RECRUITING

Starting Technology in At Risk Type 1 Diabetes Study

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

Diabetes technology has revolutionized T1D management, disparities in technology access are evident among racial-ethnic minorities, patients with lower socioeconomic status and those with poorly controlled T1D (A1c\>8.5%). In order to examine whether diabetes technology can reduce diabetes care burdens and enhance outcomes among some of highest need patients, diabetes technology clinical trials must be expanded beyond the very select populations included in studies thus far (ie., mostly White, higher SES). Therefore, the investigators propose to perform a pilot RCT of hybrid closed-loop insulin pump therapy (HCL) in 40 diverse adult patients with poorly controlled T1D (HbA1c \>8.5%) from the largest academic and safety net health systems in the Los Angeles region to determine the feasibility of a RCT in this population and identify facilitators and barriers of effective use of closed loop insulin pump therapy in patients with poorly controlled T1D.

Official Title

Starting Technology in At Risk Type 1 Diabetes (STAR-T1D) Study

Quick Facts

Study Start:2024-09-05
Study Completion:2027-06
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06453928

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:18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Type 1 Diabetes
  2. * A1c \>8.5%
  3. * Not insulin pump user
  4. * Primary language of English or Spanish
  5. * Have medical insurance coverage
  1. * No measured A1c in the past year
  2. * Have comorbidities that can result in inaccurate hemoglobin A1c
  3. * Have cognitive, physical or mental impairment precluding diabetes technology use
  4. * Limited life expectancy (\<1 year)
  5. * Pregnancy

Contacts and Locations

Study Contact

Estelle M Everett, MD, MHS
CONTACT
310-267-0625
eeverett@mednet.ucla.edu

Study Locations (Sites)

UCLA
Santa Monica, California, 90404
United States
Harbor-UCLA Medical Center
Torrance, California, 90502
United States

Collaborators and Investigators

Sponsor: University of California, Los Angeles

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 Date2024-09-05
Study Completion Date2027-06

Study Record Updates

Study Start Date2024-09-05
Study Completion Date2027-06

Terms related to this study

Keywords Provided by Researchers

  • Continuous Glucose Monitoring
  • Insulin Pump
  • Hybrid Closed Loop Systems
  • Diabetes Technology
  • Health Disparities

Additional Relevant MeSH Terms

  • Diabetes Mellitus, Type 1