Evidence map›Paper›PMID 32814165›Full record

ReviewJournal of pain and symptom management2021

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

Catherine H Saunders, Marie-Anne Durand, Peter Scalia, Kathryn B Kirkland, Meredith A MacMartin, Amber E Barnato, David W Milne, Joan Collison, Ashleigh Jaggars, Tanya Butt and 3 more

2 registry-linked trialsAbstract readReview
In one paragraph

Review in Journal of pain and symptom management, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT07024953 nanot yet recruitingnot on this mapstarted 2026, after this paper: background citation

Setting the Agenda: A Pilot Stepped Wedge Cluster Randomized Trial of a Structured Clinical Visit Agenda-Setting Intervention for Rural-Residing People With Advanced Chronic Kidney Disease

TypeinterventionalSponsorDartmouth-Hitchcock Medical CenterRan2026 to 2028Enrolled108ConditionsChronic Kidney Disease Stage 4, Chronic Kidney Disease Stage 5ArmsChronic Kidney Disease Structured Agenda-Setting Tool
NCT07221604 narecruitingnot on this mapstarted 2026, after this paper: background citation

Setting the Agenda: An Open Pilot of a Structured Clinical Visit Agenda-Setting Intervention for Rural-Residing People With Advanced Chronic Kidney Disease

TypeinterventionalSponsorDartmouth-Hitchcock Medical CenterRan2026 to 2026Enrolled30ConditionsChronic Kidney Disease Stage 4ArmsChronic Kidney Disease Structured Agenda-Setting Tool
3 · Its place in the literature

Who cites it

15 citing papers in PubMed, 1 synthesis or guideline pooled it.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors.

Catherine H SaundersThe Dartmouth Institute for Health Policy & Clinical Practice, Lebanon, New Hampshire, USA; Dartmouth-Hitchcock Medical Center, Lebanon, New Hampshire, USA. Electronic address: catherinehylassaunders@gmail.com.
Marie-Anne DurandThe Dartmouth Institute for Health Policy & Clinical Practice, Lebanon, New Hampshire, USA.
Peter ScaliaThe Dartmouth Institute for Health Policy & Clinical Practice, Lebanon, New Hampshire, USA.
Kathryn B KirklandThe Dartmouth Institute for Health Policy & Clinical Practice, Lebanon, New Hampshire, USA; Dartmouth-Hitchcock Medical Center, Lebanon, New Hampshire, USA.
Meredith A MacMartinDartmouth-Hitchcock Medical Center, Lebanon, New Hampshire, USA.
Amber E BarnatoThe Dartmouth Institute for Health Policy & Clinical Practice, Lebanon, New Hampshire, USA.
David W MilnePatient and Family Advisors, Dartmouth-Hitchcock Medical Center, Lebanon, New Hampshire, USA.
Joan CollisonPatient and Family Advisors, Dartmouth-Hitchcock Medical Center, Lebanon, New Hampshire, USA.
Ashleigh JaggarsThe Dartmouth Institute for Health Policy & Clinical Practice, Lebanon, New Hampshire, USA.
Tanya ButtDartmouth-Hitchcock Medical Center, Lebanon, New Hampshire, USA.
Garrett WaspThe Dartmouth Institute for Health Policy & Clinical Practice, Lebanon, New Hampshire, USA; Dartmouth-Hitchcock Medical Center, Lebanon, New Hampshire, USA.
Eugene NelsonThe Dartmouth Institute for Health Policy & Clinical Practice, Lebanon, New Hampshire, USA.
Glyn ElwynThe Dartmouth Institute for Health Policy & Clinical Practice, Lebanon, New Hampshire, USA.

Funding

Training Geriatric Mental Health Services ResearchersT32MH073553 · NIMH · DARTMOUTH-HITCHCOCK CLINIC · PI BRUCE, MARTHA L · 2005 to 2019
$6.4M
NIMH NIH HHS T32 MH073553
6 · The paper itself

Abstract

contextNo brief patient-reported experience measure focuses on the most significant concerns of seriously ill individuals.

objectivesThe objective of the study was to develop the consideRATE questions.

methodsThis 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).

resultsPhase 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).

conclusionOur 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.

Indexed as

FamilyUser-Centered DesignCaregiversCommunicationHumansmeasurementpalliative carepatient-reported experience measurepatient-reported outcome measureSerious illness

Identifiers

PMID32814165
PMCPMC9162500

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.