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NCT07820800Recruiting

NMR Metabolomics-Based Risk Assessment and Stratified Digital Health Interventions in Middle-Aged Adults (PREMAP)

Effectiveness and Cost-Effectiveness of NMR Metabolomics-Based Risk Assessment and Stratified Preventive Digital and Guideline-Directed Interventions in a Middle-Aged Population: A Population Cohort Study With an Embedded Pragmatic Randomised Trial and Health Economic Evaluation

Source: ClinicalTrials.gov · Last updated 6 Oct 2026

Brief summary (registry, in English)

PREMAP invites residents of the Eloisa region (South Savo, Finland) turning 45, 50, or 55 years of age in 2026 to undergo a blood-based NMR metabolomics risk assessment for five interlinked cardio-renal-metabolic conditions (type 2 diabetes, coronary heart disease/myocardial infarction, stroke/cardiovascular disease, chronic kidney disease, and fatty liver disease), alongside a mental wellbeing assessment (WHO-5 Well-Being Index). Based on this risk profile, participants are classified as low, moderate, or high multi-disease risk. Participants at moderate or high risk are individually randomized in a 1:1:1 ratio to one of three digital health interventions for up to 12 months: a habit-based lifestyle application (BitHabit), a structured digital lifestyle coaching programme (Onnikka), or a guideline-based digital self-care pathway (Oma Eloisa, comparator). Participants at high risk additionally receive a physician consultation and optimization of guideline-directed medical therapy. All participants, including the non-randomized low-risk group, are followed prospectively at baseline, 6 months, and 12 months. The study evaluates whether early risk identification and risk-stratified digital interventions reduce future disease risk and improve wellbeing and estimates the cost-effectiveness of the overall approach for the Finnish healthcare system.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
1400 (estimated)
First submitted
2 Sept 2026
Start date
Sept 2026
Primary completion date
Sept 2027
Lead sponsor
University of Eastern Finland
NCT number
NCT07820800

What you commit to

  • Study type: Interventional
  • Planned participants: 1400
  • From Sept 2026 to the primary completion date, Sept 2027
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Incarcerated or under forensic psychiatric care

Other

  • Currently pregnant or breastfeeding
  • Significantly impaired capacity for self-determination
  • Insufficient proficiency in Finnish to provide informed consent and complete study procedures
  • No Finnish personal identity code

Who the study is looking for

  • 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)

Age in the registry: 45 years to 55 years · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Wellbeing Services County of South Savo (Eloisa) (provide social and healthcare services and emergency services in the Enonkoski, Hirvensalmi, Juva, Kangasniemi, Mikkeli, Mäntyharju, Pieksämäki, Puumala, Rantasalmi, Savonlinna ja Sulkava)
Coordinator of this site? Confirm its status
SavonlinnaFinlandRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.