Summary

Eligibility
for people ages 0-16 (full criteria)
Healthy Volunteers
healthy people welcome
Location
at UC Davis
Dates
study started
completion around
Principal Investigator
by Caroline Schulmeister (ucdavis)

Description

Summary

The goal of this clinical trial is to learn if access to a diabetes coach improves quality of life (QOL) for families of children with newly diagnosed type 1 diabetes. The main questions it aims to answer are:

  1. Determine if there are beneficial effects on diabetes-related QOL at the end of the 6-month intervention.
  2. Determine if potential beneficial effects persist beyond completion of the support intervention, as measured by diabetes-related QOL at 12 months and 24 months following diagnosis

Participants assigned to the intervention group will have access to a diabetes coach for 6 months following type 1 diabetes diagnosis. They will be compared to participants who are assigned to the control group and are receiving usual care.

Official Title

Effect of Personalized Comprehensive Diabetes Support Among Families of Children With Newly Diagnosed Type 1 Diabetes

Keywords

Type 1 Diabetes, Diabetes Mellitus, Type 1 Diabetes Mellitus, personalized comprehensive diabetes support

Eligibility

You can join if…

Open to people ages 0-16

  • Families of children 16 years of age or younger with a new diagnosis
  • Stable living situation such that the same caregivers are anticipated to be caring for the child during the full 2-year study duration.

You CAN'T join if...

  • Families of children older than 16 years
  • Children from non-English speaking families

Location

  • University of California Davis
    Sacramento California 95817 United States

Lead Scientist at University of California Health

  • Caroline Schulmeister (ucdavis)
    Assistant Professor, Pediatrics, School of Medicine. Authored (or co-authored) 4 research publications

Details

Status
accepting new patients by invitation only
Start Date
Completion Date
(estimated)
Sponsor
University of California, Davis
ID
NCT06057662
Study Type
Interventional
Participants
Expecting 60 study participants
Last Updated