Skip to content

Chinese Population Health and Multimorbidity Study

The Chinese Population Health and Multimorbidity Study: Baseline Survey, and Follow-up Investigation

Status
Enrolling by invitation
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07026370
Acronym
CPHMS
Enrollment
50991
Registered
2025-06-18
Start date
2011-01-01
Completion date
2027-06-30
Last updated
2026-03-05

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

Conditions

Cardiovascular and Cerebrovascular Diseases, Chronic Respiratory Diseases, Endocrine and Metabolic Diseases, Malignant Tumors, Multimorbidities

Keywords

Multimorbidities, Epidemiological survey, Cohort, Population medicine

Brief summary

The Chinese Population Health and Multimorbidity Study (CPHMS; initially named China Pulmonary Health Study, CPHS) was a large-scale epidemiological survey designed to investigate the pulmonary health of Chinese adults aged 20 years or older leveraging a multistage stratified sampling scheme between 2011 and 2014 in mainland China. Briefly, a total number of 57,779 local residents were recruited from 10 representative provinces and municipalities and were invited to participate in the study. A final number of 50,991 adults who met the major inclusion criteria could be considered in further analyses. In order to investigate the changes of pulmonary health and disease status (e.g. occurrence and development of chronic respiratory diseases and other important relevant multimorbidities, lung function indices, etc.) and corresponding impact factors in the CPHMS study population, we plan to initiate the first round of follow-up investigation between 2025 and 2027 (planned) , i.e. more than 10 years after the baseline survey.

Interventions

None listed

Sponsors

China-Japan Friendship Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
20 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* (1) the individuals who participated in the CPHMS baseline survey; * (2) their ID number and phone number are available; * (3) sign the informed consent.

Exclusion criteria

* (1) incapable of taking pre- and post-bronchodilator spirometry tests; * (2) request to withdraw the informed consent; * (3) terminate due to medical or ethical considerations judged by the investigators and/or ethics committee.

Design outcomes

Primary

MeasureTime frameDescription
Occurrence of multimorbiditiesSince the year of baseline survey till the year of 2025 and 2027 (the first round of follow-up investigation of CPHMS)Occurrence of chronic respiratory diseases, cardiovascular and cerebrovascular diseases, malignant tumors, and/or metabolic diseases, etc.

Secondary

MeasureTime frameDescription
Changes of lung function, forced expiratory volume in one second (FEV1)Since the year of baseline survey till the year of 2025 and 2027 (the first round of follow-up investigation of CPHMS)Changes of pre- and post-bronchodilator spirometry test indices, FEV1
Changes of lung function, forced vital capacity (FVC)Since the year of baseline survey till the year of 2025 and 2027 (the first round of follow-up investigation of CPHMS)Changes of pre- and post-bronchodilator spirometry test indices, FVC
Changes of lung function, FEV1/FVCSince the year of baseline survey till the year of 2025 and 2027 (the first round of follow-up investigation of CPHMS)Changes of pre- and post-bronchodilator spirometry test indices, FEV1/FVC
Changes of lung function, the percentage of measured FEV1 value to the predicted value (FEV1%pred)Since the year of baseline survey till the year of 2025 and 2027 (the first round of follow-up investigation of CPHMS)Changes of pre- and post-bronchodilator spirometry test indices, FEV1%pred

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 6, 2026