Literature DB >> 21632913

Development of the HD-Teen Inventory.

Martha Driessnack1, Janet K Williams, J Jackson Barnette, Kathleen J Sparbel, Jane S Paulsen.   

Abstract

Adolescents, who have a parent with Huntington Disease (HD), not only are at genetic risk for HD but also are witness to its onset and devastating clinical progression as their parent declines. To date, no mechanism has been developed to direct health care providers to the atypical adolescent experiences of these teens. The purpose of this report is to describe the process of developing the HD-Teen Inventory clinical assessment tool. Forty-eight teens and young adults from 19 U.S. states participated in the evaluation of the HD-Teen Inventory tool. Following item analysis, the number of items was reduced and item frequency and reaction scales were combined, based on the strong correlation (r = .94). The resultant tool contains 15 inventory and 2 open-ended response items. The HD-Teen Inventory emerged as a more compact and efficient tool for identifying the most salient concerns of at-risk teens in HD families in research and/or clinical practice.

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Year:  2011        PMID: 21632913      PMCID: PMC3806303          DOI: 10.1177/1054773811409397

Source DB:  PubMed          Journal:  Clin Nurs Res        ISSN: 1054-7738            Impact factor:   2.075


  20 in total

Review 1.  The clinical and genetic features of Huntington disease.

Authors:  Aaron Sturrock; Blair R Leavitt
Journal:  J Geriatr Psychiatry Neurol       Date:  2010-10-05       Impact factor: 2.680

2.  A developmental perspective on adolescent health and illness: an introduction to the special issues.

Authors:  Grayson N Holmbeck
Journal:  J Pediatr Psychol       Date:  2002 Jul-Aug

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

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

4.  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

5.  Predictive genetic testing of adolescents for Huntington disease: a question of autonomy and harm.

Authors:  Fiona H Richards
Journal:  Am J Med Genet A       Date:  2008-09-15       Impact factor: 2.802

6.  Survey design from the ground up: collaboratively creating the Toronto Teen Survey.

Authors:  Sarah Flicker; Adrian Guta; June Larkin; Susan Flynn; Alycia Fridkin; Robb Travers; Jason D Pole; Crystal Layne
Journal:  Health Promot Pract       Date:  2008-03-26

Review 7.  Huntington disease: Implications for practice.

Authors:  Angela Cummins; Julia Eggert; Rosanne Pruitt; Julianne S Collins
Journal:  Nurse Pract       Date:  2011-02

8.  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

9.  How young people find out about their family history of Huntington's disease.

Authors:  Karen Forrest Keenan; Edwin van Teijlingen; Lorna McKee; Zosia Miedzybrodzka; Sheila A Simpson
Journal:  Soc Sci Med       Date:  2009-03-26       Impact factor: 4.634

10.  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

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  1 in total

1.  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

  1 in total

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