Results for 'caregiving'

931 found
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  1. Robot Caregivers: Harbingers of Expanded Freedom for All? [REVIEW]Yvette Pearson - 2010 - Ethics and Information Technology 12 (3):277-288.
    As we near a time when robots may serve a vital function by becoming caregivers, it is important to examine the ethical implications of this development. By applying the capabilities approach as a guide to both the design and use of robot caregivers, we hope that this will maximize opportunities to preserve or expand freedom for care recipients. We think the use of the capabilities approach will be especially valuable for improving the ability of impaired persons to interface more effectively (...)
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  2.  71
    Caregiving Robots and Ethical Reflection: The Perspective of Interdisciplinary Technology Assessment. [REVIEW]Michael Decker - 2008 - AI and Society 22 (3):315-330.
    Autonomous robots that are capable of learning are being developed to make it easier for human actors to achieve their goals. As such, robots are primarily a means to an end and replace human actions. An interdisciplinary technology assessment was carried out to determine the extent to which a replacement of this kind makes ethical sense in terms of technology, economics and legal aspects. Proceeding from an ethical perspective, derived from Kant’s formula of humanity, in this article we analyse the (...)
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  3. Caregiving, Carebots, and Contagion.Michael C. Brannigan - 2022 - Lexington Books.
    This work explores caring robots' lifesaving benefits, particularly during contagion, while probing the threat they pose to interpersonal engagement and genuine human caregiving. As humans, we have a binding moral responsibility to care for the Other, and genuine caring demands our embodied, human-to-human presence.
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  4.  9
    Caregiving, Self‐Care, and Contemplation: Resources From Thomas Aquinas.Emily Dubie - 2021 - New Blackfriars 102 (1099):384-400.
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  5.  3
    Caregivers, Gender, and the Law: An Analysis of Family Responsibility Discrimination Case Outcomes.Sylvia Fuller, Christina Treleaven & C. Elizabeth Hirsh - 2020 - Gender and Society 34 (5):760-789.
    As workers struggle to combine work and family responsibilities, discrimination against workers based on their status as caregivers is on the rise. Although both women and men feel the pinch, caregiver discrimination is particularly damaging for women, because care is intricately tied to gendered norms and expectations. In this article, we analyze caregiver discrimination cases resolved by Canadian Human Rights Tribunals from 1985 through 2016, to explore how work and caregiving clash. We identify issues involved in disputes and the (...)
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  6. Carebots and Caregivers: Sustaining the Ethical Ideal of Care in the Twenty-First Century.Shannon Vallor - 2011 - Philosophy and Technology 24 (3):251-268.
    In the early twenty-first century, we stand on the threshold of welcoming robots into domains of human activity that will expand their presence in our lives dramatically. One provocative new frontier in robotics, motivated by a convergence of demographic, economic, cultural, and institutional pressures, is the development of “carebots”—robots intended to assist or replace human caregivers in the practice of caring for vulnerable persons such as the elderly, young, sick, or disabled. I argue here that existing philosophical reflections on the (...)
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  7.  19
    Informal Caregiver Burnout? Development of a Theoretical Framework to Understand the Impact of Caregiving.Pierre Gérain & Emmanuelle Zech - 2019 - Frontiers in Psychology 10.
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  8.  4
    Caregivers’ Understanding of Informed Consent in a Randomized Control Trial.Dorothy Helen Boyd, Yinan Zhang, Lee Smith, Lee Adam, L. Foster Page & W. M. Thomson - 2021 - Journal of Bioethical Inquiry 18 (1):141-150.
    There are differences in caregivers’ literacy and health literacy levels that may affect their ability to consent to children participating in clinical research trials. This study aimed to explore the effectiveness, and caregivers’ understandings, of the process of informed consent that accompanied their child’s participation in a dental randomized control trial. Telephone interviews were conducted with a convenience sample of ten caregivers who each had a child participating in the RCT. Pre-tested closed and open-ended questions were used, and the findings (...)
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  9.  55
    Caregiver Influences on Emerging Emotion Regulation.S. Calkins & Ashley Hill - 2007 - In James J. Gross (ed.), Handbook of Emotion Regulation. Guilford Press. pp. 229--248.
