Patient-Reported Outcomes Version of Common Terminology Criteria (CTCPRO) Cognitive Debriefing

Completed

Conditions studied: Advanced Cancers, Hematologic Diseases, Solid Tumors

In brief

The scientific aim of this study is to evaluate patient comprehension of the 77 newly developed items as well as the extent to which the items correspond to the concepts of interest for each patient reported outcome (PRO). A secondary aim of this study is to evaluate the usability of the technology interface for collecting the PRO data of the PRO-CTCAE system once it has been built to accommodate the learning garnered during the cognitive interviews.

Key facts

Study ID

NCT00909207

Run by

M.D. Anderson Cancer Center

People needed

20

Starts

2009-07-01

Last updated by the study team

2014-07-14

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Patients must be aged 18 and over
• Able to read and understand English
• Patients with a high school education or less
• Patients who are undergoing chemotherapy or radiotherapy with curative or palliative intent.
• Patient is able to provide informed consent.
• All types of cancer diagnosis

You may not qualify if…

• Significant cognitive impairment as determined by research staff's judgment

Where it is running

• Dana-Farber Cancer Institute — Boston, Massachusetts, United States
• Memorial Sloan-Kettering Cancer Center — New York, New York, United States
• Duke University Medical Center — Durham, North Carolina, United States
• UT MD Anderson Cancer Center — Houston, Texas, United States

Full record on ClinicalTrials.gov

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