Literature DB >> 21668801

Family quality of life in 25 Belgian families: quantitative and qualitative exploration of social and professional support domains.

R Steel1, L Poppe, S Vandevelde, G Van Hove, C Claes.   

Abstract

BACKGROUND: This article reports on the results of a study conducted in Belgium on family quality of life situated within a larger project focusing on the development of support strategies for young and adolescent siblings of persons with intellectual disabilities. The objectives of this article are twofold: (1) to present the results of the measures contained in the nine domains of the Family Quality of Life Survey-2006 (FQOLS-2006) from the perspective of parents (quantitative analysis); and (2) to come to a more in-depth understanding of two important domains of the FQOLS-2006 by exploring and comparing the quantitative and qualitative data from open-ended interviews with parents.
METHOD: The FQOLS-2006 was completed by the main caregivers of 25 families living in one typical Belgian province. Subsequently, semi-structured interviews with one or both parents were conducted within the same families. Content analysis was carried out on the transcribed interviews using the qualitative software package MaxQDA.
RESULTS: A detailed analysis of the quantitative data together with data from the content analysis of the interviews revealed important issues with regard to two family quality of life domains, support from others and support from services. In general, parents were satisfied with the professional support they received, whereas they were more critical of support from others.
CONCLUSIONS: The quantitative data from the FQOLS-2006 were supported and further explained by the qualitative data. These findings highlight the importance of adequate professional support, which is a flexible and capable answer to each family's individual needs. The authors warn of the dangers of 'handicapism' and plea for a family-centred support approach that takes the whole family into account. Finally, they indicate the benefits of increased practical-pedagogical support.
© 2011 The Authors. Journal of Intellectual Disability Research © 2011 Blackwell Publishing Ltd.

Entities:  

Mesh:

Year:  2011        PMID: 21668801     DOI: 10.1111/j.1365-2788.2011.01433.x

Source DB:  PubMed          Journal:  J Intellect Disabil Res        ISSN: 0964-2633


  6 in total

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Review 2.  Variables related to the quality of life of families that have a child with severe to profound intellectual disabilities: A systematic review.

Authors:  N Luitwieler; J Luijkx; M Salavati; C P Van der Schans; A J Van der Putten; A Waninge
Journal:  Heliyon       Date:  2021-06-24

3.  Listening to families with a person with neurodegenerative disease talk about their quality of life: integrating quantitative and qualitative approaches.

Authors:  Alba Aza; María Gómez-Vela; Marta Badia; M Begoña Orgaz; Eva González-Ortega; Isabel Vicario-Molina; Estrella Montes-López
Journal:  Health Qual Life Outcomes       Date:  2022-05-07       Impact factor: 3.077

4.  Experiences of mothers caring for a child with an intellectual disability during the COVID-19 pandemic in the Netherlands.

Authors:  P Embregts; L Heerkens; N Frielink; S Giesbers; L Vromans; A Jahoda
Journal:  J Intellect Disabil Res       Date:  2021-06-02

5.  State of the Art of Family Quality of Life in Early Care and Disability: A Systematic Review.

Authors:  Carmen Francisco Mora; Alba Ibáñez; Anna Balcells-Balcells
Journal:  Int J Environ Res Public Health       Date:  2020-10-02       Impact factor: 3.390

6.  Homeward bound: Exploring the motives of mothers who brought their offspring with intellectual disabilities home from residential settings during the COVID-19 pandemic.

Authors:  Frances R Vereijken; Sanne A H Giesbers; Andrew Jahoda; Petri J C M Embregts
Journal:  J Appl Res Intellect Disabil       Date:  2021-07-02
  6 in total

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