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NCT07108426Completed

Medical Education to Improve Diabetes Care and Outcomes in Hospitalized Patients

Evaluation of the Impact of In-Person and Telemedicine-Based Medical Education on Diabetes Care and Outcomes in Hospitalized Patients

Source: ClinicalTrials.gov · Last updated 7 Aug 2025

Brief summary (registry, in English)

This clinical trial aims to evaluate whether a structured medical education strategy can improve the quality of care provided to hospitalized patients with diabetes or hyperglycemia. Internal medicine residents from four university hospitals in southern Brazil are assigned to two groups: an intervention group receiving a 30-minute online lecture and 30 days of educational follow-up via WhatsApp®, and a control group receiving no additional training. The primary goal is to assess changes in physicians' knowledge about inpatient glycemic control. Secondary goals include evaluating the quality of insulin prescriptions, rates of hyperglycemia and hypoglycemia, and hospital length of stay.

Status (registry)
Completed
Study type
Interventional
Enrollment
50 (actual)
First submitted
19 Jul 2025
Start date
1 Aug 2024
Primary completion date
31 May 2025
Lead sponsor
Catholic University of Pelotas
NCT number
NCT07108426

What you commit to

  • Study type: Interventional
  • Participants enrolled: 50
  • From 1 Aug 2024 to the primary completion date, 31 May 2025
  • 1 site 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

  • Residents on vacation during the intervention month.
  • Residents from teams supervised by endocrinologists.
  • Refusal to participate in the study.

Who the study is looking for

  • Internal medicine residents from clinical teams at the participating university hospitals in southern Brazil.
  • Residents assigned to clinical teams during the intervention month.
  • Provided informed consent to participate in the study.

Age in the registry: 20 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

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

SiteCityCountrySite status
Catholic University of Pelotas
Coordinator of this site? Confirm its status
PelotasBrazilUnknown status

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