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NCT03188055

A Communication Tool to Assist Severely Injured Older Adults

Completed NA Results posted Last updated 4 November 2025
What this trial tests

NA trial testing Best Case/Worst Case communication tool in Communication in 298 participants. Completed in 3 March 2020.

Timeline
14 July 2017
Primary endpoint
20 December 2019
3 March 2020

Quick facts

Lead sponsorUniversity of Wisconsin, Madison
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationnon randomized
Designparallel
Maskingsingle
Primary purposeother
Enrollment298
Start date14 July 2017
Primary completion20 December 2019
Estimated completion3 March 2020
Sites2 locations across United States

Drugs / interventions tested

Conditions studied

Sponsor

University of Wisconsin, Madison

Who can join

50 and older, any sex, with Communication. Patients with the condition only — healthy volunteers not accepted.

Results — posted to ClinicalTrials.gov

Per-arm endpoint measurements with 95% confidence intervals where reported. Source: trial results section.

Family Member-reported Quality of End of Life Communication (QOC) Received From Study Surgeon Primary · 72 hours after trauma unit admission

Family member-reported quality of end of life communication will be measured by the 7-item end of life subscale of the Quality of Communication scale. The QOC is a validated self-report instrument. The average score is given with a possible range of 0-10. Higher scores indicate higher perceived quality of end of life communication

GroupValue95% CI
Best Case/Worst Case Communication Tool6.6± 2.6
Usual Care4.5± 2.5
Family Member-reported General Communication (QOC) Received From Study Surgeon Primary · 72 hours after trauma unit admission

Family member-reported general quality of end communication will be measured by the 6-item general communication subscale of the Quality of Communication scale. The QOC is a validated self-report instrument. The average score is given with a possible range of 0-10. Higher scores indicate higher perceived quality of communication

GroupValue95% CI
Best Case/Worst Case Communication Tool8.5± 1.9
Usual Care8.3± 1.72
Nurse-reported Quality of End of Life Communication (QOC) Received From Study Surgeon Secondary · 72 hours after trauma unit admission

Nurse-reported quality of end of life communication will be measured by the 7-item Quality of Communication scale, end of life subscale, clinician version. The QOC is a validated self-report instrument. The average score is given with a possible range of 0-10.Higher scores indicate higher perceived quality of communication

GroupValue95% CI
Best Case/Worst Case Communication Tool6± 2.79
Usual Care4.1± 2.3
Nurse-reported General Quality of Communication (QOC) Received From Study Surgeon Secondary · 72 hours after trauma unit admission

Nurse-reported general quality of communication will be measured by the 6-item Quality of Communication scale, general communication subscale, clinician version. The QOC is a validated self-report instrument. The average score is given with a possible range of 0-10. Higher scores indicate higher perceived quality of life communication

GroupValue95% CI
Best Case/Worst Case Communication Tool7.7± 1.96
Usual Care6.7± 1.97
Family-reported Communication and Care Coordination Secondary · 10 days after trauma unit admission

Family-reported communication and care coordination as measured by the 30-item Family Inpatient Communication Survey (FICS). The FICS is a validated instrument. Scores on this instrument may range from 30 to 150 and higher scores indicate greater satisfaction with ICU care

GroupValue95% CI
Best Case/Worst Case Communication Tool114.5± 22.98
Usual Care113.8± 20.87
Family-reported Goal Concordant Care Secondary · 10 days after trauma unit admission

Family-reported goal concordant care will be assessed by 2 survey questions taken from the SUPPORT study (Question 1: If you had to make a choice at this time, would you prefer a course of treatment for your loved one that focuses on extending life as much as possible, even if it means having more pain and discomfort, or would you want a plan of care that focuses on relieving pain and discomfort as much as possible, even if that means not living as long? Question 2: Would you say that your loved one's current medical care is more focused on extending life as much as possible, even if it means

GroupValue95% CI
Best Case/Worst Case Communication Tool16
Usual Care15
Best Case/Worst Case Communication Tool8
Usual Care7
Patient-reported Trauma Quality of Life (TQoL) Secondary · 30 days after trauma unit admission

Patient-reported trauma quality of life (TQoL) as measured by the 43 Trauma Quality of Life (TQoL) survey. The TQoL is a validated measure. Scores may range from 41-172. Higher scores indicate better quality of life

GroupValue95% CI
Best Case/Worst Case Communication Tool115.3± 17.91
Usual Care126.7± 18.12
Family-reported Trauma Quality of Life (TQoL) Secondary · 30 days after trauma unit admission

Family-reported trauma quality of life (TQoL) as measured by the 43 Trauma Quality of Life (TQoL) survey, adapted for use with family members. The TQoL is a validated measure. Scores may range from 41-172. Higher scores indicate better quality of life

GroupValue95% CI
Best Case/Worst Case Communication Tool102.6± 29.63
Usual Care121.7± 12.56
Trauma Nurse-reported Moral Distress Secondary · Start of study and 30 months after study commencement

Trauma unit staff-reported moral distress will be measured by the 21-item Moral Distress Scale-Revised (MDS-R), nurse version. Scores many range from 0 to 336 and higher scores indicate greater moral distress

GroupValue95% CI
Pre-intervention Survey79.48± 47.44
Post-intervention Survey82.56± 40.86
Trauma Physician-reported Moral Distress Secondary · Start of study and 30 months after study commencement

Trauma unit staff-reported moral distress will be measured by the 21-item Moral Distress Scale-Revised (MDS-R), physician version. Scores many range from 0 to 336 and higher scores indicate greater moral distress

GroupValue95% CI
Pre-intervention Survey61.03± 32.32
Post-intervention Survey51.42± 24.03

Sponsor's own description

The purpose of this study is to test the effect of the "Best Case/Worse Case" (BC/WC) communication tool on the quality of communication with older patients admitted to two trauma units. The intervention was developed and tested with acute care surgical patients at the University of Wisconsin (UW) and we are now testing whether the intervention will work in a different setting. We will test the intervention with severely injured older adults at Oregon Health Sciences University (OHSU) and Parkland Memorial Hospital (PMH) at the University of Texas Southwestern (UTS). In the first year, UTS/PMH and OHSU will recruit and enroll 50 patients in the control arm (total, for both sites) and train trauma surgeons to use the best case/worst case tool. In the second year, UTS/PMH and OHSU will recruit and enroll 50 patients in the intervention arm (total, for both sites). UW will compare survey-reported and chart-derived measures before and after clinicians learn to use the best case/worst case tool.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Best case/worst case for the trauma ICU: Development and pilot testing of a communication tool for older adults with traumatic injury.
    Zimmermann CJ, Zelenski AB, Buffington A, Baggett ND, et al · · 2021 · cited 17× · PMID 34039930 · DOI 10.1097/ta.0000000000003281

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Other recruiting trials for Communication

Currently open trials in the same condition.

Other University of Wisconsin, Madison trials

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03188055.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing