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The number of older subjects is rapidly increasingly worldwide. As a consequence, the nature of clinical conditions is also changing. Traditional medicine and models of care have been based on the evaluation and treatment of single and usually acute conditions occurring in relatively young individuals. Today, the usual clinical manifestation of diseases is characterized by multiple and often chronic conditions affecting older people. In this scenario, frailty and dementia have been triggering special interest both in research and clinical settings due to their high prevalence, impact on the individual’s quality of life, and consequences for public health worldwide. These conditions aptly reflect the complexity of age-related pathological conditions, finding as causal factor a myriad of heterogeneous, interacting, and often still unclear pathophysiological processes. Indeed, their study is strongly affected by the difficulty to differentiate the effects of a normal aging process from eventual pathological deviations of the underlying systems. Their occurrence and trajectories over time are strongly affected by a wide array of factors and determinants that can be hardly attributed to the deficit/involvement of single biological systems and/or health domains. Moreover, environment and social factors also play a key role in the determination of phenotypes. The present Research Topic is aimed at widening our understanding of the frailty and dementia phenomena occurring with aging, in order to improve the clinical and public health approaches to these burdening conditions.
Dementia. --- Aging --- Psychological aspects. --- cognition --- caregiver --- Frailty --- dementia --- mild cognitive impairment --- aging --- cognitive frailty --- Alzheimer
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The authors have developed the ethical imagination inviting a sense of “otherness” towards the vulnerable self, rebounding care for the other as a way to understand our everyday neurotic (normal) tendency of small vices as the propensity and possibility for responsibility towards the other. The authors, inviting the reader into troublesome feelings such as laziness and anger, bring a Levinasian horizon into focus, so that even in the midst of laziness, there remains the small goodness to set the self free to care for the other, meeting the demands, challenges, hesitation, shuddering, tension and shocks of such alterity, of living “otherwise”.
Medical ethics & professional conduct --- caregiver --- philosophy --- science --- caretakers --- philosophers --- morality --- vulnerable --- neurotic --- small vices --- responsibility --- laziness --- anger --- Levinasian --- goodness --- demands --- challenges --- hesitation --- shuddering --- tension --- shock --- vulnerability of the caregiver --- vices for the virtuous caring of the caregiver --- group discussions amongst caregivers --- social sciences --- healthcare
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Old age is increasingly becoming the focus of research and development in Europe. Concerning orthopaedics and sports medicine, the elderly especially are considered as frail patients who need support to maintain the health of their musculoskeletal systems. For this reason, several interventions regarding physical activity have been investigated in recent years in order to understand whether some programs of physical activity are better than others as conservative treatments for degenerative musculoskeletal pathologies (i.e., osteoarthritis, rotator cuff arthropathy, and lower back pain). Furthermore, several investigations have been carried out to understand the best preoperative and postoperative protocols of physical activity to improve the results of orthopaedic surgery. The aim of this Special Issue was to collect the updated evidence concerning these topics in the form of a collection of systematic reviews of the literature.
aging --- cerebral cortex --- dynapenia --- elderly --- motor unit --- muscle strength --- neural --- neuroplasticity --- sarcopenia --- knee --- hip --- arthroplasty --- physical activity --- prehabilitation --- chronic low back pain --- old aged patients --- physical therapy --- walking --- global postural rehabilitation --- cycling --- hydrotherapy --- yoga --- biomarkers --- noncommunicable diseases --- hypertension --- diabetes --- active exercise --- sport --- land-based --- aquatic --- knee or hip osteoarthritis --- older people --- systematic review --- meta-analysis --- osteoarthritis --- tendinopathies --- hip arthroplasty --- knee arthroplasty --- rehabilitation --- physiotherapy --- caregiver --- orthopedic disease --- caregiver strain --- shoulder --- caregiver stress --- dyads --- replacement --- return to sport --- knee osteoarthritis --- unicompartimental knee arthroplasty --- activity --- physical exercise --- balance --- falls --- n/a
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People who have chronic diseases spend a significant amount of time in self-management in out-of-hospital environments, in their homes and in their community settings. These patients have different disease statuses and management requirements, so providing personalized care is key.Personalized care is a collaborative process that should be used in chronic condition management in which patients, caregivers, and healthcare providers identify and discuss problems caused by or related to the patient's condition and then develop plans and goals to empower patients.Personalized care can improve aspects of physical health, mental health, and the ability to self-manage conditions. Thus, a personalized care approach could greatly benefit patients with chronic conditions.In this book, we have included 20 articles that expand the current knowledge on the personalized care approach to diagnosing and treating chronically ill patients.
