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

Overview

About this study

The objective of this study is to test the acceptability and feasibility of combining a commercially available smartwatch, which tracks critical biometric data for the prediction of disease progression in individuals with cancer, with human feedback based on smartwatch activity data tailored to meet each patient’s needs.

Participation eligibility

Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.

Inclusion Criteria:

* Are able to read/speak English and are able to communicate by phone
* Are 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 electronic surveys
* Own and are willing to use a personal smartphone with regular/reliable access to the internet to sync regularly with a fitness tracker
* Are willing to wear and use a smart fitness tracker for 6 weeks and allow sharing of their fitness data with the study team
* Are not currently undergoing adjunct cancer therapy (e.g. chemotherapy, radiation) during the 12-weeks of study participation, expect oral tyrosine kinase inhibitor or hormonal therapies; and
* Are an existing Mayo patient
* Self-report that they would like to improve their physical activity during initial study coordinator contact

Exclusion Criteria:

* Live outside of the United States (U.S)
* 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
* Are on prolonged bed rest (i.e., more than half of the waking day in bed) by self-report
* Currently have any lower extremity injury that impedes them from engaging in walking for 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

Note: Other protocol defined Inclusion/Exclusion Criteria may apply.

Eligibility last updated 01/07/2025. Questions regarding updates should be directed to the study team contact.

Participating Mayo Clinic locations

Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.

Mayo Clinic Location Status Contact

Jacksonville, Fla.

Mayo Clinic principal investigator

Emma Fortune Ngufor, Ph.D.

Closed for enrollment

Contact information:

Sarah Gifford CCRP

(507) 422-5848

Gifford.Sarah@mayo.edu

Rochester, Minn.

Mayo Clinic principal investigator

Emma Fortune Ngufor, Ph.D.

Open for enrollment

Contact information:

Sarah Gifford CCRP

(507) 422-5848

Gifford.Sarah@mayo.edu

More information

Publications

Publications are currently not available
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CLS-20578870

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