Literature DB >> 19939722

Refinement and validation of the Parental Illness Impact Scale.

David Morley1, Caroline Selai, Anette Schrag, Alan J Thompson, Marjan Jahanshahi.   

Abstract

OBJECTIVE: To refine and validate the Parental Illness Impact Scale (PIIS), a questionnaire designed specifically to measure the quality of life of adolescent and adult children of neurologically affected parents.
METHODS: Key informant interviews and a literature review were conducted to ensure all relevant themes were incorporated in the revised PIIS (PIIS-R). Pre-testing was achieved through a 17 member expert panel and cognitive interviews with eight adolescent and adult children. The revised instrument was administered to 169 adolescent and adult children of people with Parkinson's disease, multiple sclerosis and stroke and subjected to psychometric analysis.
RESULTS: Principal components analysis resulted in eight subscales accounting for 60.6% of explained variance. The PIIS-R showed good concurrent and discriminant validity through correlations with established measures of quality of life and psychosocial well-being. Internal consistency was high (Cronbach's alpha .92), and test-retest reliability values for subscales (r = .59-.74) and total score (r = .79) were moderate to high.
CONCLUSIONS: The PIIS-R is a scientifically robust measurement tool for assessing the impact of parental illness, and currently shows strong psychometric properties. Longitudinal data will be required to assess predictive validity and sensitivity to change. The instrument is available to other investigators, who are encouraged to further evaluate its scientific properties. Copyright (c) 2009 Elsevier Ltd. All rights reserved.

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Year:  2009        PMID: 19939722     DOI: 10.1016/j.parkreldis.2009.11.001

Source DB:  PubMed          Journal:  Parkinsonism Relat Disord        ISSN: 1353-8020            Impact factor:   4.891


  5 in total

1.  When Mom Has Migraine: An Observational Study of the Impact of Parental Migraine on Adolescent Children.

Authors:  Elizabeth K Seng; Emily D Mauser; Maya Marzouk; Zarine S Patel; Noah Rosen; Dawn C Buse
Journal:  Headache       Date:  2018-10-31       Impact factor: 5.887

2.  Adolescent and adult children of parents with Parkinson's disease: incorporating their needs in clinical guidelines.

Authors:  David Morley; Caroline Selai; Anette Schrag; Marjan Jahanshahi; Alan Thompson
Journal:  Parkinsons Dis       Date:  2011-06-12

3.  Evaluating the psychometric properties of an e-based version of the 39-item Parkinson's Disease Questionnaire.

Authors:  David Morley; Sarah Dummett; Laura Kelly; Jill Dawson; Crispin Jenkinson
Journal:  Health Qual Life Outcomes       Date:  2015-01-23       Impact factor: 3.186

4.  Validation of the Oxford Participation and Activities Questionnaire.

Authors:  David Morley; Sarah Dummett; Laura Kelly; Jill Dawson; Ray Fitzpatrick; Crispin Jenkinson
Journal:  Patient Relat Outcome Meas       Date:  2016-06-15

5.  Administering the Routine Activities domain of the Oxford Participation and Activities Questionnaire as a stand-alone scale: the Oxford Routine Activities Measure.

Authors:  David Morley; Sarah Dummett; Laura Kelly; Crispin Jenkinson
Journal:  Patient Relat Outcome Meas       Date:  2018-07-25
  5 in total

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