- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04091035
Prevalence and Risk Factors for Common Diseases
October 4, 2019 updated by: Anna Nordström
Prevalence and Risk Factors for Common Diseases in Sweden: A Nationwide Cohort Study
By using national databases in Sweden the aim of the present project is to:
- Investigate if the incidence of our most common diseases, such as fracture and cardiovascular disease, has changed from 1970-2017
- To investigate whether the risk of death for our most common diseases have changed from 1970-2017.
- To investigate the risk of a new episode after suffering from our most common diseases from 1970-2017
- To investigate the risk factors for our most common diseases, and whether these have changed from 1970.
- To investigate how severe disease or death affects the health of a close relative.
Study Overview
Status
Unknown
Conditions
Intervention / Treatment
Detailed Description
Please see above on the summary.
Study Type
Observational
Enrollment (Anticipated)
1000000
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Peter Nordström, Professor
- Phone Number: +46907851000
- Email: peter.nordstrom@umu.se
Study Contact Backup
- Name: Anna Nordström
- Email: anna.h.nordstrom@umu.se
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
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Se above
Description
Inclusion Criteria:
- All people living in Sweden that is diagnosed with our most common diseases between 1970-2017.
Exclusion Criteria:
- None
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 |
---|---|---|
Incidence of disease
Time Frame: 1970-2017
|
To investigate the incidence of the most common diseases, and whether the incidence has changed.
|
1970-2017
|
Age at diagnosis of disease
Time Frame: 1970-2017
|
To investigate age at diagnosis of our most common diseases, and whether this has changed.
|
1970-2017
|
Risk of death or disease in relative
Time Frame: 1970-2017
|
Risk of death or disease in close relative to those diagnosed with severe disease or died.
|
1970-2017
|
Risk factors for disease or death
Time Frame: 1970-2017
|
Risk factors for our most common diseases or death
|
1970-2017
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Risk for readmission
Time Frame: 1970-2017
|
To investigate the risk of readmission for our most common diseases, and whether this risk has changed,
|
1970-2017
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Study Director: Peter Nordström, Professor, Umea 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 (Anticipated)
November 1, 2019
Primary Completion (Anticipated)
November 1, 2020
Study Completion (Anticipated)
November 1, 2020
Study Registration Dates
First Submitted
September 13, 2019
First Submitted That Met QC Criteria
September 13, 2019
First Posted (Actual)
September 16, 2019
Study Record Updates
Last Update Posted (Actual)
October 8, 2019
Last Update Submitted That Met QC Criteria
October 4, 2019
Last Verified
September 1, 2019
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- VasterbottenCounty
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.
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