Search results for "CAREGIVER"

showing 10 items of 237 documents

Predictors of caregiver burden in partners of patients with Parkinson's disease

2009

Parkinson's DiseaseSettore MED/26 - Neurologiacaregiver
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Behavioral and psychological effects of coronavirus disease-19 quarantine in patients with dementia

2020

Background: In March 2020, the World Health Organization declared a global pandemic due to the novel coronavirus SARS-CoV-2 and several governments planned a national quarantine in order to control the virus spread. Acute psychological effects of quarantine in frail elderly subjects with special needs, such as patients with dementia, have been poorly investigated. The aim of this study was to assess modifications of neuropsychiatric symptoms during quarantine in patients with dementia and their caregivers. Methods: This is a sub-study of a multicenter nation-wide survey. A structured telephone interview was delivered to family caregivers of patients with diagnosis of Alzheimer disease (AD),…

Pediatricsmedicine.medical_specialtylcsh:RC435-571IrritabilityBehavioral symptoms03 medical and health sciences0302 clinical medicinelcsh:PsychiatryPsychological symptomsmedicineDementiaApathyVascular dementiaBehavioral and psychological symptoms Behavioral symptoms Caregiver Coronavirus disease Dementia Gender Psychological symptoms QuarantineOriginal ResearchMED/26 - NEUROLOGIAPsychiatryBehavioral symptomDementia with Lewy bodiesFamily caregiversbusiness.industryBehavioral and psychological symptomsGenderBehavioral and psychological symptomCaregiver burdenmedicine.diseaseMultiinfarct dementiaCaregiver030227 psychiatryCoronavirus diseaseBehavioral and psychological symptoms; Behavioral symptoms; Caregiver; Coronavirus disease; Dementia; Gender; Psychological symptoms; QuarantinePsychiatry and Mental healthSettore MED/26 - NEUROLOGIAMED/17 - MALATTIE INFETTIVEQuarantineMED/25 - PSICHIATRIADementiaM-PSI/08 - PSICOLOGIA CLINICAPsychological symptommedicine.symptombusiness030217 neurology & neurosurgery
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Family Caregivers' Experiences in Nursing Homes: Narratives on Human Dignity and Uneasiness

2013

This qualitative study focused on dignity in nursing homes from the perspective of family caregivers. Dignity is a complex concept and central to nursing. Dignity in nursing homes is a challenge, according to research. Family caregivers are frequently involved in their family members’ daily experiences at the nursing home. Twenty-eight family caregivers were included in this Scandinavian cross-country, descriptive, and explorative study. A phenomenological-hermeneutic approach was used to understand the meaning of the narrated text. The interpretations revealed two main themes: “One should treat others as one would like others to treat oneself” and “Uneasiness due to indignity.” Dignity wa…

Personhoodmedia_common.quotation_subjectNursing homesContext (language use)PersonhoodDignityNursingHumansMedicineFamilyNarrativeMeaning (existential)General Nursingmedia_commonbusiness.industryFamily caregiversHealth PolicyPerspective (graphical)CaregiversVDP::Medisinske Fag: 700::Helsefag: 800::Sykepleievitenskap: 808Caregiving:Medisinske Fag: 700::Helsefag: 800::Sykepleievitenskap: 808 [VDP]Geriatrics and GerontologybusinessDignityGerontologyQualitative research
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Introduction and Psychometric Validation of the Resilience and Strain Questionnaire (ResQ-Care)— A Scale on the Ratio of Informal Caregivers' Resilie…

2021

Background: Informal caregivers are a particularly vulnerable population at risk for adverse health outcomes. Likewise, there are many scales available assessing individual caregiver burden and stress. Recently, resilience in caregivers gained increasing interest and scales started to assess resilience factors as well. Drawing on a homeostatic model, we developed a scale assessing both caregivers' stress and resilience factors. We propose four scales, two covering stress and two covering resilience factors, in addition to a sociodemographic basic scale. Based on the stress:resilience ratio, the individual risk of adverse health outcomes and suggestions for interventions can be derived.Metho…

Psychiatrystress awarenessDiscriminant validityRC435-571Perceived Stress ScalehealthCaregiver burdenExploratory factor analysisPsychiatry and Mental healthcounselingCronbach's alphapreventionScale (social sciences)homeostasisdiagnosticsGeriatric Depression ScalePsychologyResilience (network)Original ResearchClinical psychologyFrontiers in Psychiatry
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Informal caregiving burden in advanced non-small cell lung cancer: the HABIT study.

