Search results for "CAREGIVER"

showing 10 items of 237 documents

Optimism as a key to improving mental health in family caregivers of people living with Alzheimer’s disease

2020

Objective: The aim of the present work was to study the serial multiple mediating role of optimism, perceived social support and subjective burden in the relationship between objective burden and psychological distress in caregivers of people with Alzheimer´s Disease (AD).Method: One hundred and forty family caregivers of people living with AD were recruited from randomly selected Alzheimer Association Centres. They answered the General Health Questionnaire (GHQ), the Life Orientation Test-Revised (LOT-R), the Functional Social Support Questionnaire (DUKE.UNC), the Zarit Burden Interview (ZBI) and questions relating to gender, age and the amount of time spent on daily caregiving.Results: Re…

Mediation (statistics)media_common.quotation_subjectPsychological interventionDisease03 medical and health sciencesSocial support0302 clinical medicineOptimismCost of IllnessAlzheimer DiseaseHumansmedia_common030214 geriatricsFamily caregiversMental healthPsychiatry and Mental healthCross-Sectional StudiesMental HealthCaregiversGeriatrics and GerontologyPshychiatric Mental HealthGeneral Health QuestionnairePsychologyGerontology030217 neurology & neurosurgeryClinical psychologyAging & Mental Health
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The Religious Meaning System and Resilience in Spouse Caregivers of Cancer Patients: A Moderated Mediation Model of Hope and Affect

2021

AbstractThe character of the relationship between religiosity and resilience depends to a large extent on mediation and moderation mechanisms which rely on cognitive and emotional processes. Research conducted within hope theory and the broaden and build theory indicates that hope and affect can mediate and moderate this relationship. The present study explored whether the relationship of the religious meaning system with resilience in spouse caregivers of cancer patients can be mediated by hope and simultaneously moderated by positive and negative affect. A total of 241 spouse caregivers completed a set of questionnaires. The results revealed that hope mediated the relationship between the…

Mediation (statistics)media_common.quotation_subjectSpouse caregiversAffect (psychology)ReligiosityHopeModerated mediationNeoplasmsSurveys and QuestionnairesHumansMeaning (existential)The religious meaning systemGeneral Nursingmedia_commonOriginal PaperResiliencePositive and negative affectReligious studiesGeneral MedicineBroaden-and-buildResilience PsychologicalModerationCaregiversPsychological resiliencePsychologySocial psychologyJournal of Religion and Health
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Challenges and barriers in mental healthcare systems and their impact on the family: A systematic integrative review

2020

The aim of this systematic integrative review is to analyse the challenges and barriers found in mental healthcare systems and the impact they have on the family. Searches were made of the Web of Science, Scopus, Medline and Cochrane databases using terms relating to mental health, family care and healthcare systems. We included and critically evaluated studies published in English between 2015 and 2019 that directly or indirectly analysed public mental health policies and the consequences they have for the family. We analysed our findings following the inductive content analysis approach. A total of 32 articles that met quality indicators were identified. Very closely related structural, c…

Mental Health ServicesSociology and Political Sciencemedia_common.quotation_subjectScopusMEDLINE03 medical and health sciences0302 clinical medicineQuality of life (healthcare)NursingHealth caremedicineHumansQuality (business)030212 general & internal medicineQuality Indicators Health Caremedia_commonbusiness.industryMental Disorders030503 health policy & servicesHealth PolicyPublic Health Environmental and Occupational HealthSocial SupportMental illnessmedicine.diseaseMental healthMental HealthCaregiversContent analysisQuality of Life0305 other medical sciencebusinessPsychologySocial Sciences (miscellaneous)Health & Social Care in the Community
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Controlled education of patients after stroke (ceops)-nurse-led multimodal and long-term interventional program involving a patient''s caregiver to o…

2018

Background Setting up a follow-up secondary prevention program after stroke is difficult due to motor and cognitive impairment, but necessary to prevent recurrence and improve patients’ quality of life. To involve a referent nurse and a caregiver from the patient’s social circle in nurse-led multimodal and long-term management of risk factors after stroke could be an advantage due to their easier access to the patient and family. The aim of this study is to compare the benefit of optimized follow up by nursing personnel from the vascular neurology department including therapeutic follow up, and an interventional program directed to the patient and a caregiving member of their social circle,…

