Jensen, Sofie Bratberg http://orcid.org/0000-0002-2517-5865
Dalum, Helle Stentoft
Korsbek, Lisa
Hjorthøj, Carsten
Mikkelsen, John Hagel
Thomsen, Karin
Kistrup, Kristen
Olander, Mette
Lindschou, Jane
Mueser, Kim T.
Nordentoft, Merete
Eplov, Lene Falgaard
Funding for this research was provided by:
TrygFonden (ID-nr. 103226)
Article History
Received: 16 April 2018
Accepted: 31 January 2019
First Online: 11 February 2019
Ethics approval and consent to participate
: The trial was approved by the Ethics Committee in the Capital Region of Denmark (H-1-2010-134), reported to the Danish Data Protection Agency (RHP-2011-09), and registered on ExternalRef removed (NCT01361698) before recruitment began.The trial followed the international ethical guidelines for informed consent in clinical trials. Consent was voluntary, informed, and given both verbally and in writing. The participants did not receive a fee for their participation.
: Not applicable.
: The sponsors played no role in the study design, data collection, data analysis, data interpretation, or writing of the report. Except for Professor Kim Mueser, all authors declare that they have no conflicts of interests. Professor Kim Mueser declares that he was one of the original developers of the IMR program but holds no financial interest in its use.
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