Blar i Publikasjoner fra CRIStin på tittel
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Pain and depression are associated with more anxiety in ME/CFS: A cross-sectional cohort study between Norway and Spain.
(Journal article, 2020)Objectives: Lasting, unexplained and high levels of pain may cause anxiety in patients with chronic fatigue syndrome. The objectives of the current study were to test assumptions of the association between pain and anxiety ... -
Palliasjon og lindring – en begrepsbestemmelse ved bruk av etymologiske ordbøker og offentlige dokumenter
(Peer reviewed; Journal article, 2021)Palliasjon er et begrep som har fått økende aktualitet de senere årene. Betegnelsene palliasjon og lindring anvendes ofte i norske fagmiljøer. Imidlertid er det knyttet uklarhet til begrepene og bruken av dem i klinisk ... -
Palliative enheter i de kommunale helse- og omsorgstjenestene – en kartleggingsstudie
(Peer reviewed; Journal article, 2022)Bakgrunn: Palliative enheter i helse- og omsorgstjenestene i kommunene inngår i det særskilt organiserte palliative tilbudet i Norge. Anbefalt lokalisering, organisering, oppgaver og kompetanse for enheter er beskrevet i ... -
Parental concerns of allergy or hypersensitivity and the infant's diet
(Journal article; Peer reviewed, 2019)Aim: To investigate a possible association between children’s current diet and parents’ reported avoidance of appropriate foods in the child’s diet at the age of 10 months, due to fears of allergic or hypersensitivity ... -
Participant validation: A strategy to strengthen the trustworthiness of your study and address ethical concerns. Kap. 13
(Chapter, 2022)This open access book presents new approaches for researching values as they are performed or materialized. Values have been an important topic in academic literature for a long time; they are at the core of institutional ... -
Participant validation: Exploring a contested tool in qualitative research
(Peer reviewed; Journal article, 2020)This paper examines the use of participant validation in qualitative research, and illustrates that the process of validation can be something more than validation. It can also generate new data and provide the participants ... -
Participation in a support group from the perspective of family caregivers of Alzheimer's disease patients
(Journal article; Peer reviewed, 2017)The aim: The aim of the study was to identify, describe and analyze approaches positively affecting care provided by family caregivers to the patients with Alzheimer’s disease with focus on caregivers’ perceptions and ... -
Participation in research: experiences from collaborating with cocreators during a study among mothers of teenagers with immigrant backgrounds in Oslo
(Peer reviewed; Journal article, 2019)Abstract: In this paper, we discuss what it means to practice participatory research based on experiences from a research process with mothers of immigrant background living in three local communities in Oslo. We reflect ... -
The participation of people in vulnerable situations in interest organisations: A qualitative study of representatives views
(Peer reviewed; Journal article, 2023)People in vulnerable situations have the same right as others to participate in public spheres and influence health and welfare services. However, organisations that support these people and promote their interests are ... -
Pastoral leadership in sunday services. A qualitative case study of seven pastors in the church of Norway
(Dissertation Series for the Degree of Philosophiae Doctor (Ph.D.) at VID Specialized University;56, Doctoral thesis, 2024)This study is situated in practical theology and aims at contributing to the field of pastoral theology focusing on pastoral leadership. The research question with which this study is concerned is: “How do pastors carry ... -
Patient and public involvement in Nordic healthcare research: a scoping review of contemporary practice
(Peer reviewed; Journal article, 2023)Background: Over the past decades, there has been a growing international interest in user involvement in healthcare research. However, evidence on the management and impact of patient and public involvement in Nordic ... -
The patient experience: Informing practice through identification of meaningful communication from the patient’s perspective
(Peer reviewed; Journal article, 2018)(1) Background: There is limited empirical knowledge concerning aspects of healthcare that contribute to a good patient experience from the patient’s perspective and how patient feedback informs service development. (2) ... -
Patient is the new black. Treatmentality and resistance toward patientization
(Journal article; Peer reviewed, 2019)In this essay, I challenge the ways in which global drug policy initiatives call for more humane drug policy and decriminalization. Although these initiatives promote human dignity and agency, they also encourage a particular ... -
Patient-reported outcome measures in children, adolescents, and young adults with palliative care needs—a scoping review
(Peer reviewed; Journal article, 2023)Background: Measuring outcomes facilitates evaluation of palliative services for children, adolescents, and young adults (CAYAs) with life-limiting and/or life-threatening (LL/LT) conditions. Implementation of patient-reported, ... -
Patient-reported outcome measures in pediatric palliative care—a protocol for a scoping review
(Peer reviewed; Journal article, 2021)Background: In pediatric palliative care (PPC), there is a need to involve the child’s voice in situations regarding their symptoms and care needs. Patient-reported outcome measures (PROMs) can be tools to systematically ... -
Patients with bacterial sepsis are heterogeneous with regard to their systemic lipidomic profiles
(Peer reviewed; Journal article, 2022)Sepsis is defined as life-threatening organ dysfunction caused by a dysregulated host response to infection. In the present study, we investigated the systemic/serum lipidomic profile at the time of hospital admission for ... -
Patients with severe mental illness and the ethical challenges related to confidentiality during family involvement: a scoping review
(Peer reviewed; Journal article, 2023)Background: Despite evidence on the significant potential value of family involvement during the treatment of patients with severe mental illness, research has shown that family involvement is largely underused. The duty ... -
Patients' and nurses' experiences of caring in nursing: An integrative literature review across clinical practices
(Peer reviewed; Journal article, 2023)Aim: To summarise, interpret and synthesize research findings on patients' and nurses' experiences of caring in nursing across clinical practices. Background: Caring is a universal element of nursing; however, economic ... -
Patients' experiences with a welfare technology application for remote home care: A longitudinal study
(Peer reviewed; Journal article, 2022)Aims and Objectives: To explore the longitudinal experiences using an application named remote home care for remote palliative care among patients with cancer living at home. Background: Introducing welfare technology ... -
Patients’ experiences and effects of non-pharmacological treatment for myalgic encephalomyelitis/chronic fatigue syndrome – a scoping mixed methods review
(Peer reviewed; Journal article, 2020)Purpose: The EU COST Action 15111 collaboration on myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) aims to assess current research and identify knowledge gaps in Europe. Presently, our purpose is to map the ...