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Optimizing Management and Medication of Febrile Children in Out-of-hours Primary Care: CHILI Cluster RCT (CHILI)

2016年9月15日 更新者:Maastricht University Medical Center

Optimizing Management and Medication of Febrile Children in Out-of-hours Primary Care: the CHILI Cluster Randomised Trial

The CHILI cluster randomised controlled trial (RCT) will investigate whether the use of an interactive information booklet during consultations for febrile children at General Practice (GP) out-of-hours centres can reduce the number of antibiotic prescriptions, improve parental satisfaction and reduce intention to reconsult for childhood fever episodes.

研究概览

详细说明

A GP-parent information exchange tool in the form of an interactive booklet has the potential to provide parents with information about symptoms and fever management and consistent information during GP consultations. Thereby enhancing their self-management and providing them with safety net advice when they return home.

It is hypothesized that the use of such an interactive booklet during consultations for febrile children at GP out-of-hours centres will result in a reduced number of antibiotic prescriptions, improved parental satisfaction and reduced intention to re-consult.

The development of the interactive booklet concerned a three-stage process and is based on extensive qualitative work among parents, GPs and other professionals involved in childhood fever management. The booklet incorporates already existing information about fever, alarm symptoms, advice on use of medication and specific infectious diseases that frequently occur in childhood in combination with fever such as upper respiratory tract infections, and otitis media.

We will perform a cluster-randomised controlled trial at 20 GP out-of-hours centres in the Netherlands. GP out-of-hours centres will be stratified by size, to ensure equal distribution of size between the intervention and control group. The required number of clusters and participants was based on the following assumptions: (1) ICC of 0.01, (2) alpha of 0.05, power of 0.80, (3) proportion of antibiotic prescriptions in control group of 25% and a proportion of 19% in the intervention group (6% minimal clinical relevant difference) and (4) 10% loss to follow-up and 10% efficiency loss based on unequal cluster sizes. Based on a previous cohort study, we estimated to include 1000 children per cluster (GP out-of-hours centre) within six months, resulting in a need for 20 clusters and an effective sample size of 737 patients in the intervention and control group (1474 in total).

The booklet will be used during consultations with febrile children at the GP out-of-hours centres that are randomly allocated by computer to the intervention. The child's symptoms will determine which information and advice parents receive from the GP.

Statistical analysis will be performed based on intention to treat principle by performing multilevel logistic regression analysis using IBM SPSS version 21.0 and MLwiN software. We will determine independent factors associated with antibiotic prescriptions. The same will be done for secondary outcomes.

All data will be obtained, managed and monitored according to the guidelines of Good Clinical Practice.

研究类型

介入性

注册 (实际的)

1262

阶段

  • 不适用

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习地点

    • Limburg
      • Maastricht、Limburg、荷兰、6229 HA
        • Maastricht University

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

3个月 至 12年 (孩子)

接受健康志愿者

不

有资格学习的性别

全部

描述

Inclusion Criteria:

  • Age between three months and twelve years
  • GP decides this is a fever-related consultation

Exclusion Criteria:

  • Age under 3 months or over 12 years
  • GP decides this is NOT a fever-related consultation

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:治疗
  • 分配:随机化
  • 介入模型:并行分配
  • 屏蔽:双倍的

武器和干预

参与者组/臂
干预/治疗
实验性的:Intervention
All GPs working at the participating GP out-of-hours centres that are in the intervention group will use the GP-parent information-exchange tool (interactive booklet).
The booklet incorporates already existing information about fever, alarm symptoms, advices use of medication and specific infectious diseases that frequently occur in childhood in combination with fever such as upper respiratory tract infections, and otitis media. The difference with these existing sources of information is the fact that they until now, were not incorporated into one booklet which can be physically handed over to parents.
其他名称:
  • Interactive booklet
无干预:Control
All GPs working at the participating GP out-of-hours centres that are in the control group will provide care as usual.

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Antibiotic Prescription
大体时间:Baseline (Initial consultation)
Antibiotic prescriptions for febrile children in GP out-of-hours centres during the initial consultation (dichotomous scale; number of participants with an antibiotic prescription).
Baseline (Initial consultation)

次要结果测量

结果测量
措施说明
大体时间
Intention to re-consult
大体时间:Asked within two weeks after initial consultation
Intention to re-consult for similar illnesses among parents, number of parents with the intention to re-consult
Asked within two weeks after initial consultation
Parental satisfaction with care
大体时间:Asked within two weeks after initial consultation
VAS scale 1-10
Asked within two weeks after initial consultation
Self-reported adverse events related to the fever episode like hospital admission
大体时间:Asked within two weeks after initial consultation
Asked within two weeks after initial consultation
Antibiotic prescription rates at re-consultations
大体时间:Asked within two weeks after initial consultation
Prescription rates at re-consultations for the same illness episode (defined as a consultation for the same reason over the last two weeks)
Asked within two weeks after initial consultation
Consultation rates
大体时间:During complete study period, during 6 months of study completion
Consultation rates of fever related consultations of children below the age of 12 years between intervention and control groups, through 6 months of study completion.
During complete study period, during 6 months of study completion
Referral to secondary care
大体时间:Baseline (during initial consultation)
Number of participants with Referral to secondary care during initial consultation
Baseline (during initial consultation)

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

调查人员

  • 首席研究员:Eefje de Bont, MD, MSc、Research Institute CAPHRI, Department of Family Medicine, Maastricht University

出版物和有用的链接

负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。

一般刊物

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始

2015年11月1日

初级完成 (实际的)

2016年6月1日

研究完成 (实际的)

2016年6月1日

研究注册日期

首次提交

2015年10月26日

首先提交符合 QC 标准的

2015年10月30日

首次发布 (估计)

2015年11月3日

研究记录更新

最后更新发布 (估计)

2016年9月16日

上次提交的符合 QC 标准的更新

2016年9月15日

最后验证

2015年10月1日

更多信息

与本研究相关的术语

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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