Christine Råheim Borge

• Borge, Christine Råheim; Larsen, Marie Hamilton; Osborne, Richard H.; Aas, Eline; Kolle, Ingrid Tryland & Reinertsen, Rikke [Vis alle 15 forfattere av denne artikkelen] (2024). Impacts of a health literacy-informed intervention in people with chronic obstructive pulmonary disease (COPD) on hospitalization, health literacy, self-management, quality of life, and health costs – A randomized controlled trial. Patient Education and Counseling. ISSN 0738-3991. 123. doi: 10.1016/j.pec.2024.108220.
• Vidnes, Tone Karine; Wahl, Astrid Klopstad; Larsen, Marie Hamilton; Meyer, Käthe Birgitte; Engebretsen, Eivind & Hermansen, Åsmund [Vis alle 10 forfattere av denne artikkelen] (2024). Effectiveness of a health communication intervention on health literacy in the first year following kidney transplantation – A randomized controlled study. Patient Education and Counseling. ISSN 0738-3991. 123. doi: 10.1016/j.pec.2024.108207.
• Hermansen, Åsmund; Andersen, Marit Helen; Borge, Christine Råheim; Dahl, Kari Gire; Larsen, Marie Hamilton & Lønning, Kjersti [Vis alle 9 forfattere av denne artikkelen] (2023). Preliminary validity testing of the eHealth Literacy Questionnaire (eHLQ): a Confirmatory Factor Analysis (CFA) in Norwegian hospitalized patients. BMC Psychology. ISSN 2050-7283. 11(1). doi: 10.1186/s40359-023-01449-z. Fulltekst i vitenarkiv Vis sammendrag

  Aims: To perform the first psychometric analysis of the Norwegian version of the eHLQ using confirmative factor analysis (CFA) procedures in a population of patients admitted to hospital using a cross-sectional design. The eHLQ consists of 35 items capturing the 7-dimensional eHealth Literacy Framework (eHLF) which describes users’ attributes, user’s interaction with technologies and user’s experience with digital health systems. Methods: The 7 independent scales of the eHLQ was translated from Danish and culturally adapted into the Norwegian language following a standardised protocol. Assessment of construct validity of the eHLQ was undertaken using data from a cross-sectional survey of 260 patients hospitalized at a Norwegian University Hospital in the Oslo area during a two-week period in June 2021. The analysis included using correlation analysis (Pearsons R), internal consistency (Cronbach’s alpha) and confirmatory factor analysis (CFA). Results: All factor loadings were high to acceptable (i.e. > 0.6), except for five items which had somewhat lower loadings. Regarding internal consistency, alpha ranged from 0.73 to 0.90. For optimal CFA fit for the different scale models, correlated residuals were required for five of the seven scales. Overall our analysis shows an intermediate fit of the orginal construct. Scale intercorrelations were all below 0.8, indicating an overall acceptable discriminant validity between the 7 dimensions. Conclusions: The results from the CFA analysis indicate that for almost all 7 eHLQ scales, an acceptable model fit was achieved. The 260 hospitalized patients included in this study represented a variety of diagnoses, recruited from a geographically limited area. Further studies on psychometric properties of the Norwegian version of eHLQ in larger samples, diverse settings and by using more comprehensive approaches are warranted.

• Kolltveit, Beate-Christin Hope; Graue, Marit; Borge, Christine Råheim & Frisk, Bente (2023). Patients’ experiences with participating in a team‑based person‑centred intervention for patients at risk of or diagnosed with COPD in general practice. BMC Pilot and Feasibility Studies. ISSN 2055-5784. 9. doi: 10.1186/s40814-023-01398-9. Fulltekst i vitenarkiv
• Johansen Skogestad, Ingrid; Kottorp, Anders; Larsson, Petra; Normann Moen, Marie Therese Kristine; Gay, Caryl & Borge, Christine Råheim [Vis alle 7 forfattere av denne artikkelen] (2023). Development and evaluation of the Norwegian Fatigue Characteristics and Interference Measure (FCIM) for stroke survivors: cognitive interviews and Rasch analysis. Quality of Life Research. ISSN 0962-9343. doi: 10.1007/s11136-023-03477-z. Fulltekst i vitenarkiv
• Finbråten, Hanne Søberg; Romedal, Signegun; Borge, Christine Råheim & Eie, Anette (2023). Helsekompetanse i pasient- og pårørendeopplæring – en tematisk analyse. Sykepleien Forskning. ISSN 1890-2936. 18(91893). doi: 10.4220/Sykepleienf.2023.91893. Fulltekst i vitenarkiv Vis sammendrag

