ArticleResearch square2026
Neural Correlates of Palliative Care: A Feasibility Trial in Patients with Metastatic Gastrointestinal and Lung Cancer.
Article in Research square, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05137782 (The Science of the Art of Palliative Care Pilot), which is not on this map. Not yet cited in PubMed.
What it found
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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.
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.
The Science of the Art of Palliative Care Pilot
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
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Authors and funding
8 authors.
Funding
Abstract
Background: The fundamental affective and decisional processes by which specialty palliative care (SPC) reduces suffering and decreases aggressive treatment at the end of life are not completely understood. We sought to test the feasibility, acceptability, and tolerability of conducting a clinical trial of SPC for advanced cancer patients and their care partners involving functional magnetic resonance imaging (fMRI) to further understand the mechanisms of action of SPC. Methods: This pilot open-label, single-arm observational case series was conducted at the Dartmouth Cancer Center (DCC) in collaboration with the Dartmouth Brain Imaging Center (DBIC). Participants included patients with metastatic gastrointestinal or lung cancer, their care partners, and their palliative care physician. The intervention consisted of 8-16 weeks of specialty palliative care integrated with usual oncologic care. Assessments included two fMRI study visits involving the collection of physiological measurements during audiovisual stimulation pre- and post-SPC receipt. Results: The primary outcomes were feasibility (rates of enrollment, intervention receipt), acceptability (closed-ended start and end-of- study feedback for participants and open-ended feedback for non-enrollees), and tolerability (study burden). Of 1216 screened electronic medical records, 21 patients fulfilled the eligibility criteria, of which four patients (19%) and three care partners consented to participate in the study. One participant and their care partner completed all study procedures, one participant withdrew before the first session due to disease progression, and the other two withdrew after 6 and 3 visits, respectively, due to health-related decline, logistical challenges, or emotional concerns. Conclusion: The study did not achieve its pre-determined criteria for success. Primary reasons for infeasibility were low recruitment and high attrition rates. The study's results suggest that a more definitive mechanistic study cannot be conducted at this site without addressing critical barriers to enrollment and retention in this vulnerable clinical population. Trial registration: ClinicalTrials.gov NCT05137782, first release date 11/17/2021.
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