NCT07148765

Use of Wearables Following Cystectomy- Part II

Enrolling by Invitation
NAAges 18+InterventionalSupportive care
University of Pittsburgh
~50 participants
Updated 2025-09-26 on ClinicalTrials.gov
What's tested:Fitbit Sense 2Smartphone application survey

At a glance

Recruiting sites
0 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Proportion of participants who remain in the study from enrollment until trial completion (participant retention)
Measured over From enrollment to 30 days post-discharge following cystectomy hospitalization
+1 more outcome measured
Bladder Cancer
Neurogenic Bladder Disorder
Cystectomy
1 sites across 1 states
Pennsylvania1
  • Matthew R Epstein, MD · PRINCIPAL_INVESTIGATOR · University of Pittsburgh

This trial hasn't published a contact. View it on ClinicalTrials.gov

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Eligibility criteria

Inclusion

English-speaking
Owns a smartphone
Scheduled to undergo cystectomy with urinary diversion at a UPMC hospital

Exclusion

No reliable internet access
Concurrent enrollment in another interventional study that may interfere with outcomes
  • Proportion of participants who remain in the study from enrollment until trial completion (participant retention)From enrollment to 30 days post-discharge following cystectomy hospitalization
  • Participant wearable electronic device adherenceFrom day of discharge following cystectomy hospitalization to 30 days post-discharge

    Proportion of patients who wear and transmit data from the provided Fitbit Sense 2 device for at least 16 hours per day for more 14 days