Browsing Artikler / Articles by Title
Now showing items 840-859 of 1286
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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 ... -
Palliativ behandling: Hospice Lovisenberg
(Journal article, 2003)Artikkelen bygger på en rapport om systematisering og kvantifisering av dokumentert informasjon i pasientjournaler og sykepleierapporter fra Hospice Lovisenberg ble åpnet og ut 2000. Palliativ behandling: Hospice Lovisenberg ... -
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 ... -
Parents' perceptions of factors influencing sleep in pediatric intensive care units: A qualitative study
(Peer reviewed; Journal article, 2024)Purpose: The purpose of this study is to explore factors influencing sleep in pediatric intensive care units as perceived by parents of critically ill children. Design and methods: This descriptive qualitative study used ... -
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 and coping. A mutual dependence?
(Journal article; Peer reviewed, 2013)What implications might an understanding of a mutual dependence between the concepts of participation and coping have for professional engagement with service users? This article presents why participation is central to ... -
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 ... -
Partnership in Practice Research: a Norwegian Experience
(Journal article; Peer reviewed, 2011)This article outlines some of the issues involved in developing partnerships between service users, practitioners and researchers. It discusses these through some experience in Oslo as part of a national level agreement ... -
Partnership with Parents of Children in Care: A Study of Collective User Participation in Child Protection Services
(Journal article; Peer reviewed, 2013)This article presents the findings from a study of user participation in the Norwegian Child Protection services. Birth parents who have lost the custody of their children often feel disempowered by the authorities. The ... -
Pasienters erfaring med sjelesorg i en psykiatrisk klinikk
(Peer reviewed; Journal article, 2009)Bakgrunn: Det er en økende erkjennelse av betydningen av å ivareta pasienters religiøse og åndelige behov i behandling og rehabilitering av psykiske lidelser. I sykehus blir disse behovene oftest ivaretatt av prester. ... -
Patent Rights and Human Rights: Exploring their Relationships
(Peer reviewed; Journal article, 2007)The assessment of the relationship between patent rights and human rights has resulted in several tentative findings, such as by the UN Sub-Commission on the Promotion and Protection of Human Rights, that there are ... -
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 ...