NMR Metabolomics-Based Risk Assessment and Stratified Digital Health Interventions in Middle-Aged Adults (PREMAP)
- NCT ID
- NCT07820800
- Registry status
- Not yet recruiting
- Study type
- Not specified in the registry data
- Phase
- Not applicable
- Sponsor
- University of Eastern Finland
Overview
ClinicalTrials.gov lists this study as Not yet recruiting.
Enrollment: 1400 participants (Estimated).
What is being studied
No interventions are listed in the registry data.
Who may be eligible
- Ages
- Not specified in the registry data
- Sex
- Not specified in the registry data
- Healthy volunteers accepted
- Yes
ClinicalTrials.gov lists the following eligibility criteria.
Inclusion Criteria:
* Permanent resident of the Eloisa Wellbeing Services County (South Savo, Finland), or has selected Eloisa primary health care as their primary public care provider
* Turning 45, 50, or 55 years of age during calendar year 2026
* NMR metabolomics-based risk assessment result classified as low, moderate, or high multi-disease risk
* Able to provide written informed consent digitally
* Able to use a smartphone, tablet, or computer for digital application access
* Resident of Finland with a Finnish personal identity code (required for health register linkage)
Exclusion Criteria:
* Currently pregnant or breastfeeding
* Incarcerated or under forensic psychiatric care
* Significantly impaired capacity for self-determination
* Insufficient proficiency in Finnish to provide informed consent and complete study procedures
* No Finnish personal identity code
Study locations
No study locations are listed in the registry data.
Study details
- Start date
- September 1, 2026
- Primary completion date
- September 1, 2027
- First posted
- September 15, 2026
Source and update information
- Source
- ClinicalTrials.gov
- NCT ID
- NCT07820800
- Registry last updated
- September 15, 2026
- QualifiedStudies registry data refreshed
- September 21, 2026
View NCT07820800 on ClinicalTrials.gov
Trial information can change. Confirm current study details with the study team or the registry.
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