Exploring the experiences and outcomes of children and young people receiving support for special educational needs over time in England: a qualitative study

Background One in five school-aged children and young people (CYP) in England are identified as having a special educational need or disability (SEND) requiring additional support. Despite growing numbers of pupils receiving interventions to support the broad areas of need outlined in government guidelines, little research has asked CYP directly about their experiences of securing and receiving SEND provision or how effective they think the support was for their health and education outcomes. We answered these questions through one-to-one interviews with CYP with SEND. Methods We used a semi-structured interview format, structured with a timeline to help participants recount their whole experience. We developed and piloted our approach with a CYP's advisory group. All data collectors were trained by a senior research team. We recruited participants via an online survey about SEND provision in England. Interviews were audio-recorded, transcribed verbatim and anonymized before thematic analysis, complemented by narrative portraiture for selected cases. Results We interviewed 15 CYP aged 13–25 years (12 online, 3 in-person). Respondents had a range of SEND types, most commonly autism. Thematic analysis identified four themes that acted as enablers and barriers to SEND provision: (1) education-based factors; (2) the extent that provision matched need; (3) timing of provision; and (4) relationships, communication and decision-making. Mental health and attainment were the most common outcomes discussed. Our narrative portraitures illustrate the large number and variety of influences on the quality of SEND provision at critical educational stages, which affected their educational, mental health and life trajectories. Conclusion Late identification of SEND, and poor responsiveness of school staff in implementing provision had detrimental consequences for CYP's outcomes. Listening to them about their needs, providing prompt assessments and implementing simple tailored approaches can be hugely beneficial. The ability of CYP and families to advocate for support is a key influence over the quality of provision. Our study has policy implications, including fairer formats for academic assessment and a call for additional SEND training and toolkits for teachers. Further attention must be paid to ensure the needs of all CYP are identified and met, including those who cannot advocate for themselves.

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Publication Details

Journal
Frontiers in Education
Published
2025-09-16
DOI
https://doi.org/10.3389/feduc.2025.1564583
Citations
2
Primary Topic
Family and Disability Support Research
Type
article
Field-Weighted Citation Impact
4.61

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article

Exploring the experiences and outcomes of children and young people receiving support for special educational needs over time in England: a qualitative study

Poppy Hall, Charlotte G. Tripp, Jacob Matthews, Isaac Winterburn et al.
2 citations
Frontiers in Education
Family and Disability Support Research
4.61
article

Exploring the experiences and outcomes of children and young people receiving support for special educational needs over time in England: a qualitative study

Poppy Hall, Charlotte G. Tripp, Jacob Matthews, Isaac Winterburn, Helen Casey, Jennifer Saxton, Ania Zylbersztejn, Sarah Barnes, Tamsin Jane Ford, Kristine Black‐Hawkins
article en
2 citations

Abstract

Background One in five school-aged children and young people (CYP) in England are identified as having a special educational need or disability (SEND) requiring additional support. Despite growing numbers of pupils receiving interventions to support the broad areas of need outlined in government guidelines, little research has asked CYP directly about their experiences of securing and receiving SEND provision or how effective they think the support was for their health and education outcomes. We answered these questions through one-to-one interviews with CYP with SEND. Methods We used a semi-structured interview format, structured with a timeline to help participants recount their whole experience. We developed and piloted our approach with a CYP's advisory group. All data collectors were trained by a senior research team. We recruited participants via an online survey about SEND provision in England. Interviews were audio-recorded, transcribed verbatim and anonymized before thematic analysis, complemented by narrative portraiture for selected cases. Results We interviewed 15 CYP aged 13–25 years (12 online, 3 in-person). Respondents had a range of SEND types, most commonly autism. Thematic analysis identified four themes that acted as enablers and barriers to SEND provision: (1) education-based factors; (2) the extent that provision matched need; (3) timing of provision; and (4) relationships, communication and decision-making. Mental health and attainment were the most common outcomes discussed. Our narrative portraitures illustrate the large number and variety of influences on the quality of SEND provision at critical educational stages, which affected their educational, mental health and life trajectories. Conclusion Late identification of SEND, and poor responsiveness of school staff in implementing provision had detrimental consequences for CYP's outcomes. Listening to them about their needs, providing prompt assessments and implementing simple tailored approaches can be hugely beneficial. The ability of CYP and families to advocate for support is a key influence over the quality of provision. Our study has policy implications, including fairer formats for academic assessment and a call for additional SEND training and toolkits for teachers. Further attention must be paid to ensure the needs of all CYP are identified and met, including those who cannot advocate for themselves.

Frontiers in EducationVol. 10
University of London (GB), University of Cambridge (GB), University College London (GB)
UK Research and Innovation, National Institute for Health and Care Research, Department of Health and Social Care, Economic and Social Research Council, Programme Grants for Applied Research, NIHR Cambridge Biomedical Research Centre
Openalex Percentile: Top 5%
Family and Disability Support Research
4.61
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