Expectations of Benefit in Early-Phase Clinical Trials: Implications for Assessing the Adequacy of Informed Consent
- 31 March 2008
- journal article
- research article
- Published by SAGE Publications in Medical Decision Making
- Vol. 28 (4) , 575-581
- https://doi.org/10.1177/0272989x08315242
Abstract
Background. Participants in early-phase clinical trials have reported high expectations of benefit from their participation. There is concern that participants misunderstand the trials to which they have consented, which is based on assumptions about what patients mean when responding to questions about likelihood of benefit.Methods.Participants were 27 women and 18 men in early-phase oncology trials at 2 academic medical centers in the United States. To determine whether expectations of benefit differ depending on how patients are queried, the authors randomly assigned participants to 1 of 3 interviews corresponding to 3 questions about likelihood of benefit: frequency type, belief type, and vague. In semistructured interviews, participants were queried about how they understood and answered the question. Participants then answered and discussed 1 of the other questions.Results.Expectations of benefit in response to the belief-type question were significantly greater than expectations in response to the frequency-type and vague questions (P=0:02). The most common justifications involved positive attitude (n=27 [60%]) and references to physical health (n=23 [51%]). References to positive attitude were most common among participants with higher (> 70%) expectations (n = 11 [85%]) and least common among those with lower ( < 50%) expectations (n = 3 [27%]).Conclusions. The wording of questions about likelihood of benefit shapes the expectations that patients express. Patients who express high expectations may not do so to communicate understanding but rather to register optimism. Ongoing research will clarify the meaning of high expectations and examine methods for assessing understanding.Keywords
This publication has 20 references indexed in Scilit:
- Communication and informed consent in phase 1 trials: a review of the literatureSupportive Care in Cancer, 2006
- Therapeutic misconception in early phase gene transfer trialsSocial Science & Medicine, 2006
- Discursive Versus Information-Processing Perspectives on a Bioethical ProblemTheory & Psychology, 2004
- Ethics of Phase 1 Oncology StudiesJAMA, 2003
- Perceptions of Patients and Physicians Regarding Phase I Cancer Clinical Trials: Implications for Physician-Patient CommunicationJournal of Clinical Oncology, 2003
- The correlation between patient characteristics and expectations of benefit from Phase I clinical trialsCancer, 2003
- Consent Forms for Oncology TrialsNew England Journal of Medicine, 2003
- Descriptions of Benefits and Risks in Consent Forms for Phase 1 Oncology TrialsNew England Journal of Medicine, 2002
- Personal contact, individuation, and the better-than-average effect.Journal of Personality and Social Psychology, 1995
- Variants of uncertaintyPublished by Cambridge University Press (CUP) ,1982