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

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01628289
Enrollment
4644
Registered
2012-06-26
Start date
2009-02-28
Completion date
2010-08-31
Last updated
2012-06-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Diabetic Retinopathy

Keywords

diabetic retinopathy, screening, co-payment, health service

Brief summary

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.

Interventions

OTHERcharging a co-payment for Diabetic Retinopathy screening

The intervention is charging a co-payment of HK$60 for the Diabetic Retinopathy screening.

OTHERfree screening without charging a co-payment

The intervention is to provide free screening without charging a co-payment

Sponsors

The University of Hong Kong
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

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

Exclusion criteria

* Only if not competent to give informed consent

Design outcomes

Primary

MeasureTime frameDescription
Retinopathy profile in the two groupsthe first yearThe extent of diabetic retinopathy in two groups were measured in the first year screening.

Secondary

MeasureTime frameDescription
Subjects' attendance of the screeningthe first yearWhether the subject attends the screening was measured and the attendance rate was estimated for two groups in the first year screening.
Retinopathy profile in the two groupsthe second yearThe extent of diabetic retinopathy in two groups were measured in the second year screening.

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026