Diabetes study tests team support for better blood sugar control
NCT ID NCT05911256
First seen Jun 27, 2026 · Last updated Sep 04, 2026 · Updated 1 time
Summary
This study looks at whether a team of clinical pharmacists and community health workers can help people with type 2 diabetes improve their blood sugar levels using continuous glucose monitors (CGMs). About 318 adults aged 25-75 with high blood sugar will be enrolled. The goal is to see if this extra support leads to better blood sugar control over time.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 318 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Sep 2024
- Expected to finish
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Mar 2028
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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25 to 75 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Age 25-75. * History of T2DM \> 1 year. * Speak English or Spanish. * A1c ≥ 8% (within past 6 months) - with reduction if necessary based on recruitment. * eGFR (estimated glomerular filtration rate) \> 30. * Willingness to use continuous glucose monitoring (CGM) and work with a community health worker (including home visits) and clinical pharmacist. Exclusion Criteria: * Plans for weight reduction surgery or prescription weight loss medication (specific for weight loss, not GLP-1). * Current, recent, or planned use of CGM. * Current use of steroids. * Abuse of illicit drugs. * Pregnancy (or planned pregnancy). * Specific comorbidities (e.g., recent MI, TIA, CVA, malignancy, hemoglobinopathy, severe hypoglycemia, etc.). * Psychiatric disorder that may limit ability to perform study tasks * Skin changes that preclude use of sensor or allergy to adhesive. * Planning to leave geographic area within 12 months or distance from clinical site \> 20 miles. * Participation in another study.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
The full official record for this study. This one lists no contact details, but it is the first place any would appear.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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University of Massachusetts
Worcester, Massachusetts, 01605, United States
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