Bangladesh PRODUCTIVity in Eyecare Trial (B-PRODUCTIVE)
Primary Purpose
Diabetic Retinopathy, Diabetic Macular Edema
Status
Recruiting
Phase
Not Applicable
Locations
Bangladesh
Study Type
Interventional
Intervention
Results utilized from autonomous AI diagnostic system for diabetic retinopathy and/or diabetic macular edema
Sponsored by
About this trial
This is an interventional diagnostic trial for Diabetic Retinopathy
Eligibility Criteria
Inclusion Criteria:
Retina specialists regularly seeing patients with DR
- Routinely examines >= 20 patients with diabetes without known diabetic retinopathy or diabetic macular edema per week
- Routinely provides laser treatment or intravitreal injections to >= 3 DR patients/month
Patients
- Diagnosed with type 1 or 2 diabetes
- Presenting visual acuity >= 6/18 best corrected visual acuity in the better-seeing eye
Exclusion Criteria:
Retina specialists
- Currently using an AI system integrated into their clinical care and/or inability to provide informed consent.
Patients
- Inability to provide informed consent or understand the study; persistent vision loss, blurred vision or floaters; previously diagnosed with diabetic retinopathy or diabetic macular edema; history of laser treatment of the retina or injections into either eye, or any history of retinal surgery; contraindicated for imaging by fundus imaging systems
Sites / Locations
- Deep Eye Care FoundationRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
No Intervention
Arm Label
Intervention Group
Control Group
Arm Description
Autonomous AI results are used to evaluate if the participant needs to see the retina specialist (positive result) or not (negative result).
All participants see the retina specialist irrespective of the results of their autonomous AI evaluation.
Outcomes
Primary Outcome Measures
Number of examined participants with diabetes per retina specialist working hour
Number of examined participants with diabetes per retina specialist working hour. Numerator is the number of examined participants (including persons evaluated by autonomous AI on Intervention Days who are determined not to need to see the retina specialist). The denominator is retina specialist working time in hours.
Number of examined retina participants per retina specialist working hour
Number of examined retina participants per retina specialist working hour. Numerator is the number of examined participants (including persons evaluated by autonomous AI on Intervention Days who are determined not to need to see the retina specialist). The denominator is retina specialist working time in hours.
Secondary Outcome Measures
Change in the number of DR treatments scheduled
Change in number of patients with diabetic retinopathy per week scheduled for any treatment including injections, implants, laser or surgery.
Change in complexity score
• Change from baseline in mean complexity score of participants seen per hour per retina specialist. The complexity score is determined by external masked graders using a standard system adapted from Wilkinson et al. International Clinical Diabetic Retinopathy (DR) and Diabetic Macular Edema (DME) Severity Scales. The complexity score for an eye will be the sum of points with higher score as increased complexity (0=No or Mild Non-Proliferative DR (NPDR), 1 = Moderate NPDR or Severe NPDR, 3 = Proliferative DR (PDR), 2 = DME), and for a person it will be the sum of both eyes.
Satisfaction with autonomous AI assessed by questionnaire.
• Retina specialist, technician and participant satisfaction with autonomous AI assessed by questionnaire using a 5 point Likert scale (1 = Very Satisfied 2 = Satisfied, 3 = Dissatisfied, 4 = Very Dissatisfied and 5 = N/A).
Number of participants willing to pay for testing by autonomous AI.
Retina specialist and participant willingness to pay for testing by autonomous AI. Median amount willing to pay among those who would pay anything and percentage willing to pay anything.
Full Information
NCT ID
NCT05182580
First Posted
November 16, 2021
Last Updated
February 27, 2023
Sponsor
Orbis
Collaborators
Digital Diagnostics, Inc., Deep Eye Care Foundation (DECF)
1. Study Identification
Unique Protocol Identification Number
NCT05182580
Brief Title
Bangladesh PRODUCTIVity in Eyecare Trial
Acronym
B-PRODUCTIVE
Official Title
Assessing the Impact of Using Autonomous Artificial Intelligence (AI) for Pre-screening of Diabetic Retinopathy (DR) and Diabetic Macular Edema on Physician Productivity in Bangladesh
Study Type
Interventional
2. Study Status
Record Verification Date
February 2023
Overall Recruitment Status
Recruiting
Study Start Date
March 20, 2022 (Actual)
Primary Completion Date
June 2023 (Anticipated)
Study Completion Date
June 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Orbis
Collaborators
Digital Diagnostics, Inc., Deep Eye Care Foundation (DECF)
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Product Manufactured in and Exported from the U.S.