  10.  12
    Caregivers’ Perception of Dignity in Teenagers with Autism Spectrum Disorder.Fatemeh Mohammadi, Mahnaz Rakhshan, Zahra Molazem, Najaf Zareh & Mark Gillespie - 2019 - Nursing Ethics 26 (7-8):2035-2046.
    Introduction: Maintaining dignity is one of patients is one of the main ethical responsibilities of caregivers. However, in many cases, the dignity of patients, especially autistic teenagers is not maintained. The extent to which dignity needs are met for this group within the Iranian care system is difficult to determine as dignity is an abstract concept, and there are few related research studies reported. Objectives: The objective of this study is to find out caregivers perspectives on dignity in teenagers with (...)
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  11.  9
    Caregiving and Moral Distress for Family Caregivers During Early-Stage Alzheimer’s Disease.Chris Weigel - 2019 - International Journal of Feminist Approaches to Bioethics 12 (2):74-91.
    That diseases such as Alzheimer’s present many kinds of vulnerabilities for the afflicted is perhaps too obvious to mention given that a person with Alzheimer’s disease eventually becomes dependent on others for most basic, everyday needs. The ensuing vulnerabilities have physical, cognitive, emotional, social, and legal aspects, as well as aspects concerning autonomy. Such diseases also present a wide range of vulnerabilities for caregivers across multiple domains. Caregivers are vulnerable, for example, to social isolation, physical exhaustion, stress, and loss of (...)
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  12.  8
    Caregivers Blinded by the Care: A Qualitative Study of Physical Restraint in Pediatric Care.Bénédicte Lombart, Carla De Stefano, Didier Dupont, Leila Nadji & Michel Galinski - forthcoming - Nursing Ethics:096973301983312.
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  13. Caregivers' Attitudes and Practices: Influence on Childhood Body Weight.Fabiana Silva Costa, Daisy Lopes Del Pino & Rogério Friedman - 2011 - Journal of Biosocial Science 43 (3):369-378.
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  14.  7
    Family Caregiving and the Intergenerational Transmission of Poverty.Richard L. Kaplan - 2018 - Journal of Law, Medicine and Ethics 46 (3):629-635.
    The United States relies on uncompensated family caregivers to provide most of the long-term care required by older adults as they age. But such care comes at a significant financial cost to these caregivers in the form of lower lifetime earnings and diminished Social Security retirement benefits, ineligibility for Medicare coverage of their healthcare costs, and minimal retirement savings. To reduce the impact of uncompensated caregiving on the intergenerational transmission of poverty, this paper discusses three possible mechanisms of compensating (...)
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  15. The Real Caregivers in the Nursing Home-Certified Nursing Assistants.David B. Oliver - 1999 - Bioethics Forum 15:18-22.
     
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  16.  2
    Caregiver Choice and Caregiver Outcomes: A Longitudinal Study of Irish Spousal Dementia Caregivers.Maria M. Pertl, Aditi Sooknarine-Rajpatty, Sabina Brennan, Ian H. Robertson & Brain A. Lawlor - 2019 - Frontiers in Psychology 10.
  17.  38
    The Ethics of Robotic Caregivers.Amitai Etzioni & Oren Etzioni - 2017 - Interaction Studies 18 (2):174-190.
    As Artificial Intelligence technology seems poised for a major take-off and changing societal dynamics are creating a high demand for caregivers for elders, children and those infirmed-robotic caregivers, may well be used much more often. This article examines the ethical concerns raised by the use of AI caregivers and concludes that many of these concerns are avoided when AI caregivers operate as partners rather than substitutes. Furthermore, most of the remaining concerns are minor and are faced by human caregivers as (...)
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  18.  12
    Caregivers’ Perception of Women’s Dignity in the Delivery Room: A Qualitative Study.Fateme Mohammadi, Hadise Sadate Tabatabaei, Farzaneh Mozafari & Mark Gillespie - forthcoming - Nursing Ethics:096973301983497.
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  19. Caregiving In Transnational Context: “My Wings Have Been Cut; Where Can I Fly?”.Miriam Stewart, Karen Hughes, Margaret Harrison, Anne Neufeld & Denise Spitzer - 2003 - Gender and Society 17 (2):267-286.
    Migration often requires the renegotiation of familial and gender roles as immigrants encounter potentially competing values and demands. Employing ethnographic methods and including in-depth interviewing and participant observation, the authors explore the experiences of 29 South Asian and Chinese Canadian female family caregivers. Caregiving was central to their role as women and members of their ethnocultural community. The women were often engaged in paid labor that compressed the time available to fulfill their duties as caregivers. Women’s role in the (...)
