ArticleHealth expectations : an international journal of public participation in health care and health policy2024
Challenges and recommendations for advancing respite care for families of children and youth with special health care needs: A qualitative exploration.
Article in Health expectations : an international journal of public participation in health care and health policy, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
7 citing papers in PubMed.
- How Do Parents Experience Overnight Respite? Parent-Reported Outcomes in Families of Children With Intellectual and Developmental Disabilities.Journal of applied research in intellectual disabilities : JARID · 2026Article
- Exploring caregiver perspectives on health service delivery priorities for individuals with complex care needs: a qualitative descriptive study.BMC health services research · 2025Article
- Scoping Review on the Use of Navigation Services to Improve Accessibility of Programming for People With Intellectual Disabilities.Journal of applied research in intellectual disabilities : JARID · 2025Article
- Review
- Exploring fathers' experiences of caring for a child with complex care needs through ethnography and arts-based methodologies.BMC pediatrics · 2024Article
- Challenges and recommendations for advancing respite care for families of children and youth with special health care needs: A qualitative exploration.Health expectations : an international journal of public participation in health care and health policy · 2024Article
- Development of a Patient and Caregiver-Centered Pediatric Disease Concept Model for Kleefstra Syndrome.Sage open pediatricsArticle
Corrections and comments
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Authors and funding
4 authors.
Funding
Abstract
introductionCaring for children and youth with special health care needs (CYSHCN) is a significant undertaking for families. While respite care is intended to address this burden, demand continues to exceed supply. Exploring the perspectives of respite service providers (SPs) and stakeholders (SKs) provides unique insight into families' needs and respite care systems.
methodsWe conducted semistructured interviews with 41 respite care SPs and SKs across four Canadian provinces to ascertain perspectives on current and ideal respite care for families of CYSHCN. The analysis included delineating units of meaning from the data, clustering units of meaning to form thematic statements and extracting themes. The second-level analysis involved applying themes and subthemes to cross-functional process maps.
findingsParticipants noted the critical, but sometimes absent role of Community Service Workers, who have the ability to support families accessing and navigating respite care systems. SPs and SKs identified current respite systems as operating in crisis mode. New findings suggest an ideal respite care system would incorporate advocacy for families, empower families and value CYSHCN, their families and respite workers.
conclusionThe evidence of unmet respite care needs of families of CYSHCN across Canada has long been available. Our findings identifying respite system challenges and solutions can be used by funders and policymakers for planning and enhancing resources, and by healthcare professionals, respite care providers and SKs to understand barriers and take action to improve respite outcomes to meet the respite needs of all families and CYSHCN. PATIENT OR PUBLIC CONTRIBUTION: The research team is composed of patients, researchers, clinicians and decision-makers along with our Family Advisory Committee (FAC) composed of members of families of CYSHNC. The FAC was formed and met regularly with research team members, knowledge users and collaborators throughout the study to provide input on design, review themes and ensure findings are translated and disseminated in a meaningful way.
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