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Living With Cervical Cancer: Assessing Utilities Associated With Common Treatment Complications

Completed
Conditions
Cervical Cancer
Registration Number
NCT01039493
Lead Sponsor
University of Wisconsin, Madison
Brief Summary

The objective of this study is to establish patient preferences in regards to common complications of cervical cancer treatments, and to compare these preferences to those of medical providers who care for cervical cancer patients. These preferences will be determined via a interview using the Standard Gamble, which is a well-recognized method for establishing utilities.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
40
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.

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Utilities of complications associated with cervical cancer treatment.At time of interview
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

University of Wisconsin-Madison

🇺🇸

Madison, Wisconsin, United States

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