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Cerebral Palsy: The Caregiver’s Point Of View About Physiotherapy In Children | 44678
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Background: Cerebral palsy is described as a group of movement and posture disorders as a result of non-progressive lesions,
which occur in the still maturing nervous system. It is also called childhood chronic non-progressive encephalopathy, being
a health condition that results in changes of the structure and function of the neuromusculoskeletal system. Several studies
have already stated that caregivers approve services and therapists who can talk clearly and explain what they are doing during
therapy.
Objective: The aim of this study was to assess the overall knowledge of the caregiver regarding cerebral palsy (CP) and aspects
of the physiotherapeutic treatment used in children with CP.
Methods: For this, a qualitative study was conducted at the Bettina Ferro de Souza University Hospital (HUBFS) of the Federal
University of Para, Brazil. The data collection method chosen was the semi-structured interview, due to this methodology five
caregivers of children (maximum of thirteen years) diagnosed with cerebral palsy; who had regularly performed physiotherapy
in the department for at least three months were included in the study interviewed. The questions explored the caregiver’s
knowledge about the disease and the role of physiotherapy in cerebral palsy with a total of five questions. The interviews were
recorded and later transcribed. The data analysis was performed through contents analysis. The results obtained from the
interviews were organized and discussed according to the order of the questions asked in the study with the statements of the
caregivers categorized and grouped according to theme.
Results: Even though caregivers observe great improve regarding motor function, the low level of knowledge of caregivers
about the disease and its physiotherapeutic treatment can be observed in the results, which can compromise the treatment
and the evolution of the children, given that continuous treatment is required in this condition for improving quality of life of
children with CP.
Conclusion: As a conclusion, caregivers expressed satisfaction about the service, however more professional caregiver patient
learning and teaching interaction is necessary to increase the caregiver’s knowledge of the disease and physiotherapeutic
treatment.
Biography
Taiane do Socorro Silva Natividade is currently an Undergraduate Student at Federal Univer-sity of Para, Brazil and also an exchange student at Semmelweis University, Hungary.
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