Trial Information
Living With Cervical Cancer: Assessing Utilities Associated With Common Treatment Complications
Inclusion Criteria:
- A subject has to have been diagnosed with early cervical cancer (Stage I or II)
within the last 3 years and/or take care of patients with cervical cancer and
identify her or himself as one of the following: gynecologic oncologist, radiation
oncologist, physician's assistant or nurse.
- Subjects must be ≥18 and <61 years old.
Exclusion Criteria:
- Subjects who are unable to read and speak English proficiently will be excluded.
Proficiency will be assessed by the investigator enrolling patients.
- Subjects who do not have capacity to consent will not be included in this study.
- Subjects may not be investigators on this study.
Type of Study:
Observational
Study Design:
Time Perspective: Cross-Sectional
Outcome Measure:
Utilities of complications associated with cervical cancer treatment.
Outcome Time Frame:
At time of interview
Safety Issue:
No
Principal Investigator
Ellen M Hartenbach, MD
Investigator Role:
Principal Investigator
Investigator Affiliation:
University of Wisconsin, Madison
Authority:
United States: Institutional Review Board
Study ID:
M-2009-1240
NCT ID:
NCT01039493
Start Date:
February 2010
Completion Date:
August 2010
Related Keywords:
- Cervical Cancer
- Uterine Cervical Neoplasms
Name | Location |
University of Wisconsin-Madison |
Madison, Wisconsin 53792 |