Garmin PACT (Physical Activity Tracking in Type 1 Diabetes Using Garmin Vivosmart)

Description

The goal of this observational study is to test the Garmin Vivosmart in children and youth (8-21) with Type 1 Diabetes (T1D) and their parents. The main questions it aims to answer are: * Does the Garmin Vivosmart increase physical activity (PA)? * Does the Garmin Vivosmart improve T1D status Participants will: * Wear the Garmin Vivosmart (4 or higher) for a year * Complete surveys at the beginning, middle and end of participation asking about your T1D, T1D management, and PA * Parents of children will also complete similar surveys about T1D

Conditions

Type 1 Diabetes

Study Overview

Study Details

Study overview

The goal of this observational study is to test the Garmin Vivosmart in children and youth (8-21) with Type 1 Diabetes (T1D) and their parents. The main questions it aims to answer are: * Does the Garmin Vivosmart increase physical activity (PA)? * Does the Garmin Vivosmart improve T1D status Participants will: * Wear the Garmin Vivosmart (4 or higher) for a year * Complete surveys at the beginning, middle and end of participation asking about your T1D, T1D management, and PA * Parents of children will also complete similar surveys about T1D

Garmin PACT (Physical Activity Tracking)

Garmin PACT (Physical Activity Tracking in Type 1 Diabetes Using Garmin Vivosmart)

Condition
Type 1 Diabetes
Intervention / Treatment

-

Contacts and Locations

Kansas City

Children's Mercy, Kansas City, Missouri, United States, 64111

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.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • * Participants aged 8-21 years of age and/or parent of participant aged 8-17 years of age
  • * Participants diagnosed with T1D greater than 6 months ago
  • * Participants must be patients at the Children's Mercy Kansas City network
  • * Participants who do not meet age criteria above
  • * Participants who do not have T1D
  • * Participants who are unwilling to wear the device for at least 6 months

Ages Eligible for Study

8 Years to 21 Years

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

Children's Mercy Hospital Kansas City,

Mark Clements, MD, PRINCIPAL_INVESTIGATOR, Children's Mercy

Study Record Dates

2025-11