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Showing 1 to 15 of 20 results Save | Export
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Ghaleb H. Alnahdi; Arwa Alwadei; Susanne Schwab – International Journal of Developmental Disabilities, 2024
This comprehensive study delves into the family quality of life (FQOL) of caregivers in Saudi Arabia, focusing on those caring for individuals with autism, intellectual disabilities, and other disabilities and those without any disabilities. Employing the Arabic version of the Beach Center FQOL Scale, the research encompasses a diverse group of…
Descriptors: Foreign Countries, Family Environment, Quality of Life, Caregivers
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Valentini, Brian – International Journal of Developmental Disabilities, 2023
Currently, outcomes for people with autism and intellectual disabilities are poor, leaving some needing optimal life-long services. Little is known regarding the services provided at sustainable communities. This study's purpose is to explore the make-up of sustainable communities, those participating in them, and the services provided. One survey…
Descriptors: Caregiver Attitudes, Caregivers, Services, Autism Spectrum Disorders
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Santos, Ana; Galinha, Sónia; Cunha, Bruno – International Journal of Curriculum and Instruction, 2020
Increasingly, lifelong learning is of growing importance and it refers to the constant experiences and needs of individuals adapting to the development of their personal and social skills in relation to the contexts and circumstances in which they are inserted. For this, one of the primary requirements to be able to enjoy a high Quality of Life.…
Descriptors: Correlation, Educational Attainment, Quality of Life, Caregivers
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Bhopti, Anoo; Lentin, Primrose; Brown, Ted – Journal of Occupational Therapy, Schools & Early Intervention, 2020
Disability-related services such as Early Childhood Intervention Services (ECIS) become a part of life for families when there is a child with disability. Many parents give up their everyday occupations such as self-care and paid work to be able to provide long-term caregiving. This Australian study explored parent perspectives of their family…
Descriptors: Correlation, Quality of Life, Intervention, Preschool Children
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Craig, Jocelyn E.; Cartwright, Collen – British Journal of Learning Disabilities, 2015
Background: The concerns of older carers of an adult with disabilities have been well documented. The sudden incapacity or death of the carer can result in a crisis response rather than a planned transition to a chosen sustainable alternative care arrangement for the person with disability. Building on previous "Futures Planning"…
Descriptors: Older Adults, Caregivers, Disabilities, Planning
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Neikrug, S.; Roth, D.; Judes, J. – Journal of Intellectual Disability Research, 2011
Purpose: The purpose of this study is to describe and analyse the quality of life of Israeli families raising a child with a disability while challenged with all the usual demands of family life. Methods: Respondents were main caregivers of 103 children with disability receiving services at Beit Issie Shapiro, a service agency in Israel. The…
Descriptors: Family Life, Quality of Life, Caregivers, Parent Child Relationship
DeZonia, Krysti – Exceptional Parent, 2009
A caregiver of a child or adult with special needs, who is concerned about who will advocate for them when he/she no longer can, may want to consider developing a microboard to oversee their long-term life quality. A microboard is a legally recognized "agency" with the sole purpose of providing support to an individual with developmental or other…
Descriptors: Disabilities, Quality of Life, Caregivers, Advocacy
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Caples, Maria; Sweeney, John – British Journal of Learning Disabilities, 2011
Two-thirds of the people registered on the Irish National Intellectual Disability Database (NIDD) reside at home with family members frequently supporting them (Kelly et al., "National Intellectual Disability Database Committee Annual Report 2006," Health Research, 2007). Use of respite care services by parents with a child/adult with an…
Descriptors: Health Services, Mental Retardation, Quality of Life, Parents
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Sung, Minjung; Park, Jiyeon – International Journal of Special Education, 2012
In this study, a family support program was carried out for primary caregivers of children with disabilities. The program included respite care, recreation programs, counseling, and social support coordination based on individual needs of each family. In order to verify the intervention effects, parenting stress and family quality of life were…
Descriptors: Disabilities, Intervention, Parent Child Relationship, Quality of Life
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Hewitt, Amy; Lightfoot, Elizabeth; Bogenschutz, Matthew; McCormick, Katey; Sedlezky, Lori; Doljanac, Robert – Journal of Family Social Work, 2010
Future life planning is a growing concern among families with children with disabilities. This article presents a needs assessment evaluating feasibility of a new model for future life planning for family caregivers, Lifetime Assistance, which will provide ongoing planning and monitoring for individuals with intellectual and developmental…
Descriptors: Needs Assessment, Mental Retardation, Focus Groups, Quality of Life
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Lin, Jin-Ding; Lin, Pei-Ying; Wu, Chia-Ling – Research in Developmental Disabilities: A Multidisciplinary Journal, 2010
Little scientific research has focused on the measure of how positive wellbeing of people caring for people with disabilities. The purposes of the present study are to explore the wellbeing perception and its determinants of caregivers who caring for people with disability. We employed a cross-sectional, self-administrative structured…
Descriptors: Residential Care, Life Satisfaction, Quality of Life, Caregivers
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Riches, Vivienne C.; Parmenter, Trevor R.; Llewellyn, Gwynnyth; Hindmarsh, Gabrielle; Chan, Jeff – Journal of Applied Research in Intellectual Disabilities, 2009
Background: There is an urgent need for developing reliable, valid and practical instruments that assess and classify the support needed by persons with disability to function in their chosen living, working and social environments. I-CAN is an instrument that addresses the frequency and level of support needed (not individual skills or deficits)…
Descriptors: Emotional Response, Empowerment, Social Influences, Evaluation Methods
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Levine, Carol – Journal of Social Work Education, 2008
This is a tale of caregiving in two cities--and it was the best of times and the worst of times. In this article, the author describes the differences in the care given by nurses and social workers to her 90-year-old mother who died from metastatic colon cancer and to her husband who had traumatic brain injury in an automobile accident and was…
Descriptors: Accidents, Quality of Life, Head Injuries, Caregivers
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Henderson, Stacey; Skelton, Heather; Rosenbaum, Peter – Developmental Medicine & Child Neurology, 2008
Functional impairments can limit a child's ability to participate in the experiences of childhood. This "deprivation" can, in turn, have a negative effect on such children's development, academic performance, and quality of life, as well as on the lives of their caregivers and families. Many adults use assistive devices to overcome functional…
Descriptors: Quality of Life, Caregivers, Statistical Analysis, Assistive Technology
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Minnes, Patricia; Woodford, Lynn; Passey, Jennifer – Journal of Applied Research in Intellectual Disabilities, 2007
Background: Increasing numbers of adults with an intellectual disability are being cared for at home by ageing parents. The purpose of this study was to determine whether carer resources (i.e. social support and formal service use) and carer appraisals of ageing and stress/burden mediate the relationships between (1) maladaptive behaviour and…
Descriptors: Behavior Problems, Mental Retardation, Quality of Life, Disabilities
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