Neurologic ExaminationPatient Care TeamTime FactorsNurseSecondary prevention[SDV]Life Sciences [q-bio]Stroke RehabilitationRecovery of FunctionCombined Modality TherapyNurse's RoleMultimodal intervention;Family caregiver;Nurse;Secondary prevention;Stroke[SDV] Life Sciences [q-bio]StrokeStudy ProtocolDisability EvaluationLeadershipTreatment OutcomeCaregiversPatient Education as TopicMultimodal interventionHumansFranceFamily caregiverRandomized Controlled Trials as Topic
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Experiences faced by next of kin during their older family members’ transition into long-term care in a Norwegian nursing home

2013

Aims and objectives To describe and explore experiences of next of kin during the older persons’ transition into long-term care. Background Moving into long-term care is a challenge for both resident and next of kin. Next of kin experience transitions at the same time as they play significant parts in their family members’ transition into long-term care placement. Design Constructivist hermeneutical design. Methods Ten next of kin to newly admitted eight residents were recruited by purposeful sampling and interviewed. Periodic participant observation periods following new residents on arrival day and the first week after admission and some written documentation were the backdrops to the int…

Next of kinFrail Elderlymedia_common.quotation_subjectNorwegianParticipant observationDignityNursingAdaptation Psychologicalotorhinolaryngologic diseasesHumansMedicinehealth care economics and organizationsGeneral NursingAgedClimactericmedia_commonNorwayFamily caregiversbusiness.industryTransition (fiction)social sciencesGeneral MedicineLong-Term Carelanguage.human_languageNursing HomesLong-term careCaregiversFeelingbehavior and behavior mechanismslanguagebusinessJournal of Clinical Nursing
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Interventions aimed to increase independence and well-being in patients with Alzheimer’s disease: Review of some interventions in the Italian context

2018

Abstract Background Alzheimer's disease (AD) represents a huge social and economic burden for the society and caring for individuals with AD is a complex and challenging task that requires a multidisciplinary approach. Studies have shown that several interventions provide beneficial results, but some non-pharmacological interventions have not yet been studied in depth and clinical trials using them are still pending. This review provides a summary of interventions based on paradigms aimed to increase independence and well-being in people with AD, as well as those interventions that decrease caregiver burden in long-term facilties for AD patients in Italy. Methods Narrative review regarding …

Occupational therapyGerontologymedicine.medical_specialtybusiness.industryGeneral NeurosciencePsychological interventionContext (language use)Caregiver burdenmedicine.diseaseClinical trial03 medical and health sciencesPsychiatry and Mental health0302 clinical medicineQuality of life (healthcare)Multidisciplinary approachmedicineDementia030212 general & internal medicineNeurology (clinical)business030217 neurology & neurosurgeryNeurology, Psychiatry and Brain Research
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Support for families of patients dying with dementia: A qualitative analysis of bereaved family members' experiences and suggestions

2014

AbstractObjective:To explore and document the needs of family caregivers of patients dying with dementia and to identify how healthcare professionals can adequately support them.Method:We employed a cross-sectional survey containing open-ended questions that were analyzed using qualitative methods.Results:Receiving information about the diagnosis and disease trajectory of dementia is essential for the caregiving families of people dying with the disease. However, at present the communication of information offered by professionals is not experienced as satisfying. Further aspects that require improvement concern issues related to time constraints, as well as practical and emotional support …

Palliative careBereaved familyDiseaseQualitative analysisNursingSurveys and QuestionnairesHumansMedicineDementiaQualitative ResearchGeneral NursingTerminal Carebusiness.industryFamily caregiversCommunicationProfessional supportGeneral Medicinemedicine.diseasePsychiatry and Mental healthClinical PsychologyCross-Sectional StudiesCaregiversDementiabusinessBereavementQualitative researchPalliative and Supportive Care
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Responding to the Spiritual Needs of Palliative Care Patients: A Randomized Controlled Trial to Test the Effectiveness of the Kibo Therapeutic Interv…

