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1.
Gillian King Theresa Petrenchik Mary Law Patricia Hurley 《International Journal of Disability, Development & Education》2009,56(2):109-130
Despite the fairly extensive literature on the developmental benefits of youth's participation in organised, out‐of‐school activities, little is known about the participation of school‐aged children with physical disabilities in formal recreation and leisure activities, both in comparison with their participation in informal activities and with children who are typically developing. Enjoyment of formal and informal activities was examined for 427 children with physical disabilities and 354 children without disabilities, aged 6–14 years. It was predicted that children without disabilities would report significantly greater enjoyment of formal than informal activities, whereas this would not be the case for children with disabilities. This prediction was confirmed. Children with disabilities also participated in significantly fewer formal and informal activities, and participated in these activities less intensely than did children without disabilities. The mechanisms responsible for psychological engagement, enjoyment, and the developmental benefits of participation in activities are discussed, along with implications for research and clinical practice. 相似文献
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Gillian King Mary Law Patricia Hurley Theresa Petrenchik Heidi Schwellnus 《International Journal of Disability, Development & Education》2010,57(1):77-107
Similarities and differences were examined in the out‐of‐school recreation and leisure activity participation of 422 children with physical disabilities and 354 children without disabilities. The roles of age (six to eight years, nine to 11 years, and 12–14 years), gender, and disability status were examined with respect to the diversity, intensity, location, companionship, and enjoyment of participation in five types of activities, controlling for family income. The findings indicate that dimensions and types of activity participation are differentially influenced by age, gender, and disability. Age cohort comparisons indicated that children without disabilities experienced a widening social world characterised by more intense social participation, greater participation with non‐family members, and stable levels of enjoyment across the age groups. In contrast, children with disabilities in the various age groups were similar in their intensity of social participation and the nature of their companionship, with 12–14 year olds reporting less enjoyment of social activities than those aged six to eight years or nine to 11 years. The findings support the utility of a developmental and contextual perspective in understanding children’s patterns of participation. The information can be used by service providers and managers interested in creating centre‐based or community‐based recreational opportunities, and in providing information to parents about how to encourage children’s recreation and leisure participation. 相似文献
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Nancy L. Hutchinson Michelle Villeneuve Jennifer Dods C.J. Dalton Patricia Minnes 《Early Years: An International Journal of Research and Development》2014,34(4):348-363
Research has shown the benefits of parent involvement for student participation in education. Parent advocacy is a critical form of involvement by parents for children who are young, have disabilities, and are making transitions. Studies have classified forms of parent advocacy but have not illuminated the components necessary for effective parent advocacy. In this study of three families of children with developmental disabilities making the transition to kindergarten, we examined the applicability of Test’s conceptual framework of self-advocacy (CFSA) for guiding research and interventions for parent advocacy. The four components of CFSA were all reported in the parents’ experiences of advocacy. These cases highlight how parent advocacy is similar to, and more complex than, self-advocacy and suggest that parent advocacy is also influenced by the parent’s perceptions of the child’s needs and is context specific. In these cases, advocacy during transition reflects the parent’s priorities for the child’s inclusion. 相似文献
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Children’s biases toward their peers with intellectual disabilities tend to have negative developmental and social consequences for those with intellectual disabilities. As a result, researchers developed intervention programs to reduce biases toward children with intellectual disabilities. This meta-analysis is a quantitative summary of 59 studies and 144 hypothesis tests involving intervention programs to change children’s attitudes toward their peers with intellectual disabilities. Results revealed an overall significant effect (d = 0.44): following intervention programs, children’s attitudes toward their peers with intellectual disabilities increased. Moderators indicate that the most effective interventions were those that occurred over multiple sessions, involved active engagement in multiple strategies and social interactions, emphasized equal status contact that was unstructured or indirect, and had little adult guidance. Interventions had no effect on changing children’s perceptions of competence and participants in junior high had more negative attitudes following the interventions. Findings provide guidance for researchers, educators, and counselors who seek methodologies to reduce biases toward children with intellectual disabilities. 相似文献
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Astrid Nyquist Thomas Moser Reidun Jahnsen 《International Journal of Disability, Development & Education》2016,63(3):334-356
This study investigates the preferences for actual participation in and enjoyment of physical out-of-school activities in children with physical disabilities, including what particular activities they are actually participating in, how often, with whom, where, and how enjoyable they find these activities. The data are based on structured interviews with 149 children (67 girls (45%) and 82 boys (55%) from 6 to 17 years) who were attending three weeks of intensive rehabilitation at Beitostølen Healthsports Centre in Norway. The Children’s Assessment of Participation and Enjoyment and Preferences for Activities of Children scales were administered at the start of their rehabilitation stays. The study reveals a quite high level of participation in physical activity and a high degree of enjoyment in participating, but the children want to be even more active than they already are. They have clear preferences for activities, and these activities are to a large extent consistent with what they actually do during their leisure time. The children are most frequently active with family members, but they would prefer to be more active with peers. A prerequisite would therefore be to acquire better basic skills and competencies in a few chosen activities rather than having some experiences in a broad range of different activities. There are more similarities than differences between boys and girls and between age groups on the parameters investigated in this study. 相似文献
7.
