Chinese Population Health and Multimorbidity Study (CPHMS)

March 4, 2026 updated by: Jieping LEI, Ph.D., China-Japan Friendship Hospital

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

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.

Study Overview

Study Type

Observational

Enrollment (Estimated)

50991

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Beijing Municipality
      • Beijing, Beijing Municipality, China, 100029
        • China-Japan Friendship Hospital

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Sampling Method

Non-Probability Sample

Study Population

A total number of 50,991 adults aged 20 years or older from 10 representative provinces and municipalities of China participated in the CPHMS baseline survey between 2011 and 2014. In the follow-up investigation, ideally all the baseline participants should be contacted.

Description

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.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Occurrence of multimorbidities
Time Frame: Since 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.
Since the year of baseline survey till the year of 2025 and 2027 (the first round of follow-up investigation of CPHMS)

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Changes of lung function, forced expiratory volume in one second (FEV1)
Time Frame: 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
Since the year of baseline survey till the year of 2025 and 2027 (the first round of follow-up investigation of CPHMS)
Changes of lung function, forced vital capacity (FVC)
Time Frame: 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
Since the year of baseline survey till the year of 2025 and 2027 (the first round of follow-up investigation of CPHMS)
Changes of lung function, FEV1/FVC
Time Frame: 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/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 lung function, the percentage of measured FEV1 value to the predicted value (FEV1%pred)
Time Frame: 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
Since the year of baseline survey till the year of 2025 and 2027 (the first round of follow-up investigation of CPHMS)

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

January 1, 2011

Primary Completion (Estimated)

June 30, 2027

Study Completion (Estimated)

June 30, 2027

Study Registration Dates

First Submitted

May 30, 2025

First Submitted That Met QC Criteria

June 10, 2025

First Posted (Actual)

June 18, 2025

Study Record Updates

Last Update Posted (Actual)

March 5, 2026

Last Update Submitted That Met QC Criteria

March 4, 2026

Last Verified

March 1, 2026

More Information

Terms related to this study

Other Study ID Numbers

  • 2022-ZHCH330-01 (Other Grant/Funding Number: Chinese Academy of Medical Sciences)
  • 2016YFC1303900 (Other Grant/Funding Number: Ministry of Science and Technology of P. R. China)
  • 201002008 (Other Grant/Funding Number: Ministry of Health of P. R. China)
  • 2023FY100600 (Other Grant/Funding Number: Ministry of Science and Technology of P. R. China)

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

Clinical Trials on Malignant Tumors

Subscribe