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Parent experiences of diabetes care questionnaire (PEQ-DC): reliability and validity following a national survey in Norway

Crossref DOI link: https://doi.org/10.1186/s12913-018-3591-y

Published Online: 2018-10-12

Published Print: 2018-12

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

Authors

Iversen, Hilde Hestad https://orcid.org/0000-0002-6191-416X
Helland, Ylva

Bjertnaes, Oyvind

Skrivarhaug, Torild
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Article History

Received: 27 June 2017

Accepted: 1 October 2018

First Online: 12 October 2018

Ethics approval and consent to participate

: The study was approved by the Data Protection Authority at Oslo University hospital. Registration in the NCDR is based on informed consent from the child (above 12 years of age), and/or the child’s parents. In the consent form, the patient and/or the parents are informed that consent may result in requests to answer questionnaires on patient experiences. Return of the questionnaire constituted parent consent in the survey, which is the standard procedure in all national patient experience surveys conducted by the NIPH.

: Not applicable.

: The authors declare that they have no competing interests.

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