ReviewEcancermedicalscience2026
Patient and public involvement in cancer care and research: the Indian perspective.
Review in Ecancermedicalscience, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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.
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.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
6 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Biomedical research aims at improving human health through scientific studies, and is crucial for medical progress through identifying more effective ways to prevent, diagnose and treat disease. Patients (and public) are integral elements in medical research, and no research is meaningful unless it is patient (or person) centered. However, conventionally, the role of patients and the public has been restricted to only being participants in research. There is growing awareness that to be truly person-centered, research must include the patient and public voice at every stage of the research process, including priority setting, asking the right question, designing and conducting the study, interpreting and disseminating the results and ensuring that research informs policy. While this framework is reasonably well-established in some high-resource countries, it is at a very nascent stage in resource-poor settings. In this article, we examine the role of patient and public involvement in cancer care and research, with a focus on the Indian perspective.
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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.