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Showing 1 to 15 of 29 results Save | Export
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Sari Bar; Sara B. Stephens; M. Sunil Mathew; Sarah E. Messiah; Veronica Bordes Edgar – Journal of Autism and Developmental Disorders, 2024
Caregivers of children with attention deficit-hyperactivity disorder (ADHD) and autism spectrum disorder (ASD) experience more stress than caregivers of typically developing children but there is limited research evaluating caregivers' quality of life (QoL). This study aimed to describe the association of caregiver QoL in children with ASD and/or…
Descriptors: Caregivers, Quality of Life, Child Rearing, Attention Deficit Hyperactivity Disorder
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Olthof-Nefkens, Maria W. L. J.; Derksen, Els W. C.; Debets, Frieda; de Swart, Bert J. M.; Nijhuis-van der Sanden, Maria W. G.; Kalf, Johanna G. – International Journal of Language & Communication Disorders, 2023
Background: Communication difficulties are common in people with dementia, and often present from an early stage. However, direct treatment options for people with dementia that positively influence their daily communication are scarce. Aims: To evaluate the potential impact and feasibility of a personalized logopaedic intervention. Methods &…
Descriptors: Dementia, Caregivers, Interpersonal Communication, Communication Disorders
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Nesser, Whitney; Grace Yi, Eun-Hye; Wotring, Amy J.; Hutchins, Matthew D.; Snyder, Scott – American Journal of Health Education, 2023
Background: Significant advances in the treatment of Cystic Fibrosis (CF) have extended life expectancy, increasing the number of CF caregivers who deliver demanding daily treatment regimens and manage uncertainty. With the impact these changes have on CF caregivers, it is critical to understand CF caregiver quality of life (QoL). Purpose: To…
Descriptors: Quality of Life, Chronic Illness, Genetic Disorders, Caregivers
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Sheppard-Jones, Kathy; Kleinert, Harold; Butler, Laura; Li, Jian; Moseley, Emily; Adams, Chithra – Intellectual and Developmental Disabilities, 2022
This study reports on the results of an online survey of direct support professionals (DSPs) during the COVID-19 pandemic in June 2020 to measure their perceived quality of life, stressors, coping/resilience skills, and knowledge of health care rights directly related to the pandemic for the persons that they support. Specifically, we examined…
Descriptors: Allied Health Personnel, Caregivers, COVID-19, Pandemics
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Grey, Jillian M.; Totsika, Vasiliki; Hastings, Richard P. – Journal of Intellectual & Developmental Disability, 2020
Background: Placement behaviours of families of adults with intellectual disabilities has received little or no attention of researches to date. Methods: A prospective design was adopted to examine changes in placement decisions of 75 family carers over a 12-month period. Factors associated with changes were also examined. Results: Over 12 months,…
Descriptors: Placement, Adults, Intellectual Disability, Caregivers
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Ezeamama, Amara E.; Zalwango, Sarah K.; Tuke, Robert; Pad, Ricki Lauren; Boivin, Michael J.; Musoke, Philippa M.; Giordani, Bruno; Sikorskii, Alla – New Directions for Child and Adolescent Development, 2020
Caregiver's and child's self-reported quality of life (QOL) was defined using standardized questionnaires in a sample (N = 277) of 6-10 years old HIV-infected, HIV-exposed uninfected, and HIV-unexposed uninfected children from Uganda. Psychosocial stress (acute stress and cumulative lifetime adversity) and physiologic stress (dysregulations across…
Descriptors: Stress Variables, Stress Management, Quality of Life, Children
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Singh, Nirbhay N.; Lancioni, Giulio E.; Medvedev, Oleg N.; Hwang, Yoon-Suk; Myers, Rachel E.; Townshend, Kishani – International Journal of Developmental Disabilities, 2020
Objectives: Caring for individuals with intellectual disabilities (ID) or autism spectrum disorder (ASD) can be gratifying as well as stressful. Professional staff employed as caregivers often report compromised mental and physical wellbeing due to the stressful nature of working with clients who exhibit aggressive and destructive behaviors.…
Descriptors: Intellectual Disability, Quality of Life, Metacognition, Caregivers