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  20.  29
    Views of Caregivers on the Ethics of Assistive Technology Used for Home Surveillance of People Living with Dementia.Maurice Mulvenna, Anton Hutton, Vivien Coates, Suzanne Martin, Stephen Todd, Raymond Bond & Anne Moorhead - 2017 - Neuroethics 10 (2):255-266.
    This paper examines the ethics of using assistive technology such as video surveillance in the homes of people living with dementia. Ideation and concept elaboration around the introduction of a camera-based surveillance service in the homes of people with dementia, typically living alone, is explored. The paper reviews relevant literature on surveillance of people living with dementia, and summarises the findings from ideation and concept elaboration workshops, designed to capture the views of those involved in the care of people living (...)
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  21.  13
    Caregiver Depression and Early Child Development: A Mixed-Methods Study From Rural China.Ai Yue, Jiaqi Gao, Meredith Yang, Lena Swinnen, Alexis Medina & Scott Rozelle - 2018 - Frontiers in Psychology 9.
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  22.  39
    Care for the Caregivers? Transnational Justice and Undocumented Non-Citizen Care Workers.Zahra Meghani & Lisa Eckenwiler - 2009 - International Journal of Feminist Approaches to Bioethics 2 (1):77-101.
    In recent years, the flow of undocumented labor from the global South to richer nations has increased considerably. Many undocumented women workers find employment as caregivers for the dependent elderly, whose numbers are burgeoning in affluent countries. Here we present a profile of undocumented non-citizen caregivers in the United States and delineate some of the key injustices they suffer. After identifying the causal factors responsible for the flow of undocumented labor from the global South to richer nations like the United (...)
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  23.  24
    Kin Relationships and the Caregiving Biases of Grandparents, Aunts, and Uncles.Alexander Pashos & Donald H. McBurney - 2008 - Human Nature 19 (3):311-330.
    Paternity certainty and matrilineal family ties have been used to explain the asymmetric caregiving of grandparents and aunts and uncles. The proximate mechanisms underlying biased kin investment, however, remain unclear. A central question of the study presented here was whether the parent-kin relationship is an important link in the caregiving. In a two-generational questionnaire study, we asked subjects to estimate the intensity of their relationships to parents, grandparents, aunts, and uncles (emotional closeness, investment received in childhood). In addition, (...)
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  24.  23
    How Family Caregivers' Medical and Moral Assumptions Influence Decision Making for Patients in the Vegetative State: A Qualitative Interview Study.Katja Kuehlmeyer, Gian Domenico Borasio & Ralf J. Jox - 2012 - Journal of Medical Ethics 38 (6):332-337.
    Background Decisions on limiting life-sustaining treatment for patients in the vegetative state (VS) are emotionally and morally challenging. In Germany, doctors have to discuss, together with the legal surrogate (often a family member), whether the proposed treatment is in accordance with the patient's will. However, it is unknown whether family members of the patient in the VS actually base their decisions on the patient's wishes. Objective To examine the role of advance directives, orally expressed wishes, or the presumed will of (...)
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  25.  24
    Just Caring for Caregivers: What Society and the State Owe to Those Who Render Care.Alison Reiheld - 2015 - Feminist Philosophy Quarterly 1 (2):1-24.
    Traditional considerations of justice for those who require caregiving have centered on what is due to the dependent person. However, considerations of justice also bear strongly on what is due to the caregiver. I focus on unpaid dependency work, too long treated as a private matter rather than a public concern. More is owed to those who render care: the division of labor is unjust, the nature of dependency work creates vulnerabilities for caregivers, and unpaid caregivers are disadvantaged in (...)
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  26.  1
    Caregivers’ Sensemaking of Children’s Hereditary Angioedema: A Semiotic Narrative Analysis of the Sense of Grip on the Disease.Maria Francesca Freda, Livia Savarese, Pasquale Dolce & Raffaele De Luca Picione - 2019 - Frontiers in Psychology 10.
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  27.  10
    Caregiver Training in Mindfulness-Based Positive Behavior Supports : Effects on Caregivers and Adults with Intellectual and Developmental Disabilities.Nirbhay N. Singh, Giulio E. Lancioni, Bryan T. Karazsia & Rachel E. Myers - 2016 - Frontiers in Psychology 7.
