Evidence map›Paper›PMID 42014153›Full record

ArticleBMJ open2026

Participatory development and feasibility study of a digital intervention for detecting and treating bio-psycho-social needs of long-term cancer survivors: study protocol of the DELPHIN study.

Rieka von der Warth, Annalia Gminder, Arian Karimzadeh, Katharina Averdunk, Cosimo Döppenschmitt, Renate Pfeifer, Matthias Schmid, Ingo G H Schmidt-Wolf, Matthias Weigl, Benjamin Aretz and 2 more

Abstract read
In one paragraph

Article in BMJ open, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

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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

12 authors.

Rieka von der WarthUniversity Hospital Bonn, Institute for Family Medicine, University of Bonn, Bonn, Germany rieka.von-der-warth@ukbonn.de.ORCID http://orcid.org/0000-0003-2445-8019
Annalia GminderUniversity Hospital Bonn, Institute for Family Medicine, University of Bonn, Bonn, Germany.
Arian KarimzadehUniversity Hospital Bonn, Institute for Family Medicine, University of Bonn, Bonn, Germany.
Katharina AverdunkUniversity Hospital Bonn, Institute for Patient Safety, University of Bonn, Bonn, Germany.
Cosimo DöppenschmittGerman Foundation for Young Adults with Cancer, Meeting Point Bonn, Bonn, Germany.
Renate PfeiferPatient Representative in the Joint Federal Committee, Bonn, Germany.
Matthias SchmidUniversity Hospital Bonn, Institute for Medical Biometry, Informatics, and Epidemiology (IMBIE), University of Bonn, Bonn, Germany.
Ingo G H Schmidt-WolfUniversity Hospital Bonn, Department of Integrated Oncology Bonn, CIO Bonn, University of Bonn, Bonn, Germany.
Matthias WeiglUniversity Hospital Bonn, Institute for Patient Safety, University of Bonn, Bonn, Germany.
Benjamin AretzUniversity Hospital Bonn, Institute for Medical Biometry, Informatics, and Epidemiology (IMBIE), University of Bonn, Bonn, Germany.
Franziska GeiserUniversity Hospital Bonn, Clinic and Polyclinic for Psychosomatic Medicine and Psychotherapy, University of Bonn, Bonn, Germany.
Birgitta WeltermannUniversity Hospital Bonn, Institute for Family Medicine, University of Bonn, Bonn, Germany.ORCID http://orcid.org/0000-0002-1285-1545

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionLong-term cancer survivors may suffer from significant bio-psycho-social burden even years after treatment. Yet, a structured approach to detect and address bio-psycho-social burden of long-term cancer survivors in primary care is missing in Germany, although family physicians are the primary medical contact for most patients. In this paper, we describe the DELPHIN study aiming to develop and test a structured care model for long-term cancer survivors. The DELPHIN study and intervention will facilitate networking of regional medical and non-medical services. This protocol describes the intervention as well as the pilot study.

methodsThe DELPHIN study comprises a developmental and a feasibility phase. In the developmental phase, we will assess (1) the current care needs of long-term cancer survivors (n=1000) using a cross-sectional questionnaire survey; (2) in an additional cross-sectional questionnaire survey, we will address medical and non-medical care providers to assess current care practice for this patient group (n≥250); (3) a qualitative interview study with both long-term cancer survivors (n=12) and family physicians (n=10) will assess patients' needs and barriers for effective care. Results will then be triangulated to inform development of the DELPHIN intervention. The intervention shall include the following elements: the DELPHIN mobile app for patients with a digital screening tool, a digital treatment plan, a survivorship passport and information on regional medical and non-medical providers. Additionally, a DELPHIN website and a DELPHIN eLearning tool for family physicians will be developed. The subsequent feasibility study will follow 100 long-term cancer survivors using the DELPHIN app for 4 months, with two assessments (t DISCUSSION: The DELPHIN study seeks to address cancer survivors' unmet bio-psycho-social needs through implementing a digital mobile application. Positive results in the feasibility study will provide the basis for a future effectiveness study and integration into routine care. ETHICS AND DISSEMINATION: The study was reviewed by the Ethics Committee of the University of Bonn, Germany (No: 2024-409 BO) which did not object to the study. TRIAL REGISTRATION NUMBER: DRKS00035726.

Indexed as

Cancer SurvivorsCross-Sectional StudiesDigital HealthFeasibility StudiesFemaleGermanyHumansMaleNeeds AssessmentPilot ProjectsQuality of LifeSurveys and QuestionnairesAdult oncologyeHealthPsychosocial InterventionSocial Support

Identifiers

PMID42014153
PMCPMC13110596

What OpenQuestion holds

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LicenceCC BY-NC
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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.