RECRUITING

Know and Own Your Movement-related Metrics Via Wearable Devices

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

This study aims to promote daily physical activity in cancer survivors who are at high risk for type 2 diabetes (T2D) by using a personalized biological-based feedback strategy. T2D is one of the most common co-occurring conditions in cancer survivors and can worsen cancer-related health outcomes, especially in those who are insufficiently active. The investigators hypothesize that seeing the immediate impacts of exercise on their biological status will motivate cancer survivors to exercise. The investigators will use real-time data from continuous glucose monitor to demonstrate the acute impact of physical activity and measure daily activity levels using wearable trackers. As wearable sensor technology is constantly advancing, this study is the first step to exploring how researchers can use wearable sensors to help people make a direct connection between their daily behaviors and health outcomes.

Official Title

Personalized Feedback of Wearable Biological Sensor Data to Promote Active Living in Cancer Survivors

Quick Facts

Study Start:2023-03-29
Study Completion:2024-12-01
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT05490641

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. * be 18 years or older
  2. * have had a diagnosis of cancer
  3. * have completed curative-intended treatment for at least 3 months (except hormone therapy or long-term maintenance chemotherapy)
  4. * be at high-risk for type 2 diabetes based on the American Diabetes Association Type 2 Diabetes Risk Test
  5. * currently insufficiently active
  6. * capable of participating in moderate-vigorous intensity unsupervised exercise
  7. * have no current diagnosis or history of type 1 or 2 diabetes
  8. * able to speak, read, and write in English
  9. * have a smartphone with daily internet access
  1. * currently taking oral antidiabetic agents (OADs)
  2. * current treatment with any insulin regimen other than basal insulin, e.g. prandial or pre-mixed insulin
  3. * currently pregnant
  4. * on dialysis
  5. * have self-reported health issues that limit physical activity
  6. * work overnight shifts
  7. * unwilling to use the study devices
  8. * current participation in other exercise or weight loss-related program or intervention
  9. * currently on a low-carb diet
  10. * current use of other implanted medical devices such as pacemakers
  11. * do not have a smartphone that is compatible with the Fitbit and the LibreLink apps

Contacts and Locations

Study Contact

Yue Liao, MPH, PhD
CONTACT
18172728529
yue.liao@uta.edu

Principal Investigator

Yue Liao, MPH, PhD
PRINCIPAL_INVESTIGATOR
University of Texas at Arlington

Study Locations (Sites)

The University of Texas at Arlington
Arlington, Texas, 76010
United States

Collaborators and Investigators

Sponsor: The University of Texas at Arlington

  • Yue Liao, MPH, PhD, PRINCIPAL_INVESTIGATOR, University of Texas at Arlington

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 Date2023-03-29
Study Completion Date2024-12-01

Study Record Updates

Study Start Date2023-03-29
Study Completion Date2024-12-01

Terms related to this study

Additional Relevant MeSH Terms

  • Cancer
  • Survivorship