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EPIC-CP 先导试验研究方案:一项多中心、随机对照试验,旨在调查社会处方对澳大利亚脑瘫儿童的可行性和可接受性。

EPIC-CP pilot trial study protocol: a multicentre, randomised controlled trial investigating the feasibility and acceptability of social prescribing for Australian children with cerebral palsy.

机构信息

Community Paediatrics Research Group, Central Clinical School, The University of Sydney, Faculty of Medicine and Health, Sydney, New South Wales, Australia

Population Child Health Clinical Research Group, University of New South Wales Medicine & Health, Sydney, New South Wales, Australia.

出版信息

BMJ Open. 2024 Jul 13;14(7):e076304. doi: 10.1136/bmjopen-2023-076304.

Abstract

INTRODUCTION

The social determinants of health contribute to poorer health outcomes for children with cerebral palsy (CP) and are barriers to families accessing health services. At an individual level, social determinants of health are experienced as unmet social needs, for example, unsafe housing conditions. There is emerging evidence that clinical pathways for the systematic identification and referral to services for unmet social needs can support families to address these needs. These clinical pathways have not been implemented for children with CP. The objectives are to investigate the feasibility and acceptability of two co-designed social needs clinical pathways for parents/caregivers of children with CP-social prescribing (ie, Community Linker plus resource pack) compared with resource pack only.

METHODS AND ANALYSIS

This pilot randomised controlled trial will run at the three tertiary paediatric rehabilitation services in New South Wales, Australia. A total of 120 participants will be recruited, with randomisation stratified by study site. A survey tool will be used to identify families experiencing unmet social needs. Parents/caregivers who report one or more unmet social need/s and consent will be eligible. The active control group will receive a resource pack containing information on community services to support unmet social needs. The social prescribing intervention group will receive one-on-one Community Linker support, in addition to the resource pack. The survey tool, intervention, logic model, and resource pack were co-designed with patient families and their healthcare workers. Feasibility of the research design and the clinical pathways will be evaluated using the number/proportion of parents/caregivers who complete the survey tool, consent, engage with the intervention, and complete research measures. Acceptability will be evaluated using questionnaires and qualitative interviews.

ETHICS AND DISSEMINATION

Human research ethics approval was granted by the Sydney Children's Hospitals Network Human Research Ethics Committee (2022/ETH01688). Participants and stakeholders will receive updates and findings via regular communication channels including meetings, presentations, and publications.

TRIAL REGISTRATION NUMBER

Australia New Zealand Clinical Trials Registry: 12622001459718.

摘要

简介

健康的社会决定因素导致脑瘫(CP)患儿的健康结果较差,并且是家庭获得卫生服务的障碍。在个人层面上,健康的社会决定因素表现为未满足的社会需求,例如不安全的住房条件。有新的证据表明,用于系统识别和转介未满足的社会需求服务的临床途径可以支持家庭满足这些需求。这些临床途径尚未应用于脑瘫患儿。本研究的目的是调查两种共同设计的 CP 患儿父母/照顾者的社会需求临床途径(即社区联络者加资源包)与仅资源包相比的可行性和可接受性,社区联络者即提供社区资源信息和转介服务。

方法和分析

这项试点随机对照试验将在澳大利亚新南威尔士州的三个三级儿科康复服务机构进行。共招募 120 名参与者,按研究地点进行分层随机分组。调查工具将用于识别经历未满足社会需求的家庭。报告一个或多个未满足的社会需求/并同意的父母/照顾者有资格参加。主动对照组将获得一个包含社区服务信息的资源包,以支持未满足的社会需求。社会处方干预组除了资源包外,还将接受一对一的社区联络者支持。调查工具、干预措施、逻辑模型和资源包是与患者家庭及其医疗保健工作者共同设计的。研究设计和临床途径的可行性将通过完成调查工具、同意、参与干预和完成研究措施的父母/照顾者的数量/比例来评估。可接受性将通过问卷调查和定性访谈进行评估。

伦理和传播

悉尼儿童医院网络人类研究伦理委员会已批准人体研究伦理(2022/ETH01688)。参与者和利益相关者将通过定期沟通渠道(包括会议、演示和出版物)获得更新和研究结果。

试验注册

澳大利亚和新西兰临床试验注册中心:12622001459718。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6cc4/11255413/e9e0559b6e8a/bmjopen-14-7-g001.jpg

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