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Oruche, Ukamaka Marian; Robb, Sheri L.; Draucker, Claire Burke; Aalsma, Matt; Pescosolido, Bernice; Chacko, Anil; Ofner, Susan; Bakoyannis, Giorgos; Brown-Podgorski, Brittany – Child & Youth Care Forum, 2018
Background: Caregivers of adolescents diagnosed with Oppositional Defiant Disorder and/or Conduct Disorder (ODD/CD) experience unique challenges when interacting with child service systems involved in their adolescents' care. Absent from the literature are interventions to improve these interactions, which in the long term may improve adolescent…
Descriptors: Caregivers, Adolescents, Behavior Disorders, Intervention
Lin, Chien-chun – ProQuest LLC, 2016
Caring for a family member with intellectual developmental disability (IDD) often results in many negative impacts, such as higher levels of stress and depression, physical and/or mental issues, lower level of support, lower financial capacity, as well as less positive or more pessimistic views of their child's future, and an overall lower level…
Descriptors: Caregivers, Family Role, Intellectual Disability, Developmental Disabilities
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Herrema, Renske; Garland, Deborah; Osborne, Malcolm; Freeston, Mark; Honey, Emma; Rodgers, Jacqui – Journal of Autism and Developmental Disorders, 2017
Family members are often the primary caregiver for autistic adults and this responsibility may impact on the carer's wellbeing and quality of life. 109 family members of autistic adults completed an online survey assessing their wellbeing relating to their caring role for their autistic relative. Family members who were supporting an autistic…
Descriptors: Well Being, Mental Health, Family Environment, Adults
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Carona, C.; Crespo, C.; Canavarro, M. C. – Research in Developmental Disabilities: A Multidisciplinary Journal, 2013
This study had two main objectives: first, to examine the direct and indirect effects, via social support, of caregiving burden on the adaptation outcomes of children/adolescents with cerebral palsy and their parents; and second, to assess the invariance of such models in clinical vs. healthy subsamples. Participants were 210 dyads of…
Descriptors: Adjustment (to Environment), Adolescents, Parent Child Relationship, Quality of Life
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Khanna, Rahul; Madhavan, S. Suresh; Smith, Michael J.; Tworek, Cindy; Patrick, Julie H.; Becker-Cottrill, Barbara – Autism: The International Journal of Research and Practice, 2012
The purpose of this study was to test the psychometric properties of the Caregiver Strain Questionnaire (CGSQ) among caregivers of children with autism. The CGSQ was originally developed to assess burden experienced by parents of children and adolescents with serious emotional and behavioral disorders. Study data was collected from 304 primary…
Descriptors: Autism, Quality of Life, Caregivers, Test Validity
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Yoong, A.; Koritsas, S. – Journal of Intellectual Disability Research, 2012
Background: Because of an increase in life expectancy and de-institutionalisation, many adults with intellectual disability (ID) live with and are cared for by their parents throughout their adult lives. Because of caring demands, the quality of life (QOL) of parents may be affected. The study explored the impact of caring for an adult with ID on…
Descriptors: Mental Retardation, Quality of Life, Questionnaires, Employment Opportunities
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Weiss, Jonathan A.; Lunsky, Yona – Journal of Child and Family Studies, 2011
Parents of individuals with autism spectrum disorders (ASD) often experience stressors associated with caring for their child. These stressors can cause considerable distress for families, which at times can develop into full blown crisis, and it is important that professionals be able to quickly identify when families are approaching or are in…
Descriptors: Aggression, Autism, Quality of Life, Caregivers
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Gerkensmeyer, Janis E.; Perkins, Susan M.; Day, Jennifer; Austin, Joan K.; Scott, Eric L.; Wu, Jingwei – Journal of Child and Family Studies, 2011
As primary caregivers of children with mental health problems, mothers face challenges that put them at risk for depression, which is rarely identified or addressed. The aims of this paper were to (a) identify mean differences among demographic, stressor, threat, and resource variables specified in a theoretical model and thought to be associated…
Descriptors: Parent Child Relationship, Mothers, Quality of Life, Caregivers
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