Literature DB >> 29171008

Patient-reported outcome measures for young people with developmental disabilities: incorporation of design features to reduce cognitive demands.

Ariel E Schwartz1, Jessica M Kramer2, Angela L Longo2.   

Abstract

Use of patient-reported outcome measures (PROMs) may increase the involvement of young people with developmental disabilities in their healthcare decisions and healthcare-related research. Young people with developmental disabilities may have difficulty completing PROMs because of extraneous assessment demands that require additional cognitive processes. However, PROM design features may mitigate the impact of these demands. We identified and evaluated six pediatric PROMs of self-care and domestic life tasks for the incorporation of suggested design features that can reduce cognitive demands. PROMs incorporated an average of 6 out of 11 content, 7 out of 14 layout, and 2 out of 9 administration features. This critical review identified two primary gaps in PROM design: (1) examples and visuals were not optimized to reduce cognitive demands; and (2) administration features that support young people's motivation and self-efficacy and reduce frustration were underutilized. Because assessment demands impact the validity of PROMs, clinicians should prospectively consider the impact of these demands when selecting PROMs and interpreting scores. WHAT THIS PAPER ADDS: Patient-reported outcome measure (PROM) design features can reduce assessment demands related to cognitive processes. Pediatric PROMs underutilize design features that decrease cognitive demands of self-reporting.
© 2017 Mac Keith Press.

Entities:  

Mesh:

Year:  2017        PMID: 29171008      PMCID: PMC5771952          DOI: 10.1111/dmcn.13617

Source DB:  PubMed          Journal:  Dev Med Child Neurol        ISSN: 0012-1622            Impact factor:   5.449


  17 in total

1.  Acquiescence in interviews with people who have mental retardation.

Authors:  W M L Finlay; E Lyons
Journal:  Ment Retard       Date:  2002-02

Review 2.  Subjective quality of life in children with intellectual impairment--how can it be assessed?

Authors:  Melanie White-Koning; Catherine Arnaud; Sylvie Bourdet-Loubère; Hélène Bazex; Allan Colver; Hélène Grandjean
Journal:  Dev Med Child Neurol       Date:  2005-04       Impact factor: 5.449

3.  ICF linking rules: an update based on lessons learned.

Authors:  Alarcos Cieza; Szilvia Geyh; Somnath Chatterji; Nenad Kostanjsek; Bedirhan Ustün; Gerold Stucki
Journal:  J Rehabil Med       Date:  2005-07       Impact factor: 2.912

4.  Reducing Barriers to Patient-Reported Outcome Measures for People With Cognitive Impairments.

Authors:  Jessica M Kramer; Ariel Schwartz
Journal:  Arch Phys Med Rehabil       Date:  2017-04-08       Impact factor: 3.966

5.  The PCORI perspective on patient-centered outcomes research.

Authors:  Lori Frank; Ethan Basch; Joe V Selby
Journal:  JAMA       Date:  2014-10-15       Impact factor: 56.272

6.  Item selection in self-report measures for children and adolescents with disabilities: lessons from cognitive interviews.

Authors:  Linda Eddy; Leyla Khastou; Karon F Cook; Dagmar Amtmann
Journal:  J Pediatr Nurs       Date:  2010-08-23       Impact factor: 2.145

7.  Construction of the eight-item patient-reported outcomes measurement information system pediatric physical function scales: built using item response theory.

Authors:  Esi Morgan DeWitt; Brian D Stucky; David Thissen; Debra E Irwin; Michelle Langer; James W Varni; Jin-Shei Lai; Karin B Yeatts; Darren A Dewalt
Journal:  J Clin Epidemiol       Date:  2011-02-02       Impact factor: 6.437

8.  Differential item functioning in the Patient Reported Outcomes Measurement Information System Pediatric Short Forms in a sample of children and adolescents with cerebral palsy.

Authors:  Wendy J Coster; Pengsheng Ni; Mary D Slavin; Pamela A Kisala; Ratna Nandakumar; Mary Jane Mulcahey; David S Tulsky; Alan M Jette
Journal:  Dev Med Child Neurol       Date:  2016-04-21       Impact factor: 5.449

9.  The Questionnaire of Young People's Participation (QYPP): a new measure of participation frequency for disabled young people.

Authors:  C Tuffrey; B J Bateman; A C Colver
Journal:  Child Care Health Dev       Date:  2013-07       Impact factor: 2.508

10.  Psychometric properties of the PROMIS ® pediatric scales: precision, stability, and comparison of different scoring and administration options.

Authors:  James W Varni; Brooke Magnus; Brian D Stucky; Yang Liu; Hally Quinn; David Thissen; Heather E Gross; I-Chan Huang; Darren A DeWalt
Journal:  Qual Life Res       Date:  2013-10-02       Impact factor: 4.147

View more
  3 in total

1.  Usability and Reliability of an Accessible Patient-Reported Outcome Measure (PROM) Software: The Pediatric Evaluation of Disability Inventory-Patient-Reported Outcome (PEDI-PRO).

Authors:  Jessica M Kramer; Ariel E Schwartz; Daniel K Davies; Steven E Stock; Pengsheng Ni
Journal:  Am J Occup Ther       Date:  2021 Jan-Feb

2.  Modified Delphi procedure-based expert consensus on endpoints for an international disease registry for Metachromatic Leukodystrophy: The European Metachromatic Leukodystrophy initiative (MLDi).

Authors:  Daphne H Schoenmakers; Shanice Beerepoot; Sibren van den Berg; Laura Adang; Annette Bley; Jaap-Jan Boelens; Francesca Fumagalli; Wim G Goettsch; Sabine Grønborg; Samuel Groeschel; Peter M van Hasselt; Carla E M Hollak; Caroline Lindemans; Fanny Mochel; Peter G M Mol; Caroline Sevin; Ayelet Zerem; Ludger Schöls; Nicole I Wolf
Journal:  Orphanet J Rare Dis       Date:  2022-02-14       Impact factor: 4.123

Review 3.  Toward dynamic phenotypes and the scalable measurement of human behavior.

Authors:  Laura Germine; Roger W Strong; Shifali Singh; Martin J Sliwinski
Journal:  Neuropsychopharmacology       Date:  2020-07-06       Impact factor: 8.294

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.