CareLit Fachartikel

Patients’ willingness to provide their clinical data for research purposes and acceptance of different consent models. Findings from a representative survey of cancer patients in…

Köngeter, A.; Schickhardt, C.; Jungkunz, M.; Bergbold, S.; Mehlis, K.; Winkler, E. · Das Gesundheitswesen · 2022 · Heft 8/09 · S. 1 bis 1

Dokument
576910
CareLit-ID
Jahr
2022
Publikation
PDF
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Metadaten
DOI
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Bibliografische Angaben

Zeitschrift
Das Gesundheitswesen
Autor:innen
Köngeter, A.; Schickhardt, C.; Jungkunz, M.; Bergbold, S.; Mehlis, K.; Winkler, E.
Ausgabe
Heft 8/09 / 2022
Jahrgang 84
Seiten
1 bis 1
Erschienen: 2022-08-22 13:00:00
ISSN
0941-3790

Zusammenfassung

Einleitung Secondary use of clinical data for biomedical research purposes holds great potential for various types of non-interventional, data-driven studies. Patients’ willingness to support research with their clinical data is a crucial prerequisite for research progress. The aim of the study is to learn about patients’ attitudes and expectations regarding secondary use of their clinical data in order to inform the development of an appropriate governance framework for secondary use of clinical data for research purposes. Methoden A questionnaire was developed to assess willingness of cancer patients to provid…

Schlagworte

klinische Daten Patientenwille Forschung Einwilligungsmodelle Datenschutz Krebsregister Umfrage Datenfreigabe Patient Acceptance of Health Care Data Sharing Consent Forms Neoplasms Surveys and Questionnaires Research Support as Topic Das Gesundheitswesen