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Brief Title: Intensive Preoperative Ostomy Education for the Radical Cystectomy Patient

Intensive Preoperative Ostomy Education for the Radical Cystectomy Patient

INTRODUCTION

  • Org Study ID: STUDY00142039
  • Secondary ID: N/A
  • NTC ID: NCT03462667
  • Sponsor: University of Kansas Medical Center

BRIEF SUMMARY


The purpose of this study is to learn if the stoma boot camp is a good and effective way to
help people adapt to life with a stoma after surgery.

DETAILED DESCRIPTION


Bladder cancer is the fifth most common cancer in the USA. The primary treatment for invasive
bladder cancer is a radical cystectomy (RC) with a urinary diversion. Patients that have this
procedure must deal with a stoma that requires daily care and manual skills. A stoma is an
artificial opening that allows urine to pass from the ureters outside the body. Having a
surgery that results in a stoma can dramatically change a person's life.

This study is being done to test a new education session called the stoma boot camp. The
session was created to help people deal with changes in their post-surgery life and living
with a stoma.

The session requires a one time visit to the study site and lasts about two hours.
Participants can bring a support person to the boot camp if they choose. During the two hour
session, nurses will provide teaching, counseling, and hands on practice with an artificial
stoma.


  • Overall Status
    Recruiting
  • Start Date
    February 26, 2018
  • Phase
    N/A
  • Study Type
    Interventional

PRIMARY OUTCOMES

Primary Outcome 1 - Measure: Ostomy adjustment scale

Primary Outcome 1 - Timeframe: Change from Baseline to 30 Days After Date of Surgery

CONDITION

  • Stoma Ileostomy

ELIGIBILITY


Inclusion Criteria:

- Patients must be presumed to undergo a radical cystectomy with ileal conduit diversion

- Diagnosis of bladder cancer

Exclusion Criteria:

- Patients undergoing a radical cystectomy with ileal conduit for any reason other than
bladder cancer will not be allowed to participate

Gender: All

Minimum Age: N/A

Maximum Age: 18 Years

Healthy Volunteers: No

OFFICIAL INFORMATION

Name: Moben Mirza, MD

Role: Principal Investigator

Affiliation: University of Kansas Medical Center

Overall Contact

Name: Moben Mirza, MD

Phone: (913) 574-0847

Email: adahlgren@kumc.edu

LOCATION

Facility Status Contact
Facility: University of Kansas Medical Center
Kansas City, Kansas 66160
United States
Status: Recruiting Contact: N/A