Predicting Diabetic Retinopathy From Risk Factor Data and Digital Retinal Images

NCT ID: NCT03694145

Last Updated: 2025-02-14

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

ACTIVE_NOT_RECRUITING

Total Enrollment

300 participants

Study Classification

OBSERVATIONAL

Study Start Date

2018-10-25

Study Completion Date

2025-07-31

Brief Summary

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The objective of this study is to compare the results of a deep learning approach to diabetic retinopathy assessment with results from (1) an in-person examination with an ophthalmologist, and (2) the assessments of optometrists involved in a teleretinal screening program.

Detailed Description

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This study represents the third aim of a grant with five aims. The study will compare and evaluate the predictive accuracy of: (a) machine learning models developed to grade diabetic retinopathy and assess the presence or absence of diabetic macular edema and (b) the assessments of optometrist readers, both from digital retinal images, against standard of care dilated retinal examinations by board-certified ophthalmologists and/or retinal-specialty fellows for 300 diabetic patients utilizing a Los Angeles County reading center.

For the study, the investigators will recruit 300-500 eligible diabetic patients for in-person eye examinations performed by board certified ophthalmologists and/or retinal-specialty fellows at Los Angeles County reading centers. The study will take place over the course of two visits: a teleretinal screening and an in-person eye examination.

The in-person dilated eye examinations that the study participants will participate in and be compensated for follow the usual standard of care that patients receive in a setting that does not utilize teleretinal screening. Yearly dilated eye examinations are standard of care for all persons with diabetes.

Conditions

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Diabetic Retinopathy Diabetic Macular Edema

Study Design

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Observational Model Type

OTHER

Study Time Perspective

PROSPECTIVE

Study Groups

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Diabetic patients w. risk of retinopathy

The 300-500 patients to be enrolled for the study are diabetic patients normally seen by the Los Angeles County Department of Health Services (LACDHS) Teleretinal Diabetic Retinopathy Screening Program and Reading Center. In addition to receiving their recommended LACDHS annual teleretinal screening, for the study, participants will receive an additional in-person eye examination.

In-Person Eye Examination

Intervention Type OTHER

Dilated in-person eye examination by a board-certified ophthalmologist or retinal fellow.

Interventions

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In-Person Eye Examination

Dilated in-person eye examination by a board-certified ophthalmologist or retinal fellow.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Patients diagnosed with Type I or Type II Diabetes
* Patients who are over the age of 18 years
* Patients who have not previously been seen in the current year by the LACDHS Teleretinal Diabetic Retinopathy Screening Program and Reading Center
* Patients whose teleretinal screening exam images yield readable results

Exclusion Criteria

* Patients under the age of 18 years
* Patients with gestational diabetes
* Patients who have previously been seen in the current year by LACDHS's Teleretinal Diabetic Retinopathy Screening Program and Reading Center
* Patients whose teleretinal screening exam images do not yield readable results, as gradable images are needed for later comparison against ophthalmologist reads.
* Previously eligible patients who do not return for an in-person eye exam within 3 months of receiving a teleretinal screening (In order for the results of the teleretinal screening and in-person eye examinations to yield similar information, patients who do not return for their in-person eye exam within 3 months of their teleretinal screening will not be able to remain in the study. This is because significant eye changes not documented by the teleretinal screening may occur after a 3-month period).
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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National Library of Medicine (NLM)

NIH

Sponsor Role collaborator

Los Angeles County Department of Public Health

OTHER_GOV

Sponsor Role collaborator

University of California, Los Angeles

OTHER

Sponsor Role collaborator

Charles Drew University of Medicine and Science

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Omolola Ogunyemi, PhD

Role: PRINCIPAL_INVESTIGATOR

Charles Drew University of Medicine and Science

Locations

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Los Angeles Department of Public Health

Los Angeles, California, United States

Site Status

University of California - Los Angeles

Los Angeles, California, United States

Site Status

Charles R. Drew University of Medicine and Science

Los Angeles, California, United States

Site Status

Countries

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United States

Other Identifiers

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R01LM012309

Identifier Type: NIH

Identifier Source: secondary_id

View Link

1218589-3

Identifier Type: -

Identifier Source: org_study_id

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