  Bakgrunn: Pasienters og pårørendes muligheter til best å kunne håndtere sin egen helsetilstand kan påvirkes av i hvilken grad sykepleiere og annet helsepersonell tilpasser helseinformasjon til den enkeltes helsekompetanse. Pasienter og pårørende må dessuten ha tilstrekkelig helsekompetanse for at de skal kunne delta i samvalgsprosesser. I korthet omfatter helsekompetanse den enkeltes kompetanse i å finne, forstå, vurdere og anvende helseinformasjon og helsetjenester for å fremme og bevare god helse. Imidlertid er helsekompetanse et relativt ukjent begrep blant helsepersonell. Mange har uttrykt usikkerhet rundt innholdet i begrepet og en interesse for hvilke konsekvenser helsekompetanse kan ha for pasient- og pårørendeopplæringen. Det er lite forskning på hvordan helsepersonell selv reflekterer over betydningen av helsekompetanse i pasient- og pårørendeopplæring. Hensikt: Hensikten med studien var å beskrive helsepersonells og lederes refleksjoner om betydningen av helsekompetanse i pasient- og pårørendeopplæringen. Metode: Studien er deskriptiv-kvalitativ, der dataene ble innhentet gjennom prosessverktøyet «verdenskafé». Vi gjennomførte datasamlingen på Regional konferanse for pasient- og pårørendeopplæring i Helse Sør-Øst (HSØ) i desember 2021. Totalt deltok 54 tverrfaglige helsepersonell og ledere fra åtte helseforetak med særskilt ansvar for pasient- og pårørendeopplæringen i spesialisthelsetjenesten. I tillegg deltok brukerrepresentanter. For å analysere datamaterialet anvendte vi tematisk analyse etter inspirasjon av Braun og Clarke. Resultat: Vi identifiserte seks hovedtemaer og 27 undertemaer. Hovedtemaene omfattet: 1) Helsepersonells kompetanse, 2) Pasientens og pårørendes kompetanse og preferanser, 3) Interaksjon, 4) Ressurser og rammer, 5) Samhandling og samarbeid, 6) og Konsekvenser av helsekompetanse. Konklusjon: Helsepersonell og ledere rapporterte et behov for økt kompetanse i hvordan de kan følge opp helsekompetansebehov i pasient- og pårørendeopplæringen. Et slikt behov kan relateres til et fokus på organisatorisk helsekompetanse. Tilstrekkelige ressurser og rammer samt økt samhandling og samarbeid kan bidra til mer tilpasset pasient- og pårørendeopplæring. Mer oppmerksomhet rundt helsekompetanse kan muligens også gi styrket pasientsikkerhet.

• Lundereng, Elias David; Nes, Andrea Aparecida Gonçalves; Holmen, Heidi; Winger, Anette; Thygesen, Hilde & Jøranson, Nina [Vis alle 10 forfattere av denne artikkelen] (2023). Health Care Professionals’ Experiences and Perspectives on Using Telehealth for Home-based Palliative Care: Scoping Review. Journal of Medical Internet Research. ISSN 1438-8871. 25. doi: 10.2196/43429. Fulltekst i vitenarkiv Vis sammendrag

  Background: Telehealth seems feasible for use in home-based palliative care (HBPC). It may improve access to health care professionals (HCPs) at patients’ homes, reduce hospital admissions, enhance patients’ feelings of security and safety, and increase the time spent at home for patients in HBPC. HBPC requires the involvement of various HCPs such as nurses, physicians, allied health professionals, dietitians, psychologists, religious counselors, and social workers. Acceptance of the use of technology among HCPs is essential for the successful delivery of telehealth in practice. No scoping review has mapped the experiences and perspectives of HCPs regarding the use of telehealth in HBPC. Objective: The aim of this review was to systematically map published studies on HCPs’ experiences and perspectives on the use of telehealth in HBPC. Methods: A scoping review was conducted using the methodology of Arksey and O’Malley. The review was reported according to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses extension for scoping reviews. A systematic search was performed in AMED, CINAHL, Embase, MEDLINE, PsycINFO, and Web of Science for studies published in peer-reviewed journals between January 1, 2000, and August 23, 2022. The reference lists of the included papers were hand searched to identify additional studies. The inclusion criteria were (1) studies using qualitative, quantitative, or mixed methods; (2) studies including HCPs using telehealth with patients in HBPC; (3) studies on HCPs’ experiences and perspectives on the use of telehealth in HBPC; (4) studies published between January 1, 2000, and August 23, 2022; and (5) studies published in English, Portuguese, Norwegian, Danish, Swedish, or Spanish. Pairs of authors independently included studies and extracted data. The first 2 stages of thematic synthesis were used to thematically organize the data. Results: This scoping review included 29 papers from 28 studies. Four descriptive themes were identified: (1) easy to use but technological issues undermine confidence, (2) adds value but personal and organizational barriers challenge adoption, (3) potential to provide useful and meaningful patient-reported data, and (4) mutual trust as a prerequisite for interpersonal relationships. Conclusions: Telehealth in HBPC seems to be easy to use and may improve the coordination of care, time efficiency, clinical assessments, and help build and enhance personal and professional relationships. However, the introduction of technology in HBPC is complex, as it may not align well with the overall aim of palliative care from HCPs’ point of view. Further, changes in practice and requirements for HCPs may reduce motivation for the use of telehealth in HBPC. HCPs consider themselves to have central roles in implementing telehealth, and a lack of acceptance and motivation is a key barrier to telehealth adoption. Policy makers and telehealth developers should be aware of this potential barrier when developing or implementing new technology for use in HBPC.

