Jønsson, A. B. R.
Martiny, F. H. J.
Søndergaard, M. K.
Brodersen, J. B.
Due, T. D.
Nielsen, M. H.
Bakkedal, C.
Bardram, J. E.
Bissenbakker, K.
Christensen, I.
Doherty, K.
Kjellberg, P.
Mercer, S. W.
Reventlow, S.
Rozing, M. P.
Møller, A.
Funding for this research was provided by:
Novo Nordisk (NNF16OC0022038, NNF16OC0022038, NNF16OC0022038, NNF16OC0022038, NNF16OC0022038, NNF16OC0022038, NNF16OC0022038, NNF16OC0022038, NNF16OC0022038, NNF16OC0022038, NNF16OC0022038, NNF16OC0022038, NNF16OC0022038, NNF16OC0022038, NNF16OC0022038)
KEU Region North (No ID number available, No ID number available, No ID number available, No ID number available, No ID number available, No ID number available, No ID number available, No ID number available, No ID number available, No ID number available, No ID number available, No ID number available, No ID number available, No ID number available, No ID number available)
Royal Library, Copenhagen University Library
Article History
Received: 21 August 2022
Accepted: 5 September 2023
First Online: 5 October 2023
Declarations
:
: We applied for ethical approval of the study to the National Committee on Health Research Ethics in Denmark, which decided that the current study was to be considered a quality improvement project (cf. journal number H-20003281). According to the Danish legislation, “komitéloven” (ExternalRef removed), quality improvement projects do not require ethical approval. Still, the study was conducted in compliance with the Helsinki Declaration in its latest form and good clinical practice guidelines and followed the rules for informed consent [CitationRef removed]. Informed consent was obtained from all study participants after they had been identified in the general practices’ patient medical records and prior to their participation. All study participants, including clinical staff, general practitioners, and patients, were informed about the study before participation via written material and oral explanation. The written material was tailored to the medical personnel and patients with SMI to ensure it was understandable and relevant. The information material was designed using study information and consent form templates from the National Committee on Health Research Ethics in Denmark, supplemented with guidance from the University of Copenhagen. We collected written consent forms from all study participants.
: Not applicable.
: The authors declare no competing interests.