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Kathrine Padegaard<\/span> kathrinearke@gmail.com<\/a> Julie Schou Nissen, Selma Kaya-Mortensen, Sygeplejerskeuddannelsen – Institut for Sygeplejerske- og Ern\u00e6ringsuddannelser – Fakultet for Sundhedsuddannelser og Teknologi. Campus Nordsj\u00e6lland. BA-projekt afleveret 06.03.2026. Vejledere: Brigitte Bang og Rikke Agnete Petersen.<\/span><\/p>\n DOWNLOAD RESUM\u00c9<\/a> DOWNLOAD BACHELOR PROJEKT<\/a><\/p>\n Resum\u00e9 Metode Resultater Konklusion Implikationer for praksis Abstract Methods Results Conclusion Implications for practice Drawing on Antonovsky\u2019s salutogenic perspective and the concept of sense of coherence (SOC), nurses gain an additional clinical lens on comprehensibility, manageability and meaningfulness in patients\u2019 illness management. This underscores the need to develop and test a structured tool that combines assessments of coping ability, disease-specific quality of life, and perceived need for support, with the aim of systematically identifying patients who should be offered nurse-led consultations as part of quality improvement in outpatient clinics.<\/span><\/p>\n<\/div>\n","protected":false},"excerpt":{"rendered":" Kathrine Padegaard kathrinearke@gmail.com Julie Schou Nissen, Selma Kaya-Mortensen, Sygeplejerskeuddannelsen – Institut for Sygeplejerske- og Ern\u00e6ringsuddannelser – Fakultet for Sundhedsuddannelser og 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\n<\/span><\/strong>Psoriasis (PSO) er en kronisk inflammatorisk hudsygdom, der p\u00e5virker b\u00e5de den fysiske, psykiske og sociale trivsel. I klinisk praksis varierer patienters evne til at h\u00e5ndtere sygdommens konsekvenser betydeligt, hvilket udfordrer sygeplejerskers mulighed for systematisk at identificere st\u00f8ttebehov. P\u00e5 trods af eksisterende forskning i mestring og livskvalitet er der ikke kvantitativ viden om sammenh\u00e6ngen mellem mestringsevne, sygdomsspecifik livskvalitet og behovet for sygeplejerskesamtaler hos voksne patienter med PSO. Dette studie adresserer dette videnshul.<\/span><\/p>\n
\n<\/span><\/strong>Studiet er et kvantitativt tv\u00e6rsnitsstudie baseret p\u00e5 et digitalt sp\u00f8rgeskema. Mestringsevne blev m\u00e5lt ved OAS\u201113, sygdomsspecifik livskvalitet ved DLQI og behov for sygeplejerskesamtaler blev m\u00e5lt via selvkonstruerede sp\u00f8rgsm\u00e5l. M\u00e5lpopulationen i dette projekt er voksne patienter (\u226518 \u00e5r) i ambulatorisk behandling for PSO i Danmark.<\/span><\/p>\n
\n<\/span><\/strong>Studiet identificerer statistisk signifikante, men svage negative korrelationer mellem mestringsevne og sygdomsspecifik livskvalitet (r<\/span>s<\/span> = \u20130,264; p = 0,003) samt mellem mestringsevne og behov for sygeplejerskesamtaler (r<\/span>s<\/span> = \u20130,248; p = 0,006). Resultaterne indikerer, at h\u00f8jere mestringsevne er forbundet med bedre livskvalitet og et lavere oplevet behov for sygeplejerskesamtaler.<\/span><\/p>\n
\n<\/span><\/strong>Tv\u00e6rsnitsdesignet begr\u00e6nser muligheden for at drage kausale konklusioner, men studiet bidrager med ny viden om relationen mellem mestring, sygdomsspecifik livskvalitet og st\u00f8ttebehov hos patienter med PSO. Resultaterne peger p\u00e5 et potentiale for udvikling af kliniske redskaber, der systematisk kan identificere patienter med et \u00f8get behov for sygeplejerskesamtaler og dermed styrke den individualiserede st\u00f8tte i ambulant praksis.<\/span><\/p>\n