2007

Introduction This study's aim was to assess economic data regarding the home assistance burden for advanced non-small cell lung cancer (NSCLC) patients in Italy. Patients and Methods One hundred four NSCLC patients in second-line chemotherapy (2LC) or in supportive therapy (ST) were enrolled in 18 Italian oncology departments and were observed for 3 months. The main caregiver's workload was assessed monthly by a task scale; other caregivers' activities were also registered. Eastern Cooperative Oncology Group performance status was assessed by physicians, and patients completed the Lung Cancer Symptoms (LCS) subscale. Formal caregiving time was valued according to market prices; informal car…

Pulmonary and Respiratory MedicineAdultMalemedicine.medical_specialtyLung NeoplasmsHome Nursingmedia_common.quotation_subjectAntineoplastic Agentscaregiving burden in advanced non-small cell lung cancerNSCLCQuality of lifeCost of IllnessCarcinoma Non-Small-Cell LungmedicineHumansLung cancermedia_commonAgedAged 80 and overbusiness.industrySocial SupportWorkloadAssistance burdenHealth Care CostsMiddle Agedmedicine.diseaseOncologyCaregiversItalySocioeconomic FactorsInformal caregivingSpouseSupportive psychotherapyScale (social sciences)Family medicinePhysical therapyCosts and Cost AnalysisQuality of LifeFemaleHabitNon small cellbusiness
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Parental-caregiver perceptions of child oral health-related quality of life (P-CPQ): Psychometric properties for the peruvian spanish language.

2013

Objectives: The aim of the study was to cross-culturally adapt the Parental-Caregiver Perceptions Questionnaire (P-CPQ) to the Peruvian Spanish language and assess its reliability and validity. Study Design: To translate and cross-cultural adapt the instrument, 60 parents answered the P-CPQ in two pilot tests. The final version of the P-CPQ was evaluated in 200 parents of children aged 11 to 14 years, who were clini - cally examined for dental caries. The internal consistency was assessed by Cronbach's alpha coefficient while repeat administration of the P-CPQ on the same 200 children facilitated the test-retest reliability via intraclass correlation coefficient (ICC). Construct and discrim…

Quality of lifeMaleParentsvalidityPsychometricsAdolescentPsychometricsIntraclass correlationOdontologíaOral HealthDevelopmental psychologyQuality of life (healthcare)childrenCronbach's alphaSurveys and QuestionnairesPeruHumansChildGeneral DentistryReliability (statistics)LanguagereliabilityCultural CharacteristicsOral Medicine and PathologyResearchDiscriminant validityConstruct validityReproducibility of Results:CIENCIAS MÉDICAS [UNESCO]//purl.org/pe-repo/ocde/ford#3.02.14 [https]Ciencias de la saludOtorhinolaryngologyCaregiversScale (social sciences)UNESCO::CIENCIAS MÉDICASQuality of Lifeoral healthSurgeryFemalePsychologyClinical psychologyMedicina oral, patologia oral y cirugia bucal
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Rehabilitation for Multiple Sclerosis in Adults (I); Impairment and Impact on Functioning and Quality of Life: An Overview

