Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2021 Mar;61(3):555-565.e5.
doi: 10.1016/j.jpainsymman.2020.08.002. Epub 2020 Aug 16.

User-Centered Design of the consideRATE Questions, a Measure of People's Experiences When They Are Seriously Ill

Affiliations
Review

User-Centered Design of the consideRATE Questions, a Measure of People's Experiences When They Are Seriously Ill

Catherine H Saunders et al. J Pain Symptom Manage. 2021 Mar.

Abstract

Context: No brief patient-reported experience measure focuses on the most significant concerns of seriously ill individuals.

Objectives: The objective of the study was to develop the consideRATE questions.

Methods: This user-centered design study had three phases. We reviewed the literature and consulted stakeholders, including caregivers, clinicians, and researchers, to identify the elements of care most important to patients (Phase 1). We refined items based on cognitive interviews with patients, families, and clinicians (Phase 2). We piloted the measure with patients and families (Phase 3).

Results: Phase 1 resulted in seven questions addressing the following elements: 1) care team attention to patients' physical symptoms, 2) emotional symptoms, 3) environment of care, 4) respect for patients' priorities, 5) communication about future plans, 6) communication about financial and similar affairs, and 7) communication about illness trajectory. Phase 2 participants included eight patients, eight family members, and seven clinicians. We added an open-text comment option. We did not identify any other issues that were important enough to participants to include. Response choices ranged from one (very bad) to four (very good), with a not applicable option (does not apply). Phase 3 involved 15 patients and 16 family members and demonstrated the acceptability of the consideRATE questions. Most reported that the questions were not distressing, disruptive, or confusing. Completion time averaged 2.4 minutes (range 1-5).

Conclusion: Our brief patient-reported serious illness experience measure is based on what matters most to patients, families, and clinicians. It was acceptable to patients and families in a regional sample. It has promise for use in clinical settings.

Keywords: Serious illness; measurement; palliative care; patient-reported experience measure; patient-reported outcome measure.

PubMed Disclaimer

Figures

Fig. 1.
Fig. 1.
Iterative the consideRATE questions development.
Fig. 2.
Fig. 2.
Most important elements of serious illness care comprising the consideRATE suite constructs. Note: Based on the systematic review by Virdun et al. Numbers correspond to ranked elements of serious illness experience, according to patient priorities. Adequate environment for care and minimizing burden tied for fifth most important elements of care.
Fig. 3.
Fig. 3.
Changes in the consideRATE question instructions and items. Note: See Appendix IV for complete measure items.

References

    1. Singer AE, Meeker D, Teno JM, et al. Symptom trends in the last year of life from 1998 to 2010. Ann Intern Med 2015; 162:175. - PMC - PubMed
    1. Soothill K, Morris SM, Harman J, et al. The significant unmet needs of cancer patients: probing psychosocial concerns. Support Care Cancer 2001;9:597e605. - PubMed
    1. Krishnasamy M, Wilkie E, Haviland J. Lung cancer health care needs assessment: patients’ and informal carers’ responses to a national mail questionnaire survey. Palliat Med 2001;15:213e227. - PubMed
    1. Kelley AS, Bollens-Lund E. Identifying the population with serious illness: the “denominator” challenge. J Palliat Med 2018;21:S7eS16. - PMC - PubMed
    1. Zhang B, Wright AA, Huskamp HA, et al. Health care costs in the last week of life: associations with end-of-life conversations. Arch Intern Med 2009;169:480e488. - PMC - PubMed