Actively Recruiting

Phase Not Applicable
Age: 13Years - 21Years
All Genders
NCT07116434

Discovery Diabetes

Led by Vanderbilt University Medical Center · Updated on 2025-12-23

150

Participants Needed

1

Research Sites

102 weeks

Total Duration

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AI-Summary

What this Trial Is About

The goal of this clinical trial is to learn if the Discovery Program can help improve diabetes management in adolescents and young adults with type 1 diabetes (T1D). The main questions it aims to answer are: Does the Discovery Program lead to better glycemic control as measured by HbA1c levels? How does participation in the Discovery Program affect diabetes distress and self-management skills? Researchers will compare participants in the Discovery Program to those receiving standard diabetes care to see if the program has a positive effect on diabetes management. Participants will: Engage in a 3-month intervention that includes personalized mobile health communications and clinician support. Complete surveys and assessments at the beginning of the study, and again at 3 and 6 months. Allow the study team to access their electronic health records for additional data on diabetes management.

CONDITIONS

Official Title

Discovery Diabetes

Who Can Participate

Age: 13Years - 21Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adolescents aged 13 to 17 years and young adults aged 18 to 21 years
  • Diagnosed with type 1 diabetes for at least one year
  • Access to a smartphone
  • Have a My Health at Vanderbilt (MHAV) patient portal account
  • Ability to read, speak, and understand English
  • Have an appointment with a nurse practitioner in the VUMC Eskind Clinic within 7 months of initial contact
Not Eligible

You will not qualify if you...

  • Diagnosis of type 2 diabetes
  • Any physical, cognitive, sensory, or emotional condition that prevents participation (such as difficulty seeing or using a phone, hearing digital stories, or answering questions)

AI-Screening

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Trial Site Locations

Total: 1 location

1

Vanderbilt University

Nashville, Tennessee, United States, 37240

Actively Recruiting

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Research Team

A

Abigail Doyle, MSHI

CONTACT

D

Dina Bu, BS

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

2

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