Literature DB >> 19891814

Caregiving experiences and knowledge about dementia in Portuguese clinical outpatient settings.

Manuel Gonçalves-Pereira1, Isabel Carmo, Joaquim Alves da Silva, Ana L Papoila, Raimundo Mateos, Steven H Zarit.   

Abstract

BACKGROUND: Important public health and clinical issues remain unanswered concerning disease-related knowledge and caregiving experiences in dementia. The aim of this study is to describe these dimensions in Portuguese clinical settings and analyze the link between knowledge and burden, and also between knowledge and positive caregiving experiences.
METHODS: We studied a non-randomized sample of 116 caregivers of outpatients with ICD10-DCR diagnosis of dementia. Comprehensive assessments included Dementia Knowledge Questionnaire (DKQ), Zarit Burden Interview (ZBI), Caregiving Activity Survey (CAS), Positive Aspects of Caregiving (PAC) and General Health Questionnaire-12 (GHQ). Portuguese translations for DKQ, ZBI and PAC scales had been developed; validity aspects were documented, as well as test-retest reliability coefficients for ZBI (ICC = 0.93) and PAC (ICC = 0.85).
RESULTS: Most caregivers were close relatives, female and living with the patient. Although positive aspects of care were reported, burden and distress levels were moderate to high. Knowledge needs were not striking. Distress was moderately correlated to burden, but no associations were found between caregivers' knowledge and ZBI, PAC or GHQ. DKQ scores did not predict PAC nor ZBI scores. A relationship was found between ZBI, as dependent variable, and PAC, GHQ and CAS.
CONCLUSIONS: A large proportion of caregivers in this sample, albeit informed about dementia, were at risk of high burden and distress. Knowledge about dementia may not be protective of burden per se, nor did it influence positive aspects of caregiving.

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Year:  2009        PMID: 19891814     DOI: 10.1017/S1041610209991050

Source DB:  PubMed          Journal:  Int Psychogeriatr        ISSN: 1041-6102            Impact factor:   3.878


  6 in total

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2.  Effects of a community intervention program for dementia on mental health: the importance of secondary caregivers in promoting positive aspects and reducing strain.

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3.  Perceptions of the impact of COVID-19 on healthcare communication in a nationally representative cross-sectional survey of family caregivers.

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Journal:  BMJ Open       Date:  2022-04-13       Impact factor: 3.006

4.  Assessment of the consequences of caregiving in psychosis: a psychometric comparison of the Zarit Burden Interview (ZBI) and the Involvement Evaluation Questionnaire (IEQ).

Authors:  Manuel Gonçalves-Pereira; Eduardo González-Fraile; Borja Santos-Zorrozúa; Manuel Martín-Carrasco; Paola Fernández-Catalina; Ana I Domínguez-Panchón; Paula Muñoz-Hermoso; Javier Ballesteros
Journal:  Health Qual Life Outcomes       Date:  2017-04-05       Impact factor: 3.186

5.  Online training and support program (iSupport) for informal dementia caregivers: protocol for an intervention study in Portugal.

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6.  Feasibility of an online training and support program for dementia carers: results from a mixed-methods pilot randomized controlled trial.

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  6 in total

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