Quality of Life After Treatment for Bladder Cancer: The Bladder Cancer Survivorship Study
NCT ID: NCT06350734
Last Updated: 2025-10-20
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
704 participants
OBSERVATIONAL
2018-10-12
2029-01-31
Brief Summary
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Detailed Description
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I. To compare general and disease-specific quality of life outcomes at 6, 12, 24, and 36 months after treatment for localized bladder cancer using the PROMIS-29 and the Bladder Cancer Index (BCI) respectively.
II. To identify patient level characteristics that may influence quality of life outcomes after treatment for localized bladder cancer.
OUTLINE: This is an observational study.
Patients complete surveys and also have their medical records reviewed on study.
Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Observational
Patients complete surveys and also have their medical records reviewed on study.
Non-Interventional Study
Non-Interventional Study
Interventions
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Non-Interventional Study
Non-Interventional Study
Eligibility Criteria
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Inclusion Criteria
* Be willing to complete a survey in English before starting definitive treatment (surgery or radiation);
* Able to give consent.
18 Years
ALL
No
Sponsors
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Mayo Clinic
OTHER
Responsible Party
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Principal Investigators
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Mark D. Tyson, M.D., M.P.H.
Role: PRINCIPAL_INVESTIGATOR
Mayo Clinic
Locations
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Mayo Clinic in Arizona
Scottsdale, Arizona, United States
Mayo Clinic in Florida
Jacksonville, Florida, United States
Mayo Clinic in Rochester
Rochester, Minnesota, United States
Countries
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Facility Contacts
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Related Links
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Mayo Clinic Clinical Trials
Other Identifiers
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NCI-2024-00973
Identifier Type: REGISTRY
Identifier Source: secondary_id
18-004675
Identifier Type: OTHER
Identifier Source: secondary_id
18-004675
Identifier Type: -
Identifier Source: org_study_id
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