Evaluation of Mood Disorders in Bladder Cancer Patients and Their Primary Caregivers

INTRODUCTION

  • Org Study ID: 144280
  • Secondary ID: N/A
  • NTC ID: NCT04036877
  • Sponsor: University of Kansas Medical Center

BRIEF SUMMARY

This is a cross-sectional study evaluating mood disorders in bladder cancer patients and their caregivers across the bladder cancer trajectory

  • Overall Status
    Recruiting
  • Start Date
    September 19, 2019
  • Phase
  • Study Type
    Observational

PRIMARY OUTCOMES

Primary Outcome 1 - Measure: Severity of depression in bladder cancer patients and their caregivers: Patient-Health Questionnaire-9

Primary Outcome 1 - Timeframe: Data will be assessed through study completion, on average one year

Primary Outcome 2 - Measure: Severity of anxiety in bladder cancer patients and their caregivers: Generalized Anxiety Disorder-7

Primary Outcome 2 - Timeframe: Data will be assessed through study completion, on average one year

Primary Outcome 3 - Measure: Health-related quality of life in bladder cancer patients and their caregivers: Short Form-12

Primary Outcome 3 - Timeframe: Data will be assessed through study completion, on average one year

Primary Outcome 4 - Measure: Financial Toxicity in bladder cancer patients and their caregivers

Primary Outcome 4 - Timeframe: Data will be assessed through study completion, on average one year

CONDITION

  • Bladder Cancer

ELIGIBILITY

Inclusion Criteria:
Patients or caregiver of patient with a histologic diagnosis of bladder cancer of the following subtypes, urothelial carcinoma, adenocarcinoma, or squamous cell carcinoma, within 24 months of survey administration and received treatment at the University of Kansas Health System

- ≥ 18 years of age

- Have a patient-designated primary informal/family caregiver

- Able to speak and read English

- Willing and able to provide informed consent

- Functioning telephone number or access to one
Exclusion Criteria:
Patients or caregivers of patients with metastatic bladder cancer

- Patients who are unable to designate a primary caregiver

- Patients and caregivers who do not both consent to study participation

Gender: All

Minimum Age: 18 Years

Maximum Age: N/A

Healthy Volunteers: N/A

OFFICIAL INFORMATION

Name: N/A

Role: N/A

Affiliation: N/A

Overall Contact

Name: N/A

Phone: 913-574-0847

Email: adahlgren@kumc.edu

LOCATION

Facility Status Contact
Facility: University of Kansas Health System
Kansas City, Kansas 66160
United States
Status: Recruiting Contact: Contact
Alexandra Dahlgren
913-574-0847
adahlgren@kumc.edu