• Borge, Christine Råheim; Larsen, Marie Hamilton; Osborne, Richard H; Engebretsen, Eivind; Andersen, Marit Helen & Holter, Ingrid Asbjørnsen [Vis alle 7 forfattere av denne artikkelen] (2022). How to co-design a health literacy-informed intervention based on a needs assessment study in chronic obstructive pulmonary disease. BMJ Open. ISSN 2044-6055. 12(10). doi: 10.1136/bmjopen-2022-063022. Fulltekst i vitenarkiv Vis sammendrag

  Objective To develop a co-designed health literacy (HL)-informed intervention for people with chronic obstructive pulmonary disease (COPD) that enables them to find, understand, remember, use and communicate the health information needed to promote and maintain good health. Design This study used a co-design approach informed by the programme logic of the Ophelia (Optimising Health Literacy and Access) process. The co-design included workshops where possible solutions for an HL-informed intervention were discussed based on an HL needs assessment study. Settings Five workshops were performed in a local community setting in the specialist and municipality healthcare services in Oslo, Norway. Participants People with COPD, multidisciplinary healthcare professionals (HCPs) from the municipality and specialist healthcare services, and researchers (n=19) participated in the workshops. The co-designed HL-informed intervention was based on seven focus groups with people with COPD (n=14) and HCPs (n=21), and a cross-sectional study of people with COPD using the Health Literacy Questionnaire (n=69). Results The workshop co-design process identified 45 action points and 51 description points for possible intervention solutions to meet the HL needs of people with COPD. The final recommendation for an HL-informed intervention focused on tailored follow-up after hospitalisation, which uses motivational interviewing techniques, is based on the individual’s HL, self-management and quality of life needs and is implemented in cooperation with HCPs in both the specialist and municipality healthcare services. Conclusion During the codesign process, the workshop group generated several ideas for how to help patients find, understand, remember, use and communicate health information in order to promote and maintain good health. People with COPD need tailored follow-up based on their individual HL needs by HCPs that have knowledge of COPD and are able to motivate them for self-management tasks and help them to improve their quality of life (QOL) and decrease hospitalisation. Data availability statement No data are available. Norwegian regional ethical guidelines do not give permission to share data from research if they are not anonymous.

• Larsen, Marie Hamilton; Mengshoel, Anne Marit; Andersen, Marit Helen; Borge, Christine Råheim; Ahlsen, Birgitte & Dahl, Kari Gire [Vis alle 15 forfattere av denne artikkelen] (2022). “A bit of everything”: Health literacy interventions in chronic conditions – a systematic review. Patient Education and Counseling. ISSN 0738-3991. 105(10), s. 2999–3016. doi: 10.1016/j.pec.2022.05.008. Fulltekst i vitenarkiv
• Frisk, Bente; Sundør, Ingrid Elise; Dønåsen, Mette Ramstad; Refvem, Olav Kåre & Borge, Christine Råheim (2022). How is the organisational settings, content and availability of comprehensive multidisciplinary pulmonary rehabilitation for people with COPD in primary healthcare in Norway: A cross-sectional study. BMJ Open. ISSN 2044-6055. 12(2). doi: 10.1136/bmjopen-2021-053503. Fulltekst i vitenarkiv
• Urstad, Kristin Hjorthaug; Andersen, Marit Helen; Larsen, Marie Hamilton; Borge, Christine Råheim; Helseth, Sølvi & Wahl, Astrid Klopstad (2022). Definitions and measurement of health literacy in health and medicine research: A systematic review. BMJ Open. ISSN 2044-6055. 12(2). doi: 10.1136/bmjopen-2021-056294. Fulltekst i vitenarkiv Vis sammendrag