Ozcan Karaaslan Ibrahim Diken Gerald Mahoney 《International Journal of Disability, Development & Education》2011,58(4):359-372
The case study was conducted to examine the feasibility of an early intervention curriculum called Responsive Teaching with two five-year-old children from Turkey who had significant developmental delays. This study determined whether Turkish mothers might be successful in learning to become more responsive to their children, and whether this would result in significant improvements in their children’s development. Both dyads received 28 individual parent–child intervention sessions which were conducted over a four-month period of time. Pre-, mid-, and post-assessments indicated improvements in the mothers’ responsiveness to their children and the children’s levels of engagement with their parents. There were also improvements in the children’s language and personal social development. Mothers reported that Responsive Teaching helped them learn to interact more effectively with their children and that this resulted in longer and more enjoyable interactions with them. Results from this investigation are discussed in terms of their implications for providing developmental services to preschool-aged children with disabilities in Turkey. 相似文献
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Necdet Karasu 《欧洲特需教育杂志》2013,28(3):358-369
Active participation of parents in every step of their children with special needs’ education is crucial, and it begins with the educational assessment of the children. The parents experience with the professionals who are responsible of assessing children’s abilities might be crucial for the services that will be provided for the children with disabilities. The Guidance and Research Centers (GRCs) of Turkey are the key organisations for the services for children with special needs. This study focused on identifying the experience of the parents at the GRCs and applied qualitative research principles. The findings showed that the parents have reflected both positive and negative experience, but the majority focused on negative experiences. It might be drawn out that GRCs must be improved from several perspectives. 相似文献
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Gudrun Doll‐Tepper 《Curriculum Journal》2013,24(2):299-315
Abstract Historically, in Germany individuals with special needs have been offered participation in physical education (PE) both in segregated and increasingly in integrated settings. Specific curricula for children with disabilities (physical disabilities, hearing, and visual impairments, speech and behaviour disorders as well as intellectual disabilities) were developed in the 1960s and 1970s. They all emphasized the specific importance of physical activities for people with a disability focusing not only on motor competencies but also on the psychological and social benefits of physical education. During the 1970s so‐called model schools started to include children with disabilities in mainstream schools. Unlike developments in the United States, for example, where integrated or mainstream schooling was based on legal requirements, in Germany improved integration or inclusion was not based on federal law, but on parents’ or teachers’ initiatives in different Bundesländer (states of Germany). Parallel to these developments, new approaches to PE have accentuated a positive orientation towards ‘ability’ rather than ‘disability’. Professionals in PE in universities and in schools have been challenged to develop better diagnostic skills and more individualized programmes. On the initiative of nine European universities, a European Master's degree of Adapted Physical Activity has been developed to offer advanced training on a European scale. However, despite these positive and innovative developments serious concerns remain concerning the situation of children with disabilities in the school system. This article argues that there is still a significant lack of specially trained professionals and support staff and that the ongoing process of reducing the amount of PE in schools for all children, including those with a disability, does not contribute to improved physical and social skills or increased participation in recreational and sport activities outside schools. 相似文献
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The number of parents undertaking an intensive home training programme of children with disabilities (e.g. Applied Behavioural Analysis) has increased. It reveals a paradox in current disability research and policies. On the one hand, policies in general are aimed at inclusion through movement of social barriers for participation, grounded in the social model of disability. On the other hand, intensive home training is based on the aim of rehabilitation through intensive training of individual cognitive and social skills, an approach grounded in a bio-medical model. Intensive home training programmes are supported by political legislation that enables parents to partake the training and hire the necessary helpers. How is this paradox viewed from the perspective of the parents? From the departure of the dialectical model of disability – and its central concepts of developmental incongruence, developmental time and social agency – two mothers practising home training with their children with autism disorder were interviewed about their motives for home training and subsequent experience with their child. Results showed that the motive to home training was to create a local congruence that allowed the child to thrive. Intensive home training also restored the mothers’ sense of agency vis-à-vis their child’s development. However, home training might not abolish the need for adaptations of the child’s social practices outside the family. It is discussed how societal support to home training risks to hinder higher order reorganisation of developmental opportunities that are necessary to actualise policy statements of inclusion. 相似文献
