Evidence map›Paper›PMID 42625801›Full record

ArticleDigital health

Mobilizing participation: The first German stakeholder conference on engaging patients and self-help organizations in digital health research.

Paula Nadler, Manuel Schaper, Thomas M Duda, Hartmut Gartzke, Wiebke Papenthin, Verena Winter, Silke Schicktanz, Sabine Wöhlke

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Article in Digital health. 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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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Paula NadlerFaculty of Health, Hamburg University of Applied Sciences (HAW), Hamburg, Germany.
Manuel SchaperFaculty of Health, Hamburg University of Applied Sciences (HAW), Hamburg, Germany.ORCID https://orcid.org/0000-0002-2385-5031
Thomas M DudaPRO Retina Foundation for the Prevention of Blindness, Bonn, Germany.
Hartmut GartzkeADHS Deutschland e.V., Berlin, Germany.
Wiebke PapenthinAllianz Chronischer Seltener Erkrankungen (ACHSE) e.V., Berlin, Germany.
Verena WinterLymphselbsthilfe e.V., Herzogenaurach, Germany.
Silke SchicktanzDepartment of Medical Ethics and History of Medicine, University Medical Center Göttingen, Germany.ORCID https://orcid.org/0000-0001-9627-752X
Sabine WöhlkeFaculty of Health, Hamburg University of Applied Sciences (HAW), Hamburg, Germany.ORCID https://orcid.org/0000-0002-7679-085X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Digital transformation in the healthcare sector within the European Union (EU) raises various ethical concerns regarding the use of health research data and regarding how to address such concerns through ethical governance. Methods: This article presents the results of the first German national stakeholder conference - a structured discourse process for developing political or ethical positions through citizen participation - which included patient organizations (POs) and self-help organizations (SHOs) (N=45). Participants were asked to describe their positions regarding participation and engagement in digital health research and health research data-sharing policies in an interactive process, facilitated by researchers from health care ethics. Results: POs/SHOs emphasize the ethical relevance of patient autonomy and transparency as preconditions for trust. Therefore, data protection and transparent consent procedures are seen as a necessary part of responsible research. While recognizing the potential of large-scale data use to increase research efficiency, they stress the importance of promoting patient-centeredness through participatory approaches. Structured participation requires clear definition of tasks, empowerment of POs/SHOs, understanding of the special features of voluntary structures, and target group-oriented, barrier-free communication of research results. Their support depends on upholding strong legal safeguards and respecting individual rights. Additional demands include improved digital literacy, health literacy, and financial resources. Conclusions: Future research should focus on dynamic consent models and fair participation structures. From the start, it should be clarified to POs/SHOs whether intended research projects are oriented toward the public good or primarily commercial. This can be an important factor in their decision to participate in research.

Indexed as

data-sharingdigital health researchparticipatory health researchpatient organizationsposition paperpublic involvementstakeholder conference

Identifiers

PMID42625801
PMCPMC13490783

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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.