2020

Context The WHO recognizes the need to attend to patients' spiritual needs as being fundamental to comprehensive and high-quality end-of-life care. Spiritual needs must be attended since the resolution of biological and psychosocial issues is insufficient to reduce patients' suffering. Associations have been found between spiritual needs and other variables of importance for patients in palliative care. Despite the consensus that exists regarding the importance of assessing and attending to spiritual needs, professionals encounter many difficulties in attempting to do so. Objectives Our study aims to demonstrate the benefits that the KIBO therapeutic interview in palliative care patients ca…

Palliative caremedia_common.quotation_subjectlcsh:BF1-990Context (language use)050105 experimental psychologylaw.invention03 medical and health sciences0302 clinical medicineNursingRandomized controlled triallawIntervention (counseling)Health carePsychology0501 psychology and cognitive sciencesinterventionGeneral PsychologyOriginal Researchmedia_commonpalliative carebusiness.industryFamily caregivers05 social sciencesspiritualitylcsh:Psychologytreatment effectivenesspsychological resiliencePsychological resiliencebusinessPsychologyPsychosocial030217 neurology & neurosurgeryFrontiers in Psychology
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Validity and reliability of the Palliative Care Transition Measure for Caregivers (PCTM-C).

2018

AbstractObjectivePatients suffering from advanced disease face different care transitions. The transition from acute to palliative care is challenging and may lead to the discontinuity of care. Family caregivers become important sources of information, as patients begin to experience difficulties in coping with emotional transition events. The Care Transition Measure was developed to evaluate care transitions as experienced by the elderly. It has never been used in palliative care. The aim of this study was to test the validity and reliability of a modified version of the Palliative Care Transition Measure, specifically the Palliative Care Transition Measure for Caregivers (PCTM-C).MethodTh…

Palliative carepalliative carePsychometricsFamily caregiversnursing roleValiditytransitionGeneral MedicineSettore MED/45 - Scienze Infermieristiche Generali Cliniche E PediatricheConfirmatory factor analysisIntegrated care03 medical and health sciencesPsychiatry and Mental healthClinical Psychology0302 clinical medicineNursingCronbach's alpha030220 oncology & carcinogenesisContent validityPsychologyGeneral NursingPalliativesupportive care
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An examination of the impact of care giving styles (accommodation and skilful communication and support) on the one year outcome of adolescent anorex…

2016

Abstract Background The cognitive interpersonal model predicts that parental caregiving style will impact on the rate of improvement of anorexia nervosa symptoms. The study aims to examine whether the absolute levels and the relative congruence between mothers' and fathers' care giving styles influenced the rate of change of their children's symptoms of anorexia nervosa over 12 months. Methods Triads ( n =54) consisting of patients with anorexia nervosa and both of their parents were included in the study. Caregivers completed the Caregiver Skills scale and the Accommodation and Enabling Scale at intake. Patients completed the Short Evaluation of Eating Disorders at intake and at monthly in…

ParentsMale050103 clinical psychologyAnorexia NervosaPsychological intervention0302 clinical medicineParent-Child RelationsMaternal Behavioreducation.field_of_studyParenting05 social sciencesMultilevel modelCognitionMiddle AgedAnorexiaCare giver skillPsychiatry and Mental healthClinical PsychologyEating disordersCaregiversFemalemedicine.symptomCaregivers' congruenceSymptom changePsychologyAccommodationClinical psychologyParents/psychologyAdultParenting/psychologyAdolescentAnorexia Nervosa/psychologyPopulationAnorexiaInterpersonal communicationbehavioral disciplines and activities03 medical and health sciencesCaregivers/psychologySettore M-PSI/08 - Psicologia Clinicamental disordersmedicineHumans0501 psychology and cognitive scienceseducationPaternal Behaviorbusiness.industryAccommodatingModels Theoreticalmedicine.diseaseEnabling behaviour030227 psychiatrybusiness
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