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临床试验/NCT04490941
NCT04490941招募中不适用

The Effectiveness of Ophthalmologist-delivered Health Education on Top of Routine Community Care in Type 2 Diabetic Patients at Risk for Diabetic Retinopathy: A Parallel-group, Randomised Trial

Zhongshan Ophthalmic Center, Sun Yat-sen University1 个研究点 分布在 1 个国家目标入组 652 人开始时间: 2020年7月22日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
652
试验地点
1
主要终点
Glycated haemoglobin (HbA1c)

研究概览

简要总结

Diabetic retinopathy affects over one third of all people with diabetes and is one of the leading causes of vision loss. The management of diabetes and its complications should include screening for diabetic retinopathy. A randomised trial is therefore needed of the use of a simple and widely practicable approach to explore the integration of eye care in managing diabetes. The trial is designed as a randomised, controlled, superiority trial. The aim is to explore the effectiveness of ophthalmologist-delivered health education on top of routine community care on blood glucose and eye-related clinical outcomes in type 2 diabetic patients at risk for diabetic retinopathy.

详细描述

Diabetic retinopathy (DR) is a highly specific vascular complication of diabetes mellitus, with prevalence strongly related to a number of risk factors including the duration of diabetes, the level of glycaemic control, etc. Diabetic retinopathy affects over one third of all people with diabetes and is one of the leading causes of vision loss. It is recommended that optimising glycaemic control could reduce the risk or slow the progression of diabetic retinopathy, and that the management of diabetes and its complications should include screening for diabetic retinopathy. A randomised trial is therefore needed of the use of a simple and widely practicable approach to explore the integration of eye care in managing diabetes. The trial is designed as a randomised, controlled, superiority trial. The aim is to explore the effectiveness of ophthalmologist-delivered health education on top of routine community care on blood glucose and eye-related clinical outcomes in type 2 diabetic patients at risk for diabetic retinopathy. Participants will be randomly assigned to either control or intervention group with a 1:1 allocation as per computer-generated random numbers. A senior onsite manager will monitor participant enrolment over the course of the study. An ophthalmologist-delivered health education will be offered as the intervention in an individualised, face-to-face counselling session to build awareness on diabetes symptoms, particularly on diabetic retinopathy, and its risk factors with appropriate management. All subjects, regardless of the group allocation, will be followed up for 12 months. Baseline and follow-up profiles will be assessed and collected by clinical personnel blind to group allocation. The intervention arm will be compared against the control for all primary analysis. The study was partly supported by the Open Research Funds of the State Key Laboratory of Ophthalmology. Trial results will be disseminated to key stakeholders and the general medical community.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Double (Investigator, Outcomes Assessor)

入排标准

年龄范围
35 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age 35-80 years
  • Clinically diagnosed with type 2 diabetes
  • At risk of diabetic retinopathy (DR),e.g. no apparent DR or mild non-proliferative DR
  • On regular community care by 'family doctor team' in the context of the National basic public health service delivery

排除标准

  • With symptoms of cognitive dysfunction, dementia, severe mental disorders, or other conditions with inability to appropriately convey personal thoughts
  • Type 1 diabetes or gestational diabetes
  • Developed with eye conditions requiring timely treatment, e.g., diabetic macular edema, severe non-proliferative diabetic retinopathy, or proliferative DR
  • Have a family member (including relatives) who participated in the trial with a different group assignment
  • Currently enrol in other ongoing interventions that may exert additional effects on blood glucose control

结局指标

主要结局

Glycated haemoglobin (HbA1c)

时间窗: 12-months follow-up

Proportion of participants who had optimal control of HbA1c level at 12 months

次要结局

  • Patients' adherence(12-months follow-up)
  • triglyceride concentration(12-months follow-up)
  • Body mass index(12-months follow-up)
  • Treatment burden(12-months follow-up)
  • Blood pressure(12-months follow-up)
  • cholesterol concentration(12-months follow-up)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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