Literature DB >> 31764427

Reliability, validity and relevance of needs assessment instruments for informal dementia caregivers: a psychometric systematic review.

Stephanie Kipfer1,2, Sandrine Pihet1.   

Abstract

OBJECTIVE: The objective of this review is to identify reliable and/or valid needs assessment instruments for informal dementia caregivers which are relevant for clinical practice, research and informal caregivers.
INTRODUCTION: Informal dementia caregivers report important unmet needs at all stages of the disease. In addition, they often indicate that health care providers insufficiently attend and adapt to their multiple needs. A systematic and patient-centered assessment is needed to address this lack of knowledge and understanding. However, existing quantitative needs assessment questionnaires are limited in terms of psychometric testing. Qualitative measures are time intensive and difficult to conduct on a large scale, with growing economic pressure. Information about the methodological quality and the characteristics of needs assessment instruments are crucial for clinicians and researcher to make informed decisions about the most reliable and valid tool for their specific purpose. INCLUSION CRITERIA: This review considered studies on multidimensional needs assessment instruments for assessing the needs of informal dementia caregivers, living at home. Psychometric studies or other type of studies with sufficient data to evaluate methodological quality were included if they considered at least one outcome for reliability or validity.
METHODS: Studies in English, French or German and published until February 2019 were searched in four databases: Embase, MEDLINE, CINAHL and PsycINFO. After screening the titles, abstracts or full-texts for eligibility, the provisional included studies were assessed for methodological quality with a standardized tool for systematic reviews of measurement properties. After data extraction using a standardized tool, the quality of the measurement properties was rated and compared using predefined quality criteria.
RESULTS: Eighteen articles covering 14 different needs assessment instruments were included in the review. Eleven publications focused on the development or the evaluation of an instrument. In addition, a development report, a manual and five studies, not aimed primarily at validation but containing sufficient information about the development or the evaluation of the used instruments, were included. The systematic evaluation of the instruments revealed that half of them had excellent content validity. In contrast, structural validity was rarely examined, and mostly with an insufficient sample size or a questionable analysis. None of the instruments had an optimally tested and good internal consistency. Regarding reliability, test-retest agreement was rarely tested and inter-rater agreement was evaluated using controversial procedures. Comparing the different instruments reviewed, the "Partnering for better health - living with chronic illness: dementia" had the best psychometric evidence, and the "Questionnaire of consultation expectations" was also partly supported, while most other instruments presently had limited psychometric soundness.
CONCLUSIONS: Despite the good evidence for some psychometric properties, further developments in the field of needs assessment for informal dementia caregivers are needed, particularly regarding structural and construct validity, as well as test-retest reliability and sensitivity to change. To enhance conceptual clarity, the development of an underlying theoretical model of needs should be prioritized.

Year:  2019        PMID: 31764427     DOI: 10.11124/JBISRIR-2017-003976

Source DB:  PubMed          Journal:  JBI Database System Rev Implement Rep        ISSN: 2202-4433


  45 in total

1.  Essential information and support needs of family caregivers.

Authors:  Sarah B Wackerbarth; Mitzi M S Johnson
Journal:  Patient Educ Couns       Date:  2002-06

Review 2.  Needs of informal caregivers during transition from home towards institutional care in dementia: a systematic review of qualitative studies.

Authors:  Basema Afram; Hilde Verbeek; Michel H C Bleijlevens; Jan P H Hamers
Journal:  Int Psychogeriatr       Date:  2014-10-07       Impact factor: 3.878

3.  Development of an Item Pool for a Needs-Based Measure of Quality of Life of Carers of a Family Member with Dementia.

Authors:  Jan R Oyebode; Simon Pini; Emma Ingleson; Molly Megson; Mike Horton; Linda Clare; Hareth Al-Janabi; Carol Brayne; Penny Wright
Journal:  Patient       Date:  2019-02       Impact factor: 3.883

4.  Patient-reported and proxy-reported outcome measures for the assessment of health-related quality of life among patients receiving enteral feeding: a systematic review protocol.

Authors:  Ingeborg Simpelaere; Anne White; Geertruida E Bekkering; Bart Geurden; Gwen Van Nuffelen; Marc De Bodt
Journal:  JBI Database System Rev Implement Rep       Date:  2016-07

5.  Camberwell Assessment of Need for the Elderly (CANE). Development, validity and reliability.

Authors:  T Reynolds; G Thornicroft; M Abas; B Woods; J Hoe; M Leese; M Orrell
Journal:  Br J Psychiatry       Date:  2000-05       Impact factor: 9.319

6.  Caring for individuals with dementia and cognitive impairment, not dementia: findings from the aging, demographics, and memory study.

Authors:  Gwenith G Fisher; Melissa M Franks; Brenda L Plassman; Stephanie L Brown; Guy G Potter; David Llewellyn; Mary A M Rogers; Kenneth M Langa
Journal:  J Am Geriatr Soc       Date:  2011-03       Impact factor: 5.562

7.  Development of the risk appraisal measure: a brief screen to identify risk areas and guide interventions for dementia caregivers.

Authors:  Sara J Czaja; Laura N Gitlin; Richard Schulz; Song Zhang; Louis D Burgio; Alan B Stevens; Linda O Nichols; Dolores Gallagher-Thompson
Journal:  J Am Geriatr Soc       Date:  2009-04-21       Impact factor: 5.562

8.  Correlates of objective and subjective measures of caregiver burden among dementia caregivers: influence of unmet patient and caregiver dementia-related care needs.

Authors:  Travonia B Hughes; Betty S Black; Marilyn Albert; Laura N Gitlin; Deirdre M Johnson; Constantine G Lyketsos; Quincy M Samus
Journal:  Int Psychogeriatr       Date:  2014-08-08       Impact factor: 3.878

9.  The experience of Italians caring for family members with Alzheimer's disease.

Authors:  Ercole Vellone; Julita Sansoni; Marlene Zichi Cohen
Journal:  J Nurs Scholarsh       Date:  2002       Impact factor: 3.176

10.  Measuring caregiver activation for health care: Validation of PBH-LCI:D.

Authors:  Tatiana Sadak; Anna Korpak; Soo Borson
Journal:  Geriatr Nurs       Date:  2015-05-07       Impact factor: 2.361

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.