Roessingh Research and Development, Institute for Research in Rehabilitation Medicine and Technology, Enschede, The Netherlands.
Int J Integr Care. 2012 Jan-Mar;12:e9. doi: 10.5334/ijic.672. Epub 2012 Mar 6.
To improve communication in the integrated care setting of children with cerebral palsy, we developed a web-based system for parent-professional and inter-professional communication. The present study aimed to evaluate parents' experiences regarding the system's contribution to their communication with professionals during a six-months pilot in three Dutch care regions. In addition, factors associated with parents' system use and non-use were analyzed.
The system's functional specifications were based on key elements of the Chronic Care Model and quality dimensions formulated by the Institute of Medicine. At baseline, parents completed a T0-questionnaire on their experiences regarding sufficiency of contact, accessibility of professionals, timeliness of information exchange, consistency of information and parents' role as messenger of information and/or care coordinator. After the pilot, parents completed a T1-questionnaire on their experiences regarding the system's contribution to each of these aspects.
Of the 30 participating parents 21 had used the system, of which 20 completed the T1-questionnaire. All these parents indicated that they had experienced a contribution of the system to parent-professional communication, especially with respect to accessibility of professionals, sufficiency of contact and timeliness of information exchange, and to a lesser extent consistency of information and parents' messenger/coordinator role. In comparison with non-users, users had less positive baseline experiences with accessibility and a higher number of professionals in the child's care network.
All users indicated a contribution of the system to parent-professional communication, although the extent of the experienced contribution varied considerably. Based on the differences found between users and non-users, further research might focus on the system's value for complex care networks and problematic access to professionals.
为了改善脑性瘫痪儿童综合护理环境中的沟通,我们开发了一个基于网络的家长与专业人员及专业间沟通系统。本研究旨在评估父母在荷兰三个护理区域进行的六个月试点期间,对系统在与专业人员沟通方面的贡献的体验。此外,还分析了与父母系统使用和未使用相关的因素。
系统的功能规范基于慢性护理模型的关键要素和医学研究所制定的质量维度。在基线时,父母完成了一份关于他们在接触的充分性、专业人员的可及性、信息交换的及时性、信息的一致性以及父母作为信息传递者和/或护理协调员的角色方面的体验的 T0 问卷。在试点后,父母完成了一份关于系统对这些方面的贡献的 T1 问卷。
在 30 名参与的父母中,有 21 名使用了系统,其中 20 名完成了 T1 问卷。所有这些父母都表示,他们体验到了系统对家长与专业人员沟通的贡献,特别是在专业人员的可及性、接触的充分性和信息交换的及时性方面,在信息的一致性和父母作为信息传递者/协调员的角色方面则稍逊一筹。与非使用者相比,使用者在基线时对可及性的体验更为积极,并且孩子的护理网络中的专业人员数量更多。
所有使用者都表示系统对家长与专业人员的沟通有贡献,尽管体验到的贡献程度差异很大。基于使用者和非使用者之间发现的差异,进一步的研究可能集中在系统对复杂护理网络和专业人员难以获得的价值。