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NCT07257822Active, not recruiting

The Digital Diabetes Patient Reminder (DIPAR) Tool For Adults With Type 2 Diabetes

The Digital Diabetes Patient Reminder (DIPAR) Tool to Improve Clinical Outcomes and Process of Management in Adults With Type 2 Diabetes: A Proof-of-Concept Randomized Controlled Trial

Source: ClinicalTrials.gov · Last updated 19 Feb 2026

Brief summary (registry, in English)

Digital health tools may present an opportunity to address these challenges by enhancing care delivery, improving patient engagement, and facilitating better disease management for chronic diseases such as type 2 diabetes mellitus (T2DM). This primary objective of this randomized controlled trial is to evaluate whether the Diabetes Digital Patient Reminder (DIPAR), embedded in patient portal, can increase the proportion of T2DM patients who have their albuminuria measured at least once annually by either a general practitioner (GP) or a diabetes specialist, as documented in their hospital medical records (EMD), thereby reflecting active monitoring of diabetes-related parameters.

Status (registry)
Active, not recruiting
Study type
Interventional
Enrollment
200 (estimated)
First submitted
24 Sept 2025
Start date
6 Oct 2025
Primary completion date
Jun 2027
Lead sponsor
KU Leuven
NCT number
NCT07257822

What you commit to

  • Study type: Interventional
  • Planned participants: 200
  • From 6 Oct 2025 to the primary completion date, Jun 2027
  • 2 sites 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

  • Are unable to use a mobile phone because of mental or cognitive impairment;

Other

  • Participant is pregnant or hospitalized at the time of recruitment;
  • Deemed ineligible by the treating physicians.

Who the study is looking for

  • Voluntary written informed consent of the participant or their legally authorized representative has been obtained prior to any screening procedures;
  • Adults 18 years or older;
  • Treated and followed-up for Type 2 diabetes at the department of endocrinology at the participating hospitals;
  • Patients with (the ability to access) the MyNexuz patient portal;
  • Patients with the ability to understand Dutch, French or English.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (2)

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

SiteCityCountrySite status
University Hospital of UZ Leuven
Coordinator of this site? Confirm its status
LeuvenBelgiumUnknown status
Regional Hospital of Leuven
Coordinator of this site? Confirm its status
LeuvenBelgiumUnknown status

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