  Objectives The way health literacy is understood (conceptualised) should be closely linked to how it is measured (operationalised). This study aimed to gain insights into how health literacy is defined and measured in current health literacy research and to examine the relationship between health literacy definitions and instruments. Design Systematic review in accordance with the Preferred Reporting Items for Systematic Reviews and Meta-Analyses statement. Data sources The MEDLINE, PsycINFO, ERIC and CINAHL databases were searched for articles published during two randomly selected months (March and October) in 2019. Eligibility criteria We included articles with a quantitative design that measured health literacy, were peer-reviewed and original, were published in the English language and included a study population older than 16 years. Data extraction and synthesis Six researchers screened the articles for eligibility and extracted the data independently. All health literacy definitions and instruments were considered in relation to category 1 (describing basic reading and writing skills, disease-specific knowledge and practical skills) and category 2 (social health literacy competence and the ability to interpret and critically assess health information). The categories were inspired by Nutbeam’s descriptions of the different health literacy levels. Results 120 articles were included in the review: 60 within public health and 60 within clinical health. The majority of the articles (n=77) used instruments from category 1. In total, 79 of the studies provided a health literacy definition; of these, 71 were in category 2 and 8 were in category 1. In almost half of the studies (n=38), health literacy was defined in a broad perspective (category 2) but measured with a more narrow focus (category 1). Conclusion Due to the high degree of inconsistency between health literacy definitions and instruments in current health literacy research, there is a risk of missing important information about health literacy considered be important to the initial understanding of the concept recognised in the studies.

• Johansen Skogestad, Ingrid; Kirkevold, Marit; Larsson, Petra; Borge, Christine Råheim; Indredavik, Bent & Gay, Caryl [Vis alle 7 forfattere av denne artikkelen] (2021). Post-stroke fatigue: an exploratory study with patients and health professionals to develop a patient-reported outcome measure. Journal of Patient-Reported Outcomes. ISSN 2509-8020. 5. doi: 10.1186/s41687-021-00307-z. Fulltekst i vitenarkiv Vis sammendrag

  Background Post-stroke fatigue (PSF) is commonly reported and described as disabling by patients recovering from stroke. However, a major challenge is how to accurately diagnose and assess PSF. Therefore, the aim of this study was to explore PSF as it is experienced by stroke survivors and described by health professionals to guide future development of a PSF-specific PROM. Methods Individual semi-structured interviews were conducted with stroke survivors experiencing PSF (n = 9) and three focus groups were conducted with health professionals (n = 16). Data were analyzed through inductive content analysis. Results The analysis revealed four themes illustrating the experience and descriptions of PSF: 1) PSF characteristics, 2) interfering and aggravating factors, 3) management, and 4) PSF awareness, which refers to stroke survivors first becoming aware of PSF after their initial hospital admission. Conclusion This study highlights the complexity and multidimensionality of PSF. The results from this study will guide future development of a PSF-PROM and support its content validity.

• Borge, Christine Råheim; Larsen, Marie Hamilton; Osborne, Richard H; Engebretsen, Eivind; Andersen, Marit Helen & Holter, Ingrid Asbjørnsen [Vis alle 8 forfattere av denne artikkelen] (2021). Exploring patients’ and health professionals’ perspectives on health literacy needs in the context of chronic obstructive pulmonary disease. . Chronic Illness. ISSN 1742-3953. doi: 10.1177/1742395321999441. Vis sammendrag

  Objective Persons with chronic obstructive pulmonary disease (COPD) require complex follow-up by healthcare professionals (HCPs) and may experience several health literacy (HL) needs. This study aimed to explore such needs in people with COPD and the HCPs who care for them. Methods From October 2016 to August 2017 a qualitative study with four focus groups (FG) were performed in people with COPD (n = 14) and three in multidisciplinary HCPs (n = 21). An inductive thematic analysis was used to investigate HL needs. Results Four HL needs emerged: 1) strengthening the feeling of security; 2) combating the burden of insufficient knowledge on COPD and lack of informational flow; 3) supporting motivation for endurance and self-management; and 4) strengthening dignity. Discussion This study highlights a gap between people with COPD who express important HL needs and HCPs’ capabilities to care for these needs. For HCPs to increase HL in such cases, HCPs need to improve their own HL. It is essential to find solutions on how to improve HL in HCPs who care for people with COPD and to increase the availability of interventions that increase HL in COPD. Education programs, health organizations, and governments should be aware of HL needs in such situations.

