- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05039034
Screening and Management of High-risk Populations of Stroke in Dehui City (SAMHPSDC)
August 31, 2021 updated by: Yi Yang
This epidemiological survey is to analyze the prevalence rate of stroke and exposure rate of risk factors in sampling population aged 40 years and over (born before December 31,1975) in Dehui City, to provide scientific basis for pertinent prevention and control of stroke in Jilin Province, and to provide valuable data for the high-risk groups to carry out regular follow-up and standardized management.
Study Overview
Status
Completed
Intervention / Treatment
Study Type
Observational
Enrollment (Actual)
4100
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
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Jilin
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Changchun, Jilin, China, 130000
- First Hospital of Jilin University
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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
40 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
Target population aged 40 years and over (born before December 31,1975) was selected from Dehui City by means of group sampling.
Description
Inclusion Criteria:
- Aged 40 years and over in Dehui City
- Willing to participate in the study and follow-up visits
- Signed an informed consent
Exclusion Criteria:
- Life expectancy<3 years
- Unwilling to participate in the study and follow-up visits
- Living away from Dehui City over 6 months
- Unable to cooperate with examination and questionnaire due to mental disease
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 |
|---|---|
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Low-risk Group
Low-risk Group is defined as the population with <3 risk factors (hypertension, dyslipidemia or dyslipoproteinemia, diabetic mellitus, atrial fibrillation or valvular heart disease, smoking, lack of exercise or light manual labor, overweight or obesity and family history of stroke), but without chronic disease (hypertension, diabetic mellitus, atrial fibrillation or valvular heart disease).
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Mediate-risk Group
Mediate-risk Group is defined as the population with <3 risk factors (hypertension, dyslipidemia or dyslipoproteinemia, diabetic mellitus, atrial fibrillation or valvular heart disease, smoking, lack of exercise or light manual labor, overweight or obesity and family history of stroke), but meanwhile suffer from chronic disease (hypertension, diabetic mellitus, atrial fibrillation or valvular heart disease).
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High-risk Group
High-risk Group is defined as the population with ≥3 risk factors (hypertension, dyslipidemia or dyslipoproteinemia, diabetic mellitus, atrial fibrillation or valvular heart disease, smoking, lack of exercise or light manual labor, overweight or obesity and family history of stroke), or population with history of stroke or/and transient ischemic attack.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Prevalence rate of stroke
Time Frame: 4 months
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The proportion of stroke in the general population.
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4 months
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Prevalence rate of hypertension
Time Frame: 4 months
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The proportion of hypertension in the general population.
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4 months
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Prevalence rate of diabetes mellitus
Time Frame: 4 months
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The proportion of diabetes mellitus in the general population.
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4 months
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Prevalence rate of dyslipidemia
Time Frame: 4 months
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The proportion of dyslipidemia in the general population.
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4 months
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Study Chair: Yi Yang, M.D. Ph.D., The First Hospital of Jilin University
- Study Director: Ying-Qi Xing, M.D. Ph.D., The First Hospital of Jilin University
- Study Director: Zhen-Ni Guo, M.D., The First Hospital of Jilin University
- Principal Investigator: Fu-Liang Zhang, M.D., The First Hospital of Jilin University
- Principal Investigator: Hao-Yuan Liu, M.D., The First Hospital of Jilin University
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, 2016
Primary Completion (Actual)
March 31, 2016
Study Completion (Actual)
March 31, 2017
Study Registration Dates
First Submitted
August 30, 2021
First Submitted That Met QC Criteria
August 31, 2021
First Posted (Actual)
September 9, 2021
Study Record Updates
Last Update Posted (Actual)
September 9, 2021
Last Update Submitted That Met QC Criteria
August 31, 2021
Last Verified
August 1, 2021
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- SMDC
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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