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1.
J Intellect Disabil Res ; 56(1): 17-29, 2012 Jan.
Article in English | MEDLINE | ID: mdl-21504492

ABSTRACT

BACKGROUND: Although the Family Quality of Life Survey - 2006 (FQOLS-2006) is being used in research, there is little evidence to support its hypothesised domain structure. The purpose of this study was to test the domain structure of the survey using confirmatory factor analysis. METHOD: Samples from Australia, Canada, Nigeria and the USA were analysed using structural equation modelling. The data from Australia, Canada and the USA were combined on the assumption that these countries are similar, at least to some degree, in economic development, language and culture. The Nigerian data were analysed on its own. The analysis was undertaken in two phases. First, the hypothesis that each of nine domains of the FQOLS-2006 is a unidimensional construct that can reliably measure the dimensions Importance, Stability, Opportunities, Attainment, Stability and Satisfaction was tested. Second, the hypothesis that family quality of life (FQoL) is a single latent construct represented by the nine domains measured in the FQOLS-2006 was tested. RESULTS: In the first phase of the analysis, the Importance dimension was dropped because of skewness and lack of variance. The Stability dimension did not fit well within the individual domain model in both the Nigerian and the combined three countries' data. When Importance and Stability were excluded, the individual domain models showede good or acceptable fit when error variances of some dimensions were allowed to correlate. In the second phase of the analysis, the overall model, FQoL, represented by the nine domains of the FQOLS-2006 showed good fit in both data sets. CONCLUSIONS: The conceptual model of the FQOLS-2006 was supported with some qualifications. Each domain on the survey can be reliably measured by four dimensions Opportunities, Initiative, Attainment and Satisfaction. The dimensions of Importance and Stability, however, did not fit. Data reported on these dimensions from past and current studies should be interpreted with caution. The construct of FQoL is also reliably measured by the domains of the FQOLS-2006. Further research into the psychometric properties of the survey, particularly from a cross-cultural perspective, is needed.


Subject(s)
Caregivers/psychology , Family Health , Intellectual Disability/nursing , Psychometrics/methods , Quality of Life/psychology , Adolescent , Child , Cost of Illness , Disabled Persons/psychology , Factor Analysis, Statistical , Family/psychology , Female , Health Surveys , Humans , Intellectual Disability/psychology , Male , Models, Psychological , Parents/psychology , Psychometrics/instrumentation , Reproducibility of Results , Social Support , Surveys and Questionnaires , Young Adult
2.
J Intellect Disabil Res ; 56(1): 71-86, 2012 Jan.
Article in English | MEDLINE | ID: mdl-21883595

ABSTRACT

BACKGROUND: Family quality of life (FQOL) is a recent concept in intellectual/developmental disability research. Outcomes for the family are important to the provision of services because families, rather than institutions, are increasingly considered the primary support unit. This article presents Australian findings using the international Family Quality of Life Survey: Main Caregivers of People with Intellectual or Developmental Disabilities (FQOLS-2006). METHOD: Forty-two South Australian main caregivers of people with an intellectual/developmental disability were interviewed using the FQOLS-2006. The FQOL domains assessed were Health of the Family, Financial Well-being, Family Relationships, Support from Other People, Support from Disability-Related Services, Influence of Values, Careers, Leisure and Recreation, and Community Interaction. Domains were measured in terms of Importance, Opportunities, Attainment, Initiative, Stability and Satisfaction. The FQOLS-2006 asked about the family's practical and emotional Support from Other People together, whereas the current study separated the constructs of practical and emotional support. Questions pertaining to FQOL in the past were also added, in order to gain a broader picture of present FQOL. RESULTS: Results indicated that families considered all the FQOL domains to be important. However, Health, Family Relationships and Financial Well-being were regarded as slightly more important than Practical and Emotional Support from Others. The attainment of Family Relationships, Health, Values, and Leisure and Recreation were rated as quite a bit, but Practical Support from Other People was only rated as a little. Families were generally satisfied with all FQOL domains, but they were satisfied with their Family Relationships and they were neither satisfied or dissatisfied with their Financial Well-being. Results also indicated that there was a need to distinguish between the provision of practical and emotional support from others, because the attainment of emotional support was rated at a slightly higher level than practical support. CONCLUSIONS: The FQOLS-2006 provided a comprehensive measure of FQOL, which, with some additional modifications, could be used to better inform service provisions and ultimately enhance the quality of life of people with intellectual/developmental disabilities and their families.


Subject(s)
Caregivers/psychology , Developmental Disabilities/nursing , Disabled Persons/statistics & numerical data , Family Health/statistics & numerical data , Intellectual Disability/nursing , Quality of Life/psychology , Adolescent , Adult , Aged , Australia , Child , Child, Preschool , Cost of Illness , Cross-Cultural Comparison , Developmental Disabilities/psychology , Family/psychology , Female , Health Surveys , Humans , Intellectual Disability/psychology , Male , Middle Aged , Parents/psychology , Psychometrics/instrumentation , Psychometrics/methods , Social Support , Socioeconomic Factors , Surveys and Questionnaires , Young Adult
3.
J Intellect Disabil Res ; 56(1): 1-16, 2012 Jan.
Article in English | MEDLINE | ID: mdl-22151130

ABSTRACT

Historically, intervention programmes in intellectual and developmental disabilities have targeted the individual's special needs independent of the family and environmental context. This trend has been changing over the past two decades. This paper presents a literature review on changing trends in family support and the development of family quality of life (FQOL) and intellectual disability from a construct to a theory. The evolution of research in quality of life from the perspective of the individual with the disability to the family is described. A description of the development of FQOL measures is included, specifically an introduction and comparison of the two leading comprehensive initiatives on measuring FQOL - international FQOL project and the FQOL initiative of the Beach Center on Disability, in the USA. This paper provides the conceptual background and context to the other papers presented in this special issue, which focus on FQOL measurement in specific contexts.


Subject(s)
Cost of Illness , Developmental Disabilities/nursing , Family Health , Intellectual Disability/nursing , Psychometrics/methods , Quality of Life/psychology , Caregivers/psychology , Developmental Disabilities/psychology , Disabled Persons/psychology , Family/psychology , Health Surveys , Humans , Intellectual Disability/psychology , Parents/psychology , Psychometrics/instrumentation , Psychometrics/trends , Social Support , Surveys and Questionnaires
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