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Completed

NCT Number: NCT05648383

Promote Health With Digital Tools Among Adults With Type 2 Diabetes/Prediabetes and/or Hypertension

The goal of this hybrid type II effectiveness-implementation trial is to evaluate whether an intersectoral, digitally enabled, family-based intervention can prevent and manage type 2 diabetes mellitus (T2DM) and hypertension (HTN) in adults with intermediate hyperglycaemia or T2DM (with or without HTN), and improve growth outcomes in their children, across socioeconomically diverse communities in Albania, Bulgaria, Greece, and Spain.

The main questions it aims to answer are:

* Does the DigiCare4You intervention reduce HbA1c levels in adults with T2DM compared to enhanced standard care? * Does the DigiCare4You intervention reduce fasting plasma glucose levels in adults with intermediate hyperglycaemia compared to enhanced standard care? * Does the DigiCare4You intervention improve BMI z-scores in children linked to enrolled parents compared to enhanced standard care?

Researchers will compare the DigiCare4You intervention group to the enhanced standard care group to see if combining structured counselling, digital self-management tools, and school/community reinforcement improves cardiometabolic outcomes in adults and growth outcomes in children beyond standard national guideline-based care.

Participants will:

* Complete a two-stage screening procedure, including a digital risk questionnaire and a clinical assessment, to confirm eligibility * Attend structured assessment visits at regular intervals over 24 months, including anthropometric, biochemical, and blood pressure measurements * Receive (intervention group only) three intensive face-to-face counselling sessions in the first eight weeks, followed by ongoing digital self-management support through interoperable mobile health tools * Be encouraged to adopt healthier lifestyle behaviours as a family unit throughout the study period.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Universiteti i Mjekësisë, Tirana, Rruga E Dibrës, Albania

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About this study

DigiCare4You is an EU-funded (Horizon 2020) hybrid type II effectiveness-implementation study conducted across four European countries: Albania, Bulgaria, Greece, and Spain. The study addresses a critical gap in chronic disease prevention by combining community-based screening with a digitally supported self-management intervention targeting adults at cardiometabolic risk and their families.

Background and rationale Type 2 diabetes mellitus (T2DM) and hypertension (HTN) are among the leading causes of preventable morbidity and mortality in Europe, disproportionately affecting socioeconomically vulnerable populations. Despite their high burden, early detection and sustained management remain inconsistently delivered, particularly among groups with limited engagement in preventive healthcare. DigiCare4You was designed to address this through an equity-focused, scalable model that integrates screening, prevention, and long-term self-management support within existing health and educational infrastructures.

Study design The study uses a cluster-randomised design, with municipalities allocated 1:1 to either the DigiCare4You intervention arm or the enhanced standard care arm. Randomisation at the municipality level was chosen to minimise contamination between participants and to enable delivery through existing local healthcare and school structures.

Screening approach A novel two-stage screening procedure was embedded within existing national child growth monitoring services, using routine interactions between families and health or educational services as entry points to reach parents and caregivers who might otherwise have limited contact with preventive care. Stage 1 involved a digital self-reported risk questionnaire based on the FINDRISC score. Adults scoring ≥10 were referred to Stage 2, which included glycaemic testing, blood pressure measurement, and anthropometric assessment at local healthcare centres. Adults confirmed with intermediate hyperglycaemia or T2DM, with or without HTN, were invited to join the intervention.

Intervention The 24-month intervention combined structured face-to-face counselling with continuous digital self-management support. Counselling was guided by the Transtheoretical Model and incorporated established behaviour change techniques including self-monitoring, goal setting, barrier problem solving, relapse prevention, and self-efficacy enhancement, delivered through a shared decision-making approach. Three intensive counselling sessions were provided in the first eight weeks, followed by ongoing support through four interoperable digital tools (MetaDieta, MyDiet, MetaClinic, DiaWatch) supporting nutrition counselling, clinical monitoring, and medication adherence. School- and community-based components reinforced healthy behaviours within the broader family environment.

