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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT04910321
Other study ID # 20201221ZJS001
Secondary ID
Status Active, not recruiting
Phase
First received
Last updated
Start date December 30, 2020
Est. completion date December 31, 2029

Study information

Verified date April 2022
Source Westlake University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

The Hangzhou Hospital Staff Cohort (HHSC) is a prospective cohort study among staffs from three hospitals located in Hangzhou, China, including the Hangzhou First People's Hospital, Hangzhou Women's Hospital, and Hangzhou Red Cross Hospital. Participants recruitment and baseline survey including anthropometric, lifestyle and clinical measurement, as well as biological samples collection are initiated in January 2021. Recruited hospital staff are followed up every year during the medical examination organized by their employer. The primary aim of the HHSC study is to investigate the prospective associations of diet, physical activities, sleep, and other lifestyle factors with the long-term metabolic health of the hospital staffs. The secondary aim of the HHSC study is to integrate multi-omics data including genomics, metabolomics, proteomics and microbiome by a machine learning algorithm, to probe into the complex mediating roles of gene, metabolism and gut microbiota linking lifestyle factors with metabolic health.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 3000
Est. completion date December 31, 2029
Est. primary completion date December 31, 2029
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Participants aged 18 years or older - Serving staffs of designated hospitals Exclusion Criteria: - Participants with cancer - Participants with other serious medical disorders

Study Design


Intervention

Other:
diet, physical activities, sleep
lifestyle factors

Locations

Country Name City State
China Hangzhou First People's Hospital Hangzhou Zhejiang

Sponsors (4)

Lead Sponsor Collaborator
Westlake University First People's Hospital of Hangzhou, Hangzhou Red Cross Hospital, Hangzhou Women's Hospital

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Incidence of type 2 diabetes diagnosed as fasting blood glucose larger than 7.0 mmol/L Fasting blood glucose is measured every year during follow-up 3 years after enrollment
Primary Incidence of type 2 diabetes diagnosed as fasting blood glucose larger than 7.0 mmol/L Fasting blood glucose is measured every year during follow-up 6 years after enrollment
Primary Incidence of type 2 diabetes diagnosed as fasting blood glucose larger than 7.0 mmol/L Fasting blood glucose is measured every year during follow-up 9 years after enrollment
Secondary Change of body mass index Participants' body weight and height was measured to calculate body mass index every year during follow-up Change from baseline at 3 years
Secondary Change of body mass index Participants' body weight and height was measured to calculate body mass index every year during follow-up Change from baseline at 6 years
Secondary Change of body mass index Participants' body weight and height was measured to calculate body mass index every year during follow-up Change from baseline at 9 years
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