Literature DB >> 28321280

Does an educational workshop have an impact on caregivers' levels of knowledge about cerebral palsy? A comparative, descriptive cross-sectional survey of Zimbabwean caregivers.

Jermaine M Dambi1, Celia Mandizvidza1, Matthew Chiwaridzo1, Clement Nhunzvi1, Cathrine Tadyanemhandu1.   

Abstract

BACKGROUND: The diagnosis of a child with a life-long disability, such as cerebral palsy (CP), can be catastrophic to parents. It is often accompanied by feelings of despair, anxiety, hopelessness, and the fear of the unknown. Knowledge about CP is thus essential for caregiver adjustment and preparation for the caregiving role. However, there is a paucity of empirical evidence regarding the best method for educating caregivers. The aim of this study was therefore to evaluate the impact of an educational intervention on caregivers' knowledge about cerebral palsy.
METHODS: This cross-sectional survey included 49 caregivers of children with cerebral palsy. Convenience sampling was used to select participants from two central hospitals in Harare, Zimbabwe. The caregivers were divided into two groups based on whether or not they had attended an educational workshop. The knowledge of cerebral palsy questionnaire (KCPQ) was administered once to assess the caregivers' CP knowledge.
RESULTS: The caregivers were comparable in terms of sociodemographic characteristics. The mean KCPQ scores for caregivers who attended workshops was 17.4 (SD 1.5), versus 13.8 (SD 2.5) for those without exposure to workshops. The differences between the two groups was statistically significant (U = 77.0, Z = -4.45, and P < 0.001).
CONCLUSIONS: Our findings suggest that educational workshops may lead to improved CP knowledge among caregivers. This may better equip parents and guardians to meet the extra caregiving demands associated with CP, leading to improved health outcomes for children with CP and their caregivers.

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Year:  2016        PMID: 28321280      PMCID: PMC5348609          DOI: 10.4314/mmj.v28i4.4

Source DB:  PubMed          Journal:  Malawi Med J        ISSN: 1995-7262            Impact factor:   0.875


  23 in total

1.  Parents' perceptions of disclosure of the diagnosis of cerebral palsy.

Authors:  G Baird; H McConachie; D Scrutton
Journal:  Arch Dis Child       Date:  2000-12       Impact factor: 3.791

Review 2.  Classification systems in cerebral palsy.

Authors:  Susan A Rethlefsen; Deirdre D Ryan; Robert M Kay
Journal:  Orthop Clin North Am       Date:  2010-10       Impact factor: 2.472

3.  The psychosocial well-being of parents of children with cerebral palsy: a comparison study.

Authors:  Anna Cheshire; Julie H Barlow; Lesley A Powell
Journal:  Disabil Rehabil       Date:  2010       Impact factor: 3.033

4.  Why do we need a diagnosis? A qualitative study of parents' experiences, coping and needs, when the newborn child is severely disabled.

Authors:  A H Graungaard; L Skov
Journal:  Child Care Health Dev       Date:  2007-05       Impact factor: 2.508

5.  Impact of caring for children with cerebral palsy on the general health of their caregivers in an African community.

Authors:  Tal-hatu K Hamzat; Eluemuno L Mordi
Journal:  Int J Rehabil Res       Date:  2007-09       Impact factor: 1.479

Review 6.  Proposed definition and classification of cerebral palsy, April 2005.

Authors:  Martin Bax; Murray Goldstein; Peter Rosenbaum; Alan Leviton; Nigel Paneth; Bernard Dan; Bo Jacobsson; Diane Damiano
Journal:  Dev Med Child Neurol       Date:  2005-08       Impact factor: 5.449

7.  Parents' reactions to the diagnosis of cerebral palsy: associations between resolution, age and severity of disability.

Authors:  C Schuengel; I C M Rentinck; J Stolk; J M Voorman; G M P Loots; M Ketelaar; J W Gorter; J G Becher
Journal:  Child Care Health Dev       Date:  2009-03-23       Impact factor: 2.508

8.  The other side of the story - maternal perceptions of safety advice and information: a qualitative approach.

Authors:  J Ablewhite; D Kendrick; M Watson; I Shaw
Journal:  Child Care Health Dev       Date:  2015-01-20       Impact factor: 2.508

Review 9.  Caregiving process and caregiver burden: conceptual models to guide research and practice.

Authors:  Parminder Raina; Maureen O'Donnell; Heidi Schwellnus; Peter Rosenbaum; Gillian King; Jamie Brehaut; Dianne Russell; Marilyn Swinton; Susanne King; Micheline Wong; Stephen D Walter; Ellen Wood
Journal:  BMC Pediatr       Date:  2004-01-14       Impact factor: 2.125

10.  Psychological impact of cerebral palsy on families: The African perspective.

Authors:  Olajide A Olawale; Abraham N Deih; Raphael Kk Yaadar
Journal:  J Neurosci Rural Pract       Date:  2013-04
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