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The China National COPD Screening Program

The National Chronic Obstructive Pulmonary Disease Screening Program in China

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05480176
Enrollment
800000
Registered
2022-07-29
Start date
2021-10-09
Completion date
2025-12-31
Last updated
2022-07-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic Obstructive Pulmonary Disease

Keywords

Chronic Obstructive Pulmonary Disease, Screening, Spirometry

Brief summary

The national COPD screening program is in a cross-sectional manner at the baseline, planning to recruit a total of 800,000 participants from 160 districts or counties (5,000 for each site on average) from 31 provinces, autonomous regions or municipalities directly under the central government of China. The filtered COPD high-risk population and confirmed COPD patients will be managed and followed up according to the standardized clinical guidelines. The major aims of the program are to estimate the prevalences of COPD high-risk population and under- or miss- diagnosed COPD patients, and to manage the development and outcomes of the disease.

Interventions

OTHERComprehensive intervention and management Ⅰ

Mainly health advisory.

OTHERComprehensive intervention and management Ⅱ

Health advisory and regular follow-ups.

OTHERComprehensive intervention and management Ⅲ

Pharmaceutical and non-pharmaceutical (e.g. health advisory, rehabilitation, etc.) interventions according to standardized clinical guidelines, with regular follow-ups.

Sponsors

China-Japan Friendship Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
35 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* adults aged between 35 and 75 years; * residents living in the survey area with more than 6 months in the past year.

Exclusion criteria

* experienced myocardial infarction, stroke or shock in the past 3 months; * experienced severe cardiac insufficiency, severe arrhythmia or unstable angina pectoris in the past 4 weeks; * experienced massive hemoptysis in the past 4 weeks; * received chest, abdominal or ophthalmic surgery in the past 3 months; * have mental disorders (e.g. auditory hallucinations, visual hallucinations, taking antipsychotics, seizures requiring medication, etc.); * have cognitive impairment (e.g. dementia, comprehension impairment, etc.); * have uncontrolled hypertension (i.e. systolic blood pressure \> 200 mmHg, diastolic blood pressure \> 100 mmHg); * present with heart rate \>120 beats/min; * have aortic aneurysm; * have severe hyperthyroidism; * are pregnant or lactating women; * experienced respiratory infectious diseases (e.g. tuberculosis, influenza, etc.) in the past month.

Design outcomes

Primary

MeasureTime frameDescription
Lung function2 yearsThe changes of lung function (e.g. FEV1, FVC, FEV1/FVC, etc.) (P.S.: it is hard to assume that the lung function would be improved or decling, especially for the pre- or early-COPD population)

Secondary

MeasureTime frameDescription
Respiratory symptoms2 yearsThe appearance frequencies of respiratory symptoms (e.g. cough, sputum, wheeze, dyspnea, etc.)
Exacerbations2 yearsThe numbers of exacerbations (e.g. emergency department visit, hospital admission, etc.) that related to COPD

Countries

China

Contacts

Primary ContactJieping LEI, Ph.D.
jiepinglei@126.com010-84206408

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 8, 2026