Mothers' experiences with the Pediatric Evaluation of Disability Inventory (PEDI)
Title
Mothers' experiences with the Pediatric Evaluation of Disability Inventory (PEDI)
Creator
Rich D; Rigby P; Wright V
Identifier
Publisher
Physical & Occupational Therapy In Pediatrics
Date
2014
Subject
PEDI Study
Description
Parents of a child with a disability are often asked about their child's functioning in daily activities. One way to gather this information is through parent-report functional questionnaires such as the Pediatric Evaluation of Disability Inventory (PEDI). The purpose of this study was to explore parental experiences associated with completion of the PEDI before and after a functional therapy intervention. Semi-structured interviews were conducted with 12 mothers of children with cerebral palsy (CP) or developmental delay (DD) who had completed the PEDI within a larger study. A content analysis approach was used to code and organize the data into five themes. PEDI completion was associated with increased parental awareness of developmental patterns, and greater insight into levels of assistance they give to their child. Parents described various challenges and concerns with the PEDI that have implications for test administration processes. The findings have potential to enable more sensitive and focused PEDI use.
2014-08
Rights
Article information provided for research and reference use only. PedPalASCNET does not hold any rights over the resource listed here. All rights are retained by the journal listed under publisher and/or the creator(s).
Type
Journal Article
Citation List Month
Backlog
URL Address
Citation
Rich D; Rigby P; Wright V, “Mothers' experiences with the Pediatric Evaluation of Disability Inventory (PEDI),” Pediatric Palliative Care Library, accessed October 6, 2024, https://pedpalascnetlibrary.omeka.net/items/show/14874.