COMPLETED

InBody Band 3 Fitness Tracker to Improve Health Outcomes and Quality of Life in Black Prostate Cancer Survivors

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 clinical trial studies how well the InBody Band 3 fitness tracker works to improve physical activity, body composition, and quality of life in Black prostate cancer survivors. Prostate cancer is the most common cancer in men and Black men are more likely to be diagnosed with prostate cancer in an advanced stage. Body composition is associated with disease progression, treatment response, and survival in cancer patients. Reducing stress and maintaining healthy levels of physical activity and sleep are important for a healthy body and improving outcomes, however, there is currently little evidence available on the physical activity, stress levels and sleep patterns in this population. Wearable health activity trackers and smart watches are tools that can be used to track physical activity, stress, sleep and body composition and have been shown to have a positive impact in many patient populations. The InBody Band 3 may be an effective method to improve physical activity, body composition and quality of life in Black prostate cancer survivors.

Official Title

Bridging the Digital Divide of Wearables to Improve Health Outcomes and Quality of Life Among Black Prostate Cancer (CaP) Survivors

Quick Facts

Study Start:2024-11-04
Study Completion:2025-05-08
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:COMPLETED

Study ID

NCT06703996

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:MALE
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Able to read/speak English and are able to communicate by phone
  2. * 18 years of age or older
  3. * Self-identify as Black
  4. * Have been diagnosed with stage I-IV prostate cancer
  5. * Have an active email address and are able to regularly check emails for electronic surveys
  6. * Own and are willing to use a personal smartphone with regular/reliable access to the internet to sync regularly with a fitness tracker
  7. * Are willing to wear and use a smart fitness tracker for 6 weeks and allow sharing of their fitness data with the study team
  8. * Are not currently undergoing adjunct cancer therapy (e.g. chemotherapy, radiation) during the 6 weeks of study participation, except oral tyrosine kinase inhibitor or hormonal therapies; and
  9. * Are an existing Mayo patient
  10. * Self-report that they would like to improve their physical activity during initial study coordinator contact
  1. * Live outside of the United States (U.S)
  2. * Have an implanted medical device (e.g., pacemaker, etc.) or a life-sustaining device (e.g., patient monitoring device)
  3. * Have a self-reported history of a psychiatric disorder(s) or moderate to severe cognitive impairment precluding participation in the study intervention or preventing the ability to provide independent informed consent
  4. * Are on prolonged bed rest (i.e., more than half of the waking day in bed) by self-report
  5. * Currently have any lower extremity injury that impedes them from engaging in walking for one block
  6. * Are unable to walk for at least one block without a walking aide by self-report; or
  7. * Regularly use a wheelchair for mobility by self-report

Contacts and Locations

Principal Investigator

Emma Fortune Ngufor, PhD
PRINCIPAL_INVESTIGATOR
Mayo Clinic in Rochester

Study Locations (Sites)

Mayo Clinic in Florida
Jacksonville, Florida, 32224-9980
United States
Mayo Clinic in Rochester
Rochester, Minnesota, 55905
United States

Collaborators and Investigators

Sponsor: Mayo Clinic

  • Emma Fortune Ngufor, PhD, PRINCIPAL_INVESTIGATOR, Mayo Clinic in Rochester

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 Date2024-11-04
Study Completion Date2025-05-08

Study Record Updates

Study Start Date2024-11-04
Study Completion Date2025-05-08

Terms related to this study

Additional Relevant MeSH Terms

  • Prostate Carcinoma