‘We don’t know nearly enough’: an online survey exploring perspectives of specialists who support children with brain-based visual impairments

dc.citation.volume18
dc.contributor.authorJakubowski JS
dc.contributor.authorMay E
dc.contributor.authorFindlay R
dc.contributor.authorMcDowell N
dc.contributor.authorSimkin SK
dc.contributor.authorHamm LM
dc.contributor.editorChang M
dc.date.accessioned2025-03-27T02:05:15Z
dc.date.available2025-03-27T02:05:15Z
dc.date.issued2025-01-29
dc.description.abstractIntroduction: Children with brain-based visual impairments (some of whom have a diagnosis of Cerebral Visual Impairment, or ‘CVI’) represent a growing and underserved population within vision services. These children often have more complex needs than those with ocular visual impairments and benefit from specialist support from multiple disciplines. This study aimed to understand the perspectives of these specialists in terms of their goals, views on collaboration, and understanding of the term ‘CVI’. Methods: We invited a range of specialists who work with children with brain-based visual impairments, including educators, rehabilitation staff, clinicians, and family members, to complete an online survey between April 2023 and April 2024. Results: The analysis included 94 respondents: 51 educators, 30 rehabilitation staff, 7 clinicians, and 6 family members. Respondents shared common goals of connecting with the child (87/94, 93%) and fostering their learning and development (82/94, 93%). However, respondents also noted some specific and divergent goals, which can be at odds with each other. Professional staff frequently identified family members as the most valuable source of information about their child’s vision (36/88, 41%), though family members expressed feeling under-valued. Transdisciplinary clinics were highlighted as a helpful model to provide quality child-centered care. Of the 73 professional staff who reported being familiar with the term ‘CVI’ (73/88, 83%), most (61/73, 84%) thought it was underdiagnosed, but respondents had different perspectives on what a diagnosis meant. Only 73% of professionals familiar with CVI reported receiving formal training about it. Discussion: The varied goals and different perspectives on CVI create challenges to providing cohesive support for children with brain-based visual impairments. Increasing the availability of complementary formal training across disciplines and adopting transdisciplinary models of care are promising approaches to improve the quality of services.
dc.description.confidentialfalse
dc.edition.edition2024
dc.identifier.citationJakubowski JS, May E, Findlay R, McDowell N, Simkin SK, Hamm LM. (2024). ‘We don’t know nearly enough’: an online survey exploring perspectives of specialists who support children with brain-based visual impairments. Frontiers in Human Neuroscience. 18.
dc.identifier.doi10.3389/fnhum.2024.1510812
dc.identifier.eissn1662-5161
dc.identifier.elements-typejournal-article
dc.identifier.number1510812
dc.identifier.urihttps://mro.massey.ac.nz/handle/10179/72698
dc.languageEnglish
dc.publisherFrontiers Media S.A.
dc.publisher.urihttps://www.frontiersin.org/journals/human-neuroscience/articles/10.3389/fnhum.2024.1510812/f
dc.relation.isPartOfFrontiers in Human Neuroscience
dc.rights(c) 2025 The Author/s
dc.rightsCC BY 4.0
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.subjectbrain based visual impairment
dc.subjectCVI
dc.subjectcerebral visual impairment
dc.subjectparent perspectives
dc.subjectsurvey
dc.subjecttransdisciplinary care
dc.title‘We don’t know nearly enough’: an online survey exploring perspectives of specialists who support children with brain-based visual impairments
dc.typeJournal article
pubs.elements-id500141
pubs.organisational-groupOther

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