Blar i HVL Open på forfatter "Strømsvik, Nina"
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Ask Rosa – The making of a digital genetic conversation tool, a chatbot, about hereditary breast and ovarian cancer
Siglen, Elen; Vetti, Hildegunn Høberg; Lunde, Aslaug Beathe Forberg; Hatlebrekke, Thomas Akselberg; Strømsvik, Nina; Hamang, Anniken; Hovland, Sigrid Tronsli; Rettberg, Jill Walker; Steen, Vidar Martin; Bjorvatn, Cathrine (Peer reviewed; Journal article, 2021)Objective We aimed at developing a pilot version of an app (Rosa) that can perform digital conversations with breast or ovarian cancer patients about genetic BRCA testing, using chatbot technology, to identify best practices ... -
Ask Rosa – The making of a digital genetic conversation tool, a chatbot, about hereditary breast and ovarian cancer
Siglen, Elen; Vetti, Hildegunn Høberg; Lunde, Aslaug Beathe Forberg; Hatlebrekke, Thomas Akselberg; Strømsvik, Nina; Hamang, Anniken; Hovland, Sigrid Tronsli; Rettberg, Jill Walker; Steen, Vidar Martin; Bjorvatn, Cathrine (Peer reviewed; Journal article, 2021)Objective We aimed at developing a pilot version of an app (Rosa) that can perform digital conversations with breast or ovarian cancer patients about genetic BRCA testing, using chatbot technology, to identify best practices ... -
Assessing the relationship between patient preferences for recontact after BRCA1 or BRCA2 genetic testing and their monitoring coping style in a Norwegian sample
Ommundsen, Randi Marlene Dahle; Strømsvik, Nina; Hamang, Anniken (Peer reviewed; Journal article, 2021)Recontacting former patients regarding new genetic information is currently not standard care but might be implemented in the future. Little information is available on the implications of this practice from the point of ... -
Identifying sequence variants contributing to hereditary breast and ovarian cancer in BRCA1 and BRCA2 negative breast and ovarian cancer patients
Jarhelle, Elisabeth; Stensland, Hilde Monica Frostad Riise; Hansen, Geir Åsmund Myge; Skarsfjord, Siri; Jonsrud, Christoffer; Ingebrigtsen, Monica; Strømsvik, Nina; Van Ghelue, Marijke (Peer reviewed; Journal article, 2019)Families with breast and ovarian cancer are often tested for disease associated sequence variants in BRCA1 and BRCA2. Pathogenic sequence variants (PVs) in these two genes are known to increase breast and ovarian cancer ... -
“It was an important part of my treatment”: a qualitative study of Norwegian breast Cancer patients’ experiences with mainstreamed genetic testing
Strømsvik, Nina; Olsson, Pernilla Marie A.; Gravdehaug, Berit; Lurås, Hilde; Schlichting, Ellen; Jørgensen, Kjersti; Wangensteen, Teresia; Vamre, Tone; Heramb, Cecilie; Mæhle, Lovise Olaug; Grindedal, Eli Marie (Peer reviewed; Journal article, 2022)Background In South-Eastern Norway, genetic testing for BRCA1 and BRCA2 is offered to breast cancer patients by their treating surgeon or oncologist. Genetic counselling from a geneticist or a genetic counsellor is offered ...