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Pretorius, Chrisma; Steadman, Jacqui – Child Care in Practice, 2018
Family members of children with disabilities have become more involved in their children's care and have adopted the role of primary caregiver. Due to the varying degrees of the condition, children with cerebral palsy (CP) often require greater involvement from their caregivers. Fifteen caregivers for children with CP residing in rural communities…
Descriptors: Child Rearing, Rural Areas, Cerebral Palsy, Foreign Countries
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
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

Rimmerman, A.; And Others – International Journal of Rehabilitation Research, 1989
This study of 78 mothers of mentally retarded children and adults found that respite care acts as a differential service that can enhance coping resources and is of most benefit to high self-esteem mothers of young developmentally disabled children, especially as a home-based model. (Author/JDD)
Descriptors: Child Rearing, Coping, Developmental Disabilities, Home Programs

Abelson, A. Geoffrey – Focus on Autism and Other Developmental Disabilities, 1999
A respite care needs assessment survey was completed by 574 Iowa families of children with developmental disabilities. Results documented a void in the availability and accessibility of respite services regardless of demography, income level, or extent of disability. Respondents generally perceived that the availability of respite care service…
Descriptors: Child Rearing, Developmental Disabilities, Family Needs, Family Problems
Families of Children with Disabilities: A Review of Literature and Recommendations for Interventions
Neely-Barnes, Susan L.; Dia, David A. – Journal of Early and Intensive Behavior Intervention, 2008
Children with disabilities receive most of their support from families. While most family caregivers are mothers or fathers, grandparents are increasingly providing care for children with disabilities. In addition, family caregivers come from diverse cultural backgrounds that impact their views on disability. This paper reviews the literature on…
Descriptors: Caregivers, Disabilities, Literature Reviews, Parents
Brodin, Jane – 1995
This study surveyed how respite care services functioned for Swedish families who have children with disabilities and compared the results with a previous study made 6 years earlier. The study was based on a questionnaire completed by 245 of Sweden's municipalities. The study examined the quantity and quality of the services and respondents' views…
Descriptors: Child Rearing, Disabilities, Family Needs, Foreign Countries
Douma, J. C. H.; Dekker, M. C.; Koot, H. M. – Journal of Intellectual Disability Research, 2006
Background: Parents of children and adolescents with both intellectual disabilities (ID) and psychopathology often experience high levels of parenting stress. To support these parents, information is required regarding the types of support they need and whether their needs are met. Method: In a sample of 745 youths (aged 10-24 years) with moderate…
Descriptors: Parents, Psychopathology, Child Rearing, Anxiety
Petr, Christopher G.; Barney, David D. – 1991
In focus group interviews, 39 parents of children (ages birth to 21 years) with developmental disabilities, emotional disorders, and technology-supported needs shared their perspectives regarding special needs, crisis situations, and parent/professional relationships. The purpose of the study was to determine what is necessary to keep children…
Descriptors: Child Advocacy, Child Rearing, Children, Crisis Intervention
Drummond, Jane; McDonald, Linda; MacKenzie-Keating, Sandra; Fleming, Darcy – Developmental Disabilities Bulletin, 2004
This longitudinal study inventoried the types of services accessed by a sample of Alberta families of children with or at-risk for disabilities. We explored the role of severity of disability, parental stress, and family income on services accessed. With few exceptions, services were accessed more frequently as the children's lives progressed but…
Descriptors: Integrated Services, Family Income, Disabilities, Foreign Countries