Children with Cerebral Palsy in Bangladesh: Their Contribution to the Development of a Rehabilitation Training Programme

M. Zuurmond, Ilias Mahmud, S. Hartley
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Abstract

Purpose: Although cerebral palsy is the most prevalent health condition linked to childhood disability in Bangladesh, support and rehabilitation for this group is limited and intervention development is slow. An initiative to address these unmet needs was the development of a parent training programme for the rehabilitation of children with cerebral palsy. The aim of this study was to explore what was important in the everyday lives of children with cerebral palsy in rural Bangladesh and take their views into account in order to inform the parent/caregiver training programme. Methods: Qualitative data was collected from12 children with cerebral palsy, between 5 - 14 years of age.  The children were purposively selected from among those who attended the parent training programme. A participatory method called the ‘Feeling Dice’ was used to elicit children’s feelings about their everyday lives. The approach was easy to use, acceptable in the local context, the children enjoyed the activity, and it generated rich information.  Results: ‘Inclusion in play’ and ‘being able to attend school’ made the children happy and were their two main priorities, yet were not key issues for parents. The children were frustrated by their dependence on others for day-to-day activities such as feeding, bathing, and transport to school.  Children also played an important part in encouraging their parents to attend the training course. Conclusion: This study showed that valuable information can be gathered from children with cerebral palsy by using a simple and adaptable participatory research tool.  Children’s views and priorities sometimes differed from those of their parents and carers, and could be useful for developing more relevant and valid interventions.  Children need to be recognised as important ‘agents of change’ within their own rehabilitation. This methodology is in harmony with the UNCRPD recommendations, and supports inclusive and rights-based intervention development.
孟加拉脑瘫儿童:他们对发展康复训练计划的贡献
目的:虽然脑瘫是孟加拉国与儿童残疾有关的最普遍的健康状况,但对这一群体的支持和康复有限,干预措施进展缓慢。解决这些未得到满足的需求的一项倡议是,为脑瘫儿童的康复制定了一项家长培训方案。这项研究的目的是探索在孟加拉国农村脑瘫儿童的日常生活中什么是重要的,并考虑他们的意见,以便为父母/照顾者培训方案提供信息。方法:对12例5 ~ 14岁的脑瘫患儿进行定性分析。这些孩子是有意从参加家长培训方案的孩子中挑选出来的。一种名为“感觉骰子”的参与式方法被用来引出孩子们对日常生活的感受。这种方法易于使用,在当地环境中可以接受,孩子们喜欢这个活动,它产生了丰富的信息。结果:“融入游戏”和“能够上学”让孩子们快乐,这是他们的两个主要优先事项,但对父母来说并不是关键问题。孩子们对日常活动的依赖感到沮丧,比如吃饭、洗澡和上学的交通。孩子们在鼓励父母参加培训课程方面也发挥了重要作用。结论:本研究表明,使用一种简单、适应性强的参与式研究工具可以从脑瘫儿童中收集有价值的信息。儿童的观点和优先事项有时与他们的父母和照顾者不同,这可能有助于制定更相关和有效的干预措施。儿童需要在他们自己的康复过程中被视为重要的“变革推动者”。这一方法与《残疾人权利公约》的建议相一致,并支持包容性和基于权利的干预发展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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