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  28.  2
    Caregiving and the Abuse of Power.Joseph Walsh - 2019 - Feminist Philosophy Quarterly 5 (3).
    Caregiving relationships are often characterized by an imbalance of power between the caregiver and her cared-for. The danger that this power will be abused is a source of serious moral concern. In this article, I argue that the risk of an abuse of power sometimes stems not from the possession of power itself, but from the very nature of caring relationships. This is because carers must be prepared to exercise non-minimal amounts of power over their cared-fors, even if doing (...)
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  29.  9
    Deception in Caregiving: Unpacking Several Ethical Considerations in Covert Medication.Rosalind Abdool - 2017 - Journal of Law, Medicine and Ethics 45 (2):193-203.
    From a clinical ethics perspective, I explore several traditional arguments that deem deception as morally unacceptable. For example, it is often argued that deception robs people of their autonomy. Deception also unfairly manipulates others and is a breach of important trust-relations. In these kinds of cases, I argue that the same reasons commonly used against deception can provide strong reasons why deception can be extremely beneficial for patients who lack mental capacity. For example, deception can enhance, rather than impair, autonomy (...)
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  30.  2
    Caregiving Relationships as Evolutionary and Developmental Bases of Obligation.Rachna B. Reddy & Henry M. Wellman - 2020 - Behavioral and Brain Sciences 43.
    Obligation as defined by Tomasello requires mutually capable parties, but one-sided caregiver relationships reveal its developmental and evolutionary precursors. Specifically, “coercive” emotions may prompt protective action by caregivers toward infant primates, and infants show distress toward caregivers when they appear to violate expectations in their relationships. We argue that these early social-relational expectations and emotions may form the base of obligation.
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  31.  18
    Child-Caregiver Interaction in Two Remote Indigenous Australian Communities.Jill Vaughan, Gillian Wigglesworth, Deborah Loakes, Samantha Disbray & Karin Moses - 2015 - Frontiers in Psychology 6.
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  32.  1
    Patient Portal Access for Caregivers of Adult and Geriatric Patients: Reframing the Ethics of Digital Patient Communication.Teja Ganta, Jacob M. Appel & Nicholas Genes - forthcoming - Journal of Medical Ethics:medethics-2021-107759.
    Patient portals are poised to transform health communication by empowering patients with rapid access to their own health data. The 21st Century Cures Act is a US federal law that, among other provisions, prevents health entities from engaging in practices that disrupt the exchange of electronic health information—a measure that may increase the usage of patient health portals. Caregiver access to patient portals, however, may lead to breaches in patient privacy and confidentiality if not managed properly through proxy accounts. We (...)
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  33.  13
    Experiences of Caregivers and Relatives in Public Nursing Homes.Elisabeth Häggström & Annica Kihlgren - 2007 - Nursing Ethics 14 (5):691-701.
    The aim of the present study was, by means of discussion highlighting ethical questions and moral reasonings, to increase understanding of the situations of caregivers and relatives of older persons living in a public nursing home in Sweden. The findings show that these circumstances can be better understood by considering two different perspectives: an individual perspective, which focuses on the direct contact that occurs among older people, caregivers and relatives; and a societal perspective, which focuses on the norms, values, rules (...)
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  34.  5
    Testimonial Injustice: Considering Caregivers in Paediatric Behavioural Healthcare.Michelle Trang Pham, Eric A. Storch & Gabriel Lázaro-Muñoz - 2021 - Journal of Medical Ethics 47 (11):738-739.
    Harcourt argues that in clinical contexts, children and young people with mental health illness can experience epistemic, specifically testimonial, injustice when their perspectives are unjustifiably discounted by health service providers.1 Our goal in this commentary was to illustrate how caregivers, a critical component of CYP treatment triad, can also engage in testimonial injustice towards CYP patients. Testimonial injustice occurs when one suffers a credibility deficit and that credibility deficit is based on prejudice.2 Harcourt expands Fricker’s account of testimonial injustice by (...)
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  35.  5
    Caregiver Reactions to Neuroimaging Evidence of Covert Consciousness in Patients with Severe Brain Injury: A Qualitative Interview Study.Charles Weijer, Adrian M. Owen, Sarah Munce, Laura Elizabeth Gonzalez-Lara, Fiona Webster & Andrew Peterson - 2021 - BMC Medical Ethics 22 (1):1-13.