2010

Multiple sclerosis (MS) is a chronic, central nervous system, disabling disease. International Classification of Functioning and relevant generic and specific outcome measures are reported. Problems perceived by people with MS (PwMS) affect mobility, sight, continence, feeding, or cognitive impairment, depending on whether acute, chronic, or long-term disability was involved. The most common body function and structure impairments leading to disability and reported by health care professionals are fatigue, weakness, decreased fitness, sensory disorders, pain, upper motor neuron syndromes, ataxia and tremor, balance and postural control problems, gait pattern disorders, visual problems, and …

Quality of lifemedicine.medical_specialtyDaily life activityRehabilitationDisabilitybusiness.industrymedicine.medical_treatmentMultiple sclerosisRehabilitationPhysical Therapy Sports Therapy and Rehabilitationmedicine.diseaseCaregiverMultiple sclerosisPhysical medicine and rehabilitationQuality of life (healthcare)Physical therapyMedicinebusiness
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Narrative Medicine to integrate patients’, caregivers’ and clinicians’ migraine experiences: the DRONE multicentre project

2021

Abstract Background Although migraine is widespread and disabling, stigmatisation and poor awareness of the condition still represent barriers to effective care; furthermore, research on migraine individual and social impact must be enhanced to unveil neglected issues, such as caregiving burden. The project investigated the migraine illness experience through Narrative Medicine (NM) to understand daily life, needs and personal resources of migraneurs, their caregivers and clinicians, and to provide insights for clinical practice. Methods The project involved 13 Italian headache centres and targeted migraneurs, their caregivers and migraine specialists at these centres. Written narratives, c…

Quality of lifemedicine.medical_specialtyUnmanned Aerial DevicesMigraine Disordersmedia_common.quotation_subjectIllness experienceCoding (therapy)Illness experienceDermatologyQuality of life (healthcare)PerceptionmedicineHumansNarrativePsychiatryeducationMigrainemedia_commonNarrative medicineeducation.field_of_studyGeneral Medicinemedicine.diseaseDoctor-patient relationshipNarrative medicinePsychiatry and Mental healthCaregiversMigraineDoctor–patient relationshipOriginal ArticleNeurology (clinical)Psychology
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Age-dependency in mortality of Finnish family caregivers: a nationwide register-based study

2020

Abstract Purpose Mortality appears to be lower in family caregivers than in the general population. However, there is lack of knowledge whether the difference in mortality between family caregivers and the general population is dependent on age. The purpose of this study was to analyze all-cause mortality in relation to age in family caregivers and to study their cause-specific mortality using data from multiple Finnish national registers. Methods The data included all individuals, who received family caregiver's allowance in Finland in 2012 (n = 42 256, mean age 67 years, 71% women) and a control population matched for age, sex, and municipality of residence (n = 83 618). Information on da…

Register basedGerontologyFamily caregiversbusiness.industryPublic Health Environmental and Occupational HealthMedicine10. No inequalitybusiness3. Good healthDependency (project management)European Journal of Public Health
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'I had to help my child!': The role of emotions, risk, and trust in use of nasal decongestants in children.

2013

Recent studies suggest that a number of common cold medicines, including nasal decongestants are not suitable for small children. In Latvia nasal decongestants are primarily over-the-counter (OTC) medicines, and patient information leaflets generally permit use of these medicines for small children. The previous studies in Latvia investigating the use of medicines in cases of common cold demonstrated extensive use of decongestants in children less than six years of age, marking a necessity for more profound research. As a result a qualitative study was implemented in 2011 to identify sources of information that offer advice for the use of decongestants in children. The caregivers’ percepti…

Riskmedicine.medical_specialtyDecision MakingEmotionsPoison controlCommon ColdTrustPediatricsSuicide preventionOccupational safety and healthNursingInjury preventionMedicineHumansQualitative Researchbusiness.industryInfant NewbornHuman factors and ergonomicsInfantCommon coldmedicine.diseaseLatviaNasal decongestantNasal DecongestantsCaregiversFamily medicineChild PreschoolPediatrics Perinatology and Child HealthFemalebusinessQualitative researchJournal of child health care : for professionals working with children in the hospital and community
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