Robinson, Eirin Guldsten http://orcid.org/0000-0002-0895-7005
Gyllensten, Hanna http://orcid.org/0000-0001-6890-5162
Johansen, Jeanette Schultz http://orcid.org/0000-0001-7052-5142
Havnes, Kjerstin http://orcid.org/0000-0003-4535-8439
Granas, Anne Gerd http://orcid.org/0000-0002-6849-9421
Bergmo, Trine Strand http://orcid.org/0000-0002-9580-7688
Småbrekke, Lars http://orcid.org/0000-0001-6475-3368
Garcia, Beate Hennie http://orcid.org/0000-0002-0815-0383
Halvorsen, Kjell H. http://orcid.org/0000-0003-1562-1822
Clinical trials referenced in this document:
Documents that mention this clinical trial
A Trial-Based Cost-Utility Analysis of a Medication Optimization Intervention Versus Standard Care in Older Adults
https://doi.org/10.1007/s40266-023-01077-7
Interdisciplinary collaboration across secondary and primary care to improve medication safety in the elderly (IMMENSE study): study protocol for a randomised controlled trial
https://doi.org/10.1136/bmjopen-2017-020106
Funding for this research was provided by:
Helse Nord RHF (HST1314-16)
University of Oslo
Article History
Accepted: 10 October 2023
First Online: 22 November 2023
Declarations
:
: Open access funding provided by University of Oslo (incl Oslo University Hospital). The IMMENSE study was supported by the Northern Norway Regional Health Authority (grant number HST1314-16). The funding body has supported expenses to cover pharmacist salary and study running costs. They have no part in the collection, management, analysis, or interpretation of the data, nor in the writing and reporting of the study’s conclusions.
: Eirin Guldsten Robinson, Hanna Gyllensten, Jeanette Schultz Johansen, Kjerstin Havnes, Anne Gerd Granas, Trine Strand Bergmo, Lars Småbrekke, Beate Hennie Garcia, and Kjell H. Halvorsen have no conflicts of interest that are directly relevant to the content of this article.
: This research has been performed in accordance with ethical guidelines stated by the Helsinki declaration. The Norwegian Centre for Research Data and the Norwegian Data Protection Authority granted ethical approval (Project number 41366).
: All participants or next of kin gave written informed consent for study participation.
: Not applicable.
: The datasets generated and analyzed during the current study are not publicly available because they contain information that can compromise research participants’ privacy/consent but are available from the corresponding author on reasonable request.
: Not applicable.
: EGR provided the study design, performed the statistical analyses, drafted the manuscript, and prepared the tables and illustrations. HG contributed to the statistical analyses. BG, KHH, JSJ, KH, and LS planned and conducted the RCT and collected data. All authors contributed to the study design, writing, reviewing, and editing the manuscript, and have approved the final version.