Summary information

Study title

Autonomy, Rights and Children with Special Needs: A New Paradigm, 2017-2019

Creator

Riddell, S, Centre for Research in Education Inclusion & Diversity (CREID), University of Edinburgh

Study number / PID

854073 (UKDA)

10.5255/UKDA-SN-854073 (DOI)

Data access

Restricted

Series

Not available

Abstract

This research investigated the way in which the children's rights agenda is being implemented in practice in the field of SEN/ASN, taking into account the wider policy context of declining budgets, reduced local authority power, increasingly complex governance arrangements and policy divergence across England and Scotland. The project's specific objectives are to analyse: The extent to which children and young people with SEN/ASN in different social, geographical and educational contexts and with different types of difficulty are able to realise their rights effectively; The degree to which the rights of children and young people with SEN/ASN intersect with those of parents/carers and are driven by, or influence, the decision-making of schools and local authorities; The way in which capacity for autonomous decision-making is understood and acted upon in different social and educational contexts; The factors which promote or inhibit the realisation of rights by children and young people with SEN/ASN, including those who are looked after by the local authority; The impact of a children's rights approach on the broader education and social policy landscape. Since the late 1970s, in the field of special educational needs (SEN) in England and additional support needs (ASN) in Scotland, there has been a growing focus on parental involvement in educational decision-making. Despite the emphasis on the empowerment of children in the UN Convention on the Rights of the Child (UNCRC) and the UN Convention on the Rights of Persons with Disabilities (UNCRPD), parental rights in education have tended to trump those of children and young people. There has also been some disparity with regard to the emphasis on the educational rights of children and young people with SEN/ASN in different parts of the UK, and competing understandings of the concept of autonomy. In both England and Scotland, new legislation aims to place the rights of children and young people with SEN and ASN on a...
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Methodology

Data collection period

01/07/2017 - 14/08/2019

Country

England, Scotland

Time dimension

Not available

Analysis unit

Organization

Universe

Not available

Sampling procedure

Not available

Kind of data

Numeric
Text

Data collection mode

(1) Review of literature, policy, legislation and administrative data (April–July 2017)Electronic databases (including the British Education Research Index, ERIC, Medline, Social Science Citation Index) were searched using appropriate keywords. The literature search was restricted to English language publications and work conducted over the past 10 years. The international literature on children’s rights of participation and redress was examined, with a focus on education and other relevant spheres of social policy (e.g. youth justice, family law and health). The ‘grey’ literature (including reports of evaluations and policy reviews conducted by practitioner or policy bodies which may not be in the public domain) was also examined, as was relevant administrative data published by the Scottish Government, the Department for Education and the tribunal systems in both jurisdictions. The overall aim of this review was to locate the exercise of rights in SEN/ASN within a broader socio-legal and international context. A key concept to be explored was that of autonomy, its significance and implications for fundamental rights and the way in which children’s participatory rights are realised in different types of education systems in Europe and in a wider international context. (2) Key informant interviews (April–July 2017)Up to 20 interviews were conducted in both England and Scotland (40 in total) with key players in government and organisations promoting and delivering SEN/ASN services. Their purpose was to sensitise the research team to important themes concerning the realisation of children and young people’s rights. Key informants included: Scottish Government and DfE representatives; Commissioners for Children and Young People; organisations representing children and young people with different types of SEN/ASN; parents’/carers’ forums; local authorities; schools; dispute resolution and advocacy services. School interviewees will be drawn from local authority maintained mainstream and special schools, other special schools and (England only) academies and free schools. (3) Local authority questionnaire survey (April – August 2017) Drawing on the central themes arising in the key informant interviews, a questionnaire survey was developed and administered to the responsible officer for SEN/ASN in all English local authorities. A survey was used in our previous collaborative research and achieved a good response rate. (4) In-depth case studies of children/young people with SEN/ASN (9 months, Aug. 2017–April 2018)Six LAs were identified (3 in England and 3 in Scotland) with different social and geographical profiles and SEN/ASN policies and practices reflected in patterns of identification, placement, funding and support for children’s rights . Within each authority, eight case studies of children and young people with SEN/ASN were conducted. (48 in total; 24 in each jurisdiction). The case studies, based on semi-structured interviews and observations with children and young people and significant others, were used to explore factors affecting the exercise of rights of participation and redress. The interviews focussed on children and young people’s accounts of their involvement in decisions on matters such as school choice, educational provision, funding including individual budgets (where appropriate), the resolution of disagreements including mediation and tribunals, curriculum and planning. The sampling criteria for the child and family case studies focussed on the four most common overall official categories of SEN/ASN (Riddell et al., 2016): (1) social, emotional and behavioural difficulties (Scotland) and social, emotional and mental health difficulties (England); (2) moderate learning difficulties; (3) speech, language and communication difficulties; and (4) autistic spectrum disorder. In each authority there were two case studies (one for a child at primary education stage, the other for one at secondary stage) for each of these four categories of SEN/ASN.In addition to these variables, children and young people were drawn from different deprivation quintiles , ethnic groups and age groups, and reflected a gender balance. Cases were drawn from different types of school (local authority maintained mainstream and special; academies (England only); other special schools). Within each of the 48 case studies, we interviewed the child or young person, their parents/carers and up to two significant others, such as a teacher, educational psychologist or parent partnership officer (up to four interviews per case study, maximum of 192 interviews in total). The interviews with children/young people and parents/carers were conducted either in the home or in another setting chosen by the adult. In some cases, it may be necessary to interview the children and adults together.In order to understand the way in which the school environment supports the rights of children and young people with SEN/ASN, we undertook at least half a day’s classroom observation per child/young person (subject to permission), as well as interviews and other activities.

Funding information

Grant number

ES/P002641/1

Access

Publisher

UK Data Service

Publication year

2021

Terms of data access

The Data Collection is available for download to users registered with the UK Data Service.

Related publications

Not available