fibromyalgia --- physical functioning --- obesity --- pain catastrophizing --- pain acceptance --- chronic pain --- rehabilitation --- clinical psychology --- performance-based test --- dual-tasking --- cognitive function --- postural control --- older adults --- Parkinson disease --- personalized medicine --- clinical exercise --- exercise prescription --- boot camp --- physiotherapy --- compliance --- qualitative --- empowerment --- medication acceptability --- intentional nonadherence --- decision --- self esteem --- pharmacology --- rheumatology --- autoimmune --- adolescent --- nursing --- review literature --- sexuality --- virtual reality --- pain --- fatigue --- quality of life --- meta-analysis --- temporomandibular disorders --- surface electromyography --- aerobic exercise --- therapeutic exercise --- diabetes mellitus --- SGLT-2 inhibitors --- antidiabetic agents --- cardiovascular outcomes --- personalized therapy --- sleep --- chronic liver disease --- informal caregiver --- caregiver --- bibliometrics --- data analysis --- needs --- intervention --- patient-focused care --- aged --- disease prevention --- health promotion --- nursing education --- nursing students --- mental disorders --- mental illness --- social stigma --- students --- ageism --- stereotyping --- prejudice --- discrimination --- assessment --- aging --- stroke --- ischemia --- biomarkers --- mortality risk --- patient adherence --- glaucoma --- personalized care --- patient compliance --- child --- child abuse --- maltreatment --- neglect --- risk factors --- family --- caregivers --- child protective services --- advanced nursing practice --- rehabilitation nursing --- transitional care --- hospital discharge --- continuity of care --- hip fracture --- older person --- returning home --- safety --- n/a
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In Zambia, due to the rise of tuberculosis and the closely connected HIV epidemic, a large number of children have experienced the illness or death of at least one parent. Children as Caregivers examines how well intentioned practitioners fail to realize that children take on active caregiving roles when their guardians become seriously ill and demonstrates why understanding children's care is crucial for global health policy. Using ethnographic methods, and listening to the voices of the young as well as adults, Jean Hunleth makes the caregiving work of children visible. She shows how children actively seek to "get closer" to ill guardians by providing good care. Both children and ill adults define good care as attentiveness of the young to adults' physical needs, the ability to carry out treatment and medication programs in the home, and above all, the need to maintain physical closeness and proximity. Children understand that losing their guardians will not only be emotionally devastating, but that such loss is likely to set them adrift in Zambian society, where education and advancement depend on maintaining familial, reciprocal relationships. View a gallery of images from the book (https://www.flickr.com/photos/childrenascaregivers)
Tuberculosis --- HIV-positive persons --- AIDS (Disease) --- Child caregivers --- Consumption (Disease) --- Lungs --- Phthisis --- Pulmonary tuberculosis --- TB (Disease) --- Chest --- Mycobacterial diseases --- Mycobacterium tuberculosis --- HIV-infected persons --- HIV infections --- HIV patients --- HIV-sero-positive persons --- HIV-seropositive persons --- People living with HIV/AIDS --- Positive persons, HIV --- -Sero-positive persons, HIV --- -Seropositive persons, HIV --- -Patients --- Acquired immune deficiency syndrome --- Acquired immunodeficiency syndrome --- Acquired immunological deficiency syndrome --- Immunological deficiency syndromes --- Virus-induced immunosuppression --- Children as caregivers --- Caregivers --- Patients --- Home care --- Diseases --- HIV, aids, guardians, legal guardian, children, childhood, child, childhood studies, zambia, africa, african children, ill, illness, caregiver, caregiving, health, public policy, health policy, public health, family, family illness.
