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

Last updated: February 26, 2025
Sponsor: Mayo Clinic
Overall Status: Active - Recruiting

Phase

N/A

Condition

Prostate Disorders

Prostate Cancer

Urologic Cancer

Treatment

Discussion

Questionnaire Administration

Medical Device Usage and Evaluation

Clinical Study ID

NCT06703996
24-009203
24-009203
NCI-2024-09282
  • Ages > 18
  • Male

Study Summary

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.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Able to read/speak English and are able to communicate by phone

  • 18 years of age or older

  • Self-identify as Black

  • Have been diagnosed with stage I-IV prostate cancer

  • Have an active email address and are able to regularly check emails for electronicsurveys

  • Own and are willing to use a personal smartphone with regular/reliable access to theinternet to sync regularly with a fitness tracker

  • Are willing to wear and use a smart fitness tracker for 6 weeks and allow sharing oftheir fitness data with the study team

  • Are not currently undergoing adjunct cancer therapy (e.g. chemotherapy, radiation)during the 6 weeks of study participation, except oral tyrosine kinase inhibitor orhormonal therapies; and

  • Are an existing Mayo patient

  • Self-report that they would like to improve their physical activity during initialstudy coordinator contact

Exclusion

Exclusion Criteria:

  • Live outside of the United States (U.S)

  • Have an implanted medical device (e.g., pacemaker, etc.) or a life-sustaining device (e.g., patient monitoring device)

  • Have a self-reported history of a psychiatric disorder(s) or moderate to severecognitive impairment precluding participation in the study intervention orpreventing the ability to provide independent informed consent

  • Are on prolonged bed rest (i.e., more than half of the waking day in bed) byself-report

  • Currently have any lower extremity injury that impedes them from engaging in walkingfor one block

  • Are unable to walk for at least one block without a walking aide by self-report; or

  • Regularly use a wheelchair for mobility by self-report

Study Design

Total Participants: 20
Treatment Group(s): 3
Primary Treatment: Discussion
Phase:
Study Start date:
November 04, 2024
Estimated Completion Date:
July 15, 2025

Study Description

PRIMARY OBJECTIVES:

I. Assess the feasibility of a remote wearables-based intervention among Black prostate cancer survivors.

II. Assess the acceptability of the wearables-based intervention among Black prostate cancer survivors.

OUTLINE:

Patients wear the InBody Band 3 fitness tracker continuously and participate in check-in/goal-setting discussions over 20-30 minutes weekly for 6 weeks.

Connect with a study center

  • Mayo Clinic in Florida

    Jacksonville, Florida 32224-9980
    United States

    Site Not Available

  • Mayo Clinic in Rochester

    Rochester, Minnesota 55905
    United States

    Active - Recruiting

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