4.7 Article

A Qualitative Investigation Into What Parents Want From an Online Behavioural Sleep Intervention for Children With Epilepsy

Journal

FRONTIERS IN PSYCHOLOGY
Volume 12, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fpsyg.2021.628605

Keywords

qualitative; epilepsy; sleep; sleep intervention; parental needs; children

Funding

  1. National Institute for Health Research (NIHR) [RP-PG-0615-20007]
  2. National Health and Medical Research Council (NHMRC) [1136222]
  3. Victorian Government's Operational Infrastructure Support Program
  4. National Institutes of Health Research (NIHR) [RP-PG-0615-20007] Funding Source: National Institutes of Health Research (NIHR)

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This study aimed to identify specific considerations for parents of children with epilepsy in the content and delivery of online behavioral sleep interventions. Ten themes were identified, including the need for inclusion of other parents' experiences, understanding of changing sleep-management options, personalized suggestions, addressing child anxiety, practical advice, educational information, acknowledging parental worries, providing support for children's sleep, and involving children in the intervention. Specific adaptations and additions to online BSI content and format are necessary to meet the needs of parents of children with epilepsy.
Many of the same sleep problems seen in typically developing (TD) children are frequently experienced by children with epilepsy (CWE). Behavioural sleep interventions (BSIs) are commonly and successfully used to treat these sleep problems in TD children and in some neurodevelopmental disorder populations. Therefore, BSIs should be effective in CWE, however, there are special seizure-related considerations for CWE and their parents which may be salient to consider in any future BSI development for this group. The current study sought to identify, from parents, if there were special considerations for the content and delivery of an online BSI for parents of CWE. Semi-structured interviews were conducted with nine mothers of CWE and thematic analysis was conducted on the interview data. Ten themes were apparent which represented what parents wanted from any online BSI for CWE. Parents wanted (i) other parents' views and real-life experiences to be included, (ii) recognition of how changes over time may influence the appropriateness of using various sleep-management options, (iii) to be presented with a range of sleep management options from which they could select, (iv) personalised information and suggestions for behaviour-change options, (v) help to address child anxiety around sleep, (vi) for the advice and behaviour-change options to be practical, (vii) general educational information about sleep and the relationship between sleep and epilepsy, (viii) for parental worries and concerns to be acknowledged, (ix) to receive help, support, and reassurance around children's sleep; and (x) to include the child in the intervention. It was clear that any online BSI would require specific adaptations and additions (to content and delivery format) to best meet the needs of parents of CWE. It is hoped that having identified what parents want from on online BSI for CWE will allow these factors to be acknowledged in future intervention development, with the intention to optimise parental engagement and intervention effectiveness. Practical suggestions for how these aspects could be integrated into any online BSI are suggested.

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