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Jin Y. Shin Nguyen Viet Nhan Kathleen Crittenden S. Stavros Valenti Hoang Thi Dieu Hong 《International Journal of Disability, Development & Education》2008,55(3):239-249
The purpose of the present study was to examine agreement on childhood disability among the teachers and parents of children with cognitive delays in Vietnam. The participants were 57 teachers in kindergarten programmes (for children 2 to 6 years of age), and 106 mothers and 93 fathers of the children attending these kindergarten programmes. The data were collected using the ABILITIES Index and a demographic information form. The results indicated that teachers rated the children’s level of functioning more severely, especially in the areas of intellectual disabilities and behaviour problems, than mothers and fathers. Logistic regression that examined the factors that predicted the agreement and disagreement among parents and teachers revealed that teachers and parents were more likely to agree when the child’s disability was genetically related or physical. Screening, diagnosis and treatment issues can become more challenging for children with intellectual disabilities who do not have such physical and genetic conditions, especially when the agreement between parents and professionals on the conditions of the children is low. 相似文献
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Tsung-Yen Chuang Ming-Shiou Kuo Ping-Lin Fan Yen-Wei Hsu 《Educational technology research and development : ETR & D》2017,65(3):699-717
Sensory integration dysfunction (SID, also known as sensory processing disorder, SPD) is a condition that exists when a person’s multisensory integration fails to process and respond adequately to the demands of the environment. Children with SID (CwSID) are also learners with disabilities with regard to responding adequately to the demands made by a learning environment, and usually have performance difficulties in one or more areas of life, such as productivity, leisure and play, or activities of daily living, and this can reduce their learning motivation. This study tries to develop a motion-sensing digital game-based SID therapy to help such children become more engaged in physical training, with the hope that by improving their bodily-kinesthetic intelligence these children can be more confident of facing various learning challenges, like those associated with social participation. This research applied the Microsoft Kinect system and a specially designed motion-sensing game related to SID, and used interviews to collect responses from the children and their parents. The Chinese version of the sensory profile and clinical observation were applied to evaluate the effects of the therapy, and the triangulation method applied in the data analysis reveals the improvements of all participants in eight clinical observation items. The results imply that our approach was able to increase the learning motivation and actions of the CwSID who participated in this study, with better results than those obtained in our earlier work, which used the Nintendo Wii device and its commercially available games. 相似文献
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Kim Angeles Gärtner Verena Clara Vetter Michaela Schäferling Gitta Reuner Silke Hertel 《Metacognition and Learning》2018,13(3):241-264
Inhibitory control is considered a core component of self-regulation. Tremendous advances in early childhood have been attributed to brain maturation processes as well as environmental influences, such as parental co-regulation. Parental self-efficacy represents a key correlate of parenting behaviors and is associated with child outcomes. However, research on the interplay of parental co-regulation, parental self-efficacy and child’s inhibitory control in early childhood is scarce. In this study we explore to what extent parents’ positive (PCR) and negative co-regulation (NCR) and domain-specific (DSSE) and domain-general (DGSE) self-efficacy beliefs assessed at pre-test (T1) predict toddlers’ inhibitory control six weeks later (T2). Furthermore, we examine whether NCR mediates the link between DSSE and parent-reported inhibitory control. Results are based on data from 90 parent-child dyads (children’s age: 24–35 months). Parents’ PCR, NCR, DSSE and DGSE are assessed via questionnaire. Children’s inhibitory control is measured via the Inhibition Scale of the Behavior Rating Inventory of Executive Functions (BRIEF-IN) and a Snack Delay task. Multiple regression analyses reveal that parents’ NCR and DSSE, but not PCR and DGSE, significantly predict BRIEF-IN at T2 (controlling for covariates). The indirect effect from parents’ DSSE on BRIEF-IN via NCR is not confirmed by the data. No associations are observed regarding children’s performance in the Snack Delay task. The present study adds new and important evidence that parents’ DSSE and NCR independently predict (parent-reported) inhibitory control in toddlerhood. Parenting interventions should thus not only address parenting practices but target parental self-efficacy beliefs as an important factor, too. 相似文献
