Clinical trial Recruiting at 2 sites Interventional Ages 18 to 90

Nurse-led virtual diabetes care with a smartphone app for adults on Medicaid and insulin

Official title: Nurse-led App Intervention to Improve Glycemic Control in Patients With Insulin-treated Type 2 Diabetes on Medicaid

Run by Rutgers, The State University of New Jersey · NCT06814184 · Data updated 2026-11-12

This 12-month pilot will test whether a nurse-led program using a smartphone app, MyChart messages, and phone coaching helps adults on Medicaid who have type 2 diabetes and use insulin better manage their blood sugar.

More Type 2 Diabetes trials

Quick facts

Study typeInterventional
Ages18 Years to 90 Years
SexAll
Enrollment60 (estimated)
SponsorRutgers, The State University of New Jersey
Academic / other
Locations2 sites (New Brunswick, New Jersey and 1 other locations)
StatusRecruiting
StartedApril 1, 2026
Main results expectedDecember 1, 2028
Study endsDecember 1, 2028
Registry record updatedJuly 2, 2026
Trial IDNCT06814184 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are adults (18+) with type 2 diabetes who are on insulin, have an elevated A1C, are Medicaid or dual eligible, and can read English and use an Android or iOS smartphone.

Probably not a fit

Patients without a smartphone or smartphone skills, who are pregnant, have significant cognitive impairment, or do not read English are unlikely to benefit from this intervention.

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

What this trial studies

Guided by the Self- and Family Management Framework, this 12-month pilot delivers a nurse-led, app-based behavioral program to Medicaid-enrolled adults with type 2 diabetes on insulin. The intervention combines MyChart education and goal-setting, a clinician–patient collaborative problem-solving action plan, and remote glucose monitoring via the mySugr app. Nurses provide messaging and phone-based support to reinforce self-management behaviors and identify when treatment adjustments may be needed. The study measures changes in self-management behaviors and glycemic control compared with usual care.

Why it matters

Potential benefit: If successful, the program could improve daily diabetes self-management and lower A1C for Medicaid patients by combining digital tracking with nurse support.

How similar studies have gone: Prior nurse-led and app-based remote-monitoring programs have shown modest improvements in self-management and A1C in some populations, but results vary and Medicaid groups have been less frequently studied.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* A1C \>7 for age 18-64, A1C\>8 for age 65 or older within 12 months prior baseline
* A1C\>7 for age 18-64, A1c\>8 for age 65 or older at baseline
* Medicaid recipient or dual Medicaid and Medicare recipient
* Age 18 or older
* Type 2 diabetes
* On insulin therapy
* Owning and using Android or iOS smartphone for at least 6 months
* English proficiency
* Adequate vision to read text messages on their current smartphone
* Smartphone use proficiency. Smartphone proficiency will be self-reported and determined by telephone as the ability to use a smartphone in ways other than emailing, texting, and making phone calls.

Exclusion Criteria:

* Pregnancy
* Patients with cognitive impairment who will be screened with the Six-Item Screener to Identify Cognitive Impairment Among Potential Research Subjects.

Where it's running

  • Rutgers Health Family Medicine at Monument Square
    New Brunswick, New Jersey, United States
    Recruiting
  • University Medical Group General Internal Medicine
    New Brunswick, New Jersey, United States
    Recruiting

Study contacts

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.