A Lifecourse Map of Diseases in China

November 3, 2022 updated by: Wei Zhao, Shandong University

A Lifecourse Map of Common Diseases and Rare Diseases in China

The purpose of this study is to form a chronological map of common diseases and rare diseases in Chinese population by determining the prevalence of different diseases in each age group.

Study Overview

Status

Recruiting

Intervention / Treatment

Detailed Description

Studying the distribution of various diseases in specific populations can help explore the causes of diseases, elucidate the distribution patterns, and develop preventive and control measures. Based on an overall assessment of prevalence, the combination of relevant results with age at diagnosis for multiple diseases is important for further understanding of the distribution of diseases at the population level. Therefore, this study aims to form a chronological map of common diseases and rare diseases in Chinese population by determining the prevalence of different diseases in each age group, thus providing a reference for more effective prevention, diagnosis and treatment of diseases.

Study Type

Observational

Enrollment (Anticipated)

40000000

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

    • Shandong
      • Jinan, Shandong, China, 250012

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
  • CHILD

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

All inpatients within the period of January 1, 2017 to December 31, 2021.

Description

Inclusion Criteria:

  1. All inpatients within the period of January 1, 2017 to December 31, 2021.
  2. Patients with discharge diagnosis.
  3. Patients with accurate gender and age records.

Exclusion Criteria:

  1. Morbidity and mortality due to external causes, i.e. injuries, poisonings and other adverse events due to external environment and accidents.
  2. Pregnancy-related conditions.
  3. Symptoms, signs, abnormal clinical and laboratory findings.
  4. Traditional Chinese Medicine diagnosis records.
  5. Patients with incorrect or missing disease codes.

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

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Hospitalized patients
The diseases were included based on the results of the preliminary data exploration and standardization according to ICD-10.
Data analysis is based on a single database from the National Health Medical Data (North Center).

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
age-specific prevalence rate
Time Frame: between January 1, 2017 and December 31, 2021
Age-specific prevalence rate stratified by sex were calculated by dividing the number of incident cases with a current disease by the total number of people in the study population during that time period.
between January 1, 2017 and December 31, 2021
sex-specific prevalence rate
Time Frame: between January 1, 2017 and December 31, 2021
Sex-specific prevalence rate stratified by age for 10-year bands were calculated by dividing the number of incident cases with a current disease by the total number of people in the study population during that time period.
between January 1, 2017 and December 31, 2021

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
total cost of hospitalization
Time Frame: between January 1, 2017 and December 31, 2021
Total cost of hospitalization and deductibles for the total population and for each age group of diseases are described by mean (SD) values.
between January 1, 2017 and December 31, 2021

Collaborators and Investigators

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

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)

August 1, 2022

Primary Completion (ANTICIPATED)

July 31, 2023

Study Completion (ANTICIPATED)

July 31, 2024

Study Registration Dates

First Submitted

November 3, 2022

First Submitted That Met QC Criteria

November 3, 2022

First Posted (ACTUAL)

November 10, 2022

Study Record Updates

Last Update Posted (ACTUAL)

November 10, 2022

Last Update Submitted That Met QC Criteria

November 3, 2022

Last Verified

November 1, 2022

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 2022-DISEASE

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.

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