Literature DB >> 22821667

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

Aimee Aubeeluck1, Julie Dorey, Ferdinando Squitieri, Emilie Clay, Edward J N Stupple, Annunziata De Nicola, Heather Buchanan, Tiziana Martino, Mondher Toumi.   

Abstract

BACKGROUND: Existing research suggests that family caregivers of persons with Huntington's disease (HD) face a distinct series of problems, linked to the complex nature of the disease. Aubeeluck and Buchanan (Clin Genet, 71(5):434-445, 2007) developed and validated a disease-specific measure used to explore caregivers quality of life and assess the efficacy of therapeutic interventions. This current study builds on this research through the validation of French and Italian translations of the Huntington's disease quality of life battery for carers (HDQoL-C).
METHOD: A total of 301 family carers completed the HDQoL-C. Participants were recruited through the "Euro-HDB" study which is measuring the burden in HD across Europe and the USA.
RESULTS: Factor analysis demonstrated good internal consistency, reliability and congruent validity. Carers who cared for patients with less clinically severe symptoms reported significantly better QoL than carers of patients with more clinically severe symptoms. DISCUSSION: Findings indicate the HDQoL-C is multi-lingual, multi-cultural and easily applicable in other languages.

Entities:  

Mesh:

Year:  2012        PMID: 22821667     DOI: 10.1007/s11136-012-0227-2

Source DB:  PubMed          Journal:  Qual Life Res        ISSN: 0962-9343            Impact factor:   4.147


  17 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.  Huntington's disease--falling through the net.

Authors:  J Shakespeare; J Anderson
Journal:  Health Trends       Date:  1993

3.  Communication and Huntington's disease: qualitative interviews and focus groups with persons with Huntington's disease, family members, and carers.

Authors:  Lena Hartelius; Maria Jonsson; Anneli Rickeberg; Katja Laakso
Journal:  Int J Lang Commun Disord       Date:  2010 May-Jun       Impact factor: 3.020

4.  Family break-down and stress in Huntington's chorea.

Authors:  A Tyler; P S Harper; K Davies; R G Newcome
Journal:  J Biosoc Sci       Date:  1983-04

5.  Social perspectives in Huntington's chorea.

Authors:  M R Hayden; R Ehrlich; H Parker; S J Ferera
Journal:  S Afr Med J       Date:  1980-08-02

6.  Principles of Good Practice for the Translation and Cultural Adaptation Process for Patient-Reported Outcomes (PRO) Measures: report of the ISPOR Task Force for Translation and Cultural Adaptation.

Authors:  Diane Wild; Alyson Grove; Mona Martin; Sonya Eremenco; Sandra McElroy; Aneesa Verjee-Lorenz; Pennifer Erikson
Journal:  Value Health       Date:  2005 Mar-Apr       Impact factor: 5.725

7.  Psychosocial impact of predictive testing for Huntington disease on support persons.

Authors:  J K Williams; D L Schutte; P A Holkup; C Evers; A Muilenburg
Journal:  Am J Med Genet       Date:  2000-06-12

8.  Coordinated multidisciplinary care for Huntington's disease. An outpatient department.

Authors:  Ruth B Veenhuizen; Aad Tibben
Journal:  Brain Res Bull       Date:  2009-07-01       Impact factor: 4.077

9.  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

Review 10.  Huntington's disease: from pathology and genetics to potential therapies.

Authors:  Sara Imarisio; Jenny Carmichael; Viktor Korolchuk; Chien-Wen Chen; Shinji Saiki; Claudia Rose; Gauri Krishna; Janet E Davies; Evangelia Ttofi; Benjamin R Underwood; David C Rubinsztein
Journal:  Biochem J       Date:  2008-06-01       Impact factor: 3.857

View more
  4 in total

Review 1.  Instruments measuring the disease-specific quality of life of family carers of people with neurodegenerative diseases: a systematic review.

Authors:  Thomas E Page; Nicolas Farina; Anna Brown; Stephanie Daley; Ann Bowling; Thurstine Basset; Gill Livingston; Martin Knapp; Joanna Murray; Sube Banerjee
Journal:  BMJ Open       Date:  2017-03-29       Impact factor: 2.692

2.  An International Validation of a Clinical Tool to Assess Carers' Quality of Life in Huntington's Disease.

Authors:  Aimee Aubeeluck; Edward J N Stupple; Malcolm B Schofield; Alis C Hughes; Lucienne van der Meer; Bernhard Landwehrmeyer; Aileen K Ho
Journal:  Front Psychol       Date:  2019-07-23

3.  Analysis of the caregiver burden associated with Sanfilippo syndrome type B: panel recommendations based on qualitative and quantitative data.

Authors:  Elsa Shapiro; Charles Marques Lourenço; Neslihan Onenli Mungan; Nicole Muschol; Cara O'Neill; Suresh Vijayaraghavan
Journal:  Orphanet J Rare Dis       Date:  2019-07-08       Impact factor: 4.123

4.  Exploring the Reliability and Validity of the Huntington's Disease Quality of Life Battery for Carers (HDQoL-C) within A Polish Population.

Authors:  Agnieszka Bartoszek; Aimee Aubeeluck; Edward Stupple; Adrian Bartoszek; Katarzyna Kocka; Barbara Ślusarska
Journal:  Int J Environ Res Public Health       Date:  2019-06-30       Impact factor: 3.390

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.