Erfassung und Verarbeitung von persönlichen Daten zur Evaluation von Krebsfrüherkennungsprogrammen - Ergebnisse einer Bevölkerungsbefragung im Kontext des Krebsfrüherkennungs- und -registergesetzes

F. Greiner; S. Nolte; A. Waldmann; A. Katalinic; E. W. Breitbart

doi:10.1055/s-0033-1355420

Erfassung und Verarbeitung von persönlichen Daten zur Evaluation von Krebsfrüherkennungsprogrammen - Ergebnisse einer Bevölkerungsbefragung im Kontext des Krebsfrüherkennungs- und -registergesetzes

Translated title of the contribution: 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

F. Greiner^*, S. Nolte, A. Waldmann, A. Katalinic, E. W. Breitbart

^*Corresponding author for this work

Institute of Social Medicine and Epidemiology

2 Citations (Scopus)

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.

Translated title of the contribution	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
Original language	German
Journal	Gesundheitswesen
Volume	75
Issue number	11
Pages (from-to)	751-753
Number of pages	3
ISSN	0941-3790
DOIs	https://doi.org/10.1055/s-0033-1355420
Publication status	Published - 18.10.2013

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

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10.1055/s-0033-1355420

Cite this

@article{c9a4c0c24e4c4f84b556bd5c44296ebb,

title = "Erfassung und Verarbeitung von pers{\"o}nlichen Daten zur Evaluation von Krebsfr{\"u}herkennungsprogrammen - Ergebnisse einer Bev{\"o}lkerungsbefragung im Kontext des Krebsfr{\"u}herkennungs- und -registergesetzes",

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 regis{\^A}-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.",

author = "F. Greiner and S. Nolte and A. Waldmann and A. Katalinic and Breitbart, \{E. W.\}",

year = "2013",

month = oct,

day = "18",

doi = "10.1055/s-0033-1355420",

language = "Deutsch",

volume = "75",

pages = "751--753",

journal = "Gesundheitswesen",

issn = "0941-3790",

publisher = "Georg Thieme Verlag",

number = "11",

}

Erfassung und Verarbeitung von persönlichen Daten zur Evaluation von Krebsfrüherkennungsprogrammen - Ergebnisse einer Bevölkerungsbefragung im Kontext des Krebsfrüherkennungs- und -registergesetzes. / Greiner, F.; Nolte, S.; Waldmann, A. et al.
In: Gesundheitswesen, Vol. 75, No. 11, 18.10.2013, p. 751-753.

Research output: Journal Articles › Journal articles › Research › peer-review

TY - JOUR

T1 - Erfassung und Verarbeitung von persönlichen Daten zur Evaluation von Krebsfrüherkennungsprogrammen - Ergebnisse einer Bevölkerungsbefragung im Kontext des Krebsfrüherkennungs- und -registergesetzes

AU - Greiner, F.

AU - Nolte, S.

AU - Waldmann, A.

AU - Katalinic, A.

AU - Breitbart, E. W.

PY - 2013/10/18

Y1 - 2013/10/18

N2 - 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.

AB - 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.

UR - https://www.scopus.com/pages/publications/84889096780

U2 - 10.1055/s-0033-1355420

DO - 10.1055/s-0033-1355420

M3 - Zeitschriftenaufsätze

C2 - 24142370

AN - SCOPUS:84889096780

SN - 0941-3790

VL - 75

SP - 751

EP - 753

JO - Gesundheitswesen

JF - Gesundheitswesen

IS - 11

ER -

Erfassung und Verarbeitung von persönlichen Daten zur Evaluation von Krebsfrüherkennungsprogrammen - Ergebnisse einer Bevölkerungsbefragung im Kontext des Krebsfrüherkennungs- und -registergesetzes

Abstract

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SCREEN: Evaluation of the model project for skin cancer screening

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Erfassung und Verarbeitung von persönlichen Daten zur Evaluation von Krebsfrüherkennungsprogrammen - Ergebnisse einer Bevölkerungsbefragung im Kontext des Krebsfrüherkennungs- und -registergesetzes

Abstract

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Projects

SCREEN: Evaluation of the model project for skin cancer screening

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