Schmidt, Tanja https://orcid.org/0000-0003-2476-8711
Gramkow, Marie Christoffersen
Poulsen, Dorthe Varning
Miller, Louise Holm
Wermuth, Lene
Stigsdotter, Ulrika K.
Funding for this research was provided by:
Velux Fonden (00027383)
Article History
Received: 5 August 2022
Accepted: 8 October 2022
First Online: 23 October 2022
Declarations
:
: All interview participants will be asked to provide a written informed consent. Workshop participants will provide oral consent before the start of each workshop. A researcher will explain the purpose and procedures of the study and explicitly ask each workshop participant if he or she has understood everything and wants to participate. It is important that the workshop participants feel at ease, and we therefore aim at creating a conversational atmosphere, which we feel a written consent will disturb. Also, no identifiable information will be collected on workshop participants. Asking people with severe dementia for written or oral consent can be challenging and, in many cases, not applicable. Instead, we will ask the next of kin or primary care person to give consent, and to participate in everything the person with dementia is participating in, to make sure that he or she seems happy and not distressed by participating. All participants can withdraw from the study at any time and data will be collected in accordance with the Helsinki declaration. The study and its data-management procedures have been approved by the Universities Research & Innovation Organization (10.804). Formal ethical approval was not required according to the Danish National Committee on Health Research Ethics.
: Not applicable.
: The authors declare that they have no competing interests.