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Published in: Supportive Care in Cancer 7/2007

01-07-2007 | Original Article

Phase I participants’ views of quality of life and trial participation burdens

Authors: Marlene Zichi Cohen, Jacquelyn Slomka, Rebecca D. Pentz, Anne L. Flamm, David Gold, Roy S. Herbst, James L. Abbruzzese

Published in: Supportive Care in Cancer | Issue 7/2007

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Abstract

Purpose

Participants’ perception of quality of life (QOL) and respondent burden have significant implications for investigators’ ethical responsibilities to their subjects in phase I cancer trials. To address these responsibilities, analysis was conducted on participants’ views of their experiences of a phase I trial, including the associated burdens and what constitutes QOL.

Patients and methods

One hundred potential participants of the endostatin trial were surveyed. Sixteen of the 18 trial participants were interviewed extensively about their experiences on the trial.

Results

Participants described ‘normality’ as a baseline ability to function, be productive, and be free from symptoms of disease and side effects of treatment. Reflecting the relative nontoxicity of the study drug, participants contrasted their current QOL with their negative experience of previous cancer treatments and viewed their QOL as fairly good. However, participants emphasized that indirect and procedural burdens of trial participation had a significant impact on their current QOL.

Conclusions

Candid descriptions of a trial’s practical demands, in addition to potential physical complications in a trial, could improve the quality of informed consent.
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Metadata
Title
Phase I participants’ views of quality of life and trial participation burdens
Authors
Marlene Zichi Cohen
Jacquelyn Slomka
Rebecca D. Pentz
Anne L. Flamm
David Gold
Roy S. Herbst
James L. Abbruzzese
Publication date
01-07-2007
Publisher
Springer-Verlag
Published in
Supportive Care in Cancer / Issue 7/2007
Print ISSN: 0941-4355
Electronic ISSN: 1433-7339
DOI
https://doi.org/10.1007/s00520-007-0216-0

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