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Starting soon Not applicable

Screening for Diabetic RETINopathy Using a Non-mydriatic Retinograph Funduscope in Occupational MEDicine

NCT07828821 · tracked via the Priya Life Science France tracker
Phase
Not applicable
Started
2026-10
Last updated
2026-09-18

Condition(s) studied

Diabetic Retinopathy

Investigational drug(s) / intervention(s)

Non-mydriatic retinographySelf-administered questionnaire

Non-mydriatic retinography: Retinophotography will be performed using the non-mydriatic retinograph FundusScope FC161. The retinal images will subsequently be analyzed by the Ophthalmology Department. Screened workers will be informed of their results and will be redirected to the care pathway if necessary.

Self-administered questionnaire: Participants will complete a self-administered questionnaire, administered online via REDCap® or in paper version for individuals who may have difficulty using computers. The questionnaire will collect information about diabetes, occupational characteristics, sociodemographic characteristics, visual analog scales of stress at work, stress at home, anxiety, sleep quality, fatigue, mood/morale, burnout, autonomy at work, workload, support from the hierarchy, support from colleagues and satisfaction at work in relation to efforts deployed, and lifestyle variables including sitting, physical activity, alcohol and tobacco.

Study summary

Diabetic retinopathy is a complication of diabetes that can affect vision. Early detection and appropriate management can help prevent or delay vision loss. However, some people with diabetes do not receive the recommended regular eye examinations.

The RETINOMED study is a pilot study designed to evaluate the feasibility of offering diabetic retinopathy screening to workers with diabetes through an Occupational Health service.

Participants will attend a single study visit at the Occupational Health Department of Clermont-Ferrand University Hospital. During this visit, retinal photographs will be taken using a non-mydriatic retinal camera, which does not require pupil dilation. Participants will also complete a questionnaire about their sociodemographic and occupational characteristics, lifestyle, and diabetes.

The study will assess the acceptability of this screening program among eligible workers. It will also estimate the prevalence of diabetic retinopathy among screened workers and explore participant characteristics that may be associated with diabetic retinopathy.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Worker * Adult (≥18 years old) * Diabetic * Affiliated with a Social Security scheme * Able to give informed consent to participate in the research Exclusion Criteria: * Protected persons (minors, guardianship, curatorship, deprived of freedoms, safeguard of justice) * Pregnant or breastfeeding women; these women may be offered participation after pregnancy and/or breastfeeding * Non-voluntary person

Primary outcome measure(s)

  • Acceptability of diabetic retinopathy screening in an Occupational Health setting — Day 1
    Proportion of eligible workers who consent to undergo the proposed retinal screening during their Occupational Health visit.

Trial sites (1)

FacilityCityRegionStatus
CHU de Clermont-Ferrand Clermont-Ferrand France
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07828821 on ClinicalTrials.gov ↗ ← All trials in France