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Showing 1 to 15 of 26 results Save | Export
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Altay, Burçak – Educational Gerontology, 2017
In design disciplines, an affective understanding of users' everyday lives can increase designer sensitivity and awareness, leading to higher-quality design outcomes. Developing students' empathic understanding within design education is required to accomplish this goal. This article discusses learning strategies that enhance students' empathic…
Descriptors: Empathy, Older Adults, Design, Foreign Countries
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Tait, Kathleen; Hussain, Rafat – International Journal of Disability, Development and Education, 2017
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…
Descriptors: Foreign Countries, Quality of Life, Family Environment, Parent Attitudes
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Miller, E.; Buys, L.; Woodbridge, S. – Journal of Intellectual Disability Research, 2012
Background: Caring for a child with a disability can be a unique and challenging experience, with families often relying on informal networks for support. Often, grandparents are key support resources, yet little is known about their roles and experiences. Reporting on data collected in a larger Australian study, this article explores…
Descriptors: Child Rearing, Family Needs, Quality of Life, Disabilities
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Holloway, Susan D.; Domínguez-Pareto, Irenka; Cohen, Shana R.; Kuppermann, Miriam – Journal of Mental Health Research in Intellectual Disabilities, 2014
Previous studies indicate that families construct daily routines that enable the household to function smoothly and promote family quality of life. However, we know little about how activities are distributed between parents caring for a child with an intellectual disability (ID), particularly in Latino families. To address this gap, we…
Descriptors: Hispanic Americans, Mental Retardation, Family Environment, Interviews
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Hong, Joo Young; Turnbull, Ann – International Journal of Special Education, 2013
Beginning in the mid-to-late 1980s, the focus on individual quality of life expanded to family quality of life (FQOL) in the field of intellectual disabilities. However, few studies examined FQOL for families who have children with hearing loss. Furthermore, most studies focused on mothers' perceptions of FQOL. The purpose of this study is to…
Descriptors: Quality of Life, Family Environment, Hearing Impairments, Mothers
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Moyson, T.; Roeyers, H. – Journal of Intellectual Disability Research, 2012
Background: The concept of family quality of life is becoming increasingly important in family support programmes. This concept describes the quality of life of all family members and the family system as a whole, but only the opinion of the parents has been included. The opinion of the siblings has been incorporated in the opinions of the…
Descriptors: Grounded Theory, Siblings, Qualitative Research, Mental Retardation
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Bergstrom, H.; Hochwalder, J.; Kottorp, A.; Elinder, L. S. – Journal of Intellectual Disability Research, 2013
Background: In the context of a health intervention among people with intellectual disabilities (ID), there was a need to assess satisfaction with some aspects of life, in order to monitor both potential positive and negative effects of the intervention. The aim of the present study was to develop and evaluate an easily administered scale for…
Descriptors: Psychometrics, Life Satisfaction, Intervention, Social Indicators
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Phillips, Linda R.; Reed, Pamela G. – Gerontologist, 2010
Purpose: To describe caregivers' constructions of their caregiving role in providing care to elders they knew were dying from life-limiting illnesses. Design and Methods: Study involved in-depth interviews with 27 family caregivers. Data were analyzed using constant comparative analysis. Results: Four categories were identified: centering life on…
Descriptors: Quality of Life, Caregivers, Death, Caregiver Role
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Bertelli, M.; Bianco, A.; Rossi, M.; Scuticchio, D.; Brown, I. – Journal of Intellectual Disability Research, 2011
Background: There is substantial literature investigating quality of life (QoL) of individuals with intellectual disability (ID). QoL of families of people with ID is emerging as an important field of research. Despite this, there is a lack of studies regarding their relationship. Aim: The present paper aimed to study the relationship between QoL…
Descriptors: Mental Retardation, Family Programs, Quality of Life, Questionnaires
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Tellier, Myriam; Rochette, Annie; Lefebvre, Helene – International Journal of Rehabilitation Research, 2011
Clients with mild stroke may present subtle deficits that have an impact on complex activities and roles. The purpose of this study was to explore the perceived quality of life of spouses, 3 months after the client with stroke was discharged to go home from acute care. A qualitative design based on a constructivist paradigm was used. Interviews…
Descriptors: Spouses, Quality of Life, Disabilities, Content Analysis
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Moyson, Tinneke; Roeyers, Herbert – Exceptional Children, 2011
This study investigated how siblings of children with autism spectrum disorder (ASD) describe and define their quality of life. Using a qualitative research design, the authors collected data through a 4-stage process which included in-depth interviews of 17 children ages 6 to 14 and focus groups. All of the children with ASD were male and between…
Descriptors: Grounded Theory, Siblings, Qualitative Research, Autism
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Brown, R. I.; Geider, S.; Primrose, A.; Jokinen, N. S. – Journal of Intellectual Disability Research, 2011
Introduction: Since the development of inclusion and integration, parents have increasingly become the major, and sometimes the only, carers of their children with disabilities. Many families speak of stress and frustration with service and community support, and some have turned to residential and specialised day care services to overcome…
Descriptors: Residential Care, Siblings, Mental Retardation, Family Life
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Poon, K. K. – Journal of Intellectual Disability Research, 2011
Background: This study sought to describe the activities and participation of adolescents with autism spectrum disorders (ASD) in Singapore and to examine the suitability of the Activity and Participation component of the International Classification of Functioning, Disability and Health for achieving this purpose. This information may guide the…
Descriptors: Special Schools, Autism, Quality of Life, Rating Scales
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Chou, Yueh-Ching; Chiao, Chi; Fu, Li-Yeh – Journal of Intellectual & Developmental Disability, 2011
Background: Primary family carers of adults with profound intellectual and multiple disabilities (PIMD) experience a range of considerable demands. Method: A census survey was conducted in a city of Taiwan; 796 family carers of adults (aged 18 or older) diagnosed with intellectual disability and/or with multiple disabilities living with the family…
Descriptors: Family Income, Severe Disabilities, Multiple Disabilities, Mental Retardation
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Reid, Allison; Imrie, Heather; Brouwer, Emily; Clutton, Shannon; Evans, Jan; Russell, Diane; Bartlett, Doreen – Physical & Occupational Therapy in Pediatrics, 2011
In this study we investigated experiences of parents of children with cerebral palsy (CP) to identify areas in which health care providers and educators could improve practice. A second objective was to create educational material for parents of young children newly diagnosed with CP. A purposive sample of nine parents, who previously participated…
Descriptors: Parent Materials, Quality of Life, Cerebral Palsy, Parents
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