\n<\/span><\/strong>Projektets resultater peger p\u00e5 et potentiale for en mere struktureret tilgang til vurdering af patienters mestringsevne, livskvalitet og oplevet st\u00f8tte i ambulante psoriasisforl\u00f8b. En systematisk vurdering kan styrke grundlaget for at planl\u00e6gge og m\u00e5lrette sygeplejesamtaler til de patienter, der har st\u00f8rst behov for st\u00f8tte. Med afs\u00e6t i Antonovsky’s salutogenetiske perspektiv og begrebet oplevelse af sammenh\u00e6ng (OAS) f\u00e5r sygeplejersken et supplerende klinisk blik p\u00e5 begribelighed, h\u00e5ndterbarhed og meningsfuldhed i patientens sygdomsh\u00e5ndtering. Dette peger p\u00e5 relevansen af at udvikle og afpr\u00f8ve et struktureret redskab, der kombinerer vurdering af mestringsevne, sygdomsspecifik livskvalitet og oplevet st\u00f8ttebehov, med henblik p\u00e5 systematisk at identificere patienter, der b\u00f8r tilbydes sygeplejesamtaler som led i kvalitetsudviklingen i ambulatorier.<\/span><\/p>\nAssociation between coping ability, disease-specific quality of life and need for nurse consultations among adults with psoriasis \u2013 A quantitative cross-sectional study<\/span><\/h3>\n
\nClinical dissertation by Kathrine Padegaard, Julie Schou Nissen, Selma Kaya-Mortensen<\/span> submitted 06.03.2026 . Copenhagen University College Nursing programme – Department of Nursing and Nutrition, Faculty of Health Sciences and Technology. <\/span>Supervisors: Brigitte Bang and Rikke Agnete Petersen.<\/span><\/p>\n
\n<\/span>Introduction
\n<\/span><\/strong>Psoriasis (PSO) is a chronic inflammatory skin disease that affects physical, psychological, and social well-being. In clinical practice, patients vary considerably in their ability to manage the consequences of the disease, which challenges nurses\u2019 ability to systematically identify support needs. Despite existing research on coping and quality of life (QoL), no quantitative evidence exists on the associations among coping ability, disease-specific QoL, and the need for nurse consultations (NC) in adults with PSO.<\/span><\/p>\n
\n<\/span><\/strong>The study is a quantitative cross-sectional design based on a digital questionnaire. Coping ability was measured using the SOC-13, disease-specific QoL using the DLQI, and the need for NC was assessed using self-constructed questions. The target population was adults (\u226518 years) receiving outpatient treatment for PSO in Denmark.<\/span><\/p>\n
\n<\/span><\/strong>The study identified statistically significant but weak negative correlations between coping ability and disease-specific QoL (r<\/span>s<\/span> = \u20130.264; p = 0.003), as well as between coping ability and the need for NC (r<\/span>s <\/span>= \u20130.248; p = 0.006). The results indicate that higher coping ability is associated with better QoL and a lower perceived need for NC.<\/span><\/p>\n
\n<\/span><\/strong>The cross-sectional design limits the ability to draw causal conclusions, but the study contributes new knowledge on the relationships among coping, disease-specific QoL, and support needs in patients with PSO. The results point to the potential to develop clinical tools that systematically identify patients with an increased need for NC, thereby strengthening individualised support in outpatient practice.<\/span><\/p>\n
\n<\/span><\/strong>The findings indicate a potential for a more structured approach to assessing patients\u2019 coping ability, disease-specific quality of life and perceived support in ambulatory psoriasis care. A systematic assessment can strengthen the basis for planning and targeting nurse-led consultations towards patients with the greatest need for support. <\/span><\/p>\n