Abstract
In a representative German sample, 62.1% of participants of cancer screening interventions indicated willingness to provide personal data for data-linkage with cancer registries. An agreement of over 90% is deemed necessary to conduct a meaningful population-based evaluation. The 'early detection of cancer and cancer regisÂ-tries' bill proposed a procedure based on the use of pseudonyms only. This way personal consent is not required but participants are granted the right to object.
Titel in Übersetzung | Collection and processing of personal data to evaluate cancer screening programmes - Results of a survey of the German population in light of the bill 'early detection of cancer and cancer registries |
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Originalsprache | Deutsch |
Zeitschrift | Gesundheitswesen |
Jahrgang | 75 |
Ausgabenummer | 11 |
Seiten (von - bis) | 751-753 |
Seitenumfang | 3 |
ISSN | 0941-3790 |
DOIs | |
Publikationsstatus | Veröffentlicht - 18.10.2013 |