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- Klinische proef NCT07820800
NMR Metabolomics-Based Risk Assessment and Stratified Digital Health Interventions in Middle-Aged Adults (PREMAP) (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
Studie Overzicht
Toestand
Conditie
Interventie / Behandeling
Gedetailleerde beschrijving
The study addresses an evidence gap: no published pragmatic, randomized trial has directly compared digital lifestyle intervention platforms in a population prospectively risk-stratified through NMR metabolomics in a real-world public-sector setting. PREMAP combines a prospective, population-based cohort (all enrolled participants, followed regardless of risk group) with an embedded pragmatic, open-label, three-arm randomized controlled trial restricted to participants classified as moderate or high multi-disease risk. The non-randomized low-risk group receives its risk result and general health information and is followed as a naturalistic reference group; withholding a risk result or randomizing this group to an active digital intervention was judged neither scientifically nor ethically justified.
At the population cohort level, the study evaluates change from baseline to 6 months in the five NMR-derived disease-specific risk predictions and in the WHO-5 wellbeing score across all enrolled participants. Within the embedded randomised substudy, the three digital health arms are compared head-to-head on the same two outcome domains at 6 months, adjusting for guideline-directed medical therapy status and relevant covariates. Secondary objectives include patient-reported outcomes (health-related quality of life, work productivity, health activation, life satisfaction), clinical and health-register-based outcomes (incident diagnoses, new prescriptions, hospitalization, sickness absence) over at least 12 months, and a health economic evaluation using patient-level Monte Carlo microsimulation to estimate cost per quality-adjusted life year (QALY) gained, from both healthcare payer and societal perspectives.
Studietype
Inschrijving (Geschat)
Fase
- Niet toepasbaar
Contacten en locaties
Studiecontact
- Naam: Janne Martikainen, PhD, Professor
- Telefoonnummer: +3583552600
- E-mail: janne.martikainen@uef.fi
Deelname Criteria
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
- Volwassen
Accepteert gezonde vrijwilligers
Beschrijving
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
Studie plan
Hoe is de studie opgezet?
Ontwerpdetails
- Primair doel: Preventie
- Toewijzing: Gerandomiseerd
- Interventioneel model: Parallelle opdracht
- Masker: Enkel
Wapens en interventies
Deelnemersgroep / Arm |
Interventie / Behandeling |
|---|---|
|
Experimenteel: Arm 1: BitHabit
Digital, self-directed lifestyle behavior-change smartphone application based on habit-formation and behavioral-economics principles.
Provides personalized, small, achievable habit suggestions targeting physical activity, nutrition, sleep, stress management and recovery.
Active engagement up to 6 months from randomization; app access continues to 12 months.
|
Arm 1: BitHabit digital lifestyle app (12 months); Arm 2: Onnikka digital lifestyle coaching (12 months); Arm 3: Oma Eloisa digital self-care pathway (comparator).
High-risk participants additionally receive physician consultation + Guideline-Directed Medical Treatment (GDMT) optimisation in the high-risk arm.
Andere namen:
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Experimenteel: Arm 2: Onnikka
Digital lifestyle coaching programme grounded in cognitive behavioral therapy and acceptance and commitment therapy, focused on sustainable weight management and metabolic risk reduction through structured programme modules, automated check-ins and optional peer support.
Active engagement up to 12 months from randomization.
|
Arm 1: BitHabit digital lifestyle app (12 months); Arm 2: Onnikka digital lifestyle coaching (12 months); Arm 3: Oma Eloisa digital self-care pathway (comparator).
High-risk participants additionally receive physician consultation + Guideline-Directed Medical Treatment (GDMT) optimisation in the high-risk arm.
Andere namen:
|
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Actieve vergelijker: Arm 3: Oma Eloisa
Structured digital self-care pathway based on national clinical guidelines, providing lifestyle information, guidance and self-monitoring tools without personalized coaching or professional support.
Represents the current standard of digital support available in the Eloisa region and is used as the comparator arm; low-risk participants also use this pathway on a non-randomized basis.
Continuous access throughout the follow-up period (up to 12 months).
|
Arm 1: BitHabit digital lifestyle app (12 months); Arm 2: Onnikka digital lifestyle coaching (12 months); Arm 3: Oma Eloisa digital self-care pathway (comparator).
High-risk participants additionally receive physician consultation + Guideline-Directed Medical Treatment (GDMT) optimisation in the high-risk arm.
Andere namen:
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Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
|
NMR-derived disease-specific 10-year risk predictions
Tijdsspanne: Baseline to 6 months
|
Change from baseline in NMR-derived disease-specific 10-year risk predictions (type 2 diabetes, coronary heart disease/myocardial infarction, stroke/cardiovascular disease, chronic kidney disease, fatty liver disease)
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Baseline to 6 months
|
|
The World Health Organization-Five Well-Being Index (WHO-5)
Tijdsspanne: Baseline to 6 months (primary); baseline to 12 months (secondary time point)
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Change from baseline in WHO-5 Well-Being Index.
A percentage score ranging from zero to 100; zero represents worst possible mental well-being; a score of 100 represents best possible mental well-being.
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Baseline to 6 months (primary); baseline to 12 months (secondary time point)
|
Secundaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
|
EuroQoL 5-Dimension 5-Level (EQ-5D-5L)
Tijdsspanne: baseline and at 6 and 12 months
|
EQ-5D-5L index score (obtained applying the Nordic value sets (Denmark, Norway, Sweden)) ranging from -0.285 to one; -0.285 indicates condition worse than death and one full health.
|
baseline and at 6 and 12 months
|
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Incident diagnoses of the five target conditions
Tijdsspanne: Over at least 12 months
|
Unit of measurement is incidence of Chronic Kidney Disease, Type 2 Diabetes, Myocardial Infarction, Stroke, and Fatty Liver Disease (MASLD).
