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Diabetic Retinopathy Screening in Private Practice

2018年10月10日 更新者:The University of Hong Kong

The Feasibility of Screening for Diabetic Retinopathy in Private Practice Hong Kong

Introduction: Diabetic mellitus (DM) is a prevalent disease in Hong Kong (HK) and diabetic retinopathy (DR) is one of the most common complications of DM. Screening for DR is a cost-effective method to identify patients who are at risk of vision loss so that timely treatment can be provided to patients. In Hong Kong, the Hospital Authority has recently set up screening services (RAMP) in the government outpatient clinics and all DM patients attending these clinics will be screened at least once every two years and some every six months, according to their individual risks. However, those diabetic patients who attend the private sector for their primary care may not have access to this service.

Aim: This study from the University of Hong Kong aims to determine the characteristics of a sustainable approach to setting up an effective and quality-controlled screening service for DR in the private primary care sector of Hong Kong and to estimate the potential benefit to be gained in terms of impact on avoidable vision loss, costs of care and potential for further development of this model in chronic disease care.

Methods:A screening centre is being set up and a randomised study carried out in which screening will be offered at three different fee levels to subjects recruited by their general practitioner (GP). The following data will be collected (a) willingness to attend screening at the different fee levels (b) screening findings in terms of DR and other eye diseases (c) risk factors and other characteristics of those screened and unscreened. The information will allow us to estimate the level of fee which best combines effectiveness with sustainability in the longer term.

研究概览

研究类型

介入性

注册 (实际的)

238

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、香港
        • Department of Ophthalmology, 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

18年 及以上 (成人、年长者)

接受健康志愿者

有资格学习的性别

全部

描述

Inclusion Criteria:

  • Patients diagnosed to have diabetic mellitus
  • Able to give informed consent

Exclusion Criteria:

  • Pregnant women

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:无(打开标签)

武器和干预

参与者组/臂
干预/治疗
有源比较器:Free screening group
Subjects in this group receive free diabetic retinopathy screening.
The intervention provide Diabetic Retinopathy screening without charging a fee.
有源比较器:Pay screening group ($150)
Subjects in this group receiving diabetic retinopathy screening will be charged HK$150.
The intervention is charging HK$150 for the Diabetic Retinopathy screening.
有源比较器:Pay screening group ($300)
Subjects in this group receiving diabetic retinopathy screening will be charged HK$300.
The intervention is charging HK$300 for the Diabetic Retinopathy screening.

研究衡量的是什么?

主要结果指标

结果测量
大体时间
The overall, & at different fee level, uptake (as a percentage of participants) of screening from those at-risk patients who attend private GP's
大体时间:one year
one year

次要结果测量

结果测量
大体时间
Percentage of participants with diabetes who are only under the care of a private GP, or also attend specialist service, and have had access to DR screening
大体时间:one year
one year
Prevalence of DR (overall, and for sight-threatening diabetic retinopathy) among diabetic patients in private primary care
大体时间:one year
one 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:Jonathan Cheuk Hung Chan, MBBS、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 (实际的)

2016年9月1日

初级完成 (实际的)

2017年12月13日

研究完成 (实际的)

2018年6月1日

研究注册日期

首次提交

2016年7月27日

首先提交符合 QC 标准的

2016年8月10日

首次发布 (估计)

2016年8月15日

研究记录更新

最后更新发布 (实际的)

2018年10月11日

上次提交的符合 QC 标准的更新

2018年10月10日

最后验证

2018年10月1日

更多信息

与本研究相关的术语

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

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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