• Wahl, Astrid Klopstad; Osborne, Richard H; Larsen, Marie Hamilton; Andersen, Marit Helen; Holter, Ingrid Asbjørnsen & Borge, Christine Råheim (2021). Exploring health literacy needs in chronic obstructive pulmonary disease (COPD): Associations between demographic, clinical variables, psychological well-being and health literacy . Heart & Lung. ISSN 0147-9563. 50(3), s. 417–424. doi: 10.1016/j.hrtlng.2021.02.007. Vis sammendrag

  Background The World Health Organization (WHO) points to health literacy as an important factor in prevention and control of non-communicable diseases (NCDs), including COPD. Objective To investigate associations between selected demographic and clinical variables, psychological well-being and health literacy. Methods Health literacy was measured using the nine domain Health Literacy Questionnaire (HLQ) and one domain from the eHealth Literacy Questionnaire (eHLQ). Using data from a cross-sectional sample of 158 people with COPD, recruited from a hospital-based patient list period (2014-2016), multiple regression analyses were performed. Results The strongest associated variables with health literacy were psychological well-being, measured by the WHO-5 well-being index and education, indicating that higher psychological well-being and educational level are associated with higher levels of health literacy. Conclusion The present study highlights the importance of specifically looking to psychological factors in determining potentially health literacy needs among people with COPD.

• Larsen, Marie Hamilton; Hermansen, Åsmund; Borge, Christine Råheim; Strumse, Yndis A. Staalesen; Andersen, Marit Helen & Wahl, Astrid Klopstad (2021). Health literacy profiling in persons with psoriasis – A cluster analysis. Skin Health and Disease (SHD). ISSN 2690-442X. 1(2). doi: 10.1002/ski2.17. Fulltekst i vitenarkiv
• Holmen, Heidi; Larsen, Marie Hamilton; Sallinen, Merja Helena; Thoresen, Lisbeth; Ahlsen, Birgitte & Andersen, Marit Helen [Vis alle 10 forfattere av denne artikkelen] (2020). En balansegang: helsepersonells erfaringer med mennesker med kronisk sykdom - en oversiktsartikkel av kvalitative studier . BestPractice Nordic. ISSN 1902-7583.
• Larsen, Marie Hamilton; Staalesen, Yndis; Borge, Christine Råheim; Andersen, Marit Helen & Wahl, Astrid Klopstad (2020). Relevant associations between alexithymia and health-literacy in persons with psoriasis. Journal of dermatological treatment (Print). ISSN 0954-6634. doi: 10.1080/09546634.2020.1756204. Fulltekst i vitenarkiv Vis sammendrag

  Strumse heter Staalesen Strumse og P er på Staalesen

• Holmen, Heidi; Larsen, Marie Hamilton; Sallinen, Merja Helena; Thoresen, Lisbeth; Ahlsen, Birgitte & Andersen, Marit Helen [Vis alle 10 forfattere av denne artikkelen] (2020). Working with patients suffering from chronic diseases can be a balancing act for health care professionals - a meta-synthesis of qualitative studies. BMC Health Services Research. ISSN 1472-6963. doi: 10.1186/s12913-019-4826-2. Fulltekst i vitenarkiv
• Larsen, Marie Hamilton; Strumse, Yndis A. Staalesen; Andersen, Marit Helen; Borge, Christine Råheim & Wahl, Astrid Klopstad (2019). Associations between disease education, self-management support, and health literacy in psoriasis. Journal of dermatological treatment (Print). ISSN 0954-6634. 2:6, s. 603–609. doi: 10.1080/09546634.2019.1688233.
• Haraldstad, Kristin; Wahl, Astrid Klopstad; Andenæs, Randi; Andersen, John Roger; Andersen, Marit Helen & Beisland, Elisabeth Grov [Vis alle 24 forfattere av denne artikkelen] (2019). A systematic review of quality of life research in medicine and health sciences. Quality of Life Research. ISSN 0962-9343. 28(10), s. 2641–2650. doi: 10.1007/s11136-019-02214-9. Fulltekst i vitenarkiv Vis sammendrag

  Purpose Quality of life (QOL) is an important concept in the field of health and medicine. QOL is a complex concept that is interpreted and defined differently within and between disciplines, including the fields of health and medicine. The aims of this study were to systematically review the literature on QOL in medicine and health research and to describe the country of origin, target groups, instruments, design, and conceptual issues. Methods A systematic review was conducted to identify research studies on QOL and health-related quality of life (HRQOL). The databases Scopus, which includes Embase and MEDLINE, CINAHL, and PsycINFO were searched for articles published during one random week in November 2016. The ten predefined criteria of Gill and Feinstein were used to evaluate the conceptual and methodological rigor. Results QOL research is international and involves a variety of target groups, research designs, and QOL measures. According to the criteria of Gill and Feinstein, the results show that only 13% provided a definition of QOL, 6% distinguished QOL from HRQOL. The most frequently fulfilled criteria were: (i) stating the domains of QOL to be measured; (ii) giving a reason for choosing the instruments used; and (iii) aggregating the results from multiple items. Conclusion QOL is an important endpoint in medical and health research, and QOL research involves a variety of patient groups and different research designs. Based on the current evaluation of the methodological and conceptual clarity of QOL research, we conclude that the majority QOL studies in health and medicine have conceptual and methodological challenges