Yes
5. Study Description
Brief Summary
The purpose of this study is to assess the impact of using autonomous artificial intelligence (AI) system for identification of diabetic retinopathy (DR) and diabetic macular edema on productivity of retina specialists in Bangladesh.
Globally, the number of people with diabetes mellitus is increasing. Diabetic retinopathy is a chronic, progressive complication of diabetes mellitus that affects the microvasculature of the retina, which if left untreated can potentially result in vision loss. Early detection and treatment of diabetic retinopathy can prevent potential blindness.
Study Aim: To assess the impact of using autonomous artificial intelligence (AI) system for detection of diabetic retinopathy (DR) and diabetic macular edema on physician productivity in Bangladesh.
Main study question: Will ophthalmologists with clinic days randomized to use autonomous AI DR detection for all persons with diabetes (diagnosed or un-diagnosed) visiting their clinic system have a greater number of examined patients with diabetes (by either AI or clinical exam), and a greater complexity of examined patients on a recognized grading scale, per physician working hour than those randomized not to have autonomous AI screening for their diabetes population?
The investigators anticipate that this study will demonstrate an increase in physician productivity, supporting efficiency for both physicians and patients, while also addressing increased access for DR screening; ultimately, preventing vision loss amongst diabetic patients. The study has the potential to contribute to the evidence base on the benefits of AI for physicians and patients. Additionally, the study has the potential to demonstrate the benefits (and/or challenges) of implementing AI in resource-constrained settings, such as Bangladesh.
Detailed Description
Bangladesh PRODUCTIVity in Eyecare (B-PRODUCTIVE) Trial
Study Aim: To assess the impact of using autonomous artificial intelligence (AI) for identification of diabetic retinopathy (DR) and diabetic macular edema on productivity of retina specialists in Bangladesh.
Hypothesis: Autonomous AI increases retina specialist productivity
Main Study Question: Will retina specialists complete a greater number of diabetic eye exams per working hour (including persons reviewed by AI whom the retina specialist does not need to see personally) when they use autonomous AI in a randomized clinical trial?
Design: Cluster-randomized (by clinic day) controlled trial.
Randomization: By clinic day. Each morning the clinic manager will open an opaque envelope, which informs the manager if it is an Intervention (AI) or Control (non-AI) day.
Interventions: All patients in both groups go through the eligibility checklist. If approved, they will be evaluated by autonomous AI. This is done to decrease potential bias (neither patients nor physicians know the group assignment of participants) and concealment (so that neither patients nor doctors can arrange visits on a known "Intervention Day").
Intervention Group: On randomly selected "Intervention" clinic days, if patients screen positive or have insufficient image quality, they continue to the ophthalmologist. If not eligible for autonomous AI, they proceed straight to the ophthalmologist without autonomous AI evaluation. If patients receive a negative result, they do not see the retina specialist, and are referred for a visit at the regular eye clinic (not the retina clinic) in 3 months.
Control Group: On randomly-selected "Control Days," all patients see the ophthalmologist, irrespective of the results of autonomous AI evaluation.
Masking: The retina doctors are masked both patient group assignment (that is, whether autonomous AI was used for pre-screening or not on the particular clinic day) and also masked to the results of the AI on Intervention days. Patients are also masked to group assignment and autonomous AI results.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diabetic Retinopathy, Diabetic Macular Edema
7. Study Design
Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Cluster-randomized (by clinic day) controlled trial.
Masking
ParticipantCare Provider
Masking Description
The retina specialists are masked both to patient group assignment (that is, whether autonomous AI results were used or not on the particular clinic day) and also masked to the results of the autonomous AI on Intervention days. Patients are also masked to group assignment and autonomous AI screening results.
Allocation
Randomized
Enrollment
924 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Intervention Group
Arm Type
Experimental
Arm Description
Autonomous AI results are used to evaluate if the participant needs to see the retina specialist (positive result) or not (negative result).
