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NCT06487962Enrolling by invitation

Pilot RCT: FQHC Intervention for Uptake of CGM in Low-Income Adults With T1D

Source: ClinicalTrials.gov · Last updated 12 Aug 2025 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

Low-income adults with type 1 diabetes (T1D), despite their disproportionate burden of acute complications (hypoglycemia and diabetes ketoacidosis) and related emergency department visits, hospitalizations, and death, remain largely disenfranchised from continuous glucose monitoring (CGM), an efficacious technology to mitigate these inequities. To increase CGM uptake in low-income, adults with T1D receiving diabetes management in federally qualified health centers (FQHCs), this pilot randomized control trial (RCT), will assess the feasibility of our study protocol, including our multi-level intervention informed by the Socio-Ecological Model.

Status (registry)
Enrolling by invitation
Study type
Interventional
Enrollment
30 (estimated)
First submitted
13 Jun 2024
Start date
28 May 2024
Primary completion date
1 Aug 2026
Lead sponsor
University of Connecticut
NCT number
NCT06487962

What you commit to

  • Study type: Interventional
  • Planned participants: 30
  • From 28 May 2024 to the primary completion date, 1 Aug 2026
  • 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

  • Serious illness that may prevent study participation (e.g., severe depression)
  • Uncorrected hearing or vision impairment

Other

  • Pregnancy or planning to become pregnant
  • Lactation
  • Less than 6 months life expectancy
  • Alcohol abuse or dependence

Who the study is looking for

  • Low-income status
  • Documented diagnosis of T1D
  • 18 years of age or older
  • Federally Qualified Health Center (FQHC) primary care provider
  • English or Spanish-speaking And at intervention sites
  • Willingness to wear a CGM sensor
  • Adult family member or friend, who will give consent to participate in the study and co-attend the 4-week intervention sessions
  • Reported difficulty in using CGM if current or past use of CGM

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. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Community Health Center, Inc.
Coordinator of this site? Confirm its status
MiddletownUnited StatesUnknown status
Treasure Coast Community Health
Coordinator of this site? Confirm its status
Vero BeachUnited StatesUnknown status

Related publications

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