• Larsen, Marie Hamilton; Staalesen, Yndis; Borge, Christine Råheim; Osborne, Richard H; Andersen, Marit Helen & Wahl, Astrid Klopstad (2019). Health literacy - a new piece of the puzzle in psoriasis care? - results from a cross-sectional study . British Journal of Dermatology. ISSN 0007-0963. 06(18), s. 1506–1516. doi: 10.1111/bjd.17595. Fulltekst i vitenarkiv
• Steindal, Simen Alexander; Torheim, Henny; Oksholm, Trine; Christensen, Vivi Lycke; Lee, Kathryn A & Lerdal, Anners [Vis alle 10 forfattere av denne artikkelen] (2018). The effectiveness of nursing interventions for breathlessness in people with chronic obstructive pulmonary disease: A systematic review and meta-analysis. Journal of Advanced Nursing. ISSN 0309-2402. doi: 10.1111/jan.13902. Fulltekst i vitenarkiv
• Larsson, Petra; Borge, Christine Råheim; Nygren-Bonnier, Malin; Lerdal, Anners & Edvardsen, Anne (2018). An evaluation of the short physical performance battery following pulmonary rehabilitation in patients with chronic obstructive pulmonary disease. BMC Research Notes. ISSN 1756-0500. 11(348). doi: 10.1186/s13104-018-3458-7.
• Leine, Marit; Wahl, Astrid Klopstad; Borge, Christine Råheim; Hustavenes, Magne Mikal & Bondevik, Hilde (2017). Feeling safe and motivated to achieve better health: Experiences with a partnership-based nursing practice programme for in-home patients with chronic obstructive pulmonary disease. Journal of Clinical Nursing (JCN). ISSN 0962-1067. 26(17-18), s. 2755–2764. doi: 10.1111/jocn.13794.
• Borge, Christine Råheim; Mengshoel, Anne Marit; Moum, Torbjørn Åge & Wahl, Astrid Klopstad (2016). Fluctuating patterns in quality of life outcomes among patients with moderate and severe stages of chronic obstructive pulmonary disease. Quality of Life Research. ISSN 0962-9343. 25, s. 2041–2051. doi: 10.1007/s11136-016-1227-4.
• Borge, Christine Råheim; Mengshoel, Anne Marit; Omenaas, Ernst; Moum, Torbjørn Åge; Ekman, Inger & Lein, Martha Pauline [Vis alle 8 forfattere av denne artikkelen] (2015). Effect of guided deep breathing on breathlessness and the breathing pattern in chronic obstructive pulmonary disease: A double-blind randomized control trial. Patient Education and Counseling. ISSN 0738-3991. 98(2), s. 182–190. doi: 10.1016/j.pec.2014.10.017.
• Saltnes, Solfrid Sørgjerd; Storhaug, Kari; Borge, Christine Råheim; Enmarker, Ingela & Willumsen, Tiril (2015). Oral health-related quality-of-life and mental health in individuals with chronic obstructive pulmonary disease (COPD). Acta Odontologica Scandinavica. ISSN 0001-6357. 73(1), s. 14–20. doi: 10.3109/00016357.2014.935952.
• Borge, Christine Råheim; Hagen, Kåre Birger; Mengshoel, Anne Marit; Omenaas, Ernst; Moum, Torbjørn Åge & Wahl, Astrid Klopstad (2014). Effects of controlled breathing exercises and respiratory muscle training in people with chronic obstructive pulmonary disease: results from evaluating the quality of evidence in systematic reviews. BMC Pulmonary Medicine. ISSN 1471-2466. 14:184. doi: 10.1186/1471-2466-14-184.
• Borge, Christine Råheim; Moum, Torbjørn Åge; Lein, Martha Pauline; Austegard, Elise Lynn & Wahl, Astrid Klopstad (2014). Illness perception in people with chronic obstructive pulmonary disease. Scandinavian Journal of Psychology. ISSN 0036-5564. 55(5), s. 456–463. doi: 10.1111/sjop.12150. Vis sammendrag

