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“It is always me against the Norwegian system.” barriers and facilitators in accessing and using dementia care by minority ethnic groups in Norway: a qualitative study

Crossref DOI link: https://doi.org/10.1186/s12913-020-05801-6

Published Online: 2020-10-15

Published Print: 2020-12

Update policy: https://doi.org/10.1007/springer_crossmark_policy

Authors

Czapka, Elżbieta Anna http://orcid.org/0000-0001-8548-0346
Sagbakken, Mette
Funding

Funding for this research was provided by:

Stiftelsen Dam
License Information

Text and Data Mining valid from 2020-10-15

Version of Record valid from 2020-10-15
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Article History

Received: 14 June 2020

Accepted: 5 October 2020

First Online: 15 October 2020

Ethics approval and consent to participate

: The study was considered to be outside the remit of the Act on Medical and Health Research and could be implemented without the approval of the REK (the Regional Committees for Medical and Health Research Ethics). It was reported to the Norwegian Data Protection Officer for Research (NSD). The researchers followed Oslo Metropolitan University’s data security guidelines. All the participants were informed about the aims of the study and that they could withdraw their participation without giving any reason. They all gave written consent to participate in the study. The consent form was approved by the NSD (Norwegian Centre for Research Data).

: Not applicable.

: The authors declare that they have no competing interests.

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