MedPath

Prostate Cancer Survey

Completed
Conditions
Prostate Cancer
Registration Number
NCT03128710
Lead Sponsor
University of Maryland, Baltimore
Brief Summary

There have been calls from patients, payers, healthcare providers, and policy makers for an evaluation of newer, high-cost radiation technologies compared to conventional forms of radiation therapy. National attention has focused on the use of intensity modulated radiation therapy (IMRT) into routine daily clinical practice for prostate cancer. The goal of the present study is to determine whether the type of radiation treatment received by the patients can result in a reduction in patient-relevant side effects following prostate irradiation. The analysis will be performed by obtaining patient answered surveys looking at side effects.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
Male
Target Recruitment
224
Inclusion Criteria
  • Participant is 18 years or older
  • Has been diagnosed with prostate cancer
  • Able to speak and read English
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Exclusion Criteria
  • Participant is not being seen for prostate cancer
  • Under the age of 18
Read More

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To determine patient preference weights for side effect reduction in radiation treatment of prostate cancer3 years

Investigators will use an anonymous survey and results from multiple focus groups to quantify the relative importance/significance of commonly encountered side effects experienced by patients following external beam radiation therapy. We will complete descriptive statistics as a means of understanding the data obtained by survey responses. Additionally, comparative analyses may be undertaken to evaluate differences between different side effects experienced.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

UMMC

🇺🇸

Baltimore, Maryland, United States

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