  Illness perception (IP) concerns how patients evaluate living with a disease. To get a broader understanding of IP in patients with chronic obstructive pulmonary disease (COPD), we investigated whether breathlessness is an important precursor of IP and whether IP in its turn is related to mental health, physical health and global quality of life (QOL). One hundred and fifty-four patients with COPD participated in a cross-sectional survey. Participants underwent pulmonary function testing, provided socio-demographic and clinical information, and completed the following standardized instruments: Brief Illness Perception Questionnaire, Respiratory Quality of Life Questionnaire, Short-Form 12 Health Survey and the Quality of Life Scale. Multiple regression analyses were performed. A high IP score indicates that a patient believes that his/her illness represents a threat. Participants with a high score on the IP dimensions consequences, identity, concern and emotional representation, experienced more breathlessness. High scores on the IP dimensions consequences, identity and concern were associated with impaired physical health and high scores on the IP dimensions consequences, identity and emotional representation were associated with impaired mental health. Impaired global QOL was associated with high scores on the IP dimensions consequences, identity, concern, coherence and emotional representation. The strength of the associations between breathlessness and physical/mental health and global QOL decreased when certain dimensions of IP were included as predictors, indicating that IP to some extent acts as a mediating factor. These findings may have practical implications of patient counseling by helping COPD patients to cope with their disease by restructuring their personal models of illness.

• Borge, Christine Råheim; Wahl, Astrid Klopstad & Moum, Torbjørn (2011). Pain and quality of life with chronic obstructive pulmonary disease. Heart & Lung. ISSN 0147-9563. 40(3), s. 90–101. doi: 10.1016/j.hrtlng.2010.10.009.
• Hope, Håvar Blich; Medhus, Asle Wilhelm; Sandstad, Olav; Borge, Christine Råheim & Skar, Viggo Øystein (2011). Reduced C-13-D-xylose absorption in alcoholics is more likely caused by alterations in small intestinal mucosa than delayed gastric emptying. Scandinavian Journal of Gastroenterology. ISSN 0036-5521. 46(4), s. 414–419. doi: 10.3109/00365521.2010.536252.
• Borge, Christine Råheim; Wahl, Astrid Klopstad & Moum, Torbjørn (2010). Association of breathlessness with multiple symptoms in chronic obstructive pulmonary disease. Journal of Advanced Nursing. ISSN 0309-2402. 66(12), s. 2688–2700. doi: 10.1111/j.1365-2648.2010.05447.x.

Se alle arbeider i Cristin

• Oksholm, Trine & Borge, Christine Råheim (2021). Lungesykepleie. Fagbokforlaget. ISBN 9788245033939. 259 s.

