ArticleScientific reports2026
Pressure and coping strategies of caregivers of children with autism spectrum disorder in rural areas: a qualitative study.
Article in Scientific reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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.
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Who cites it
1 citing paper in PubMed.
- Applying self-determination theory to understand maternal well-being in autism caregiving: a mini review.Frontiers in child and adolescent psychiatry · 2026Review
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Authors and funding
6 authors.
Funding
Abstract
The prevalence of autism spectrum disorders in children is on the rise. Medical rehabilitation resources in rural areas are relatively scarce, and rural family caregivers often bear greater pressure. This study deeply understood the pressure faced by caregivers of children with autism spectrum disorders in rural areas and their coping strategies, and provided references for improving their physical and mental health and social support system. Using purposive sampling method in qualitative research, 14 caregivers of rural autism spectrum disorder children were selected for semi-structured interviews. Colaizzi analysis method was used to summarize the topics of the interview data, and the caregivers’ stressors and coping strategies were systematically analyzed. Six themes were extracted, (a) economic pressure and lack of resources, (b) internal family conflict and emotional burden, (c) social isolation and associated stigma, (d) lack of knowledge and rehabilitation system, (e) psychological resilience and positive coping, (f) and the construction and improvement of support network. Caregivers of rural autism spectrum disorder children face multiple pressures, with heavy economic burden, obvious stigma and weak social support. It is necessary to strengthen policy implementation and resource preference, provide professional rehabilitation guidance, build a family community government collaborative support network, and pay attention to caregivers’ negative emotions to promote their positive coping.
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