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This Special Issue of the journal Children constitutes an opportune moment to reflect on the psychosocial needs of children living with rare diseases and of their families. As medical advances, treatments, and developments have enabled many of these children to survive infancy and to live into adulthood, progress brings with it concerns and opportunities to enhance the psychosocial quality of life of children living with rare diseases, and of their families. This Special Issue reflects the current state of psychosocial research, which is primarily qualitative in nature. There are no scientifically rigorous randomized clinical trials to create an evidence base of effective psychosocial interventions for the provision of care to children with rare diseases and to their families; nevertheless, the papers within this Special Issue provide a reflection on the state of the science, including ideas about future research and practice. In this next section we share observations about the contributions made by each of the 13 articles, which cover a diverse range of topics.
Psychology --- cancer --- childhood cancer --- adaptation --- psychological --- neoplasm --- oncology --- sibling --- social support --- social adjustment --- palliative care --- end-of-life care --- equity --- public health approach --- compassionate communities --- caregiving --- parents --- psychosocial support --- rare disease --- advance care planning --- decision-making --- family caregiver --- psychosocial care --- communication --- pediatric --- adolescents and young adults --- healthcare needs --- chronic illness --- AYA transition --- Beckwith–Wiedemann syndrome --- emotional-behavioral problems --- psychosocial difficulties --- psychomotor development --- preschool-age children --- pediatric chronic illness --- rare diseases --- family caregivers --- gender differences --- genetic or rare diseases --- health outcomes --- illness perception --- parenting stress --- siblings --- bereavement --- emotions --- psychosocial distress --- pediatrics --- complex chronic conditions --- pediatric to adult transition --- special needs --- interventions --- care coordination --- transition readiness --- family burden --- parental need --- urea cycle disorders --- E-IMD --- inherited metabolic diseases --- medullary thyroid carcinoma --- psychosocial --- young adults --- life-limiting conditions --- adolescents --- age-appropriate --- development --- cognitive functions --- children --- families --- medical complexity --- policy --- advocacy --- n/a --- Beckwith-Wiedemann syndrome
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Phenylketonuria (PKU) is an established inherited amino acid disorder with a very traditional dietary therapy, but there is still more to learn and verify about its nutritional composition, application and overall effectiveness. Although in the 1950s, the first patient successfully treated with diet therapy patently established the role of a low phenylalanine protein substitute, in present times, it is still necessary to characterise the most effective source of artificial protein; defining its optimal amino acid profile; and identifying nutrient modulation that will improve the functionality of protein substitutes. It is also important to understand the impact of a life-long synthetic diet on gut microbiota, metabolomics and inflammatory status. In early-treated patients with PKU, it is unclear if co-morbidities such as overweight, obesity, hypertension and diabetes are higher than in the general population and if these are associated with increased cardiovascular risk. It is also uncertain if overweight and obesity in PKU is related to early dietary practices, the nutritional composition of protein substitutes and special low-protein foods, impact of the dietary treatment on satiety, disordered eating patterns, non-adherence with the low phenylalanine diet and poor metabolic control, or if this is even a consequence of the disorder. In a generation of ageing patients, the impact of intermittent and suboptimal dietary adherence on nutritional status deserves systematic study.
Research & information: general --- Biology, life sciences --- Food & society --- phenylketonuria --- special low protein foods --- nutritional composition --- UK --- macronutrients --- phenylketonuria (PKU) --- consensus --- Delphi method --- food labelling --- phenylalanine --- Phe --- protein --- exchanges --- PKU --- glycomacropeptide --- amino acid --- absorption --- diet therapy --- protein substitute --- gastrointestinal symptoms --- prolonged release --- satiety --- macronutrient intake --- protein content --- free from --- gluten free --- aspartame --- sugar tax --- phenylalanine hydroxylase deficiency --- hyperphenylalaninemia --- medical formula --- amino acid mixture --- tetrahydrobiopterin --- sapropterin --- BH4 --- body composition --- bone mineral density --- bone turnover markers --- osteoporosis --- blood biochemistry --- casein glycomacropeptide --- amino acid protein substitute --- low-protein diet --- newborn screening --- metabolic control --- guidelines --- nitrogen balance --- amino acid catabolism --- blood urea nitrogen --- body mass index --- obesity --- overweight --- phenylalanine restriction --- phenylalanine-restricted diet --- food --- school --- IHCP --- parent/caregiver experiences --- England --- prescribing patterns --- costs --- adult phenylketonuria --- standard operating procedure --- inherited metabolic disorders --- dietary management --- eating out --- low protein food --- restaurants --- amino acids --- adherence --- epigenetics --- health --- preconception --- women --- dietary patterns --- food frequency questionnaire --- validation --- reproducibility
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The use of Information and Communication Technologies (ICT) to deliver psychological services has been emerging as an effective way of increasing individual access to mental health promotion, prevention, and treatment. This Special Issue brings together different contributions focusing on the acceptability and feasibility, (cost-)effectiveness, potentialities, and limitations of ICT-based psychological services for mental health promotion, prevention, and treatment. In each paper, the implications for the implementation of ICT tools in different settings (e.g., primary care services) and for future research are discussed.
