Literature DB >> 29214414

Understanding the need for assistance with survey completion in people with Huntington disease.

Elizabeth A Hahn1, Nancy R Downing2, Julie C Stout3, Jane S Paulsen4, Becky Ready5, Siera Goodnight6, Jin-Shei Lai7, Jennifer A Miner6, Noelle E Carlozzi6.   

Abstract

PURPOSE: In Huntington disease (HD), motor, cognitive, and psychiatric changes can have a detrimental impact on health-related quality of life (HRQOL). The purpose of this paper is to describe the extent and type of assistance needed to complete online HRQOL surveys, and the impact of assistance on HRQOL scores.
METHODS: A patient-reported outcome measurement system was developed for HD-specific HRQOL. Individuals across the prodromal and diagnosed disease severity spectrum (n = 532) completed surveys by computer, and reported the amount and type of assistance they received.
RESULTS: Some participants (n = 56; 10.5%) did not complete all surveys; this group had larger proportions with late stage disease, racial/ethnic minority status, low education and single marital status, and poorer motor, independence and cognitive function compared to those who completed all surveys (n = 476). Overall, 72% of individuals did not receive assistance, 11% received computer assistance only, and 17% received assistance answering the survey questions. The majority of late stage individuals (78%) received some assistance compared to early stage (29%) and prodromal individuals (< 1%). Those who received assistance had higher proportions with late stage disease, were older, had less education, and had poorer functional and cognitive skills. Before and after adjustment for sociodemographic and clinical characteristics, those who received assistance had poorer scores on some HRQOL outcomes than those who did not receive assistance.
CONCLUSIONS: Computer-based assessments are feasible for many persons with HD, although other methods may also be needed. Clinicians and researchers should develop strategies to assist people with HD to complete HRQOL surveys.

Entities:  

Keywords:  Health-related quality of life; Huntington disease; Patient-reported outcomes; Surveys and questionnaires

Mesh:

Year:  2017        PMID: 29214414      PMCID: PMC5845783          DOI: 10.1007/s11136-017-1747-6

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


  35 in total

1.  Huntington disease: clinical care and evaluation.

Authors:  I Shoulson; S Fahn
Journal:  Neurology       Date:  1979-01       Impact factor: 9.910

2.  Developing the World Health Organization Disability Assessment Schedule 2.0.

Authors:  T Bedirhan Ustün; Somnath Chatterji; Nenad Kostanjsek; Jürgen Rehm; Cille Kennedy; Joanne Epping-Jordan; Shekhar Saxena; Michael von Korff; Charles Pull
Journal:  Bull World Health Organ       Date:  2010-05-20       Impact factor: 9.408

3.  Quality of life in Huntington's disease: a comparative study investigating the impact for those with pre-manifest and early manifest disease, and their partners.

Authors:  Joy Read; Rebecca Jones; Gail Owen; Blair R Leavitt; Allison Coleman; Raymund A C Roos; Eve M Dumas; Alexandra Durr; Damian Justo; Miranda Say; Julie C Stout; Sarah J Tabrizi; David Craufurd
Journal:  J Huntingtons Dis       Date:  2013

4.  Neuro-QOL: quality of life item banks for adults with neurological disorders: item development and calibrations based upon clinical and general population testing.

Authors:  Richard C Gershon; Jin Shei Lai; Rita Bode; Seung Choi; Claudia Moy; Tom Bleck; Deborah Miller; Amy Peterman; David Cella
Journal:  Qual Life Res       Date:  2011-08-27       Impact factor: 4.147

Review 5.  The incidence and prevalence of Huntington's disease: a systematic review and meta-analysis.

Authors:  Tamara Pringsheim; Katie Wiltshire; Lundy Day; Jonathan Dykeman; Thomas Steeves; Nathalie Jette
Journal:  Mov Disord       Date:  2012-06-12       Impact factor: 10.338

6.  Health-related quality of life in Huntington's disease: Which factors matter most?

Authors:  Aileen K Ho; Abigail S Gilbert; Sarah L Mason; Anna O Goodman; Roger A Barker
Journal:  Mov Disord       Date:  2009-03-15       Impact factor: 10.338

Review 7.  Huntington disease: clinical, genetic, and social aspects.

Authors:  M A Nance
Journal:  J Geriatr Psychiatry Neurol       Date:  1998       Impact factor: 2.680

8.  The development of a new computer adaptive test to evaluate chorea in Huntington disease: HDQLIFE Chorea.

Authors:  N E Carlozzi; N R Downing; S G Schilling; J-S Lai; S M Goodnight; J A Miner; S A Frank
Journal:  Qual Life Res       Date:  2016-05-03       Impact factor: 4.147

9.  HDQLIFE: the development of two new computer adaptive tests for use in Huntington disease, Speech Difficulties, and Swallowing Difficulties.

Authors:  N E Carlozzi; S G Schilling; J-S Lai; J S Perlmutter; M A Nance; J F Waljee; J A Miner; S K Barton; S M Goodnight; P Dayalu
Journal:  Qual Life Res       Date:  2016-04-01       Impact factor: 4.147

10.  WHODAS 2.0 in prodromal Huntington disease: measures of functioning in neuropsychiatric disease.

Authors:  Nancy R Downing; Ji-In Kim; Janet K Williams; Jeffrey D Long; James A Mills; Jane S Paulsen
Journal:  Eur J Hum Genet       Date:  2013-12-11       Impact factor: 4.246

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  1 in total

Review 1.  The State of Web Accessibility for People with Cognitive Disabilities: A Rapid Evidence Assessment.

Authors:  Sara Gartland; Paul Flynn; Maria Ana Carneiro; Greg Holloway; Jose de Sousa Fialho; Joe Cullen; Emma Hamilton; Amy Harris; Clare Cullen
Journal:  Behav Sci (Basel)       Date:  2022-01-26
  1 in total

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