    BackgroundSevere brain injury is a leading cause of death and disability. Diagnosis and prognostication are difficult, and errors occur often. Novel neuroimaging methods can improve diagnostic and prognostic accuracy, especially in patients with prolonged disorders of consciousness. Yet it is currently unknown how family caregivers understand this information, raising ethical concerns that disclosure of neuroimaging results could result in therapeutic misconception or false hope.MethodsTo examine these ethical concerns, we conducted semi-structured interviews with caregivers of patients with PDoC who were enrolled (...)
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  36. Caregiving: The Divided Meaning of Being Human and the Divided Self of the Caregiver.Arthur Kleinman - 2010 - In J. Michelle Molina, Donald K. Swearer & Susan Lloyd McGarry (eds.), Rethinking the Human. Center for the Study of World Religions, Harvard Divinity School. pp. 17--31.
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  37.  12
    Levinasian Caregiving.Jonathan Yahalom - 2017 - Philosophy in the Contemporary World 24 (1):51-62.
    This article reviews the work of philosopher Emmanuel Levinas to explore caregiving for dementia. It defends a dual thesis whereby it first articulates how Levinas provides a phenomenological description to account for why caregiving is subjectively dreadful and, second, how caregiving invites a fresh re-reading of Levinasian thought. The article introduces two different forms of otherness represented by death and dementia, respectively. This re-reading shows how dementia forces us to more immediately reckon with the intensity Levinas attributes (...)
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  38.  43
    Caregiver–Chimpanzee Interactions with Species-Specific Behaviors.Mary Lee A. Jensvold, Jacquelyn C. Buckner & Gina B. Stadtner - 2010 - Interaction Studies 11 (3):396-409.
    The relationships between captive primates and their caregivers are critical ones and can affect animal welfare. This study tested the effect of caregivers using chimpanzee behaviors or not, in daily interactions with captive chimpanzees. In the Chimpanzee Behavior condition the caregiver presented chimpanzee behaviors. In the Human Behavior condition the caregiver avoided using chimpanzee behaviors. The chimpanzees had individual patterns of response and had significant differences in their responses to each condition. These data are compared to a similar study conducted (...)
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  39.  6
    Extreme Caregiving: The Moral Work of Raising Children with Special Needs by Lisa Freitag.Jessica Miller - 2020 - International Journal of Feminist Approaches to Bioethics 13 (1):170-173.
    Modern medical technology has made it possible for babies to survive with conditions that would have ended their lives only half a century ago. But complex health care interventions and regimens are not enough. These children require support, caregiving, and constant vigilance from their families, especially their parents. Sometimes referred to as children with "special needs," their dependency and vulnerability may stem from genetic disorders, premature births, serious accidents, or illness. This includes conditions such as severe autism spectrum disorder, (...)
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  40.  47
    The Intervention of Robot Caregivers and the Cultivation of Children’s Capability to Play.Yvette Pearson & Jason Borenstein - 2013 - Science and Engineering Ethics 19 (1):123-137.
    In this article, the authors examine whether and how robot caregivers can contribute to the welfare of children with various cognitive and physical impairments by expanding recreational opportunities for these children. The capabilities approach is used as a basis for informing the relevant discussion. Though important in its own right, having the opportunity to play is essential to the development of other capabilities central to human flourishing. Drawing from empirical studies, the authors show that the use of various types of (...)
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  41. Acknowledging Caregivers’ Vulnerability in the Managment of Challenging Behaviours to Reduce Control Measures in Psychiatry.Jean Lefèvre-Utile, Marjorie Montreuil, Amélie Perron, Aymeric Reyre & Franco Carnevale - 2022 - Nursing Ethics 29 (3):758-779.
    Background: The management of challenging behaviours in inpatient with intellectual disability and/or autism spectrum disorders can lead to an escalation of control measures. In these complex situations where patients have an intellectual disability/autism spectrum disorder accompanied by a psychiatric comorbidity, the experiences of caregivers related to the crisis management have rarely been studied. Purpose: This study examined the moral experiences of caregivers related to challenging behaviours’ management and alternatives to control measures. Research design: Using Charles Taylor’s hermeneutic framework, a 2-month (...)
