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The Cost-effectiveness of Screening for Diabetic Retinopathy in Hong Kong

2012年6月21日 更新者:The University of Hong Kong

Introduction: There is no debate that people with diabetes should be screened for the development of retinopathy which can threaten their sight. However, there is no routine screening for retinopathy in Hong Kong at present. Many overseas countries find that they miss a large proportion of their target population and, with reliance on co-payments for screening, as is the case with the limited opportunistic screening at present, the cost-effectiveness of any routine service in Hong Kong could be reduced as is predicted by Hart's inverse care law.

Aim: This study will determine the potential cost-effectiveness of screening for retinopathy in Hong Kong under a free system and one in which a co-payment is charged.

Methods: Primary care patients attending General Outpatient Clinics on Hong Kong Island for their routine diabetic care will randomly be offered screening either at no charge or with the normal co-payment of $65. Those who are willing and unwilling to be screened will be compared for their clinical, lifestyle and socioeconomic characteristics and those unwilling will be asked their reasons. The uptake of screening at no fee and with a payment will be compared as will the prevalence of retinopathy in the two fee groups. Subsequent screening at one year will be offered at the same fee and uptake again compared.

The principal analyses will (a) identify the characteristics of those willing to be screened and reasons for not being screened (b) the uptake of screening when a co-payment is charged compared to when it is free (c) whether there is a difference in the prevalence of retinopathy between the group willing to pay and those who accept free screening and (d) the uptake of re-screening in year 2.

The resulting cost-effectiveness model will use these data, the cost data collected during the study and overseas data on benefits of treatment to model the cost-effectiveness of screening for retinopathy in Hong Kong if it were to be offered free or with a co-payment. This information will be important to determine the most cost-effective means of implementing this preventative strategy to preserve sight and quality of life.

研究概览

研究类型

介入性

注册 (实际的)

4644

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

      • Hong Kong、中国
        • Aberdeen General Outpatient Clinic,Hospital Authority
      • Hong Kong、中国
        • Department of Community Medicine,The University of Hong Kong
      • Hong Kong、中国
        • Eye Institute, Faculty of Medicine, The University of Hong Kong, Hong Kong

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

  • 孩子
  • 成人
  • 年长者

接受健康志愿者

不

有资格学习的性别

全部

描述

Inclusion Criteria:

  • All diabetic patients who attend the clinic during the study period.

Exclusion Criteria:

  • Only if not competent to give informed consent

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:卫生服务研究
  • 分配:随机化
  • 介入模型:并行分配
  • 屏蔽:单身的

武器和干预

参与者组/臂
干预/治疗
其他:free screening group
Subjects in this group receive free diabetic retinopathy screening.
The intervention is to provide free screening without charging a co-payment
其他:Pay screening group
Subjects in this group receive diabetic retinopathy screening with charging a co-payment.
The intervention is charging a co-payment of HK$60 for the Diabetic Retinopathy screening.

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
Retinopathy profile in the two groups
大体时间:the first year
The extent of diabetic retinopathy in two groups were measured in the first year screening.
the first year

次要结果测量

结果测量
措施说明
大体时间
Subjects' attendance of the screening
大体时间:the first year
Whether the subject attends the screening was measured and the attendance rate was estimated for two groups in the first year screening.
the first year
Retinopathy profile in the two groups
大体时间:the second year
The extent of diabetic retinopathy in two groups were measured in the second year screening.
the second year
Subjects' attendance of the screening
大体时间:the second year
Whether the subject attends the screening was measured and the attendance rate was estimated for two groups in the second year screening.
the second year

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:Sarah M McGhee, PhD、The University of Hong Kong

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

2009年2月1日

初级完成 (实际的)

2009年8月1日

研究完成 (实际的)

2010年8月1日

研究注册日期

首次提交

2012年6月15日

首先提交符合 QC 标准的

2012年6月21日

首次发布 (估计)

2012年6月26日

研究记录更新

最后更新发布 (估计)

2012年6月26日

上次提交的符合 QC 标准的更新

2012年6月21日

最后验证

2012年6月1日

更多信息

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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