ClinicalTrials.Veeva

Menu

Quality of Life After Treatment for Bladder Cancer: The Bladder Cancer Survivorship Study

Mayo Clinic logo

Mayo Clinic

Status

Enrolling

Conditions

Stage II Bladder Cancer AJCC v8
Stage IIIA Bladder Cancer AJCC v8
Stage 0a Bladder Cancer AJCC v8
Stage I Bladder Cancer AJCC v8
Stage 0is Bladder Cancer AJCC v8

Treatments

Other: Non-Interventional Study

Study type

Observational

Funder types

Other

Identifiers

NCT06350734
NCI-2024-00973 (Registry Identifier)
18-004675 (Other Identifier)

Details and patient eligibility

About

This study evaluates the effect of bladder cancer treatment on quality of life.

Full description

PRIMARY OBJECTIVES:

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.

Enrollment

704 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Have pathologically confirmed, clinically localized, bladder cancer
  • Be willing to complete a survey in English before starting definitive treatment (surgery or radiation);
  • Able to give consent.

Exclusion criteria

  • Does not meet inclusion criteria

Trial design

704 participants in 1 patient group

Observational
Description:
Patients complete surveys and also have their medical records reviewed on study.
Treatment:
Other: Non-Interventional Study

Trial contacts and locations

3

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems