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Showing 1 to 15 of 20 results Save | Export
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Christi, Rebecca A.; Roy, Daniel; Heung, Raywin; Flake, Eric – Journal of Autism and Developmental Disorders, 2023
Objective: Parenting an autistic child can affect a family's well-being. Finding resources is critical. This pilot study looked at respite's impact on parental stress, anxiety, and depression in military families and demographic factors associated with presence of respite care. Method: Participants completed three surveys on anonymous basis,…
Descriptors: Parents, Military Personnel, Military Service, Children
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Coleman, Jeanine; Thompson, Talia; Riley, Karen; Allen, Korrie; Michalak, Claire; Shields, Rebecca; Berry-Kravis, Elizabeth; Hessl, David – Journal of Applied Research in Intellectual Disabilities, 2023
Background: Parenting children and young adults with intellectual disabilities, including individuals with fragile X syndrome and Down syndrome, is challenging, joyful, and complicated. Exploring how parents talk about their children, and the quality of the parent/child relationship can provide insight into the home environment and interactional…
Descriptors: Genetic Disorders, Intellectual Disability, Congenital Impairments, Parents
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Norton, Michelle; Dyches, Tina Taylor; Harper, James M.; Roper, Susanne Olsen; Caldarella, Paul – Journal of Autism and Developmental Disorders, 2016
Parents of children with disabilities are at risk for high stress and low marital quality; therefore, this study surveyed couples (n = 112) of children with Down syndrome (n = 120), assessing whether respite hours, stress, and uplifts were related to marital quality. Structural equation modeling indicated that respite hours were negatively related…
Descriptors: Stress Variables, Marital Satisfaction, Down Syndrome, Structural Equation Models
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McConkey, Roy; Kelly, Fionnola; Mannan, Hasheem; Craig, Sarah – American Journal on Intellectual and Developmental Disabilities, 2011
A cohort of nearly 11,000 persons was traced over 8 years to determine those who had moved from family care and those who had remained. The majority (85%) continued to live with families, and, for two thirds (67%), no future move was deemed necessary. The 2 main predictors of moving were as follows: A need had been previously recorded and the…
Descriptors: Mental Retardation, Respite Care, Longitudinal Studies, Family Environment
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Harper, Amber; Dyches, Tina Taylor; Harper, James; Roper, Susanne Olsen; South, Mikle – Journal of Autism and Developmental Disorders, 2013
Parents of children with autism spectrum disorders (ASD) are at risk for having higher stress and lower marital quality than other parents. Survey data regarding respite care, marital quality, and daily hassles and uplifts were obtained from 101 mother-father dyads who were together raising at least one child with ASD (total # of children = 118).…
Descriptors: Respite Care, Pervasive Developmental Disorders, Autism, Parents
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McConkey, Roy; Gent, Clare; Scowcroft, Emma – Journal of Applied Research in Intellectual Disabilities, 2013
Background: Specialist short break services aim to provide enhanced support to family carers as a means of preventing children whose behaviours severely challenge from being placed in full-time residential care. To date, there is limited evidence as to the functioning and effectiveness of such services. Methods: In all, 17 children were selected…
Descriptors: Behavior Disorders, Child Behavior, Disabilities, Family Programs
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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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Thompson, David; Emira, Mahmoud – Disability & Society, 2011
This paper analyses the experiences and perceptions of parents and carers with respect to children accessing a variety of leisure activities, as well as short breaks and respite care. The children in question have wide-ranging needs and, for example, will be across the Autistic Spectrum Disorder (ASD). The findings are based upon focus group…
Descriptors: Autism, Focus Groups, Disabilities, Respite Care
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Burton-Smith, Rosanne; McVilly, Keith R.; Yazbeck, Marie; Parmenter, Trevor R.; Tsutsui, Takako – Journal of Intellectual & Developmental Disability, 2009
Background: As part of an international, multicentre project, the service and support needs of Australian family carers were investigated. Method: A sample of 1,390, 448 family carers completed a self-report survey, including an adaptation of the Family Needs Survey (FNS) and several open-ended questions. A mixed method design was used, employing…
Descriptors: Family Needs, Access to Information, Respite Care, Foreign Countries
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Young, April; Ruble, Lisa; McGrew, John – Research in Autism Spectrum Disorders, 2009
Very little research has been conducted on insurance type (private vs. public funded) and costs, accessibility, and use of services of children with autism. Analysis of five parent reported outcomes: (a) out-of-pocket expenditures, (b) variety of services used, (c) access to services, (d) child and family service outcomes, and (e) satisfaction…
Descriptors: Autism, Caregivers, Behavior Modification, Speech Language Pathology
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Sullivan, Ruth Christ – Journal of Autism and Developmental Disorders, 1979
An article is presented on the "burn-out" of parents, particularly those of autistic children (i.e., the exhaustion of their psychological and/or physical resources as a result of long and intense caring for their children), along with the comments and responses of five parents and professionals. (DLS)
Descriptors: Autism, Coping, Emotional Adjustment, Parent Attitudes
Rimstidt, Suzie – Exceptional Parent, 1983
Parents of severely disabled or chronically ill children need to find competent baby-sitters for respite as well as opportunities to spend time with other family members. Baby-sitters, who may be found among supportive professionals, community groups, and college sutdents, may be trained to deal with specific child care concerns. (CL)
Descriptors: Child Caregivers, Parents, Respite Care, Severe Disabilities
Cobb, Polyxane S. – Exceptional Parent, 1987
Designed for parents who wish to develop local respite care services for families with disabled children, this primer outlines strategies for: evaluating current available services and programs; pulling people together; conducting a needs assessment; raising money; and writing a proposal. (CB)
Descriptors: Children, Coping, Disabilities, Needs Assessment
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Aldgate, Jane – Children & Society, 1998
Explored use of respite care by 60 families to help prevent family breakdown. Found that after nine months, parents were more in control of their lives and had reduced family problems. Ninety-two percent of families remained intact. Social workers were more satisfied with the intervention in less-complex than in more-complex cases. Children…
Descriptors: Caregiver Child Relationship, Case Studies, Children, Family Programs
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