A5009041804- Interprofessional Education and Collaboration
- Diabetes Management and Education
- Mental Health and Patient Involvement
- Patient-Provider Communication in Healthcare
- Health Policy Implementation Science
- Cancer survivorship and care
- Traumatic Brain Injury Research
- Posttraumatic Stress Disorder Research
- Musculoskeletal pain and rehabilitation
- Healthcare Systems and Technology
- Patient Dignity and Privacy
- Health, psychology, and well-being
- Health and Medical Research Impacts
- Patient Satisfaction in Healthcare
- Community Health and Development
- Childhood Cancer Survivors' Quality of Life
- European and International Law Studies
- Economic and Financial Impacts of Cancer
University of Southern Denmark
2016-2021
Frederiksberg Hospital
2021
University of Birmingham
2021
Bispebjerg Hospital
2017
Kalmyk Institute for Humanities Research
2016-2017
Background: Patient empowerment (PE) may be defined as the opportunity for patients to master issues important their own health. The aim of this study was conceptualize PE and how concept manifests itself cancer attending follow-up, in order develop a relevant sensitive questionnaire population.Material methods: A theoretical model made, based on Zimmerman's theory psychological empowerment. Patients who were follow-up after first line treatment (n = 16) interviewed about experiences with...
This paper reports on the process of involving former and current cancer patients carers as co-researchers in a Danish mixed methods research project patient empowerment follow up (The Empowerment study 2015–2019). User-Involvement health care is relatively new practice Denmark was one first to systematically involve its design, conduct reporting. The has two aims: first, it provides detailed account second, presents findings from workshop held with academic researchers discuss their...
Abstract Background A range of benefits have been reported from engaging peer interviewers in qualitative interviews, but little systematic evaluation exists to assess their impact on both process and outcomes interviews health research. Objective To investigate the involving patient representatives as a research project empowerment. Design 18 were carried out part wider study, seven by academic researcher alone eleven jointly with interviewer. The analysed quantitatively qualitatively...
Patient-centred care (PCC) including collaborative practices is the core component of modern health care. Despite this, it has proven difficult to implement.To examine (1) healthcare professionals' (HCPs') perception whether they perceive a PCC culture, their attitudes towards involving patients in decisions and experiences barriers for PCC; (2) variables that may contribute explain differences perceived person-centred culture.A questionnaire survey HCPs from 27 different departments two...
presents the evaluative mixed methods
Abstract Background Posttraumatic stress disorder (PTSD) symptoms are common in chronic Whiplash associated disorders (WAD) and have been found to be with higher levels of pain disability. Theoretical frameworks suggested that PTSD not only coexist, but also mutually maintain one another. Although the comorbidity has subject increasing quantitative research, patients’ experiences symptom interaction remain largely uninvestigated using qualitative methods. Objective The present study set out...
Abstract PurposeTo investigate levels of empowerment, possibilities for empowerment and perceived importance among Danes in cancer follow-up. MethodsFrom nation-wide registers a randomly selected group people diagnosed with one ten different diagnoses between five years ago were invited to complete the newly developed ‘Cancer Patient Empowerment Questionnaire’ (CPEQ). Respondents who reported that they follow-up program included analysis. Frequencies answers items questionnaire calculated....