60 and older, any sex, with Hematologic Neoplasms. 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.
Content Validity of Best-Worst Scaling (BWS) SurveyPrimary· 3 months after treatment decision
Cognitive interviewing will be used to evaluate the content validity of using a BWS survey to quantify the preferences of older patients with hematologic malignancies at the point-of-care. BWS survey asks patients a series of questions where they choose one attribute as best and one as worst - the 7 included in this survey are maintaining usual activities, living longer, avoiding dependence on others, avoiding short-term side effects, avoiding long-term side effects, avoiding hospitalizations, and avoiding high out-of-pocket costs.
Participants who were able to accurately define each attribute and reported no missing domains.
Group
Value
95% CI
Qualitative Interviews
10
Participants who could not define attributes or reported missing domains.
Group
Value
95% CI
Qualitative Interviews
0
Acceptability of Best-Worst Scaling (BWS) Survey to PatientsSecondary· Up to 7 days after treatment decision
Number of patients who respond with agree/strongly agree to "I found survey acceptable to clarify my preferences"
Group
Value
95% CI
Pilot Testing: Participants With Newly-diagnosed Hematologic Malignancies
13
Preliminary Efficiency of Best-Worst Scaling (BWS) SurveySecondary· Up to 7 days after treatment decision
Number of patients who respond moderately effective/very affective to "how effective was the survey to help you and your doctor choose a treatment that was consistent with your goals?"
Group
Value
95% CI
Pilot Testing:
9
Completion Rate Over TimeSecondary· Up to 1 year
The completion rate over time will be reported by the number of patients who complete the BWS survey at each time point, in 3 months intervals.
consented
Group
Value
95% CI
All Participants
51
started BWS instrument at baseline
Group
Value
95% CI
All Participants
27
completed BWS instrument at baseline
Group
Value
95% CI
All Participants
26
completed study-associated surveys after their treatment encounter at least 1 time
Group
Value
95% CI
All Participants
19
completed study-associated surveys after their treatment encounter more than 1 time (median 8 times)
Group
Value
95% CI
All Participants
16
Sponsor's own description
This study will evaluate the validity of using a survey to quantify patient preferences at the point-of-care and the potential effectiveness of the survey to improve goal-concordant care. The primary hypothesis is that by identifying the strength of patient preferences for outcomes with this survey clinicians will be able to improve goal-concordant care by aligning clinical recommendations with patients' preferences. This study will have 50 patients with newly diagnosed hematologic malignancy complete the survey throughout their disease course (up to 2 years) and conduct qualitative interviews with a subset (n = 20) of participants. The information obtained from these participants will be used to refine the survey. Interviews with oncologists and palliative care specialists (up to 10) will inform implementation.
Publications & conference data
1 peer-reviewed publication reference this trial (live from Europe PMC):
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Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
Sponsor: as reported to ClinicalTrials.gov by UNC Lineberger Comprehensive Cancer Center
Last refreshed: 27 December 2024
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/NCT05061095.