Arm Title
Control Group
Arm Type
No Intervention
Arm Description
All participants see the retina specialist irrespective of the results of their autonomous AI evaluation.
Intervention Type
Diagnostic Test
Intervention Name(s)
Results utilized from autonomous AI diagnostic system for diabetic retinopathy and/or diabetic macular edema
Intervention Description
If patients receive a negative result they do not see the retina specialist
Primary Outcome Measure Information:
Title
Number of examined participants with diabetes per retina specialist working hour
Description
Number of examined participants with diabetes per retina specialist working hour. Numerator is the number of examined participants (including persons evaluated by autonomous AI on Intervention Days who are determined not to need to see the retina specialist). The denominator is retina specialist working time in hours.
Time Frame
summed weekly from baseline through study completion, 1 year
Title
Number of examined retina participants per retina specialist working hour
Description
Number of examined retina participants per retina specialist working hour. Numerator is the number of examined participants (including persons evaluated by autonomous AI on Intervention Days who are determined not to need to see the retina specialist). The denominator is retina specialist working time in hours.
Time Frame
summed weekly from baseline through study completion, 1 year
Secondary Outcome Measure Information:
Title
Change in the number of DR treatments scheduled
Description
Change in number of patients with diabetic retinopathy per week scheduled for any treatment including injections, implants, laser or surgery.
Time Frame
from baseline through study completion, 1 year
Title
Change in complexity score
Description
• Change from baseline in mean complexity score of participants seen per hour per retina specialist. The complexity score is determined by external masked graders using a standard system adapted from Wilkinson et al. International Clinical Diabetic Retinopathy (DR) and Diabetic Macular Edema (DME) Severity Scales. The complexity score for an eye will be the sum of points with higher score as increased complexity (0=No or Mild Non-Proliferative DR (NPDR), 1 = Moderate NPDR or Severe NPDR, 3 = Proliferative DR (PDR), 2 = DME), and for a person it will be the sum of both eyes.
Time Frame
from baseline through study completion, 1 year
Title
Satisfaction with autonomous AI assessed by questionnaire.
Description
• Retina specialist, technician and participant satisfaction with autonomous AI assessed by questionnaire using a 5 point Likert scale (1 = Very Satisfied 2 = Satisfied, 3 = Dissatisfied, 4 = Very Dissatisfied and 5 = N/A).
Time Frame
through study completion, 1 year
Title
Number of participants willing to pay for testing by autonomous AI.
Description
Retina specialist and participant willingness to pay for testing by autonomous AI. Median amount willing to pay among those who would pay anything and percentage willing to pay anything.
Time Frame
through study completion, 1 year
10. Eligibility
Sex
All
Minimum Age & Unit of Time
22 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Retina specialists regularly seeing patients with DR
Routinely examines >= 20 patients with diabetes without known diabetic retinopathy or diabetic macular edema per week
Routinely provides laser treatment or intravitreal injections to >= 3 DR patients/month
Patients
Diagnosed with type 1 or 2 diabetes
Presenting visual acuity >= 6/18 best corrected visual acuity in the better-seeing eye
Exclusion Criteria:
Retina specialists
Currently using an AI system integrated into their clinical care and/or inability to provide informed consent.
Patients
Inability to provide informed consent or understand the study; persistent vision loss, blurred vision or floaters; previously diagnosed with diabetic retinopathy or diabetic macular edema; history of laser treatment of the retina or injections into either eye, or any history of retinal surgery; contraindicated for imaging by fundus imaging systems
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Nathan Congdon, MD, MHP
Phone
+447748751393
Email
ncongdon@gmail.com
First Name & Middle Initial & Last Name or Official Title & Degree
Hunter Cherwek, MD
Phone
+1646-961-7283
Email
hunter.cherwek@orbis.org
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Nathan Congdon, MD, MPH
Organizational Affiliation
Orbis
Official's Role
Study Chair
Facility Information:
Facility Name
Deep Eye Care Foundation
City
Rangpur
Country
Bangladesh
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Sajidul Huq
Email
sajidul.decf@gmail.com
12. IPD Sharing Statement
Plan to Share IPD
No
IPD Sharing Plan Description
We do not plan to share IPD
Learn more about this trial
Bangladesh PRODUCTIVity in Eyecare Trial
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