Literature DB >> 17489849

The Huntington's disease quality of life battery for carers: reliability and validity.

A Aubeeluck1, H Buchanan.   

Abstract

Research into the experience of the Huntington Disease (HD) spousal carer has established that carers experience several unique obstacles within their care-giving role. However, there is still a need to establish methodically the factors that impact on the HD spousal carers' situation and ultimately their quality of life. The aim of this pilot study, which was a result of three previous exploratory studies, was to validate a HD-specific quality-of-life (QoL) measure, the Huntington disease quality-of-life battery for carers (HDQoL-C) for use (initially) with spousal carers of HD patients. Eighty-seven HD spousal carers took part in the piloting of the HDQoL-C to assess its reliability and validity as a tool for use within QoL research. Results established the HDQoL-C as a multidimensional and psychometrically sound disease-specific and subjective QoL assessment tool that incorporates the individual's physical health, psychological state, level of independence, social relationships and personal beliefs. The HDQoL-C demonstrates good internal consistency, test-re-test reliability and congruent validity.

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Year:  2007        PMID: 17489849     DOI: 10.1111/j.1399-0004.2007.00784.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.438


  19 in total

1.  Huntington disease: families' experiences of healthcare services.

Authors:  Heather Skirton; Janet K Williams; J Jackson Barnette; Jane S Paulsen
Journal:  J Adv Nurs       Date:  2010-03       Impact factor: 3.187

2.  A new scale to measure family members' perception of community health care services for persons with Huntington disease.

Authors:  Valmi D Sousa; Janet K Williams; Jack J Barnette; David A Reed
Journal:  J Eval Clin Pract       Date:  2010-03-11       Impact factor: 2.431

3.  Further evidence of reliability and validity of the Huntington's disease quality of life battery for carers: Italian and French translations.

Authors:  Aimee Aubeeluck; Julie Dorey; Ferdinando Squitieri; Emilie Clay; Edward J N Stupple; Annunziata De Nicola; Heather Buchanan; Tiziana Martino; Mondher Toumi
Journal:  Qual Life Res       Date:  2012-07-21       Impact factor: 4.147

4.  Family carer personal concerns in Huntington disease.

Authors:  Janet K Williams; Heather Skirton; James Jackson Barnette; Jane S Paulsen
Journal:  J Adv Nurs       Date:  2011-06-12       Impact factor: 3.187

5.  'All the burden on all the carers': exploring quality of life with family caregivers of Huntington's disease patients.

Authors:  Aimee Victoria Aubeeluck; Heather Buchanan; Edward J N Stupple
Journal:  Qual Life Res       Date:  2011-11-13       Impact factor: 4.147

6.  The emotional experiences of family carers in Huntington disease.

Authors:  Janet K Williams; Heather Skirton; Jane S Paulsen; Toni Tripp-Reimer; Lori Jarmon; Meghan McGonigal Kenney; Emily Birrer; Bonnie L Hennig; Joann Honeyford
Journal:  J Adv Nurs       Date:  2009-02-09       Impact factor: 3.187

7.  Patient and caregiver quality of life in Huntington's disease.

Authors:  Rebecca E Ready; Melissa Mathews; Anne Leserman; Jane S Paulsen
Journal:  Mov Disord       Date:  2008-04-15       Impact factor: 10.338

8.  Huntington's disease from the patient, caregiver and physician's perspectives: three sides of the same coin?

Authors:  Krzysztof Banaszkiewicz; Emilia J Sitek; Monika Rudzińska; Witold Sołtan; Jarosław Sławek; Andrzej Szczudlik
Journal:  J Neural Transm (Vienna)       Date:  2012-03-08       Impact factor: 3.575

9.  Health-related quality of life in Huntington's disease patients: a comparison of proxy assessment and patient self-rating using the disease-specific Huntington's disease health-related quality of life questionnaire (HDQoL).

Authors:  Mevhibe B Hocaoglu; E A Gaffan; Aileen K Ho
Journal:  J Neurol       Date:  2012-03-06       Impact factor: 4.849

10.  Disease Burden of Huntington's Disease (HD) on People Living with HD and Care Partners in Canada.

Authors:  Eileen Shaw; Michelle Mayer; Paul Ekwaru; Suzanne McMullen; Erin Graves; Jennifer W Wu; Nathalie Budd; Bridget Maturi; Tara Cowling; Tiago A Mestre
Journal:  J Huntingtons Dis       Date:  2022
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