Measurement tool from health registers (Eloisa´s EHR system, AvoHilmo, Hilmo).
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Over at least 12 months
|
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Cost-effectiveness
Tijdsspanne: Over at least 12 months
|
Incremental cost per quality-adjusted life year (QALY) gained across the three intervention arms and at the population level, estimated via microsimulation, from healthcare payer and societal perspectives
|
Over at least 12 months
|
|
Work Productivity and Activity Impairment - General Health (WPAI-GH)
Tijdsspanne: Baseline to 6 and 12 months
|
Four WPAI-GH subscales: absenteeism, presenteeism, overall work impairment, and activity impairment.
All subscales range from zero to 100% with zero indicating no impairment and 100% indicating full impairment.
|
Baseline to 6 and 12 months
|
|
Consumer Health Activation Index (CHAI)
Tijdsspanne: Baseline to 6 and 12 months
|
The ten-item CHAI score ranges from 0 to 100, with higher scores indicating greater health activation.
A score of 0 indicates the lowest level of health activation, while a score of 100 indicates the highest level of health activation.
|
Baseline to 6 and 12 months
|
|
Vitality (TARMO)
Tijdsspanne: Baseline to 6 and 12 months
|
One question with five levels.
Range 1-5, 0ne indicates full vitality and five no vitality.
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Baseline to 6 and 12 months
|
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Self-rated health
Tijdsspanne: Baseline to 6 and 12 months
|
One question with five levels.
Range 1-5, one indicate good health and 5 indicates poor health.
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Baseline to 6 and 12 months
|
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Net Promoter Score (NPS)
Tijdsspanne: Baseline to 6 and 12 months
|
NPS score is measured with a single-question survey and reported with a number ranging from -100 to +100, where a higher score is desirable.
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Baseline to 6 and 12 months
|
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New relevant prescriptions
Tijdsspanne: Over at least 12 months
|
Proportion of patients with new prescriptions for antidiabetic, antihypertensive, lipid-lowering, and renal protective drugs (Eloisa's EHR system, Kela medicine reimbursement register).
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Over at least 12 months
|
|
Work absenteeism
Tijdsspanne: Over at least 12 months
|
Number of sickness allowance days (Eloisa's EHR system, Kela register).
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Over at least 12 months
|
|
Work disability
Tijdsspanne: Over at least 12 months
|
Number of disability pension days (ETK register).
|
Over at least 12 months
|
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Hospitalization
Tijdsspanne: Over at least 12 months
|
Number of all-cause and cause-specific hospitalization days (Eloisa's EHR system, Hilmo, THL).
|
Over at least 12 months
|
|
Primary care visit rates
Tijdsspanne: Over at least 12 months
|
Primary care visit rates (Eloisa's EHR system, AvoHilmo, THL)
|
Over at least 12 months
|
|
Completion of the digital pathway
Tijdsspanne: Baseline
|
Indicator (0/1) of digital pathway successfully initiated for the participant.
Zero indicates not initiated and one successful initiation.
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Baseline
|
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Completion of blood sampling
Tijdsspanne: Baseline and 6 months
|
Indicator (0/1) of NMR blood sampling completed as planned for the participant.
Zero indicates not completed and one successful completion.
|
Baseline and 6 months
|
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Completion of risk-report delivery
Tijdsspanne: Baseline and 6 months
|
Indicator (0/1) of risk report successfully returned to the participant.
Zero indicates no return and one successful return.
|
Baseline and 6 months
|
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Correct intervention allocation relative to risk stratum
Tijdsspanne: Baseline
|
Indicator (0/1) of correct intervention allocation relative to risk stratum.
Zero indicates false and one correct intervention allocation.
|
Baseline
|
Medewerkers en onderzoekers
Studie record data
Bestudeer belangrijke data
Studie start (Geschat)
Primaire voltooiing (Geschat)
Studie voltooiing (Geschat)
Studieregistratiedata
Eerst ingediend
Eerst ingediend dat voldeed aan de QC-criteria
Eerst geplaatst (Werkelijk)
Updates van studierecords
Laatste update geplaatst (Werkelijk)
Laatste update ingediend die voldeed aan QC-criteria
Laatst geverifieerd
Meer informatie
Termen gerelateerd aan deze studie
Trefwoorden
Aanvullende relevante MeSH-voorwaarden
- Urogenitale ziekten
- Endocriene systeemziekten
- Hersenziekten
- Ziekten van het centrale zenuwstelsel
- Ziekten van het zenuwstelsel
- Vaatziekten
- Hart-en vaatziekten
- Pathologische processen
- Mannelijke urogenitale ziekten
- Nier Ziekten
- Urologische ziekten
- Vrouwelijke urogenitale ziekten
- Vrouwelijke urogenitale ziekten en zwangerschapscomplicaties
- Hartziekten
- Chronische ziekte
- Ziekte attributen
- Metabole ziekten
- Ziekten van het spijsverteringsstelsel
- Glucosemetabolismestoornissen
- Suikerziekte
- Infarct
- Necrose
- Lever Ziekten
- Nierinsufficiëntie
- Myocardiale ischemie
- Ischemie
- Vette lever
- Pathologische aandoeningen, tekenen en symptomen
- Voedings- en stofwisselingsziekten
- Hartinfarct
- Diabetes mellitus, type 2
- Niet-alcoholische leververvetting
- Nierinsufficiëntie, chronisch
- Hart-en vaatziekte
- Cerebrovasculaire aandoeningen
- Myocardinfarct
Andere studie-ID-nummers
- 189/2026
Plan Individuele Deelnemersgegevens (IPD)
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Beschrijving IPD-plan
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