Swiss Longitudinal Cohort
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Cardiovascular Risk Factors
- Sponsor
- Hypertension Excellence Centre Lucerne
- Enrollment
- 1000
- Locations
- 3
- Primary Endpoint
- Mortality
- Status
- Recruiting
- Last Updated
- 6 years ago
Overview
Brief Summary
The planned research project is a prospective population-based cohort study, similar to the well-known Framingham study in the United States. So far, there is no similar research project in Switzerland.
It is planned to examine of three Swiss municipalities. Recruitment in a first Swiss municipality (Lostallo/Cama GR) started 2014 and ended in 2019. Overall, 496 participants were recruited in this municipality. The five-year follow-up in this municipality started in 2019. It is planned to start recruitment in a second Swiss municipality (Uznach SG) in 2020.
The examinations embrace a broad spectrum of measurements (for details the investigators refer to the published study protocol).
Investigators
Eligibility Criteria
Inclusion Criteria
- •Resident of Cama GR, Lostallo GR, or Uznach SG
- •Age ≥6 years (no upper age limit), for voluntary blood sample ≥18 years
- •Willing to participate in long-term study
- •Written informed consent (in participants ≥6 years and \<18 years signed by parents)
Exclusion Criteria
- •No exclusion criteria
Outcomes
Primary Outcomes
Mortality
Time Frame: 10 years
Secondary Outcomes
- Heart function(10 years)
- Cardiovascular events(10 years)
- Autonomy(10 years)
- Cognitive function(10 years)
- Kidney function(10 years)
- Nursing home admission(10 years)