Evidence map›Paper›PMID 41709015›Full record

ArticleQuality of life research : an international journal of quality of life aspects of treatment, care and rehabilitation2026

Balancing ideals and realities: health care professionals' perspectives of and attitudes toward digital patient-centered cancer care.

Elias David Lundereng, Alen Brkic, Kate Absolom, Elisabeth Andvik, Kim Beernaert, Kathrin Cresswell, Olav Faisal Dajani, Nienke De Glas, Marie Fallon, Victoria Freitas-Durks and 12 more

Abstract read
In one paragraph

Article in Quality of life research : an international journal of quality of life aspects of treatment, care and rehabilitation, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

22 authors.

Elias David LunderengEuropean Palliative Care Research Centre (PRC), Department of Oncology, Oslo University Hospital, and Institute of Clinical Medicine, University of Oslo, Oslo, Norway. eliasdl@uio.no.ORCID http://orcid.org/0000-0002-7483-3174
Alen BrkicEuropean Palliative Care Research Centre (PRC), Department of Oncology, Oslo University Hospital, and Institute of Clinical Medicine, University of Oslo, Oslo, Norway.
Kate AbsolomLeeds Institute of Health Services Research, Leeds Institute of Medical Research, University of Leeds, Leeds, UK.
Elisabeth AndvikBI Norwegian Business School, Bergen, Norway.
Kim BeernaertEnd-of-Life Care Research Group, Vrije Universiteit Brussel (VUB) & Ghent University, Brussels, Belgium.
Kathrin CresswellUsher Institute, The University of Edinburgh, College of Medicine and Veterinary Medicine, University of Edinburgh, Edinburgh, UK.
Olav Faisal DajaniEuropean Palliative Care Research Centre (PRC), Department of Oncology, Oslo University Hospital, and Institute of Clinical Medicine, University of Oslo, Oslo, Norway.
Nienke De GlasDepartment of Medical Oncology, Helse Førde, Svanehaugvegen 2, 6812, Førde, Norway.
Marie FallonInstitute of Genetics and Cancer, University of Edinburgh, Edinburgh, UK.
Victoria Freitas-DurksINCLIVA Instituto de Investigación Sanitaria, Valencia, Spain.
Kristin Vassbotn GuldhavDepartment of Medical Oncology, Helse Førde, Svanehaugvegen 2, 6812, Førde, Norway.
Marianne Jensen HjermstadEuropean Palliative Care Research Centre (PRC), Department of Oncology, Oslo University Hospital, and Institute of Clinical Medicine, University of Oslo, Oslo, Norway.
Stein KaasaEuropean Palliative Care Research Centre (PRC), Department of Oncology, Oslo University Hospital, and Institute of Clinical Medicine, University of Oslo, Oslo, Norway.
Geana Paula KuritaDepartment of Clinical Medicine, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
Jo-Åsmund LundMATRIX, Norwegian Centre for Clinical Cancer Research, Oslo, Norway.
Nicoleta MitreaDepartment of Fundamental Disciplines and Clinical Prevention, Faculty of Medicine, University of Transilvania, Brasov, Romania.
Steven Olde DaminkDepartment of Surgery, Maastricht University Medical Centre, Maastricht, The Netherlands.
Ørnulf PaulsenMATRIX, Norwegian Centre for Clinical Cancer Research, Oslo, Norway.
Guro Meldre PedersenDNV AS, Oslo, Norway.
Terese Solvoll SkåreDepartment of Health Sciences Ålesund, Faculty of Medicine and Health Sciences, Norwegian University of Science and Technology, Ålesund, Norway.
Tonje LundebyEuropean Palliative Care Research Centre (PRC), Department of Oncology, Oslo University Hospital, and Institute of Clinical Medicine, University of Oslo, Oslo, Norway.
The MyPath consortium

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposePatient-centered care (PCC) improves quality of life, symptom management and healthcare outcomes in oncology. However, integration into routine cancer care remains limited. Digital solutions using patient-reported outcome measures (PROMs) offer a potential mechanism to operationalize PCC. This study explored healthcare professionals' (HCPs) pre-implementation perspectives on using digital PROMs to support PCC in Norwegian oncology outpatient clinics, informing the design and implementation strategies of the European MyPath digital solution.

methodsSemi-structured interviews (n = 29) and three focus groups (n = 16) were conducted with varied HCPs across four Norwegian hospitals. Interviews explored perceptions of PCC, experiences with PROMs, and requirements for digital implementation. Data were analyzed using thematic analysis, combining inductive and deductive coding guided by the TPOM framework.

resultsFour themes emerged: (1) balancing PCC with disease-centered practices, (2) integrating PCC into daily routines, (3) customization and patient acceptance of digital tools, and (4) combining patient-reported data with clinical autonomy. HCPs viewed digital PROMs as promising for facilitating PCC but emphasized that successful implementation requires workflow alignment, adaptable digital solutions, and strong stakeholder engagement. Concerns included patient digital literacy, workload implications, and overreliance on PROMs at the expense of direct patient interaction.

conclusionOur findings highlight a tension between HCPs' needs for technical functionality and workflow alignment, and the support required to adapt their practice to fully realize PCC through digital tools. Integrating PCC successfully requires organizational, cultural, and workflow adaptations, alongside active HCP engagement in design and implementation. These changes are essential to reposition PCC as an integral rather than competing component of high-quality cancer care.

Indexed as

Attitude of Health PersonnelHealth PersonnelNeoplasmsPatient-Centered CarePatient Reported Outcome MeasuresAdultDigital HealthDigital MediaFemaleFocus GroupsHumansInterviews as TopicMaleMiddle AgedNorwayQualitative ResearchDigital healthImplementation scienceOncologyPatient-centered carePROMsQualitative researchQuality of life

Identifiers

PMID41709015
PMCPMC12916892

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.