Ilvig, Pia Maria
Bredahl, Thomas Viskum Gjelstrup
Justesen, Just Bendix
Jones, Dorrie
Lundgaard, Jonna Benner
Søgaard, Karen
Christensen, Jeanette Reffstrup http://orcid.org/0000-0002-2412-5989
Article History
Received: 18 January 2018
Accepted: 23 November 2018
First Online: 4 December 2018
Ethics approval and consent to participate
: The FRIDOM program was approved by the The Regional Scientific Ethical Committees for Southern Denmark – number S20130157 and was conducted in accordance with the Helsinki declaration. The SPIRIT 2013 Checklist was thoroughly reviewed, and the guidelines were followed. The feasibility and RCT parts were retrospectively registered in the Clinical Trial Registration – number NCT02843269. To reach all eligible participants, 11 introductory one-hour meetings were held in the end of 2013. After the meetings, the employees filled out a screening questionnaire including the question “<i>Do you want to participate in the FINALE-study</i>”. Employees who did not attend the meetings, were given written information and screening questionnaires from their closest manager. Questionnaires and possible consent were returned in a sealed envelope. At the baseline test, all employees who wanted to participate filled out a declaration of consent. The participants took a copy home and the originals were placed in a locked file cabinet at the university. The participants were informed, both verbally and in writing, that their consent could be redrawn at any time and without any questions asked. This information was repeated when asked if the participants wanted to participate in an interview. All nine participants consented yet again.
: Not applicable.
: The authors declare that they have no competing interests.
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