NCT06487962
Pilot RCT: FQHC Intervention for Uptake of CGM in Low-Income Adults With T1D
Enrolling by Invitation
NAAges 18+InterventionalUniversity of ConnecticutInvestigator-initiated
~30 participants
Updated 2025-08-12 on ClinicalTrials.gov
What's tested:CGM InterventionSMBG Control Condition
At a glance
Recruiting sites
0 of 2 listed sites are recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Number of days CGM worn
Measured over 3 months and 6 months
+1 more outcome measured
Conditions
Where it's being run
2 sites across 2 statesConnecticut1
Florida1
Who to contact
This trial hasn't published a contact. View it on ClinicalTrials.gov
Do you actually qualify for this trial?
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Eligibility criteria
Inclusion
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
Exclusion
Pregnancy or planning to become pregnant
Lactation
Serious illness that may prevent study participation (e.g., severe depression)
Less than 6 months life expectancy
Alcohol abuse or dependence
Uncorrected hearing or vision impairment
What this trial measures
- Number of days CGM worn3 months and 6 months
The total number of days CGM worn. Data will be collected from Ambulatory Glucose Profile Reports.
- Percentage of time the CGM is active3 months and 6 months
The percentage of time the CGM is active. Data will be collected from Ambulatory Glucose Profile Reports.