RECRUITING

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

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