Se alle arbeider i Cristin

• Khalid, Saliha; Kristoffersen, Agnete Egilsdatter; Stub, Trine; Borge, Christine Råheim; Qureshi, Samera Azeem & Alpers, Lise-Merete (2024). Health and Illness Beliefs and Practices among Pakistani Immigrants in Norway: An Application of The Health Traditions Model.
• Finbråten, Hanne Søberg; Borge, Christine Råheim; Romedal, Signegun & Eie, Anette (2023). Refleksjoner over betydningen av helsekompetanse i pasient- og pårørendeopplæring.
• Finbråten, Hanne Søberg; Romedal, Signegun; Borge, Christine Råheim & Eie, Anette (2023). Helsepersonell og ledere sine refleksjoner rundt helsekompetanse i pasient- og pårørendeopplæring. .
• Khalid, Saliha; Kristoffersen, Agnete Egilsdatter; Alpers, Lise-Merete; Qureshi, Samera Azeem; Borge, Christine Råheim & Stub, Trine (2023). Tradisjonell medisin brukt blant pakistanske innvandrere i Norge.
• Borge, Christine Råheim & Seljelid, Berit (2023). Helsekompetanse.
• Seljelid, Berit & Borge, Christine Råheim (2023). Pasient- og pårørendeopplæring - refleksjon over teori og praksis.
• Frisk, Bente; Refvem, Olav Kåre; Sundfør, Ingrid Elise & Borge, Christine Råheim (2022). LUNGEREHABILITERINGSTILBUD I NORSKE KOMMUNER FOR PERSONER MED KRONISK OBSTRUKTIV LUNGESYKDOM - KARTLEGGINGSSTUDIE.
• Torheim, Henny & Borge, Christine Råheim (2021). Kartlegging av symptomer og kliniske tegn. I Oksholm, Trine & Borge, Christine Råheim (Red.), Lungesykepleie. Fagbokforlaget. ISSN 9788245033939. s. 52–76.
• Holmen, Heidi; Mengshoel, Anne Marit; Thoresen, Lisbeth; Larsen, Marie Hamilton; Eik, Hedda & Borge, Christine Råheim (2021). En ubetydelig brikke. Dagsavisen. ISSN 1503-2892.
• Lundereng, Elias David; Nes, Andrea Aparecida Goncalves; Holmen, Heidi; Winger, Anette; Thygesen, Hilde & Jøranson, Nina [Vis alle 11 forfattere av denne artikkelen] (2021). Health care professionals' experiences and perspectives on using telehealth for home-based palliative care: Protocol for a scoping review. JMIR Research Protocols. ISSN 1929-0748. 10(10). doi: 10.2196/33305.
• Larsen, Marie Hamilton; Strumse, Yndis S.S.; Borge, Christine Råheim; Andersen, Marit Helen & Wahl, Astrid Klopstad (2020). Viktige sammenhenger mellom aleksitymi og helsekompetanse hos pasienter med psoriasis som har deltatt i klimabehandling. BestPractice Nordic. ISSN 1902-7583.
• Mandal, H.T.; Aaby, A; Bonnen, A; Debussche, X; Borge, Christine Råheim & Kolarcik, P [Vis alle 10 forfattere av denne artikkelen] (2019). Symposium: “WHO National Health Literacy Demonstration Projects (NHLDPs): European Action Network for intervention development and implementation.
• Borge, Christine Råheim (2019). Helsekompetanse. Nøkkelen til helse for personer med kronisk obstruktiv lungesykdom (kols). Et samarbeidsprosjekt mellom Lovisenberg Diakonale Sykehus, Helsekonferansen 9 mai 2019. Presentasjon.
• Bakker, M; Putrik, P; Aaby, A; Debussche, X; Morrissey, J & Borge, Christine Råheim [Vis alle 10 forfattere av denne artikkelen] (2019). Acting together –WHO National Health literacy demonstration projects (NHLDPs) adress health literacy needs in the Eruopen Region. . Public Health Panorama. 5, s. 2–3.
• Larsen, Marie Hamilton; Borge, Christine Råheim; Staalesen, Yndis & Wahl, Astrid Klopstad (2018). Health literacy - a new pierce of The puzzle in psoriasis? .
• Steindal, Simen Alexander; Oksholm, Trine; Torheim, Henny; Christensen, Vivi Lycke; Lee, Kathryn & Lerdal, Anners [Vis alle 10 forfattere av denne artikkelen] (2017). A systematic review of nursing interventions for breathlessness in COPD. European Clinical Respiratory Journal. ISSN 2001-8525. 50. doi: 10.1183/1393003.congress-2017.PA2582.
• Steindal, Simen Alexander; Oksholm, Trine; Torheim, Henny; Christensen, Vivi Lycke; Lee, Kathryn A & Lerdal, Anners [Vis alle 10 forfattere av denne artikkelen] (2017). A systematic review of nursing interventions for breathlessness in COPD.
• Borge, Christine Råheim (2016). Pustekontroll hos personer med kronisk obstruktiv lungesykdom.
• Borge, Christine Råheim; Mengshoel, Anne Marit; Omenaas, Ernst; Moum, Torbjørn Åge; Ekman, Inger & Lein, Martha Pauline [Vis alle 8 forfattere av denne artikkelen] (2016). Effektn på tung pust ved hjelp av pusteveiledning av pasienter med moderat og alvorlig kols -en dobbelblindet, randomisert kontrollstudie. BestPractice Lungemedicin.
• Borge, Christine Råheim; Wahl, Astrid Klopstad & Moum, Torbjørn Åge (2013). Multiple symptoms and quality of life in people with Chronic Obstructive Pulmonary Disease.
• Borge, Christine Råheim; Moum, Torbjørn Åge; Austegard, Elise Lynn; Lein, Martha Pauline & Wahl, Astrid Klopstad (2013). Illness perception among people with Chronic Obstructive Pulmonary Disease.
• Borge, Christine Råheim; Moum, Torbjørn Åge & Wahl, Astrid Klopstad (2012). Smerter hos personer med KOLS. BestPractice Nordic. ISSN 1902-7583.
• Borge, Christine Råheim; Austegard, Elise Lynn & Wahl, Astrid Klopstad (2010). Compliance to inhalation medication in relation to illness perception, quality of life and predicted pulmonary function in COPD patients.
• Borge, Christine Råheim; Wahl, Astrid Klopstad & Miaskowski, Christine (2009). Subjective symptoms and functional performances in chronic obstructive pulmonary diseases (COPD).
• Borge, Christine Råheim; Wahl, Astrid Klopstad & Miaskowski, Christine (2008). Pain in people with Chronic Obstructive Pulmonary Disease (COPD).

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