 minutes after the cold air exercise test and 24 hours and 1 week post-exposure. A maximal fall of 10% will be considered as positive response

次要结局

  • Biomarkers for airway inflammation(Pre-exposure and 24 hours and 1 week post-exposure)
  • Changes in respiratory symptom score(Pre-exposure and immediately, 24 hours and 1 week post-exposure)
  • Bronchial hyperreactivity(Pre-exposure and 1 week post-exposure)
  • Nasal hyperreactivity(Pre-exposure and immediately and 24 hours post-exposure)
  • Airway inflammation(Pre-exposure and 24 hours and 1 week post-exposure)
  • Nasal inflammation(Pre-exposure and immediately and 24 hours post-exposure)
  • Evaluation of the heart rate pattern(Pre-exposure and during the 90 minutes cold air exposure)
  • Changes in microbiome in lung and nose(Pre-exposure and 1 week post-exposure)
  • Determining the exercise capacity(Pre-exposure)
  • Cough hypersensitivity(Pre-exposure and 24 hours and 1 week post-exposure)
  • Cytokine pattern in the airways(Pre-exposure and 24 hours and 1 week post-exposure)
  • Systemic inflammation(Pre-exposure and immediately, 24 hours and 1 week post-exposure)
  • Changes in asthma control(Pre-exposure and immediately, 24 hours and 1 week post-exposure)
  • Biomarkers for systemic inflammation(Pre-exposure and immediately, 24 hours and 1 week post-exposure)

研究者

发起方
KU Leuven
申办方类型
Other
责任方
Principal Investigator
主要研究者

Tatjana Decaesteker

Co-Principal Investigator

KU Leuven

研究点 (2)

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