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Children's Services
Social Policy, Research, and Practice
Volume 5, 2002 - Issue 2
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Original Articles

The Influence of Respite Care on Psychological Distress in Parents of Children With Developmental Disabilities: A Longitudinal Study

Pages 123-138 | Published online: 15 Jun 2010

Keep up to date with the latest research on this topic with citation updates for this article.

Read on this site (4)

Elizabeth Spruin, Nicola Abbott & Nicole Holt. (2018) Examining the Experiences of a Short Break Scheme amongst Adolescents with Disabilities (Service Users) and their Parents. International Journal of Disability, Development and Education 65:2, pages 148-162.
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CarlL. Algood, Cynthia Harris & Jun Sung Hong. (2013) Parenting Success and Challenges for Families of Children with Disabilities: An Ecological Systems Analysis. Journal of Human Behavior in the Social Environment 23:2, pages 126-136.
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Yueh‐Ching Chou, Ping‐Yi Tzou, Cheng‐Yun Pu, Teppo Kröger & Wan‐Ping Lee. (2008) Respite care as a community care service: Factors associated with the effects on family carers of adults with intellectual disability in Taiwan. Journal of Intellectual & Developmental Disability 33:1, pages 12-21.
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Lisa J. Meltzer & Suzanne Bennett Johnson. (2004) Summer Camps for Chronically Ill Children: A Source of Respite Care for Mothers. Children's Health Care 33:4, pages 317-331.
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Articles from other publishers (20)

Shaneha Patel, Mélina Rivard, Catherine Mello & Diane Morin. (2022) Parenting stress within mother-father dyads raising a young child with autism spectrum disorder. Research in Autism Spectrum Disorders 99, pages 102051.
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Marielle Weyland, Pauline Maes, Mikhail Kissine & Pierre Defresne. (2022) Impact of Belgian COVID-19 lockdown restrictions on autistic individuals’ socio-communicative behaviors and their parents’ quality of life. PLOS ONE 17:8, pages e0273932.
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Genevieve Graaf, Philip Baiden, George Boyd & Latocia Keyes. (2022) Barriers to Respite Care for Children with Special Health Care Needs. Journal of Developmental & Behavioral Pediatrics 43:3, pages 117-129.
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Petra Benešová & Lucie Sikorová. (2021) How do parents of children with disabilities perceive stresss and burden in comparison with parents of children without a disabilities. Pediatrie pro praxi 22:6, pages 417-419.
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Pamela K. DonohueErin P. WilliamsLaura Wright-SextonRenee D. Boss. (2018) “It's Relentless”: Providers' Experience of Pediatric Chronic Critical Illness. Journal of Palliative Medicine 21:7, pages 940-946.
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Kim E. Whitmore. (2017) The Concept of Respite Care. Nursing Forum 52:3, pages 180-187.
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Cameron L. Neece & Neilson Chan. 2017. Parental Stress and Early Child Development. Parental Stress and Early Child Development 107 124 .
Michelle Norton, Tina Taylor Dyches, James M. Harper, Susanne Olsen Roper & Paul Caldarella. (2016) Respite Care, Stress, Uplifts, and Marital Quality in Parents of Children with Down Syndrome. Journal of Autism and Developmental Disorders 46:12, pages 3700-3711.
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Kim E. Whitmore. (2016) Respite Care and Stress Among Caregivers of Children With Autism Spectrum Disorder: An Integrative Review. Journal of Pediatric Nursing 31:6, pages 630-652.
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Tina Taylor Dyches, Ruthann Christensen, James M. Harper, Barbara Mandleco & Susanne Olsen Roper. (2015) Respite Care for Single Mothers of Children with Autism Spectrum Disorders. Journal of Autism and Developmental Disorders 46:3, pages 812-824.
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Brandi Lindsey. (2016) Therapeutic Camps and Their Impact on the Family of Children with Special Health Care Needs: A Mixed Method Study. Open Journal of Nursing 06:09, pages 722-740.
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Sylvie Tétreault, Sophie Blais-Michaud, Pascale Marier Deschênes, Pauline Beaupré, Hubert Gascon, Normand Boucher & Monique Carrière. (2014) How to support families of children with disabilities? An exploratory study of social support services. Child & Family Social Work 19:3, pages 272-281.
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최희경. (2014) A Phenomenological Study on Experiences of Participants in Parents' Movement of Children with Developmental Disabilities. Family and Culture 26:2, pages 38-79.
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Geneviève Piérart, Sylvie Tétreault, Pascale Marier Deschênes & Sophie Blais-Michaud. (2014) Handicap, famille et soutien. Regard croisé Québec-Suisse. Enfances, Familles, Générations:20, pages 128-147.
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Karine N. Tremblay, Alain Côté, Lise Lachance & Louis Richer. (2012) Utilisation des services en déficience intellectuelle et satisfaction des parents à leur égard. Revue francophone de la déficience intellectuelle 23, pages 56-63.
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Janet Robertson, Chris Hatton, Emma Wells, Michelle Collins, Susanne Langer, Vicki Welch & Eric Emerson. (2011) The Impacts of short break provision on families with a disabled child: an international literature review. Health & Social Care in the Community 19:4, pages 337-371.
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Julie A. Strunk. (2010) Respite Care for Families of Special Needs Children: A Systematic Review. Journal of Developmental and Physical Disabilities 22:6, pages 615-630.
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Hedda Meadan, James W. Halle & Aaron T. Ebata. (2010) Families with Children Who Have Autism Spectrum Disorders: Stress and Support. Exceptional Children 77:1, pages 7-36.
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Beth M. Lessenberry & Ruth Anne Rehfeldt. (2016) Evaluating Stress Levels of Parents of Children with Disabilities. Exceptional Children 70:2, pages 231-244.
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Irene Carter & Rob Wilson. (2006) Reflections on Face-to-Face and Online Self-Help Group Participation: Comparing the Views of Persons with Autism with Those of Parents Speaking for Their Autistic Children. International Journal of Self Help and Self Care 5:4, pages 353-369.
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