Literature DB >> 28083952

Family-oriented services in pediatric rehabilitation: a scoping review and framework to promote parent and family wellness.

G King1, L Williams2, S Hahn Goldberg3.   

Abstract

Family-oriented services are not as common as one would expect, given the widespread endorsement of family-centred care, the role of parents in supporting optimal child outcomes, and legislation and literature indicating that parent outcomes are important in their own right. There are no published service delivery frameworks describing the scope of services that could be delivered to promote parent and family wellness. A scoping review was conducted to identify types of family-oriented services for parents of children with physical disabilities and/or intellectual impairments. This information was then synthesized into a conceptual framework of services to inform service selection and design. A scoping review of the recent literature was performed to capture descriptions of services targeting parents/families of children with physical disabilities and/or intellectual impairments, published in a six-year period (2009 to 2014). Six databases were searched and 557 retrieved articles were screened using inclusion and exclusion criteria. Thirty six relevant articles were identified. Based on descriptions of services in these articles, along with seminal articles describing the nature of desirable services, we propose a needs-based and capacity-enhancing framework outlining a continuum of family-oriented services for parents of children with disabilities. The framework includes six types of services to meet parent/family needs, organized as a continuum from fundamental information/education services, to those supporting parents to deliver services to meet their child's needs, to a variety of services addressing parents' own needs (support groups, psychosocial services and service coordination). The framework provides pediatric rehabilitation service organizations with a way to consider different possible family-oriented services. Implications include the particular importance of providing information resources, support groups and psychosocial services to meet parents' needs, enhance capacity and promote family wellness. There is also an opportunity to provide composite parent-child services to address the needs of both parents and children.
© 2017 John Wiley & Sons Ltd.

Entities:  

Keywords:  caregiver needs; disability; engagement; family; outcomes; parent; service delivery; service design

Mesh:

Year:  2017        PMID: 28083952     DOI: 10.1111/cch.12435

Source DB:  PubMed          Journal:  Child Care Health Dev        ISSN: 0305-1862            Impact factor:   2.508


  12 in total

Review 1.  Barriers to the access of people with disabilities to health services: a scoping review.

Authors:  Karina Aparecida Padilha Clemente; Simone Vieira da Silva; Gislene Inoue Vieira; Maritsa Carla de Bortoli; Tereza Setsuko Toma; Vinícius Delgado Ramos; Christina May Moran de Brito
Journal:  Rev Saude Publica       Date:  2022-07-01       Impact factor: 2.772

2.  Family-centred care in early intervention: Examining caregiver perceptions of family-centred care and early intervention service use intensity.

Authors:  Beth M McManus; Natalie J Murphy; Zachary Richardson; Mary A Khetani; Margaret Schenkman; Elaine H Morrato
Journal:  Child Care Health Dev       Date:  2019-12-18       Impact factor: 2.508

3.  Functioning and Disability Profile of Children with Microcephaly Associated with Congenital Zika Virus Infection.

Authors:  Haryelle Náryma Confessor Ferreira; Veronica Schiariti; Isabelly Cristina Rodrigues Regalado; Klayton Galante Sousa; Silvana Alves Pereira; Carla Patrícia Novaes Dos Santos Fechine; Egmar Longo
Journal:  Int J Environ Res Public Health       Date:  2018-05-29       Impact factor: 3.390

Review 4.  Parenting a Child with a Neurodevelopmental Disorder.

Authors:  Peter L Rosenbaum; Monika Novak-Pavlic
Journal:  Curr Dev Disord Rep       Date:  2021-11-20

5.  Information and Empowerment of Families of Children With Cerebral Palsy in Brazil: The Knowledge Translation Role of Nossa Casa Institute.

Authors:  Marina J Airoldi; Beatriz S Vieira; Rachel Teplicky; Deborah Chalfun; Rafael G A S Bonfim; Marisa C Mancini; Peter Rosenbaum; Marina B Brandão
Journal:  Front Rehabil Sci       Date:  2021-07-19

6.  Parental involvement and empowerment in paediatric critical care: Partnership is key!

Authors:  Agnes van den Hoogen; Marjolijn Ketelaar
Journal:  Nurs Crit Care       Date:  2022-05       Impact factor: 2.897

7.  Reconceptualizing the Family to Improve Inclusion in Childhood Disability Research and Practice.

Authors:  Michelle Phoenix; Meaghan Reitzel; Rachel Martens; Jeanine Lebsack
Journal:  Front Rehabil Sci       Date:  2021-09-10

8.  Role of parents in fatigue of children with a chronic disease: a cross-sectional study.

Authors:  Niels Kramer; Sanne L Nijhof; Elise M van de Putte; Marjolijn Ketelaar; Martha A Grootenhuis; Kors van der Ent; Joost F Swart; Martine van Grotel; Geertje W Dalmeijer; Merel M Nap-van der Vlist
Journal:  BMJ Paediatr Open       Date:  2021-05-21

9.  Mental Health and Health Behaviour Changes for Mothers of Children with a Disability: Effectiveness of a Health and Wellbeing Workshop.

Authors:  Helen M Bourke-Taylor; Kahli S Joyce; Sarah Grzegorczyn; Loredana Tirlea
Journal:  J Autism Dev Disord       Date:  2021-03-16

10.  Family-centeredness of services for young children with Down syndrome: an observational study from Turkey

Authors:  Emine Bahar Bingöler Pekcici; Ezgi Özalp Akin; Funda Akpinar; Gamze Hayran; Cansu Keleş; Betül Yağbasan; Nazmiye Kurşun; İlgi Ertem
Journal:  Turk J Med Sci       Date:  2021-02-26       Impact factor: 0.973

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