RECRUITING

GO TEAM: Glucose Optimization Through Technology Assisted Management

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

Black/African American children and young adults with type 1 diabetes are less likely to use diabetes technologies, such as continuous glucose monitors, insulin pumps, and automated insulin delivery systems, compared to White children and young adults. The investigators are working to find ways to make sure that all patients with type 1 diabetes are equally able to use these technologies. The purpose of this study is to find out if a new computer program for the diabetes team, along with a smartphone app (called Glucosano) for patients/parents, as well as a community health worker, are accepted and used by Black/African American patients and parents living with type 1 diabetes, and if this can help decrease racial disparities in the use of diabetes technologies.

Official Title

GO TEAM INTERVENTION PROTOCOL: GLUCOSE OPTIMIZATION THROUGH TECHNOLOGY ASSISTED MANAGEMENT: Use of a Diabetes Dashboard and Community Health Worker to Decrease Disparities in Technology Use in Pediatric T1D

Quick Facts

Study Start:2024-01-29
Study Completion:2026-10-01
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06074458

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:8 Years to 18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:CHILD, ADULT
Inclusion CriteriaExclusion Criteria
  1. * Self-reported as Non-Hispanic Black
  2. * Clinical diagnosis of T1D requiring treatment with insulin at the time of consent
  3. * Not currently (within the past 3 months) using an automated insulin delivery system \\
  4. * Willingness to wear a continuous glucose monitor for 10 days at 3 different time points, and willingness to consider use of a personal continuous glucose monitor
  1. * Clinical diagnosis of Type 2 or monogenic diabetes
  2. * Completed high school
  3. * Non-English speaking guardians
  4. * Automated insulin delivery system use within the past 3 months
  5. * Custody of children and family services

Contacts and Locations

Study Contact

Sarah MacLeish, DO
CONTACT
216-844-3661
sarah.macleish2@uhhospitals.org
Paul McGuigan, RN, CDCES
CONTACT
216-844-7139
paul.mcguigan@uhhospitals.org

Study Locations (Sites)

University Hospitals Cleveland Medical Center
Cleveland, Ohio, 44106
United States

Collaborators and Investigators

Sponsor: Sarah MacLeish

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2024-01-29
Study Completion Date2026-10-01

Study Record Updates

Study Start Date2024-01-29
Study Completion Date2026-10-01

Terms related to this study

Keywords Provided by Researchers

  • Pediatric
  • Diabetes Technology
  • Disparities

Additional Relevant MeSH Terms

  • Type 1 Diabetes