Actively Recruiting

Phase Not Applicable
Age: 16Years - 24Years
All Genders
NCT07270016

Pilot-Testing Real-Time Engagement for Learning to Effectively Control Type 2 Diabetes

Led by University of Pittsburgh · Updated on 2026-02-20

30

Participants Needed

1

Research Sites

41 weeks

Total Duration

On this page

Sponsors

U

University of Pittsburgh

Lead Sponsor

S

San Diego State University

Collaborating Sponsor

AI-Summary

What this Trial Is About

The goal of this study is to pilot test features of a new smartphone app and to gather feedback related to wearing a continuous glucose monitor (CGM) and a Fitbit device, as well as to obtain input on health behavior-focused messages delivered through the app. The study will enroll English-speaking participants aged 16-24 years who were diagnosed with type 2 diabetes before age 18. Participants will be asked to fill out surveys about diabetes, physical activity, and diet before and after wearing a CGM for 30 days. At the end of wearing the CGM, participants will complete an interview about their experience.

CONDITIONS

Official Title

Pilot-Testing Real-Time Engagement for Learning to Effectively Control Type 2 Diabetes

Who Can Participate

Age: 16Years - 24Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Ages 16-24 years, any sex or gender
  • Diagnosis of type 2 diabetes in childhood (younger than 18 years of age)
  • English-speaking (app in English)
  • Possession of personal smartphone that is compatible with FreeStyle Libre app
Not Eligible

You will not qualify if you...

  • Cognitive impairment or severe psychiatric conditions that could interfere with participation in behavioral intervention for diabetes self-management

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Children's Hospital of Pittsburgh

Pittsburgh, Pennsylvania, United States, 15224

Actively Recruiting

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Research Team

M

Mary Ellen Vajravelu, MD, MSHP

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

OTHER

Number of Arms

1

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