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王冰 《湖州师范学院学报》2014,(9):101-104
随着城市80后独生子女为人父为人母,工作环境竞争的日益激烈,越来越多的年轻父母或因为工作压力大,或因为逃避养育责任等选择把孩子交给保姆或孩子的祖父母、外祖父母甚至其他亲戚代为抚养,这种代为抚养的儿童称为“城市寄养儿童”。和完整家庭的孩子相比,寄养儿童的家庭教育在一定程度上是不完整的,尤其在心理情感、教育内容和教育观念等方面存在严重问题,提前建立抚养人和寄养儿童的感情、强化抚养人的家庭功能以及强化学校对寄养儿童的教育与关怀是解决城市寄养儿童家庭教育问题的主要途径。 相似文献
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Kathleen Tait Rafat Hussain 《International Journal of Disability, Development & Education》2017,64(3):328-344
Australian education service provision includes the delivery of quality educational programmes to rural and remote living children. However, according to their parents, many children with developmental disabilities (such as Down Syndrome and Autism Spectrum Disorders) who are living in rural country areas in New South Wales (NSW) still do not have access to an acceptable education programme. This study aimed to use quality of life factors via a family quality of life scale to explore 51 parents’ experience of educational service provision for their children with developmental disabilities in rural NSW. The results indicated that successful engagement with the school system is strongly affected by the views, assumptions, expertise and prejudices of teaching and care professionals. Further research into how local educational service providers may assist rural Australian families with a child with IDD in rural and remote locations is warranted. 相似文献
18.
The study aimed to deepen the understanding of parental sensitivity to their children’s abilities and the nature of their scaffolding during writing tasks. We compared the parent–child writing interactions of three groups: precocious readers (PRs), same age preschoolers (SA), and older children with the same reading level (SRL) as the PRs. Each of 60 parent child-dyads was videotaped during three writing activities that varied in their structure level: word writing, writing a birthday invitation, and free writing within a wordless children’s book. Interactions were analyzed for parental literacy-specific, social-emotional, and general cognitive support. Results demonstrated parents’ sensitivity to their children’s developmental level and skills. Parents of PRs showed levels of literacy-specific support similar to parents of older children with the SRL, and higher than parents of SA non-reading children. Parents of PRs resembled parents of SA preschoolers and provided their children with more social-emotional support than parents of the older SRL children. The general cognitive support of parents of PRs was higher than that of the two other groups. Moreover, parents of PRs referred to writing conventions and showed more responsiveness than parents in the other two groups. Parents in all three groups emphasized literacy-specific support during the more structured writing tasks (words and invitation), and placed greater emphasis on the social-emotional and general cognitive support during the least structured task (free writing within the wordless book). Beyond these differences, parents demonstrated a consistent support style. We discuss parent–child writing interactions as a context for early literacy development. 相似文献
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幼儿天生就爱在户外玩耍,户外活动不仅能促进幼儿身体的健康发育,而且能够有效促进幼儿社会性以及智力的发展,家庭户外活动更能促进亲子间的感情。通过文献法、问卷调查法、访谈法对幼儿家庭户外活动进行六方面的调查,包括幼儿家庭户外活动的时间、场所、内容、伙伴、家长参与情况以及家长态度。研究发现,幼儿家庭户外活动存在家长对幼儿户外活动认识不足、幼儿户外活动场地和内容局限单一以及存在诸多安全隐患等问题。建议家长应合理规划,增加幼儿户外活动的多样性和趣味性;注重参与,优化幼儿户外活动的体验与成效;多重保障,提升幼儿户外活动的安全性。 相似文献
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《Early childhood research quarterly》2002,17(2):148-166
The free-play social behaviors of 24 children with special needs in two discovery-oriented, inclusive preschool programs were compared with their typically-developing classmates who were matched by age and sex. Children who, for various reasons, used little or no productive language spent more time in solitary pursuits, seldom initiated interactions and, when they did, used a different entry strategy than any other group. Children who were incapable of independent locomotion were largely dependent on adults for initiating changes in their activities and for social exchanges. Although they received more adult support than children developing typically, perhaps because of limited sample size, children with disabilities who were capable of independent locomotion and displayed sufficient language to make their needs and intents clear did not differ significantly from the children who were developing typically. Adults’ behavior varied according to child condition and activity. From observing a single, 20-minute videotape of free play, naı̈ve observers agreed with our classifications of over 78% of the children. 相似文献