A Trial on Ophthalmologist-delivered Health Education on Top of Routine Community Care
Primary Purpose
Diabetes Mellitus, Type 2
Status
Recruiting
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
Ophthalmologist-delivered health education
Usual care
Sponsored by
About this trial
This is an interventional prevention trial for Diabetes Mellitus, Type 2
Eligibility Criteria
Inclusion Criteria:
- 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
Exclusion Criteria:
- 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
Sites / Locations
- Zhongshan Ophthalmic Center, Sun Yat-sen UniversityRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Other
Arm Label
Intervention group
Control group
Arm Description
Outcomes
Primary Outcome Measures
Glycated haemoglobin (HbA1c)
Proportion of participants who had optimal control of HbA1c level at 12 months
Secondary Outcome Measures
Treatment burden
Use of treatment burden questionnaire to quantify item scores for each domain, in detail and together, on treatment burden of patients
Patients' adherence
Use of adherence questionnaire to examine the extent to which physician advice, in detail and together, are adhered to by patients
Body mass index
Use of weight and height to report body mass index in kg/m^2
Blood pressure
Use of systolic and diastolic blood pressure to report blood pressure profile in mmHg
cholesterol concentration
Use of cholesterol concentration to report lipid profile in mmol/L
triglyceride concentration
Use of triglyceride concentration to report lipid profile in mmol/L
Full Information
NCT ID
NCT04490941
First Posted
July 22, 2020
Last Updated
February 8, 2022
Sponsor
Zhongshan Ophthalmic Center, Sun Yat-sen University
Collaborators
Sun Yat-sen University
1. Study Identification
Unique Protocol Identification Number
NCT04490941
Brief Title
A Trial on Ophthalmologist-delivered Health Education on Top of Routine Community Care
Official Title
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
Study Type
Interventional
2. Study Status
Record Verification Date
February 2022
Overall Recruitment Status
Recruiting
Study Start Date
July 22, 2020 (Actual)
Primary Completion Date
December 31, 2024 (Anticipated)
Study Completion Date
December 31, 2024 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Zhongshan Ophthalmic Center, Sun Yat-sen University
Collaborators
Sun Yat-sen University
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
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.
Detailed Description
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.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diabetes Mellitus, Type 2
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
InvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
652 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Intervention group
Arm Type
Experimental
Arm Title
Control group
Arm Type
Other
Intervention Type
Other
Intervention Name(s)
Ophthalmologist-delivered health education
Intervention Description
The educational intervention will be conducted on-site by a qualified, experienced ophthalmologist at an ophthalmic center with goals of building awareness on diabetes symptoms, particularly on diabetic retinopathy, and its risk factors with appropriate management.
Intervention Type
Other
Intervention Name(s)
Usual care
Intervention Description
Usual care follows standard procedure on diabetes management similar to the routine service provision.
Primary Outcome Measure Information:
Title
Glycated haemoglobin (HbA1c)
Description
Proportion of participants who had optimal control of HbA1c level at 12 months
Time Frame
12-months follow-up
Secondary Outcome Measure Information:
Title
Treatment burden
Description
Use of treatment burden questionnaire to quantify item scores for each domain, in detail and together, on treatment burden of patients
Time Frame
12-months follow-up
Title
Patients' adherence
Description
Use of adherence questionnaire to examine the extent to which physician advice, in detail and together, are adhered to by patients
Time Frame
12-months follow-up
Title
Body mass index
Description
Use of weight and height to report body mass index in kg/m^2
Time Frame
12-months follow-up
Title
Blood pressure
Description
Use of systolic and diastolic blood pressure to report blood pressure profile in mmHg
Time Frame
12-months follow-up
Title
cholesterol concentration
Description
Use of cholesterol concentration to report lipid profile in mmol/L
Time Frame
12-months follow-up
Title
triglyceride concentration
Description
Use of triglyceride concentration to report lipid profile in mmol/L
Time Frame
12-months follow-up
10. Eligibility
Sex
All
Minimum Age & Unit of Time
35 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
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
Exclusion Criteria:
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
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Yuting LI, MPH
Phone
+86-020-87334687
Email
liyuting@gzzoc.com
Facility Information:
Facility Name
Zhongshan Ophthalmic Center, Sun Yat-sen University
City
Guangzhou
State/Province
Guangdong
ZIP/Postal Code
510000
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Yuting LI, MPH
Phone
+86-020-87334687
Email
liyuting@gzzoc.com
12. IPD Sharing Statement
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A Trial on Ophthalmologist-delivered Health Education on Top of Routine Community Care
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