The intervention was delivered by existing multidisciplinary healthcare teams (internists, general practitioners, diabetologists, nurses, and dietitians) within primary care settings, trained using standardised materials and operating procedures. All digital tools are classified as medical devices under EU MDR 2017/745 and were adapted to each national context prior to deployment.

Enhanced standard care Participants in the enhanced standard care arm received structured assessment and care consistent with national clinical guidelines, including regular monitoring visits with anthropometric, biochemical, and blood pressure measurements and feedback, at intervals appropriate to their metabolic status (every 12 months for intermediate hyperglycaemia; every 3-6 months for T2DM).

Evaluation The study simultaneously evaluates clinical effectiveness and implementation outcomes using a mixed-methods approach guided by three complementary frameworks: PRECEDE-PROCEED, RE-AIM, and CFIR. Primary effectiveness outcomes are changes in HbA1c (T2DM subgroup), fasting plasma glucose (intermediate hyperglycaemia subgroup), and BMI z-scores in children. Implementation outcomes include reach, adoption, fidelity, feasibility, and sustainability. Economic evaluation includes cost-effectiveness and budget impact analyses using Markov modelling over a lifetime horizon.

Study structure The project spans five and a half years across three phases: Phase 1 (context analysis, needs assessment, and participatory co-design with stakeholder advisory boards); Phase 2 (intervention implementation and evaluation); and Phase 3 (cost-effectiveness, scalability, and transferability assessment). Findings are intended to inform evidence-based recommendations for scaling the DigiCare4You model across European health systems.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • People who have their permanent residence within the prefecture/region of the relevant facility participating in the clinical study.
  • People having children at primary and/ or secondary education.
  • People who are physically and mentally able to provide their informed consent to participate.
  • People with a FINDRISC ≥10
  • People with a fasting plasma glucose (FPG) ≥ 100 mg/dL and /or glycated hemoglobin (HbA1c) ≥ 5.7%

Exclusion criteria

  • People suffering from a health condition where adherence to the intervention will be contraindicated or improbable.
  • People unable to express a free and informed consent for medical and/or psychological conditions, mental incapacity.

Treatment and study plan

mHealth self-management intervention

Behavioral

A 24-month mHealth self-management intervention combining structured face-to-face counselling (n=5-7) with continuous digital support. Counselling follows the Transtheoretical Model, incorporating self-monitoring, goal setting, barrier problem solving, relapse prevention, and self-efficacy enhancement via shared decision-making. Three additional intensive sessions are delivered in weeks 2, 4, and 8, followed by ongoing support through four interoperable digital tools, supporting nutrition counselling, clinical monitoring, blood glucose and blood pressure self-monitoring, and medication adherence. Delivery is by multidisciplinary primary care teams using standardised operating procedures. Intervention intensity and visit schedules differ by metabolic subgroup (intermediate hyperglycaemia vs T2DM).

Standard Care

Behavioral

Participants will receive standard care, including lifestyle recommendations.

Primary outcomes

  1. Change from Baseline in fasting plasma glucose [FPG] at 12 months (1st follow-up)

    Time frame: Baseline and 12 months (1st follow-up)

    Fasting plasma glucose [FPG] is measured in participants with T2DM and in participants with intermediate hyperglycaemia at 12 months (1st follow-up) from baseline.

  2. Change from Baseline in fasting plasma glucose [FPG] at 24 months (2nd follow-up)

    Time frame: Baseline and 24 months (2nd follow-up)

    Fasting plasma glucose [FPG] is measured in participants with T2DM and in participants with intermediate hyperglycaemia at 24 months (2nd follow-up) from baseline.

  3. Change from Baseline in glycated hemoglobin [HbA1c] at 12 months (1st follow-up)

    Time frame: Baseline and 12 months (1st follow-up)

    Glycated hemoglobin [HbA1c] is measured in participants with T2DM and in participants with intermediate hyperglycaemia at 12 months (1st follow-up) from baseline.

