- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03799653
A Nurse Cohort Study in Xiamen, China
A Prospective Cohort Study of Common Chronic Diseases on Nurses in Xiamen, China: Nurse Cohort Study Xiamen (NCSX)
Study Overview
Detailed Description
Objectives: To establish a cohort of about 10,000 registered nurses (aged 20 or over) in Xiamen, China; to describe the baseline major risk factors; to analyze their interrelationships; and to examine the risks of incidence and progression of major chronic diseases, such as hypertension, stroke, CKD and cancers, and all-cause and cause-specific mortality by different levels of the risk factors after about 5 years follow-up.
Design: A prospective cohort study. Setting: 7 public hospitals in Xiamen, China. Participants: About 10,000 registered nurses (aged 20 or over) who work in public hospitals in Xiamen, China.
Main outcome: Incidences of common chronic diseases, such as CVD, diabetes, chronic kidney disease, and cancers; progression of these diseases; all cause and specific-cause mortality.
Hypothesis: Relative risks of major risk factors. Results of the study should have strong impact on prevention and control of these diseases and promoting nurses'health in the local population.
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Zhibin Li, Ph.D.
- Phone Number: 86592-2137364
- Email: zhibinli33@hotmail.com
Study Contact Backup
- Name: Haihua Zhu, Master
- Phone Number: 86592-2137278
Study Locations
-
-
Fujian
-
Xiamen, Fujian, China, 361003
- Recruiting
- The First Affiliated Hospital of Xiamen University
-
Contact:
- Zhibin Li, Ph.D.
- Phone Number: 86592-2137364
- Email: zhibinli33@hotmail.com
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Sampling Method
Study Population
- Registered nurses in public hospitals in Xiamen, China;
- Aged 20 years or over and living in Xiamen for at least 1 year and will not move out of Xiamen for at least 5 years;
Description
Inclusion Criteria:
- Registered nurses of public hospitals in Xiamen, China;
- aged 20 years or over;
- Working in the public hospitals for at least 1 year;
- Signed the informed consent and agreed to participate in the study;
- Assuming not moved out of Xiamen for at least 5 years;
Exclusion Criteria:
- who are unambulatory;
- who are receiving treatment modalities, which , if omitted, may result in immediate life threatening risk such as chemotherapy or radiotherapy for cancer, or dialysis for renal failure.
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
Nurses
All subjects are registered nurses in Xiamen, China
|
This is a prospective observational study, and there is no intervention.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Incidence rate
Time Frame: 2019.1.21-2024.12.31
|
The incidence rates of common chronic diseases, such as hypertension, The stroke, CKD and cancers
|
2019.1.21-2024.12.31
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Mortality
Time Frame: 2019.1.21-2024.12.31
|
All-cause and cause-specific mortality
|
2019.1.21-2024.12.31
|
Collaborators and Investigators
Investigators
- Study Chair: Weihua Li, Ph.D., The First Affiliated Hospital of Xiamen University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- KYH2019-002
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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.
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