ISRCTN23547970已完成未知
A feasibility randomised controlled trial investigating the clinical and cost effectiveness of a complex intervention to improve the management of children presenting to primary care with acute respiratory tract infection
niversity of Bristol (UK)0 个研究点目标入组 500 人开始时间: 2014年6月27日最近更新:
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 500
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 性别
- All
入选标准
- •Clinicians:
- •GPs and prescribing nurses are eligible to recruit children to the study
- •GP practices will be included if they have at least Internet Explorer version 8 on their IT systems
- •Children can be included into the study if they meet the following criteria:
- •1. Children aged =3 months and <12 years
- •2. Presenting with an acute RTI with cough for =28 days as a main symptom (including exacerbation of asthma)
- •3. Presenting with illnesses such as RTI and epilepsy or diabetes, including infective exacerbation of asthma (non-infective exacerbation of asthma is an exclusion criterion)
- •Target Gender: Male & Female; Upper Age Limit 11 years ; Lower Age Limit 3 months
排除标准
- •Children will not be eligible for the study if:
- •1. They are aged < 3 months or = 12 years
- •2. The parent/carer/children are unable or unwilling to assist with study
- •3. The child has already been successfully recruited to the CHICO study
- •4. They present with acute non-infective exacerbations of asthma
- •5. They present with RTI without cough or symptoms >28 days
- •6. They are at greater risk of serious infection; they have chronic diseases/multi-morbidities that increase the risk of RTI complications
研究者
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