Literature DB >> 20806651

Development of the Huntington disease family concerns and strategies survey from focus group data.

Janet K Williams1, J Jackson Barnette, David Reed, Valmi D Sousa, Debra L Schutte, Meghan McGonigal-Kenney, Lori Jarmon, Emily Phillips, Toni Tripp-Reimer, Jane S Paulsen.   

Abstract

Health concerns and management strategies among families of young and middle-age adults with Huntington's disease (HD) are unknown. This study developed and tested psychometric properties of the Huntington Disease Family Concerns and Strategies Survey (HDFCSS). Focus group data from 91 adult family members were used to develop content. Content analysis yielded four domains that were transferred into Personal, Person With HD, Community Health Care Services, and Strategies scales. Focus group data, expert validation, and cognitive interviews demonstrated survey content validity. Cronbach's alpha internal consistency coefficients for the scales were 0.83 or above. The measure can be used to generate reliable and valid data to identify adult family members' health-related concerns and management strategies for themselves and persons with HD.

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Year:  2010        PMID: 20806651      PMCID: PMC3807610          DOI: 10.1891/1061-3749.18.2.83

Source DB:  PubMed          Journal:  J Nurs Meas        ISSN: 1061-3749


  39 in total

Review 1.  Whatever happened to qualitative description?

Authors:  M Sandelowski
Journal:  Res Nurs Health       Date:  2000-08       Impact factor: 2.228

2.  Capturing the insights of family caregivers: survey item generation with a coupled interview/focus group process.

Authors:  Sarah B Wackerbarth; Megan E Streams; Melissa K Smith
Journal:  Qual Health Res       Date:  2002-10

3.  Qualitative methods and the development of clinical assessment tools.

Authors:  Jane F Gilgun
Journal:  Qual Health Res       Date:  2004-09

4.  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

Review 5.  Cognitive interviewing: verbal data in the design and pretesting of questionnaires.

Authors:  Jonathan Drennan
Journal:  J Adv Nurs       Date:  2003-04       Impact factor: 3.187

6.  Retest effects and cognitive decline in longitudinal follow-up of patients with early HD.

Authors:  A C Bachoud-Lévi; P Maison; P Bartolomeo; M F Boissé; G Dalla Barba; A M Ergis; S Baudic; J D Degos; P Cesaro; M Peschanski
Journal:  Neurology       Date:  2001-04-24       Impact factor: 9.910

7.  Behavioral changes in Huntington Disease.

Authors:  D Craufurd; J C Thompson; J S Snowden
Journal:  Neuropsychiatry Neuropsychol Behav Neurol       Date:  2001 Oct-Dec

8.  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

9.  United Kingdom experience with presymptomatic testing of individuals at 25% risk for Huntington's disease.

Authors:  C M Benjamin; A Lashwood
Journal:  Clin Genet       Date:  2000-07       Impact factor: 4.438

10.  The Caregiver Vigilance Scale: application and validation in the Resources for Enhancing Alzheimer's Caregiver Health (REACH) project.

Authors:  Diane Feeney Mahoney; Richard N Jones; David W Coon; Aaron B Mendelsohn; Laura N Gitlin; Marcia Ory
Journal:  Am J Alzheimers Dis Other Demen       Date:  2003 Jan-Feb       Impact factor: 2.035

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  9 in total

1.  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

2.  Onset of Huntington's disease: can it be purely cognitive?

Authors:  Jane S Paulsen; Jeffrey D Long
Journal:  Mov Disord       Date:  2014-08-20       Impact factor: 10.338

Review 3.  Cognitive impairment in Huntington disease: diagnosis and treatment.

Authors:  Jane S Paulsen
Journal:  Curr Neurol Neurosci Rep       Date:  2011-10       Impact factor: 5.081

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.  Mutation-related magnetization-transfer, not axon density, drives white matter differences in premanifest Huntington disease: Evidence from in vivo ultra-strong gradient MRI.

Authors:  Chiara Casella; Maxime Chamberland; Pedro L Laguna; Greg D Parker; Anne E Rosser; Elizabeth Coulthard; Hugh Rickards; Samuel C Berry; Derek K Jones; Claudia Metzler-Baddeley
Journal:  Hum Brain Mapp       Date:  2022-04-09       Impact factor: 5.399

6.  Strategies used by teens growing up in families with Huntington disease.

Authors:  Janet K Williams; Martha Driessnack; J Jackson Barnette; Kathleen J H Sparbel; Anne Leserman; Sean Thompson; Jane S Paulsen
Journal:  J Pediatr Nurs       Date:  2013-03-24       Impact factor: 2.145

7.  Caregiving by teens for family members with Huntington disease.

Authors:  Janet K Williams; Lioness Ayres; Janet Specht; Kathleen Sparbel; Mary Lou Klimek
Journal:  J Fam Nurs       Date:  2009-05-22       Impact factor: 3.818

8.  Use of the nominal group technique to identify stakeholder priorities and inform survey development: an example with informal caregivers of people with scleroderma.

Authors:  Danielle B Rice; Mara Cañedo-Ayala; Kimberly A Turner; Stephanie T Gumuchian; Vanessa L Malcarne; Mariët Hagedoorn; Brett D Thombs
Journal:  BMJ Open       Date:  2018-03-02       Impact factor: 2.692

Review 9.  Novel targets for Huntington's disease: future prospects.

Authors:  Sarah L Mason; Roger A Barker
Journal:  Degener Neurol Neuromuscul Dis       Date:  2016-05-04
  9 in total

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