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临床试验/NCT07472738
NCT07472738招募中不适用

An Observational Study for the Investigation and Classification of Treatable Traits in Patients With Chronic Airway Diseases

Beijing Chao Yang Hospital1 个研究点 分布在 1 个国家目标入组 950 人开始时间: 2025年5月7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
950
试验地点
1
主要终点
Distribution of Dyspnea Perception Scores

研究概览

简要总结

This research study focuses on chronic airway diseases, such as Chronic Obstructive Pulmonary Disease (COPD) and asthma. These conditions make it difficult for patients to breathe, but breathing difficulty (dyspnea) is often perceived very differently. Some patients may feel severe distress with mild breathing problems, while others might not notice significant breathing issues even when lung function is poor. This difference in perception is termed "dyspnea perception."

The main goal of this study is to understand how dyspnea perception varies among patients with chronic airway diseases. The investigators aim to determine if patients can be grouped into different subtypes based on the perception of breathing difficulties. The study will also investigate how these subtypes relate to other treatable characteristics, such as blood cell counts, allergy test results, and findings from lung function tests and brain scans.

Approximately 800 patients with COPD or asthma and 150 healthy volunteers will participate. Participants will answer questionnaires, undergo lung function tests, provide blood samples, and a subset will undergo a special brain scan (functional MRI). No new treatments will be assigned; instead, these characteristics will be observed and measured over time.

It is hoped that this study will help doctors better understand chronic airway diseases and lead to more personalized management strategies for patients in the future.

详细描述

Participants: The study aims to enroll approximately 800 patients with physician-diagnosed COPD (according to GOLD 2022 criteria) or asthma (according to GINA 2022 criteria), aged 20-75 years, and 150 age-matched healthy controls.

Interventions/Assessments: No investigational interventions will be assigned. Participants will undergo comprehensive assessments at baseline and follow-up visits, including:

Dyspnea perception measurement (using standardized scales). Spirometry, lung volume, and diffusion capacity tests. Fractional exhaled nitric oxide (FeNO) measurement. Blood tests (including complete blood count, total IgE, allergen screening). Health-related quality of life questionnaires (CAT, mMRC, AQLQ, SGRQ). High-resolution computed tomography (HRCT) of the chest. Functional magnetic resonance imaging (fMRI) of the brain (in a subset of participants).

Data on exacerbations, comorbidities, and current medications will be collected.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

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

入选标准

  • Inclusion Criteria for Chronic Airway Disease Patients:
  • Age 20-75 years.
  • Meets the diagnostic criteria for COPD according to the 2022 GOLD guidelines OR meets the diagnostic criteria for asthma according to the 2022 GINA guidelines.
  • Willing and able to provide informed consent.
  • Inclusion Criteria for Healthy Controls:
  • Age ≥20 years.
  • No history of asthma symptoms or diagnosis of chronic respiratory diseases such as asthma or COPD.
  • Willing and able to provide informed consent and comply with the study protocol.

排除标准

  • (applies to all participants):
  • Respiratory tract infection, COPD acute exacerbation, or asthma acute exacerbation within the past 3 months.
  • Presence of other diseases causing significant lung tissue destruction, such as severe bronchiectasis or tuberculosis.
  • History of thoracic or abdominal surgery within the past 3 months.
  • Heart rate >120 beats per minute.
  • Ongoing anti-tuberculosis treatment.
  • Presence of other severe, uncontrolled systemic diseases.
  • Pregnant or lactating women.

研究组 & 干预措施

Chronic Airway Diseases Cohort

Patients with physician-diagnosed COPD or asthma

干预措施: Comprehensive Clinical Assessment (Other)

Healthy Control Cohort

Age-matched healthy volunteers without chronic respiratory diseases

干预措施: Comprehensive Clinical Assessment (Other)

结局指标

主要结局

Distribution of Dyspnea Perception Scores

时间窗: Baseline

The distribution of dyspnea perception scores at baseline in the chronic airway disease cohort, as measured by the Borg Category-Ratio 10 (CR10) Scale (range 0-10, where higher scores indicate more severe dyspnea) or the Visual Analog Scale (VAS) (range 0-100 mm, where higher scores indicate a worse outcome/greater breathing difficulty).

Clinical Phenotypes Based on Dyspnea Perception

时间窗: Through study completion, an average of 3 years

Identification of distinct clinical phenotypes derived from cluster analysis of dyspnea perception scores in combination with other clinical traits and biomarkers

次要结局

未报告次要终点

研究者

发起方
Beijing Chao Yang Hospital
申办方类型
Other
责任方
Sponsor

研究点 (1)

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