Clinical trial Recruiting at 2 sites Observational Ages 18 and up

ECHO Diabetes program for Federally Qualified Health Centers

Official title: Extension for Community Health Outcomes (ECHO) Diabetes Federally Qualified Health Centers (FQHCs)

Run by University of Florida · NCT07417865 · Data updated 2026-11-12

This program will test whether a 6-month tele-education series for primary care teams at Federally Qualified Health Centers helps lower very high HbA1c rates and increases use of diabetes technology in adults with diabetes.

Quick facts

Study typeObservational
Ages18 Years and up
SexAll
Enrollment18 (estimated)
SponsorUniversity of Florida
Academic / other
Locations2 sites (Miami, Florida and 1 other locations)
StatusRecruiting
StartedJanuary 22, 2026
Main results expectedJuly 31, 2028
Study endsJuly 31, 2028
Registry record updatedFebruary 18, 2026
Trial IDNCT07417865 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal participants are Federally Qualified Health Centers that are members of Health Choice Network or AllianceChicago and their adult patients with diabetes whose de-identified aggregate data can be shared for monitoring.

Probably not a fit

Patients served at clinics that are not FQHCs or not part of HCN or AllianceChicago, and those under 18 who are excluded from the adult aggregate datasets, are unlikely to benefit from this program.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

The program uses a hub-and-spoke tele-education model delivering one-hour ECHO sessions twice monthly over six months to PCP teams at participating FQHCs, plus onboarding, real-time case support, and an online resource library. The multidisciplinary hub includes endocrinologists, CDCES, a psychologist, dietitian, exercise physiologist, PCPs, and health services researchers and offers CME credits. Eighteen spokes drawn from two Health Center Controlled Networks will be randomized into three staggered cohorts in a stepped-wedge design, with covariate-constrained randomization guiding assignment. Program effects will be measured using provider pre/post surveys and center-level aggregate clinical data, focusing on glycemic control and technology adoption.

Why it matters

Potential benefit: If successful, FQHC primary care teams could better manage diabetes so fewer patients have very high HbA1c and more patients gain access to CGM and insulin pumps.

How similar studies have gone: Project ECHO programs, including earlier ECHO Diabetes efforts, have generally improved provider knowledge and care processes, though patient-level outcome effects have been mixed across studies.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria: Federally Qualified Health centers (spokes) are eligible to participate that are part of Health Choice Network (HCN) or Alliance Chicago (AC). All people living with diabetes 18 and older are included in aggregate data sharing to evaluate outcomes.

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Exclusion Criteria:

* Non FQHC, not part of HCN or AC

Where it's running

  • Health Choice Network
    Miami, Florida, United States
    Recruiting
  • Alliance Chicago
    Chicago, Illinois, United States
    Recruiting

Study contacts

  • Principal investigator: Ashby F Walker, Ph.D. — University of Florida
  • Study coordinator: Ashby F Walker, Ph.D.
  • Email: afwalker@ufl.edu
  • Phone: 352-273-8278

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.