Blar i Bergen Open Research Archive på forfatter "Hamang, Anniken"
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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 (Journal article; Peer reviewed, 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 (Journal article; Peer reviewed, 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 ... -
General anxiety, depression, and physical health in relation to symptoms of heart-focused anxietya cross sectional study among patients living with the risk of serious arrhythmias and sudden cardiac death
Hamang, Anniken; Eide, Geir Egil; Rokne, Berit; Nordin, Karin; Øyen, Nina (Peer reviewed; Journal article, 2011-11-14)Objective: To investigate the role of three distinct symptoms of heart-focused anxiety (cardio-protective avoidance, heart-focused attention, and fear about heart sensations) in relation to general anxiety, depression and ... -
Health status in patients at risk of inherited arrhythmias and sudden unexpected death compared to the general population
Hamang, Anniken; Eide, Geir Egil; Nordin, Karin; Rokne, Berit; Bjorvatn, Cathrine; Øyen, Nina (Peer reviewed; Journal article, 2010-02-17)Background The possibilities in the molecular genetics of long QT syndrome (LQTS) and hypertrophic cardiomyopathy (HCM) has made family screening, with diagnostic and predictive genetic testing part of the health care offer ... -
“Sudden Death-Genetic Risk”: Living with the risk of serious arrhythmias and sudden cardiac death -A prospective multicenter-study on patient-reported outcomes in individuals with familial Long QT syndrome and Hypertrophic cardiomyopathy who received genetic investigation and counseling in Norway, 2005-2007.
Hamang, Anniken (Doctoral thesis, 2012-03-09)Background: Patients with a clinical diagnosis or a family history of the two distinct entities Long QT syndrome (LQTS) and Hypertrophic cardiomyopathy (HCM) have a higher genetically based risk of serious arrhythmias and ...