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NCT05854069Active, not recruiting

Adapting FAMS to Optimize CGM Use Among Emerging Adults With Type 1 Diabetes

Source: ClinicalTrials.gov · Last updated 3 Nov 2026

Brief summary (registry, in English)

The goal of this clinical trial is to evaluate the efficacy of an adapted FAMS (Family/friend Activation to Motivate Self-care) intervention on CGM use among study participants who are CGM users. We will leverage the infrastructure of an NIDDK-funded RCT evaluating FAMS-T1D among N=280 emerging adults with T1D who have elevated hemoglobin A1c or elevated diabetes distress (NCT05820477). We anticipate at least 50% using CGM to be included in these analyses.

Status (registry)
Active, not recruiting
Study type
Interventional
Enrollment
140 (estimated)
First submitted
24 Apr 2023
Start date
30 Apr 2023
Primary completion date
31 Jan 2027
Lead sponsor
Vanderbilt University Medical Center
NCT number
NCT05854069

What you commit to

  • Study type: Interventional
  • Planned participants: 140
  • From 30 Apr 2023 to the primary completion date, 31 Jan 2027
  • 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

  • PERSONS WITH DIABETES
  • Has a condition that would prohibit study completion (intellectual disability, blindness or auditory limitations, severe mental illness)
  • Shares a phone with the person with diabetes

Other

  • Plans to live outside the country during the study period
    • SUPPORT PERSONS
  • Plans to live outside of the country during the study period

Who the study is looking for

  • PERSONS WITH DIABETES
  • Ages 18-24
  • Have a diagnosis of T1D and has been taking insulin for at least one year
  • Comfortable sending and receiving texts
  • Can speak, read, and write in English
  • Meets one of the following two criteria: 1) has a most recent A1c value in the EHR that is 7.5% or higher (or missing) OR 2) screen positive for diabetes distress on the two-item Diabetes Distress Screen (DDS-2)
  • Using a continuous glucose monitor (CGM)
    • SUPPORT PERSONS
  • Age 18 or older
  • Can speak, read, and write in English or Spanish
  • Comfortable sending and receiving texts

Age in the registry: 18 years to 24 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
Children's Hospital of Los Angeles
Coordinator of this site? Confirm its status
Los AngelesUnited StatesUnknown status
University of Utah
Coordinator of this site? Confirm its status
Salt Lake CityUnited StatesUnknown status

Related publications

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