Clinical Trials Directory

Trials / Enrolling By Invitation

Enrolling By InvitationNCT06593704

Proactive Population Health Management of Cardiovascular Disease in Primary Care Using the PROSPERA-program.

Proactive Population Health Management of Cardiovascular Disease in Primary Care Using a Multilevel Guideline Adherence Toolkit (the PROSPERA-program).

Status
Enrolling By Invitation
Phase
N/A
Study type
Interventional
Enrollment
848 (estimated)
Sponsor
Leiden University Medical Center · Academic / Other
Sex
All
Age
40 Years – 90 Years
Healthy volunteers
Not accepted

Summary

The PROSPERA-program is a complex multilevel approach that includes training for healthcare providers, a risk assessment process, and decision support tools to help match patients with the appropriate treatment based on their care needs. The goal of this clinical trial is to determine if the PROSPERA-program can improve the cardiovascular risk profile in patients aged 40-90 years enrolled in primary care programs for increased cardiovascular risk, such as cardiovascular disease, increased vascular risk, or diabetes. The main question it aims to answer is: • Does the cardiovascular risk profile improve for patients using the PROSPERA-program? Researchers will compare the PROSPERA-program with standard cardiovascular care to see if the program enhances cardiovascular population health in primary care. Additionally, the study will assess how well the PROSPERA-program fits into the workflow of primary care providers and supports shared decision-making. Participants will: * Receive a consultation with their general practitioner or practice nurse according to the PROSPERA-program. * Have their routinely collected healthcare data used for evaluation. * Be asked to complete a questionnaire or participate in an interview (for a subset of patients).

Conditions

Interventions

TypeNameDescription
OTHERPROSPERA-programThe PROSPERA-program consists of the following components: 1. Health care provider training and education about U-Prevent and cardiovascular risk communication. 2. Risk stratification: proactive selection of cardiovascular patients through the PROSPERA-empanelment procedure - for the population with increased cardiovascular risk, prior to consultation. 3. Decision support tools: use of the Lifestylecheck and the U-Prevent clinical decision support tool to guide motivated shared decision making towards appropriate care matched to the care complexity of the patient - for the individual patient, during consultation.

Timeline

Start date
2025-02-17
Primary completion
2026-07-09
Completion
2026-07-09
First posted
2024-09-19
Last updated
2025-07-04

Locations

1 site across 1 country: Netherlands

Source: ClinicalTrials.gov record NCT06593704. Inclusion in this directory is not an endorsement.