Hearing parents' voices: A priority-setting workshop to inform a suite of psychological resources for parents of children with rare genetic epilepsies

Objective: To understand parents' of children with developmental and epileptic encephalopathies needs and preferences for psychological resources. Methods: Using a person-based approach, a multidisciplinary panel of clinician and researchers (n = 9) hosted a priority-setting workshop to 1) unde...

Full description

Saved in:
Bibliographic Details
Main Authors: Suzanne M. Nevin (Author), Claire E. Wakefield (Author), Ann Dadich (Author), Fleur LeMarne (Author), Rebecca Macintosh (Author), Erin Beavis (Author), Rani Sachdev (Author), Ann Bye (Author), Kenneth Nunn (Author), Elizabeth E. Palmer (Author)
Format: Book
Published: Elsevier, 2022-12-01T00:00:00Z.
Subjects:
Online Access:Connect to this object online.
Tags: Add Tag
No Tags, Be the first to tag this record!

MARC

LEADER 00000 am a22000003u 4500
001 doaj_fb656a0c8d884597b7d2d91ffcd2bb03
042 |a dc 
100 1 0 |a Suzanne M. Nevin  |e author 
700 1 0 |a Claire E. Wakefield  |e author 
700 1 0 |a Ann Dadich  |e author 
700 1 0 |a Fleur LeMarne  |e author 
700 1 0 |a Rebecca Macintosh  |e author 
700 1 0 |a Erin Beavis  |e author 
700 1 0 |a Rani Sachdev  |e author 
700 1 0 |a Ann Bye  |e author 
700 1 0 |a Kenneth Nunn  |e author 
700 1 0 |a Elizabeth E. Palmer  |e author 
245 0 0 |a Hearing parents' voices: A priority-setting workshop to inform a suite of psychological resources for parents of children with rare genetic epilepsies 
260 |b Elsevier,   |c 2022-12-01T00:00:00Z. 
500 |a 2772-6282 
500 |a 10.1016/j.pecinn.2021.100014 
520 |a Objective: To understand parents' of children with developmental and epileptic encephalopathies needs and preferences for psychological resources. Methods: Using a person-based approach, a multidisciplinary panel of clinician and researchers (n = 9) hosted a priority-setting workshop to 1) understand parents' needs and preferences for psychological resources and 2) to develop 'guiding principles' to inform a future suite of psychological resources. The multidisciplinary panel analysed the parent priority-setting workshop data, using a combination of thematic and lexical analysis. Results: Thematic analysis identified six key domains wherein parents (n = 8) prioritised a need for psychological resources to support adaptation to their child's genetic DEE diagnosis. Lexical analysis revealed that connection to diagnosis-specific resources provided a pathway to promote enhanced psychological adaptation, by reducing social isolation and reorienting parents towards feelings of hope. Combination of both analyses generated six thematic informed 'guiding principles'. Conclusion: Codesigned psychological resources may help parents to cope with the unique and complex interplay of stressors associated with their child's DEE diagnosis and treatment. Our 'guiding principles' will be translated to inform a future suite of tailored psychological resources. Innovation: This study demonstrates an innovative codesign approach to inform tailored psychological resources for families of children with rare genetic conditions. 
546 |a EN 
690 |a Person-based 
690 |a Qualitative research 
690 |a Codesign 
690 |a Positive psychology 
690 |a Parent mental health 
690 |a Public aspects of medicine 
690 |a RA1-1270 
655 7 |a article  |2 local 
786 0 |n PEC Innovation, Vol 1, Iss , Pp 100014- (2022) 
787 0 |n http://www.sciencedirect.com/science/article/pii/S2772628221000145 
787 0 |n https://doaj.org/toc/2772-6282 
856 4 1 |u https://doaj.org/article/fb656a0c8d884597b7d2d91ffcd2bb03  |z Connect to this object online.