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NCT05394844Completed

Diabetes Education With Real-time Continuous Glucose Monitoring

Study of a Culturally Tailored Diabetes Education Curriculum With Real-time Continuous Glucose Monitoring in a Latinx Population With Type 2 Diabetes (The CUTDM With CGM Study)

Source: ClinicalTrials.gov · Last updated 1 Dec 2025

Brief summary (registry, in English)

Determine the impact of the Compañeros en Salud (Partners in Health) curriculum in conjunction with RT-CGM on glycemic control in Latinx patients with T2D. Participants will be randomized to receive the Companeros en Salud diabetes self-management education and support (DSMES) intervention with or without RT-CGM

Status (registry)
Completed
Study type
Interventional
Enrollment
120 (actual)
First submitted
19 Apr 2022
Start date
11 Nov 2022
Primary completion date
30 Jul 2024
Lead sponsor
University of Washington
NCT number
NCT05394844

What you commit to

  • Study type: Interventional
  • Participants enrolled: 120
  • From 11 Nov 2022 to the primary completion date, 30 Jul 2024
  • 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.

Age

  • Exclusion Criteria.
    • Duration of diabetes \>15 years
    • Type 1 diabetes or latent autoimmune diabetes
    • Current use of prandial insulin
    • Any condition that prevents walking at least 1 city block
    • History of serious mental illness other than adequately treated depression
    • History of bariatric surgery or current participation in a weight management program
    • Current diagnosis of cancer or other serious or systemic medical condition
    • Significant active cardio- or cerebrovascular disease after review by PI
    • Pregnancy
    • know history x of of hypoglycemia unawareness
    • Unable to read, understand, and sign the Informed Consent Form (ICF) and if applicable, an Authorization to Use and Disclose Protected Health Information form (consistent with Health Insurance Portability and Accountability Act of 1996 \[HIPAA\] legislation), communicate with the investigator, and understand and comply with protocol requirements

Who the study is looking for

  • Participants adults 18-60 years old
  • Self-identify as Latinx
  • Have had a clinical diagnosis of T2D within the last 15 years with or without medication use
  • Have an A1C ≥8.0% at screening
  • Own or have routine access to a personal device that allows attending educational sessions virtually
  • Be physically and cognitively able to use the home CGM monitoring device
  • Be willing and able to follow all other study procedures

Age in the registry: 18 years to 60 years · 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 of Washington
Coordinator of this site? Confirm its status
SeattleUnited StatesUnknown status
University of Washington Diabetes Institute
Coordinator of this site? Confirm its status
SeattleUnited StatesUnknown status

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