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

Children's Mercy Hospital Kansas City logo

Children's Mercy Hospital Kansas City

Status

Terminated

Conditions

Type 1 Diabetes

Treatments

Other: Garmin physical activity tracker

Study type

Observational

Funder types

Other

Identifiers

NCT05992350
STUDY00002582

Details and patient eligibility

About

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

Enrollment

45 patients

Sex

All

Ages

8 to 21 years old

Volunteers

No Healthy Volunteers

Inclusion 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

Exclusion criteria

  • 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

Trial design

Trial documents
2

Trial contacts and locations

1

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Central trial contact

Priscilla Connell, MPH; Emily DeWit

Data sourced from clinicaltrials.gov

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