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  42.  1
    Professional Caregivers: Stress and Coping in the Face of Loss and Trauma.D. Machando, V. Maasdorp, C. Wogrin, G. Javangwe & K. C. Muchena - 2019 - Indo-Pacific Journal of Phenomenology 19 (2):81-90.
    Professional caregivers who work with the trauma and suffering of others, such as doctors, nurses and psychologists, may face significant challenges along with the risk of adverse, long-term mental and physical health problems. Caregivers with responsibility for dependants outside their professional work reported more stress. This finding is of particular relevance in respect of caregivers in under-developed countries such as Zimbabwe, where many households have taken in additional children who have been orphaned, whose parents are ill, or whose parents have (...)
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  43. Caregiver Access to Services-Helping Caregivers Self-Identify.C. Rugg - 2003 - Bioethics Forum 19:7-10.
     
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  44.  17
    Caregiving, Emotion, and Concern for Others.Carolyn Zahn-Waxler - 2001 - Behavioral and Brain Sciences 25 (1):48-49.
    Few individuals are constitutionally incapable of showing concern for others at an early age, and malleability is possible. Individual variations will be best understood through study of the representational prerequisites of empathy in close conjunction with caregiving environments and affective underpinnings.
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  45.  1
    Caregivers’ Perception of Teenagers’ Dignity in End of Life Stages: A Phenomenological Study.Fateme Mohammadi, Khodayar Oshvandi, Masoud Khodaveisi, Fatemeh Cheraghi, Tayebeh Hasan Tehrani, Arash Khalili & Hazel Kyle - forthcoming - Nursing Ethics:096973302210857.
    Introduction: Maintaining patient dignity in a caregiving environment is one of the most important moral responsibilities for caregivers. Nonetheless, there are vulnerable groups, specifically teenagers, who in their final stages of life are prone to their dignity being threatened. Moreover, dignity is an abstract concept and there is no studies done on teenagers’ dignity in the final stages of life available in Iran.Purpose: The purpose of this study is to describe the caregivers’ experiences regarding teenagers’ dignity in the final (...)
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  46.  8
    Caregiver–Chimpanzee Interactions with Species-Specific Behaviors.Mary Lee A. Jensvold, Jacquelyn C. Buckner & Gina B. Stadtner - 2010 - Interaction Studies. Social Behaviour and Communication in Biological and Artificial Systemsinteraction Studies / Social Behaviour and Communication in Biological and Artificial Systemsinteraction Studies 11 (3):396-409.
    The relationships between captive primates and their caregivers are critical ones and can affect animal welfare. This study tested the effect of caregivers using chimpanzee behaviors or not, in daily interactions with captive chimpanzees. In the Chimpanzee Behavior condition the caregiver presented chimpanzee behaviors. In the Human Behavior condition the caregiver avoided using chimpanzee behaviors. The chimpanzees had individual patterns of response and had significant differences in their responses to each condition. These data are compared to a similar study conducted (...)
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  47.  17
    Caregiving Men of Alzheimer’s Disease Sufferers in Nuevo Leo´N : Experiences and Meanings.J. Azoh Barry - 2014 - Vulnerable Groups and Inclusion 5.
  48.  10
    Physicians and Caregivers Do Differ in Ethical Attitudes to Daily Clinical Practice.Patrik Kjærsdam Telléus, Dorte Møller Holdgaard & Birthe Thørring - 2018 - Clinical Ethics 13 (4):209-219.
    It is commonly assumed that there are differences in physicians’ and caregivers’ ethical attitudes towards clinical situations. The assumption is that the difference is driven by different values, views and judgements in specific situations. At Aalborg University Hospital, Denmark, we aimed to investigate these assumptions by conducting a large quantitative study. The study design, based on the Factorial Survey Method, was a carefully constructed survey with 50 questions designed to test which factors influenced the respondents’ ethical reasoning. The factors were (...)
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  49. Untangling Caregiving Role From Parent Gender in Coparenting Research: Insights From Gay Two-Father Families.Nicola Carone & Vittorio Lingiardi - 2022 - Frontiers in Psychology 13.
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  50.  12
    Caregivers’ Role in Maternal–Fetal Conflict.Ercan Avci - 2015 - Narrative Inquiry in Bioethics 5 (1):67-76.
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