Skip to main content
OpenTrials
Recruiting

NCT Number: NCT07608926

Cardiovascular Prevention Supported by Digital Technology: Comparison With the Traditional Model

Cardiovascular diseases represent one of the leading causes of morbidity and mortality worldwide. Prevention in patients at cardiovascular risk is essential to reduce the incidence of cardiovascular events and slow the progression of risk.

This study aims to evaluate the effectiveness and feasibility of a cardiovascular prevention pathway delivered remotely through a digital application, comparing it with a traditional in-person care pathway.

Recruiting

Interested in participating?

Request Info

Key information

Age range

40 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Maria Cecilia Hospital

Cotignola, Ravenna, 48033, Italy

Location status: Recruiting

Location contact

Anna Maria Malagoni, Dr

CONTACT

[email protected]

+390545217213

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Age between 40 and 75 years
  • hypertension
  • hyperglycaemia
  • type 2 diabetes not requiring insulin therapy
  • dyslipidaemia
  • active smoking
  • overweight/grade I obesity
  • Willingness to participate in follow-up visits over 24 months

Exclusion criteria

  • previous myocardial infarction
  • stroke
  • transient ischemic attack
  • coronary artery diseas
  • peripheral arterial occlusive disease
  • heart failure
  • Type 1 or type 2 diabetes mellitus on insulin therapy
  • Advanced chronic kidney disease (eGFR < 30 mL/min/1.73 m²)
  • Active cancer disease
  • Severe obesity
  • Inability to use digital tools
  • Pregnancy

Treatment and study plan

Recommendations to the patient.

Other

Recommendations to the patient

Primary outcomes

  1. Blood pressure

    Time frame: 12 months

    Systolic and diastolic in millimeters of mercury

  2. number of cigarettes

    Time frame: 24 months

Secondary outcomes

  1. body weigh

    Time frame: 24 months

  2. number of daily steps

    Time frame: 24 months

Sponsors and collaborators

Lead sponsor

Maria Cecilia Hospital

Other

Registry information

Acronym: DIGITAL PREV

Important dates

Study start
2025
Primary completion
2028
Study completion
2028
First posted
May 27, 2026
Registry last updated
May 27, 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.

Published trials that share one or more normalized conditions with this study.