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首页> 外文期刊>Child: care, health and development >Two sides of the mirror: parents' and service providers' view on the family-centredness of care for children with cerebral palsy.
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Two sides of the mirror: parents' and service providers' view on the family-centredness of care for children with cerebral palsy.

机译:镜子的两面:父母和服务提供者对以家庭为中心的脑瘫儿童照料的看法。

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BACKGROUND: In order to best meet the needs of both families and their children with cerebral palsy, many rehabilitation service providers have adopted a family-centred service (FCS) approach. In FCS parents are seen as experts on their child's needs, and the family and professionals collaborate in the rehabilitation process. However, parents and service providers might look at FCS from different points of view, i.e. look into the mirror from two different sides. The objective of this study was to explore the degree to which parents experience the service as being family-centred and to which extent the service providers experience their service provision as family-centred. METHODS: A translated version of The Measure of Processes of Care 20 (MPOC-20) questionnaire was used to evaluate parents' experience of FCS, and a Measures of Processes of Care for Service Providers (MPOC-SP) questionnaire was used to evaluate the FCS provided by professionals. Parents visiting two university hospital neuropediatric wards (n= 67) during a 2-month period and who were willing to participate received the questionnaire. Also the service providers working on the same wards (n= 49) were invited to participate. RESULTS: A total of 53 families and 29 service providers completed the questionnaires. Both parents and professionals generally rated the FCS positively. General information was rated lowest and respectful treatment the highest by both parents and professionals. The results revealed that written information about the child's condition, the possibility to choose when to receive information, and contact with other families in the same situation are areas in need of improvement. CONCLUSIONS: The possibility to regularly evaluate services both from the families' and the professionals' perspectives should be part of quality development. Providing general information is a challenge for all service providers. The MPOC questionnaires can be used to highlight important areas of improvement in FCS.
机译:背景:为了最好地满足家庭及其患脑瘫儿童的需求,许多康复服务提供者采用了以家庭为中心的服务(FCS)方法。在FCS中,父母被视为满足孩子需求的专家,家庭和专业人士在康复过程中进行合作。但是,父母和服务提供商可能会从不同的角度看待FCS,即从两个不同的角度看镜子。这项研究的目的是探讨父母对服务的理解程度,以家庭为中心,服务提供者在多大程度上以家庭为中心来体验他们提供的服务。方法:使用翻译过的《护理过程测量标准》(MPOC-20)问卷评估父母对FCS的经历,并使用《服务提供者护理过程测量标准》(MPOC-SP)问卷评估父母的FCS经历。 FCS由专业人员提供。家长在两个月内访问了两个大学医院的神经儿科病房(n = 67),并且愿意参加调查。还邀请了在同一病房(n = 49)工作的服务提供商参加。结果:总共53个家庭和29个服务提供者完成了问卷。父母和专业人士通常对FCS给予积极评价。父母和专业人员对一般信息的评价最低,对父母的尊重也最高。结果表明,有关孩子状况的书面信息,选择何时接收信息的可能性以及与处于相同情况的其他家庭的联系都是需要改进的地方。结论:从家庭和专业人员的角度定期评估服务的可能性应该是质量发展的一部分。提供一般信息对于所有服务提供商都是一个挑战。 MPOC问卷可用于强调FCS改进的重要领域。

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