Enhancing decision making about participation in cancer clinical trials: development of a question prompt list. Academic Article uri icon

Overview

abstract

  • PURPOSE: Slow accrual to cancer clinical trials impedes the progress of effective new cancer treatments. Poor physician-patient communication has been identified as a key contributor to low trial accrual. Question prompt lists (QPLs) have demonstrated a significant promise in facilitating communication in general, surgical, and palliative oncology settings. These simple patient interventions have not been tested in the oncology clinical trial setting. We aimed to develop a targeted QPL for clinical trials (QPL-CT). METHOD: Lung, breast, and prostate cancer patients who either had (trial experienced) or had not (trial naive) participated in a clinical trial were invited to join focus groups to help develop and explore the acceptability of a QPL-CT. Focus groups were audio-recorded and transcribed. A research team, including a qualitative data expert, analyzed these data to explore patients' decision-making processes and views about the utility of the QPL-CT prompt to aid in trial decision making. RESULTS: Decision making was influenced by the outcome of patients' comparative assessment of perceived risks versus benefits of a trial, and the level of trust patients had in their doctors' recommendation about the trial. Severity of a patient's disease influenced trial decision making only for trial-naive patients. CONCLUSION: Although patients were likely to prefer a paternalistic decision-making style, they expressed valuation of the QPL as an aid to decision making. QPL-CT utility extended beyond the actual consultation to include roles both before and after the clinical trial discussion.

publication date

  • July 1, 2010

Research

keywords

  • Clinical Trials as Topic
  • Decision Making
  • Neoplasms
  • Patient Education as Topic
  • Patient Participation

Identity

PubMed Central ID

  • PMC4834985

Scopus Document Identifier

  • 80051578589

Digital Object Identifier (DOI)

  • 10.1007/s00520-010-0942-6

PubMed ID

  • 20593202

Additional Document Info

volume

  • 19

issue

  • 8