Evidence map›Paper›PMID 39783791›Full record

ArticleHealth expectations : an international journal of public participation in health care and health policy2025

What I Wish I Had Known: Examining Parent Accounts of Managing the Health of Their Child With Intellectual Disability.

Thom Nevill, Jessica Keely, Rachel Skoss, Rachel Collins, Katherine Langdon, Jaquie Mills, Jenny Downs

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Article in Health expectations : an international journal of public participation in health care and health policy, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 3 papers.

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0cells of the map it votes in
3citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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.

2 · The registry

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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors.

Thom NevillThe Kids Research Institute Australia, Centre for Child Health Research, University of Western Australia, Perth, Australia.
Jessica KeelyThe Kids Research Institute Australia, Centre for Child Health Research, University of Western Australia, Perth, Australia.
Rachel SkossThe Kids Research Institute Australia, Centre for Child Health Research, University of Western Australia, Perth, Australia.
Rachel CollinsCAHS Transition Service, Perth Children's Hospital, Perth, Australia.
Katherine LangdonKids Rehab, Perth Children's Hospital, Perth, Australia.
Jaquie MillsMicroboards Australia, Perth, Australia.
Jenny DownsThe Kids Research Institute Australia, Centre for Child Health Research, University of Western Australia, Perth, Australia.ORCID 0000-0001-7358-9037

Funding

This study was funded by the National Health and Medical Research Council (GTN2015902).
6 · The paper itself

Abstract

backgroundAppropriate support for the health of children with an intellectual disability by parents and healthcare professionals is pivotal, given the high risk of chronic conditions. However, there is limited research that has collected important insights from parents on their learnings for supporting their child's evolving healthcare needs.

aimThis study focuses on parents' experiences and learnings from managing and supporting the health of their child with intellectual disability. It aims to understand what parents wish they had known earlier, the essential knowledge and skills they needed to manage their child's health.

methodA qualitative study was carried out using semi-structured interviews with 21 parents of adolescents and young people with intellectual disability. The children had chronic health conditions that fell into six health domains, including (1) difficulties with movement and physical activity, (2) epilepsy, (3) dental care, (4) respiratory health and infection, (5) behaviour, mental health or sleep and (6) gastrointestinal health.

resultsThematic analysis yielded five themes: (1) optimising mutual engagement between healthcare professionals and families; (2) planning and practising effective healthcare; (3) having the right information at the right time; (4) finding the support that was needed and (5) navigating healthcare and disability systems. Over time, parents developed specific skills and knowledge for managing their child's health effectively. Some parents expressed regret for not seeking support and information about their child's health conditions earlier. Parents described how mutual engagement between healthcare professionals and parents optimised the management of their child's healthcare.

conclusionThe study found that managing the health of a child with intellectual disability is complex. The themes were consistent across health comorbidities, indicating important common experiences. The themes aligned with conceptualisations of health literacy, suggesting that improving health literacy skills can help parents better manage their children's health conditions. PATIENT OR PUBLIC CONTRIBUTION: We developed the project in consultation with members of the public who have lived experience of parenting a child with intellectual disability. They commented on the study aims, interview schedule, participant recruitment and provided feedback on the analysis and discussion.

Indexed as

Intellectual DisabilityInterviews as TopicParentsQualitative ResearchAdolescentAdultChildChronic DiseaseFemaleHumansMaleMiddle AgedYoung Adultchronic conditionshealth literacyhealth managementIntellectual disabilityparent perspectiveyoung people

Identifiers

PMID39783791
PMCPMC11713037

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.