information and communication technologies --- outcome monitoring --- therapist feedback --- measurement-based care --- mental health --- pregnancy --- personality --- depression --- adjustment --- social support --- dating apps --- Tinder --- Grindr --- Big Five --- Dark Core --- university students --- nonprofessional caregiver --- prevention --- cognitive --- behavioral --- telephone --- app --- web-based intervention --- be a mom --- randomized controlled trial --- positive mental health --- flourishing --- postpartum period --- usability --- speech interfaces --- cognitive impairment --- ICT --- elderly --- cognitive decline --- emotional disorders --- transdiagnostic --- online group format --- unified protocol --- bariatric surgery --- obesity --- therapeutic alliance --- online interventions --- therapeutic outcomes --- satisfaction with the treatment --- chronic pain --- smartphone app --- telemonitoring --- ecological momentary assessment --- digital information and communication technologies --- psychological counseling --- therapy --- COVID-19 --- coronavirus SARS-CoV-2 --- digital literacy --- web-based interventions --- internalizing symptoms --- depressive symptoms --- adolescents --- primary care --- internet-based intervention --- positive affect --- iUP-A --- i-CBT --- AMTE --- anxiety --- online therapy --- postpartum depression --- cognitive–behavioral therapy --- blended treatment --- Be a Mom --- study protocol --- psychological capital intervention --- online self-learning --- job satisfaction --- turnover intention --- job embeddedness --- cost-effectiveness --- maternal depression --- referral --- recruitment --- mobile intervention --- clinical trials --- n/a --- cognitive-behavioral therapy
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In diesem Buch wird eine Auswahl von Erhebungs- und Auswertungsinstrumenten zur Erfassung relevanter Facetten institutioneller (schrift-)sprachlicher Bildung vorgestellt. Die sieben Verfahren fokussieren unterschiedliche Aspekte der Sprachbildung sowie Sprach- und Leseförderung in Kindertageseinrichtungen und Schulen und adressieren unterschiedliche Zielgruppen (pädagogische Fachkräfte, Lehrkräfte, Kinder). Die Instrumente, die im Rahmen der Initiative "Bildung durch Sprache und Schrift" (BiSS) entwickelt wurden, sind primär für Forschungszwecke, aber auch in der Aus- und Weiterbildung von pädagogischen Fach- und Lehrkräften einsetzbar. Ein Online-Anhang stellt die Instrumente sowie alle notwendigen Materialien zur Verfügung.
BISS
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Heterogenität
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Kindertagesstätte
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Inklusion
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KITA
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"Bildung durch Sprache und Schrift"
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Lehrerprofessionalisierung
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Bildungsforschung
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Lehrerinnenbildung
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Schriftsprachliche Bildung
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Lehrerbildung
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Erziehungswissenschaft
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"Qualitätsentwicklung Bildungswesen"
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Vorschule
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Vorschulpädagogik
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Forschung
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Hochschule
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Schriftsprache
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Sprachbildung
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Sprachförderung
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Leseförderung
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Diagnostik
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Förderungsmaßnahme
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Sprachentwicklung
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Schriftspracherwerb
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Förderdiagnostik
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Förderung
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Sprachstandsforschung
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Lesekompetenz
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Sprachkompetenz
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Sprachdiagnostik
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Fachdidaktik
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Sprachgebrauch
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Kompetenzmessung
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Handlungskompetenz
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Fachwissen
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Wissen
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Professionalisierung
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Profession
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Kompetenz
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Wissenstest
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Mathematikunterricht
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Deutschunterricht
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Fachunterricht
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Fachsprache
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Reflexion
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