  4. Change from Baseline in glycated hemoglobin [HbA1c] at 24 months (2nd follow-up)

    Time frame: Baseline and 24 months (2nd follow-up)

    Glycated hemoglobin [HbA1c] is measured in participants with T2DM and in participants with intermediate hyperglycaemia at 24 months (2nd follow-up) from baseline.

Secondary outcomes

  1. Change from Baseline in blood pressure [BP] (both systolic and diastolic) at 12 months (1st follow-up)

    Time frame: Baseline and 12 months (1st follow-up)

    Blood pressure [BP] is measured in participants with T2DM and in participants with intermediate hyperglycaemia at 12 months (1st follow-up) from baseline.

  2. Change from Baseline in blood pressure [BP] (both systolic and diastolic) at 24 months (2nd follow-up)

    Time frame: Baseline and 24 months (2nd follow-up)

    Blood pressure [BP] is measured in participants with T2DM and in participants with intermediate hyperglycaemia at 24 months (2nd follow-up) from baseline.

  3. Change from Baseline in body weight [BW] at 12 months (1st follow-up)

    Time frame: Baseline and 12 months (1st follow-up)

    Body weight [BW] is measured in participants with T2DM and in participants with intermediate hyperglycaemia at 12 months (1st follow-up) from baseline.

  4. Change from Baseline in body weight [BW] at 24 months (2nd follow-up)

    Time frame: Baseline and 24 months (2nd follow-up)

    Body weight [BW] is measured in participants with T2DM and in participants with intermediate hyperglycaemia at 24 months (2nd follow-up) from baseline.

  5. Change from Baseline in waist circumference [WC] at 12 months (1st follow-up)

    Time frame: Baseline and 12 months (1st follow-up)

    Waist circumference [WC] is measured in participants with T2DM and in participants with intermediate hyperglycaemia at 12 months (1st follow-up) from baseline.

  6. Change from Baseline in waist circumference [WC] at 24 months (2nd follow-up)

    Time frame: Baseline and 24 months (2nd follow-up)

    Waist circumference [WC] is measured in participants with T2DM and in participants with intermediate hyperglycaemia at 24 months (2nd follow-up) from baseline.

Other outcomes

  1. Change form Baseline in the BMI z-score of children at 12 months (1st follow-up)

    Time frame: Baseline and 12 months (1st follow-up)

    Although children will not directly receive any intervention, their BMI z-score will be calculated at 12 months (1st follow-up) of the intervention for both groups. Change = (Month 12 score - Baseline score)

  2. Change form Baseline in the BMI z-score of children at 24 months (2nd follow-up)

    Time frame: Baseline and 24 months (2nd follow-up)

    Although children will not directly receive any intervention, their BMI z-score will be calculated at 24 months (2nd follow-up) of the intervention for both groups. Change = (Month 24 score - Baseline score)

Sponsors and collaborators

Lead sponsor

Harokopio University

Other

Collaborators

  • Baker Heart and Diabetes Institute
  • Centre for Research and Technology Hellas
  • EUROPEAN UNION'S HORIZON 2020 RESEARCH AND INNOVATION PROGRAMME (Project Number: 945246)
  • International Diabetes Federation
  • La Trobe University
  • METEDA SRL
  • Medical University of Varna
  • Monash University
  • NYU Langone Health
  • National and Kapodistrian University of Athens
  • PRIVANOVA SAS
  • STICHTING INTERNATIONAL FOUNDATION FORINTEGRATED CARE
  • Sant'Anna School of Advanced Studies
  • Universidad de Zaragoza
  • University Ghent
  • University of Medicine, Tirana

Registry information

Official study title

An Intersectoral Innovative Solution Involving DIGItal Tools, Empowering Families and Integrating Community CARE Services for the Prevention and Management of Type 2 Diabetes and Hypertension

Acronym: DigiCare4You

Important dates

Study start
2022
Primary completion
2025
Study completion
2025
First posted
Dec 13, 2022
Registry last updated
Jun 9, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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